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L. Kojom, Vineeta Singh (2020)
A Review on Emerging Infectious Diseases Prioritized Under the 2018 WHO Research and Development Blueprint: Lessons from the Indian Context.Vector borne and zoonotic diseases
Laura Muñoz, B. Parra, C. Pardo (2017)
Neurological Implications of Zika Virus Infection in AdultsThe Journal of Infectious Diseases, 216
Jiannan Ma, Ting Zhang, Li Jiang (2017)
Japanese encephalitis can trigger anti-N-methyl-d-aspartate receptor encephalitisJournal of Neurology, 264
( PetersenLR BraultAC NasciRS . West Nile virus: review of the literature. JAMA 2013; 310: 308–315.23860989)
PetersenLR BraultAC NasciRS . West Nile virus: review of the literature. JAMA 2013; 310: 308–315.23860989PetersenLR BraultAC NasciRS . West Nile virus: review of the literature. JAMA 2013; 310: 308–315.23860989, PetersenLR BraultAC NasciRS . West Nile virus: review of the literature. JAMA 2013; 310: 308–315.23860989
D. Morens, A. Fauci (2020)
Emerging Pandemic Diseases: How We Got to COVID-19Cell, 182
( GoatesC TsuhaS WorkingS , et al. Seronegative West Nile virus infection in a patient treated with rituximab for rheumatoid arthritis. Am J Med 2017; 130: e257–e258.28163051)
GoatesC TsuhaS WorkingS , et al. Seronegative West Nile virus infection in a patient treated with rituximab for rheumatoid arthritis. Am J Med 2017; 130: e257–e258.28163051GoatesC TsuhaS WorkingS , et al. Seronegative West Nile virus infection in a patient treated with rituximab for rheumatoid arthritis. Am J Med 2017; 130: e257–e258.28163051, GoatesC TsuhaS WorkingS , et al. Seronegative West Nile virus infection in a patient treated with rituximab for rheumatoid arthritis. Am J Med 2017; 130: e257–e258.28163051
( LeeVJ AguileraX HeymannD , et al. Preparedness for emerging epidemic threats: a Lancet Infectious Diseases Commission. Lancet Infect Dis 2020; 20: 17–19.31876487)
LeeVJ AguileraX HeymannD , et al. Preparedness for emerging epidemic threats: a Lancet Infectious Diseases Commission. Lancet Infect Dis 2020; 20: 17–19.31876487LeeVJ AguileraX HeymannD , et al. Preparedness for emerging epidemic threats: a Lancet Infectious Diseases Commission. Lancet Infect Dis 2020; 20: 17–19.31876487, LeeVJ AguileraX HeymannD , et al. Preparedness for emerging epidemic threats: a Lancet Infectious Diseases Commission. Lancet Infect Dis 2020; 20: 17–19.31876487
( HawkesMA CarabenciovID WijdicksEFM , et al. Outcomes in patients with severe West Nile neuroinvasive disease. Crit Care Med 2018; 46: e955–e958.29985213)
HawkesMA CarabenciovID WijdicksEFM , et al. Outcomes in patients with severe West Nile neuroinvasive disease. Crit Care Med 2018; 46: e955–e958.29985213HawkesMA CarabenciovID WijdicksEFM , et al. Outcomes in patients with severe West Nile neuroinvasive disease. Crit Care Med 2018; 46: e955–e958.29985213, HawkesMA CarabenciovID WijdicksEFM , et al. Outcomes in patients with severe West Nile neuroinvasive disease. Crit Care Med 2018; 46: e955–e958.29985213
( BoberminLD Quincozes-SantosA SantosCL , et al. Zika virus exposure affects neuron-glia communication in the hippocampal slices of adult rats. Sci Rep 2020; 10: 21604.33303883)
BoberminLD Quincozes-SantosA SantosCL , et al. Zika virus exposure affects neuron-glia communication in the hippocampal slices of adult rats. Sci Rep 2020; 10: 21604.33303883BoberminLD Quincozes-SantosA SantosCL , et al. Zika virus exposure affects neuron-glia communication in the hippocampal slices of adult rats. Sci Rep 2020; 10: 21604.33303883, BoberminLD Quincozes-SantosA SantosCL , et al. Zika virus exposure affects neuron-glia communication in the hippocampal slices of adult rats. Sci Rep 2020; 10: 21604.33303883
Petra Bogovič, F. Strle (2015)
Tick-borne encephalitis: A review of epidemiology, clinical characteristics, and management.World journal of clinical cases, 3 5
( JaniC WalkerA Al OmariO , et al. Acute transverse myelitis in West Nile Virus, a rare neurological presentation. Idcases 2021; 24: e01104.33868926)
JaniC WalkerA Al OmariO , et al. Acute transverse myelitis in West Nile Virus, a rare neurological presentation. Idcases 2021; 24: e01104.33868926JaniC WalkerA Al OmariO , et al. Acute transverse myelitis in West Nile Virus, a rare neurological presentation. Idcases 2021; 24: e01104.33868926, JaniC WalkerA Al OmariO , et al. Acute transverse myelitis in West Nile Virus, a rare neurological presentation. Idcases 2021; 24: e01104.33868926
I. Familiar, M. Boivin, J. Magen, Jose Azcorra, Colton Phippen, E. Barrett, Sydney Miller, H. Ruiseñor-Escudero (2020)
Neurodevelopment outcomes in infants born to women with Zika virus infection during pregnancy in Mexico.Child: care, health and development
( SimonLV SandhuDS GoyalA , et al. Japanese encephalitis. Treasure Island, FL: StatPearls, 2021, http://www.ncbi.nlm.nih.gov/books/NBK470423/ (accessed 19 July 2021).)
SimonLV SandhuDS GoyalA , et al. Japanese encephalitis. Treasure Island, FL: StatPearls, 2021, http://www.ncbi.nlm.nih.gov/books/NBK470423/ (accessed 19 July 2021).SimonLV SandhuDS GoyalA , et al. Japanese encephalitis. Treasure Island, FL: StatPearls, 2021, http://www.ncbi.nlm.nih.gov/books/NBK470423/ (accessed 19 July 2021)., SimonLV SandhuDS GoyalA , et al. Japanese encephalitis. Treasure Island, FL: StatPearls, 2021, http://www.ncbi.nlm.nih.gov/books/NBK470423/ (accessed 19 July 2021).
Mya Tun, R. Muthugala, T. Nabeshima, Aung Soe, S. Dumre, Lakmali Rajamanthri, Dulani Jayawardana, Shanthi Attanayake, S. Inoue, K. Morita (2020)
Complete genome analysis and characterization of neurotropic dengue virus 2 cosmopolitan genotype isolated from the cerebrospinal fluid of encephalitis patientsPLoS ONE, 15
( YadavHM Dutta MajumderP BiswasJ . Dengue associated choroiditis: a rare entity. J Ophthalmic Inflamm Infect 2017; 7: 14.28560576)
YadavHM Dutta MajumderP BiswasJ . Dengue associated choroiditis: a rare entity. J Ophthalmic Inflamm Infect 2017; 7: 14.28560576YadavHM Dutta MajumderP BiswasJ . Dengue associated choroiditis: a rare entity. J Ophthalmic Inflamm Infect 2017; 7: 14.28560576, YadavHM Dutta MajumderP BiswasJ . Dengue associated choroiditis: a rare entity. J Ophthalmic Inflamm Infect 2017; 7: 14.28560576
F. Farrar (2013)
West Nile virus: an infectious viral agent to the central nervous system.Critical care nursing clinics of North America, 25 2
( PiersonTC DiamondMS . The continued emerging threat of Flaviviruses. Nat Microbiol 2020; 5: 796–812.32367055)
PiersonTC DiamondMS . The continued emerging threat of Flaviviruses. Nat Microbiol 2020; 5: 796–812.32367055PiersonTC DiamondMS . The continued emerging threat of Flaviviruses. Nat Microbiol 2020; 5: 796–812.32367055, PiersonTC DiamondMS . The continued emerging threat of Flaviviruses. Nat Microbiol 2020; 5: 796–812.32367055
Qi Meng, Y. Zou, H. Bu, Jun-ying He (2014)
Imaging and cytological analysis of 92 patients with Japanese encephalitisNeuroimmunology and Neuroinflammation, 1
( RoosKL TylerKL . Encephalitis. In: JamesonJL FauciAS KasperDL , et al. (eds) Harrison’s principles of internal medicine. 20th ed. New York: McGraw-Hill Education, 2018, accessmedicine.mhmedical.com/content.aspx?aid=1163580317 (accessed 23 July 2021).)
RoosKL TylerKL . Encephalitis. In: JamesonJL FauciAS KasperDL , et al. (eds) Harrison’s principles of internal medicine. 20th ed. New York: McGraw-Hill Education, 2018, accessmedicine.mhmedical.com/content.aspx?aid=1163580317 (accessed 23 July 2021).RoosKL TylerKL . Encephalitis. In: JamesonJL FauciAS KasperDL , et al. (eds) Harrison’s principles of internal medicine. 20th ed. New York: McGraw-Hill Education, 2018, accessmedicine.mhmedical.com/content.aspx?aid=1163580317 (accessed 23 July 2021)., RoosKL TylerKL . Encephalitis. In: JamesonJL FauciAS KasperDL , et al. (eds) Harrison’s principles of internal medicine. 20th ed. New York: McGraw-Hill Education, 2018, accessmedicine.mhmedical.com/content.aspx?aid=1163580317 (accessed 23 July 2021).
( LiF WangY YuL , et al. Viral infection of the central nervous system and neuroinflammation precede blood-brain barrier disruption during Japanese encephalitis virus infection. J Virol 2015; 89: 5602–5614.25762733)
LiF WangY YuL , et al. Viral infection of the central nervous system and neuroinflammation precede blood-brain barrier disruption during Japanese encephalitis virus infection. J Virol 2015; 89: 5602–5614.25762733LiF WangY YuL , et al. Viral infection of the central nervous system and neuroinflammation precede blood-brain barrier disruption during Japanese encephalitis virus infection. J Virol 2015; 89: 5602–5614.25762733, LiF WangY YuL , et al. Viral infection of the central nervous system and neuroinflammation precede blood-brain barrier disruption during Japanese encephalitis virus infection. J Virol 2015; 89: 5602–5614.25762733
( TilleyPAG FoxJD JayaramanGC , et al. Nucleic acid testing for West Nile virus RNA in plasma enhances rapid diagnosis of acute infection in symptomatic patients. J Infect Dis 2006; 193: 1361–1364.16619182)
TilleyPAG FoxJD JayaramanGC , et al. Nucleic acid testing for West Nile virus RNA in plasma enhances rapid diagnosis of acute infection in symptomatic patients. J Infect Dis 2006; 193: 1361–1364.16619182TilleyPAG FoxJD JayaramanGC , et al. Nucleic acid testing for West Nile virus RNA in plasma enhances rapid diagnosis of acute infection in symptomatic patients. J Infect Dis 2006; 193: 1361–1364.16619182, TilleyPAG FoxJD JayaramanGC , et al. Nucleic acid testing for West Nile virus RNA in plasma enhances rapid diagnosis of acute infection in symptomatic patients. J Infect Dis 2006; 193: 1361–1364.16619182
Lin Zhang, Luhua Wei, Zhaoxia Wang, Yining Huang, G. Schwarz, V. Wheelock (2020)
COVID-19: Neuroinvasiveness, Neurotropism and NeurovirulenceJournal of Neuropathology and Experimental Neurology, 6
( Japanese encephalitis. CDC, 2019, https://www.cdc.gov/japaneseencephalitis/index.html (accessed 16 July 2021).)
Japanese encephalitis. CDC, 2019, https://www.cdc.gov/japaneseencephalitis/index.html (accessed 16 July 2021).Japanese encephalitis. CDC, 2019, https://www.cdc.gov/japaneseencephalitis/index.html (accessed 16 July 2021)., Japanese encephalitis. CDC, 2019, https://www.cdc.gov/japaneseencephalitis/index.html (accessed 16 July 2021).
( Calderón-PeláezMA Velandia-RomeroML Bastidas-LegardaLY , et al. Dengue virus infection of blood–brain barrier cells: consequences of severe disease. Front Microbiol 2019; 10: 1435.31293558)
Calderón-PeláezMA Velandia-RomeroML Bastidas-LegardaLY , et al. Dengue virus infection of blood–brain barrier cells: consequences of severe disease. Front Microbiol 2019; 10: 1435.31293558Calderón-PeláezMA Velandia-RomeroML Bastidas-LegardaLY , et al. Dengue virus infection of blood–brain barrier cells: consequences of severe disease. Front Microbiol 2019; 10: 1435.31293558, Calderón-PeláezMA Velandia-RomeroML Bastidas-LegardaLY , et al. Dengue virus infection of blood–brain barrier cells: consequences of severe disease. Front Microbiol 2019; 10: 1435.31293558
( TiwariS SinghRK TiwariR , et al. Japanese encephalitis: a review of the Indian perspective. Braz J Infect Dis 2012; 16: 564–573.23141974)
TiwariS SinghRK TiwariR , et al. Japanese encephalitis: a review of the Indian perspective. Braz J Infect Dis 2012; 16: 564–573.23141974TiwariS SinghRK TiwariR , et al. Japanese encephalitis: a review of the Indian perspective. Braz J Infect Dis 2012; 16: 564–573.23141974, TiwariS SinghRK TiwariR , et al. Japanese encephalitis: a review of the Indian perspective. Braz J Infect Dis 2012; 16: 564–573.23141974
( ClarkMB SchaeferTJ . West Nile virus. Treasure Island, FL: StatPearls, 2021, http://www.ncbi.nlm.nih.gov/books/NBK544246/ (accessed 21 July 2021).)
ClarkMB SchaeferTJ . West Nile virus. Treasure Island, FL: StatPearls, 2021, http://www.ncbi.nlm.nih.gov/books/NBK544246/ (accessed 21 July 2021).ClarkMB SchaeferTJ . West Nile virus. Treasure Island, FL: StatPearls, 2021, http://www.ncbi.nlm.nih.gov/books/NBK544246/ (accessed 21 July 2021)., ClarkMB SchaeferTJ . West Nile virus. Treasure Island, FL: StatPearls, 2021, http://www.ncbi.nlm.nih.gov/books/NBK544246/ (accessed 21 July 2021).
( FernandezE KoseN EdelingMA , et al. Mouse and human monoclonal antibodies protect against infection by multiple genotypes of Japanese encephalitis virus. Mbio 2018; 9: e00008–e00018.29487230)
FernandezE KoseN EdelingMA , et al. Mouse and human monoclonal antibodies protect against infection by multiple genotypes of Japanese encephalitis virus. Mbio 2018; 9: e00008–e00018.29487230FernandezE KoseN EdelingMA , et al. Mouse and human monoclonal antibodies protect against infection by multiple genotypes of Japanese encephalitis virus. Mbio 2018; 9: e00008–e00018.29487230, FernandezE KoseN EdelingMA , et al. Mouse and human monoclonal antibodies protect against infection by multiple genotypes of Japanese encephalitis virus. Mbio 2018; 9: e00008–e00018.29487230
( VermaS LoY ChapagainM , et al. West Nile virus infection modulates human brain microvascular endothelial cells tight junction proteins and cell adhesion molecules: transmigration across the in vitro blood-brain barrier. Virology 2009; 385: 425–433.19135695)
VermaS LoY ChapagainM , et al. West Nile virus infection modulates human brain microvascular endothelial cells tight junction proteins and cell adhesion molecules: transmigration across the in vitro blood-brain barrier. Virology 2009; 385: 425–433.19135695VermaS LoY ChapagainM , et al. West Nile virus infection modulates human brain microvascular endothelial cells tight junction proteins and cell adhesion molecules: transmigration across the in vitro blood-brain barrier. Virology 2009; 385: 425–433.19135695, VermaS LoY ChapagainM , et al. West Nile virus infection modulates human brain microvascular endothelial cells tight junction proteins and cell adhesion molecules: transmigration across the in vitro blood-brain barrier. Virology 2009; 385: 425–433.19135695
( Diagnostic testing West Nile virus. CDC, 2021, https://www.cdc.gov/westnile/healthcareproviders/healthCareProviders-Diagnostic.html (accessed 18 January 2022).)
Diagnostic testing West Nile virus. CDC, 2021, https://www.cdc.gov/westnile/healthcareproviders/healthCareProviders-Diagnostic.html (accessed 18 January 2022).Diagnostic testing West Nile virus. CDC, 2021, https://www.cdc.gov/westnile/healthcareproviders/healthCareProviders-Diagnostic.html (accessed 18 January 2022)., Diagnostic testing West Nile virus. CDC, 2021, https://www.cdc.gov/westnile/healthcareproviders/healthCareProviders-Diagnostic.html (accessed 18 January 2022).
( WHO and Publication. Vaccines against tick-borne encephalitis: WHO position paper – Recommendations. Vaccine 2011; 29: 8769–8770.21777636)
WHO and Publication. Vaccines against tick-borne encephalitis: WHO position paper – Recommendations. Vaccine 2011; 29: 8769–8770.21777636WHO and Publication. Vaccines against tick-borne encephalitis: WHO position paper – Recommendations. Vaccine 2011; 29: 8769–8770.21777636, WHO and Publication. Vaccines against tick-borne encephalitis: WHO position paper – Recommendations. Vaccine 2011; 29: 8769–8770.21777636
Ravi Mehta, C. Soares, R. Medialdea-Carrera, M. Ellul, M. Silva, A. Rosala-Hallas, M. Jardim, G. Burnside, L. Pamplona, M. Bhojak, Radhika Manohar, Gabriel Silva, Marcus Adriano, P. Brasil, R. Nogueira, C. Santos, L. Turtle, Patricia Sequeira, D. Brown, M. Griffiths, A. Filippis, T. Solomon (2018)
The spectrum of neurological disease associated with Zika and chikungunya viruses in adults in Rio de Janeiro, Brazil: A case seriesPLoS Neglected Tropical Diseases, 12
( AlliA OrtizJF AtootA , et al. Management of West Nile encephalitis: an uncommon complication of West Nile virus. Cureus 2021; 13: e13183.33717727)
AlliA OrtizJF AtootA , et al. Management of West Nile encephalitis: an uncommon complication of West Nile virus. Cureus 2021; 13: e13183.33717727AlliA OrtizJF AtootA , et al. Management of West Nile encephalitis: an uncommon complication of West Nile virus. Cureus 2021; 13: e13183.33717727, AlliA OrtizJF AtootA , et al. Management of West Nile encephalitis: an uncommon complication of West Nile virus. Cureus 2021; 13: e13183.33717727
A. Patabendige, B. Michael, A. Craig, T. Solomon (2018)
Brain microvascular endothelial-astrocyte cell responses following Japanese encephalitis virus infection in an in vitro human blood-brain barrier modelMolecular and Cellular Neurosciences, 89
Estefania Fernandez, Nurgun Kose, M. Edeling, J. Adhikari, G. Sapparapu, Susana Lazarte, C. Nelson, Jennifer Govero, M. Gross, D. Fremont, J. Crowe, M. Diamond (2018)
Mouse and Human Monoclonal Antibodies Protect against Infection by Multiple Genotypes of Japanese Encephalitis VirusmBio, 9
( CurrenEJ LehmanJ KolsinJ , et al. West Nile virus and other nationally notifiable arboviral diseases – United States, 2017. Morb Mortal Wkly Rep 2018; 67: 1137–1142.)
CurrenEJ LehmanJ KolsinJ , et al. West Nile virus and other nationally notifiable arboviral diseases – United States, 2017. Morb Mortal Wkly Rep 2018; 67: 1137–1142.CurrenEJ LehmanJ KolsinJ , et al. West Nile virus and other nationally notifiable arboviral diseases – United States, 2017. Morb Mortal Wkly Rep 2018; 67: 1137–1142., CurrenEJ LehmanJ KolsinJ , et al. West Nile virus and other nationally notifiable arboviral diseases – United States, 2017. Morb Mortal Wkly Rep 2018; 67: 1137–1142.
M. Mayxay, Phouvieng Douangdala, Chanthala Vilayhong, Koukeo Phommasone, Vilada Chansamouth, M. Vongsouvath, S. Rattanavong, Ko Chang, Onanong Sengvilaipaseuth, A. Chanthongthip, Soulignasack Thongpaseuth, P. Newton, A. Dubot-Pérès (2020)
Outcome of Japanese Encephalitis Virus (JEV) Infection in Pediatric and Adult Patients at Mahosot Hospital, Vientiane, Lao PDRThe American Journal of Tropical Medicine and Hygiene, 104
( de AraújoTVB XimenesRAA Miranda-FilhoDB , et al. Association between microcephaly, Zika virus infection, and other risk factors in Brazil: final report of a case-control study. Lancet Infect Dis 2018; 18: 328–336.29242091)
de AraújoTVB XimenesRAA Miranda-FilhoDB , et al. Association between microcephaly, Zika virus infection, and other risk factors in Brazil: final report of a case-control study. Lancet Infect Dis 2018; 18: 328–336.29242091de AraújoTVB XimenesRAA Miranda-FilhoDB , et al. Association between microcephaly, Zika virus infection, and other risk factors in Brazil: final report of a case-control study. Lancet Infect Dis 2018; 18: 328–336.29242091, de AraújoTVB XimenesRAA Miranda-FilhoDB , et al. Association between microcephaly, Zika virus infection, and other risk factors in Brazil: final report of a case-control study. Lancet Infect Dis 2018; 18: 328–336.29242091
(2021)
Riedel S, Hobden JA, Miller S (eds) Jawetz, Melnick, & Adelberg’s medical microbiology, 28e
( World Health Organization. Dengue: guidelines for diagnosis, treatment, prevention and control. Geneva: World Health Organization, 2009, 159p.)
World Health Organization. Dengue: guidelines for diagnosis, treatment, prevention and control. Geneva: World Health Organization, 2009, 159p.World Health Organization. Dengue: guidelines for diagnosis, treatment, prevention and control. Geneva: World Health Organization, 2009, 159p., World Health Organization. Dengue: guidelines for diagnosis, treatment, prevention and control. Geneva: World Health Organization, 2009, 159p.
( SinghH PannuAK BhallaA , et al. Dengue: uncommon neurological presentations of a common tropical illness. Indian J Crit Care Med 2019; 23: 274–275.31435146)
SinghH PannuAK BhallaA , et al. Dengue: uncommon neurological presentations of a common tropical illness. Indian J Crit Care Med 2019; 23: 274–275.31435146SinghH PannuAK BhallaA , et al. Dengue: uncommon neurological presentations of a common tropical illness. Indian J Crit Care Med 2019; 23: 274–275.31435146, SinghH PannuAK BhallaA , et al. Dengue: uncommon neurological presentations of a common tropical illness. Indian J Crit Care Med 2019; 23: 274–275.31435146
( SolomonT DungNM VaughnDW , et al. Neurological manifestations of dengue infection. The Lancet 2000; 355: 1053–1059.)
SolomonT DungNM VaughnDW , et al. Neurological manifestations of dengue infection. The Lancet 2000; 355: 1053–1059.SolomonT DungNM VaughnDW , et al. Neurological manifestations of dengue infection. The Lancet 2000; 355: 1053–1059., SolomonT DungNM VaughnDW , et al. Neurological manifestations of dengue infection. The Lancet 2000; 355: 1053–1059.
( GaoX LiuH LiX , et al. Changing geographic distribution of Japanese encephalitis virus genotypes, 1935–2017. Vector Borne Zoonotic Dis 2019; 19: 35–44.30207876)
GaoX LiuH LiX , et al. Changing geographic distribution of Japanese encephalitis virus genotypes, 1935–2017. Vector Borne Zoonotic Dis 2019; 19: 35–44.30207876GaoX LiuH LiX , et al. Changing geographic distribution of Japanese encephalitis virus genotypes, 1935–2017. Vector Borne Zoonotic Dis 2019; 19: 35–44.30207876, GaoX LiuH LiX , et al. Changing geographic distribution of Japanese encephalitis virus genotypes, 1935–2017. Vector Borne Zoonotic Dis 2019; 19: 35–44.30207876
( GooL DebbinkK KoseN , et al. A potently neutralizing human monoclonal antibody targeting an epitope in the West Nile virus E protein preferentially recognizes mature virions. Nat Microbiol 2019; 4: 71–77.30455471)
GooL DebbinkK KoseN , et al. A potently neutralizing human monoclonal antibody targeting an epitope in the West Nile virus E protein preferentially recognizes mature virions. Nat Microbiol 2019; 4: 71–77.30455471GooL DebbinkK KoseN , et al. A potently neutralizing human monoclonal antibody targeting an epitope in the West Nile virus E protein preferentially recognizes mature virions. Nat Microbiol 2019; 4: 71–77.30455471, GooL DebbinkK KoseN , et al. A potently neutralizing human monoclonal antibody targeting an epitope in the West Nile virus E protein preferentially recognizes mature virions. Nat Microbiol 2019; 4: 71–77.30455471
( KozlovaIV DeminaTV TkachevSE , et al. Characteristics of the Baikal subtype of tick-borne encephalitis virus circulating in eastern Siberia. Acta Biomed Sci 2018; 3: 53–60.)
KozlovaIV DeminaTV TkachevSE , et al. Characteristics of the Baikal subtype of tick-borne encephalitis virus circulating in eastern Siberia. Acta Biomed Sci 2018; 3: 53–60.KozlovaIV DeminaTV TkachevSE , et al. Characteristics of the Baikal subtype of tick-borne encephalitis virus circulating in eastern Siberia. Acta Biomed Sci 2018; 3: 53–60., KozlovaIV DeminaTV TkachevSE , et al. Characteristics of the Baikal subtype of tick-borne encephalitis virus circulating in eastern Siberia. Acta Biomed Sci 2018; 3: 53–60.
M. Tarbe, W. Dong, Guang Hu, Yongfen Xu, Jing Sun, S. Grayo, Xianyang Chen, C. Qin, Jincun Zhao, Li Liu, Xiuzhen Li, Q. Leng (2020)
Japanese Encephalitis Virus Vaccination Elicits Cross-Reactive HLA-Class I-Restricted CD8 T Cell Response Against Zika Virus InfectionFrontiers in Immunology, 11
S. Upreti, S. Hills, T. Sedai, Murari Shrestha, Sanjaya Shrestha, Robert Gibbons, W. Schluter, Brad Biggerstaff, Geeta Shakya, Kristen Janusz, M. Fischer, Ram Bichha (2013)
Estimation of the impact of a Japanese encephalitis immunization program with live, attenuated SA 14-14-2 vaccine in Nepal.The American journal of tropical medicine and hygiene, 88 3
( West Nile virus, https://www.who.int/news-room/fact-sheets/detail/west-nile-virus (accessed 20 July 2021).)
West Nile virus, https://www.who.int/news-room/fact-sheets/detail/west-nile-virus (accessed 20 July 2021).West Nile virus, https://www.who.int/news-room/fact-sheets/detail/west-nile-virus (accessed 20 July 2021)., West Nile virus, https://www.who.int/news-room/fact-sheets/detail/west-nile-virus (accessed 20 July 2021).
Sang-Im Yun, Seok‐Yong Kim, W. Choi, J. Nam, Y. Ju, Keun-Yong Park, Hae‐wol Cho, Young-Min Lee (2003)
Molecular characterization of the full-length genome of the Japanese encephalitis viral strain K87P39.Virus research, 96 1-2
( MisraUK KalitaJ . Movement disorders in Japanese encephalitis. J Neurol 1997; 244: 299–303.9178154)
MisraUK KalitaJ . Movement disorders in Japanese encephalitis. J Neurol 1997; 244: 299–303.9178154MisraUK KalitaJ . Movement disorders in Japanese encephalitis. J Neurol 1997; 244: 299–303.9178154, MisraUK KalitaJ . Movement disorders in Japanese encephalitis. J Neurol 1997; 244: 299–303.9178154
( ThompsonA KutzS . Introduction to the special issue on ‘emerging zoonoses and wildlife. Int J Parasitol Parasites Wildl 2019; 9: 322.31341770)
ThompsonA KutzS . Introduction to the special issue on ‘emerging zoonoses and wildlife. Int J Parasitol Parasites Wildl 2019; 9: 322.31341770ThompsonA KutzS . Introduction to the special issue on ‘emerging zoonoses and wildlife. Int J Parasitol Parasites Wildl 2019; 9: 322.31341770, ThompsonA KutzS . Introduction to the special issue on ‘emerging zoonoses and wildlife. Int J Parasitol Parasites Wildl 2019; 9: 322.31341770
N. Lindsey, J. Sejvar, Amy Bode, W. Pape, G. Campbell (2012)
Delayed mortality in a cohort of persons hospitalized with West Nile virus disease in Colorado in 2003.Vector borne and zoonotic diseases, 12 3
( de WispelaereM DesprèsP ChoumetV . European Aedes albopictus and Culex pipiens are competent vectors for Japanese encephalitis virus. PLoS Negl Trop Dis 2017; 11: e0005294.28085881)
de WispelaereM DesprèsP ChoumetV . European Aedes albopictus and Culex pipiens are competent vectors for Japanese encephalitis virus. PLoS Negl Trop Dis 2017; 11: e0005294.28085881de WispelaereM DesprèsP ChoumetV . European Aedes albopictus and Culex pipiens are competent vectors for Japanese encephalitis virus. PLoS Negl Trop Dis 2017; 11: e0005294.28085881, de WispelaereM DesprèsP ChoumetV . European Aedes albopictus and Culex pipiens are competent vectors for Japanese encephalitis virus. PLoS Negl Trop Dis 2017; 11: e0005294.28085881
( BasumataryLJ RajaD BhuyanD , et al. Clinical and radiological spectrum of Japanese encephalitis. J Neurol Sci 2013; 325: 15–21.23260319)
BasumataryLJ RajaD BhuyanD , et al. Clinical and radiological spectrum of Japanese encephalitis. J Neurol Sci 2013; 325: 15–21.23260319BasumataryLJ RajaD BhuyanD , et al. Clinical and radiological spectrum of Japanese encephalitis. J Neurol Sci 2013; 325: 15–21.23260319, BasumataryLJ RajaD BhuyanD , et al. Clinical and radiological spectrum of Japanese encephalitis. J Neurol Sci 2013; 325: 15–21.23260319
A. Hinckley, Daniel O’Leary, E. Hayes (2007)
Transmission of West Nile Virus Through Human Breast Milk Seems to Be RarePediatrics, 119
Huanyu Wang, Yi-xing Li, Xiaofeng Liang, G. Liang (2009)
Japanese encephalitis in mainland china.Japanese journal of infectious diseases, 62 5
Guo-hong Li, Zhiziong Ning, Yi-Ming Liu, Xiao-hong Li (2017)
Neurological Manifestations of Dengue InfectionFrontiers in Cellular and Infection Microbiology, 7
M. Martín-Acebes, J. Saiz (2012)
West Nile virus: A re-emerging pathogen revisited.World journal of virology, 1 2
M. Calderón-Peláez, M. Velandia-Romero, Leidy Bastidas-Legarda, E. Beltrán, Sigrid Camacho-Ortega, J. Castellanos (2019)
Dengue Virus Infection of Blood–Brain Barrier Cells: Consequences of Severe DiseaseFrontiers in Microbiology, 10
( MaJ ZhangT JiangL . Japanese encephalitis can trigger anti-N-methyl-D-aspartate receptor encephalitis. J Neurol 2017; 264: 1127–1131.28470592)
MaJ ZhangT JiangL . Japanese encephalitis can trigger anti-N-methyl-D-aspartate receptor encephalitis. J Neurol 2017; 264: 1127–1131.28470592MaJ ZhangT JiangL . Japanese encephalitis can trigger anti-N-methyl-D-aspartate receptor encephalitis. J Neurol 2017; 264: 1127–1131.28470592, MaJ ZhangT JiangL . Japanese encephalitis can trigger anti-N-methyl-D-aspartate receptor encephalitis. J Neurol 2017; 264: 1127–1131.28470592
I.R.F. Silva, J. Frontera, A. Filippis, O. Nascimento (2017)
Neurologic Complications Associated With the Zika Virus in Brazilian AdultsJAMA Neurology, 74
( PastelH ChakrabartyB SainiL , et al. A case of anti- N-methyl-D-aspartate (NMDA) receptor encephalitis possibly triggered by an episode of Japanese B encephalitis. Neurol India 2017; 65: 895–897.28681777)
PastelH ChakrabartyB SainiL , et al. A case of anti- N-methyl-D-aspartate (NMDA) receptor encephalitis possibly triggered by an episode of Japanese B encephalitis. Neurol India 2017; 65: 895–897.28681777PastelH ChakrabartyB SainiL , et al. A case of anti- N-methyl-D-aspartate (NMDA) receptor encephalitis possibly triggered by an episode of Japanese B encephalitis. Neurol India 2017; 65: 895–897.28681777, PastelH ChakrabartyB SainiL , et al. A case of anti- N-methyl-D-aspartate (NMDA) receptor encephalitis possibly triggered by an episode of Japanese B encephalitis. Neurol India 2017; 65: 895–897.28681777
( MustafáYM MeurenLM CoelhoSVA , et al. Pathways exploited by flaviviruses to counteract the blood-brain barrier and invade the central nervous system. Front Microbiol 2019; 10: 525.30984122)
MustafáYM MeurenLM CoelhoSVA , et al. Pathways exploited by flaviviruses to counteract the blood-brain barrier and invade the central nervous system. Front Microbiol 2019; 10: 525.30984122MustafáYM MeurenLM CoelhoSVA , et al. Pathways exploited by flaviviruses to counteract the blood-brain barrier and invade the central nervous system. Front Microbiol 2019; 10: 525.30984122, MustafáYM MeurenLM CoelhoSVA , et al. Pathways exploited by flaviviruses to counteract the blood-brain barrier and invade the central nervous system. Front Microbiol 2019; 10: 525.30984122
( SoverowJE WelleniusGA FismanDN , et al. Infectious disease in a warming world: how weather influenced West Nile virus in the United States (2001–2005). Environ Health Perspect 2009; 117: 1049–1052.19654911)
SoverowJE WelleniusGA FismanDN , et al. Infectious disease in a warming world: how weather influenced West Nile virus in the United States (2001–2005). Environ Health Perspect 2009; 117: 1049–1052.19654911SoverowJE WelleniusGA FismanDN , et al. Infectious disease in a warming world: how weather influenced West Nile virus in the United States (2001–2005). Environ Health Perspect 2009; 117: 1049–1052.19654911, SoverowJE WelleniusGA FismanDN , et al. Infectious disease in a warming world: how weather influenced West Nile virus in the United States (2001–2005). Environ Health Perspect 2009; 117: 1049–1052.19654911
( ShaikRS NetravathiM NitishLK , et al. A rare case of Japanese encephalitis-induced anti-N-methyl-d-aspartate receptor encephalitis. Neurol India 2018; 66: 1495.30233032)
ShaikRS NetravathiM NitishLK , et al. A rare case of Japanese encephalitis-induced anti-N-methyl-d-aspartate receptor encephalitis. Neurol India 2018; 66: 1495.30233032ShaikRS NetravathiM NitishLK , et al. A rare case of Japanese encephalitis-induced anti-N-methyl-d-aspartate receptor encephalitis. Neurol India 2018; 66: 1495.30233032, ShaikRS NetravathiM NitishLK , et al. A rare case of Japanese encephalitis-induced anti-N-methyl-d-aspartate receptor encephalitis. Neurol India 2018; 66: 1495.30233032
( SethiM DasT TomarN , et al. Japanese encephalitis virus-induced neuropathology in mouse model infected through the conjunctival route. Indian J Med Res 2019; 150: 498–503.31939394)
SethiM DasT TomarN , et al. Japanese encephalitis virus-induced neuropathology in mouse model infected through the conjunctival route. Indian J Med Res 2019; 150: 498–503.31939394SethiM DasT TomarN , et al. Japanese encephalitis virus-induced neuropathology in mouse model infected through the conjunctival route. Indian J Med Res 2019; 150: 498–503.31939394, SethiM DasT TomarN , et al. Japanese encephalitis virus-induced neuropathology in mouse model infected through the conjunctival route. Indian J Med Res 2019; 150: 498–503.31939394
( FreitasDA Souza-SantosR CarvalhoLMA , et al. Congenital Zika syndrome: a systematic review. PLoS ONE 2020; 15: e0242367.33320867)
FreitasDA Souza-SantosR CarvalhoLMA , et al. Congenital Zika syndrome: a systematic review. PLoS ONE 2020; 15: e0242367.33320867FreitasDA Souza-SantosR CarvalhoLMA , et al. Congenital Zika syndrome: a systematic review. PLoS ONE 2020; 15: e0242367.33320867, FreitasDA Souza-SantosR CarvalhoLMA , et al. Congenital Zika syndrome: a systematic review. PLoS ONE 2020; 15: e0242367.33320867
Alexander Platonov, Giacomo Rossi, L. Karan, Mironov Ko, Luca Busani, G. Rezza (2012)
Does the Japanese encephalitis virus (JEV) represent a threat for human health in Europe? Detection of JEV RNA sequences in birds collected in Italy.Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin, 17 32
U. Misra, J. Kalita (1997)
Movement disorders in Japanese encephalitisJournal of Neurology, 244
( PatrickMK JohnstonJB PowerC . Lentiviral neuropathogenesis: comparative neuroinvasion, neurotropism, neurovirulence, and host neurosusceptibility. J Virol 2002; 76: 7923–7931.12133996)
PatrickMK JohnstonJB PowerC . Lentiviral neuropathogenesis: comparative neuroinvasion, neurotropism, neurovirulence, and host neurosusceptibility. J Virol 2002; 76: 7923–7931.12133996PatrickMK JohnstonJB PowerC . Lentiviral neuropathogenesis: comparative neuroinvasion, neurotropism, neurovirulence, and host neurosusceptibility. J Virol 2002; 76: 7923–7931.12133996, PatrickMK JohnstonJB PowerC . Lentiviral neuropathogenesis: comparative neuroinvasion, neurotropism, neurovirulence, and host neurosusceptibility. J Virol 2002; 76: 7923–7931.12133996
Mélissanne Wispelaere, P. Desprès, V. Choumet (2017)
European Aedes albopictus and Culex pipiens Are Competent Vectors for Japanese Encephalitis VirusPLoS Neglected Tropical Diseases, 11
P. Karagianni, H. Alexopoulos, A. Sourdi, D. Papadimitriou, A. Dimitrakopoulos, H. Moutsopoulos (2019)
West Nile Virus infection triggering autoimmune encephalitis: Pathophysiological and therapeutic implications.Clinical immunology
M. Sethi, T. Das, N. Tomar, J. John, Z. Dubal, K. Rajak, Rajendra Singh, G. Saikumar (2019)
Japanese encephalitis virus-induced neuropathology in mouse model infected through the conjunctival routeThe Indian Journal of Medical Research, 150
( SinghDAK MehtaDA KushwahaDKP , et al. Minocycline trial in japanese encephalitis: a double blind, randomized placebo study. Pediatr Rev Int J Pediatr Res 2016; 3: 371–377.)
SinghDAK MehtaDA KushwahaDKP , et al. Minocycline trial in japanese encephalitis: a double blind, randomized placebo study. Pediatr Rev Int J Pediatr Res 2016; 3: 371–377.SinghDAK MehtaDA KushwahaDKP , et al. Minocycline trial in japanese encephalitis: a double blind, randomized placebo study. Pediatr Rev Int J Pediatr Res 2016; 3: 371–377., SinghDAK MehtaDA KushwahaDKP , et al. Minocycline trial in japanese encephalitis: a double blind, randomized placebo study. Pediatr Rev Int J Pediatr Res 2016; 3: 371–377.
L. Basumatary, D. Raja, D. Bhuyan, Marami Das, Munindra Goswami, A. Kayal (2013)
Clinical and radiological spectrum of Japanese encephalitisJournal of the Neurological Sciences, 325
( GuzmanMG HarrisE. Dengue. The Lancet 2015; 385: 453–465.)
GuzmanMG HarrisE. Dengue. The Lancet 2015; 385: 453–465.GuzmanMG HarrisE. Dengue. The Lancet 2015; 385: 453–465., GuzmanMG HarrisE. Dengue. The Lancet 2015; 385: 453–465.
F. Artal (2019)
[Neurological complications associated with dengue virus infection].Revista de neurologia, 69 3
J. Anaya, C. Ramírez-Santana, Ignacio Salgado-Castaneda, Christopher Chang, A. Ansari, M. Gershwin (2016)
Zika virus and neurologic autoimmunity: the putative role of gangliosidesBMC Medicine, 14
( PlatonovAE RossiG KaranLS , et al. Does the Japanese encephalitis virus (JEV) represent a threat for human health in Europe? Detection of JEV RNA sequences in birds collected in Italy. Eurosurveillance 2012; 17: 20241.22913940)
PlatonovAE RossiG KaranLS , et al. Does the Japanese encephalitis virus (JEV) represent a threat for human health in Europe? Detection of JEV RNA sequences in birds collected in Italy. Eurosurveillance 2012; 17: 20241.22913940PlatonovAE RossiG KaranLS , et al. Does the Japanese encephalitis virus (JEV) represent a threat for human health in Europe? Detection of JEV RNA sequences in birds collected in Italy. Eurosurveillance 2012; 17: 20241.22913940, PlatonovAE RossiG KaranLS , et al. Does the Japanese encephalitis virus (JEV) represent a threat for human health in Europe? Detection of JEV RNA sequences in birds collected in Italy. Eurosurveillance 2012; 17: 20241.22913940
V. Chan, A. Minalyan, Patrick Ottman, A. Raza, A. Tewary (2019)
Falling for a Diagnosis: West Nile Myelitis without EncephalitisCureus, 11
B. Nosal, R. Pellizzari (2016)
West Nile VirusCMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne, 168 11
L. Bobermin, André Quincozes-Santos, Camila Santos, A. Varela, T. Teixeira, K. Wartchow, L. Lissner, Amanda Silva, Natalie Thomaz, L. Santi, W. Beys-da-Silva, P. Roehe, P. Sesterheim, J. Guimarães, C. Gonçalves, D. Souza (2020)
Zika virus exposure affects neuron-glia communication in the hippocampal slices of adult ratsScientific Reports, 10
( Martín-AcebesMA SaizJ-C . West Nile virus: a re-emerging pathogen revisited. World J Virol 2012; 1: 51–70.24175211)
Martín-AcebesMA SaizJ-C . West Nile virus: a re-emerging pathogen revisited. World J Virol 2012; 1: 51–70.24175211Martín-AcebesMA SaizJ-C . West Nile virus: a re-emerging pathogen revisited. World J Virol 2012; 1: 51–70.24175211, Martín-AcebesMA SaizJ-C . West Nile virus: a re-emerging pathogen revisited. World J Virol 2012; 1: 51–70.24175211
( RiedelS HobdenJA MillerS , et al. Arthropod-Borne and Rodent-Borne viral diseases. In: RiedelS HobdenJA MillerS (eds) Jawetz, Melnick, & Adelberg’s medical microbiology, 28e. New York: McGraw-Hill Education, 2019, accessmedicine.mhmedical.com/content.aspx?aid=1163283301 (accessed 27 July 2021).)
RiedelS HobdenJA MillerS , et al. Arthropod-Borne and Rodent-Borne viral diseases. In: RiedelS HobdenJA MillerS (eds) Jawetz, Melnick, & Adelberg’s medical microbiology, 28e. New York: McGraw-Hill Education, 2019, accessmedicine.mhmedical.com/content.aspx?aid=1163283301 (accessed 27 July 2021).RiedelS HobdenJA MillerS , et al. Arthropod-Borne and Rodent-Borne viral diseases. In: RiedelS HobdenJA MillerS (eds) Jawetz, Melnick, & Adelberg’s medical microbiology, 28e. New York: McGraw-Hill Education, 2019, accessmedicine.mhmedical.com/content.aspx?aid=1163283301 (accessed 27 July 2021)., RiedelS HobdenJA MillerS , et al. Arthropod-Borne and Rodent-Borne viral diseases. In: RiedelS HobdenJA MillerS (eds) Jawetz, Melnick, & Adelberg’s medical microbiology, 28e. New York: McGraw-Hill Education, 2019, accessmedicine.mhmedical.com/content.aspx?aid=1163283301 (accessed 27 July 2021).
R. Pimentel, Shaveta Khosla, J. Rondón, F. Peña, Gwyneth Sullivan, Martha Pérez, S. Mehta, M. Brito (2021)
Birth Defects and Long-Term Neurodevelopmental Abnormalities in Infants Born During the Zika Virus Epidemic in the Dominican RepublicAnnals of Global Health, 87
( MengQ ZouY-L BuH , et al. Imaging and cytological analysis of 92 patients with Japanese encephalitis. Neuroimmunol Neuroinflammation 2014; 1: 29–34.)
MengQ ZouY-L BuH , et al. Imaging and cytological analysis of 92 patients with Japanese encephalitis. Neuroimmunol Neuroinflammation 2014; 1: 29–34.MengQ ZouY-L BuH , et al. Imaging and cytological analysis of 92 patients with Japanese encephalitis. Neuroimmunol Neuroinflammation 2014; 1: 29–34., MengQ ZouY-L BuH , et al. Imaging and cytological analysis of 92 patients with Japanese encephalitis. Neuroimmunol Neuroinflammation 2014; 1: 29–34.
J. Sejvar, Amy Bode, A. Marfin, G. Campbell, David Ewing, M. Mazowiecki, Pierre Pavot, J. Schmitt, J. Pape, B. Biggerstaff, L. Petersen (2005)
West Nile Virus–associated Flaccid ParalysisEmerging Infectious Diseases, 11
( LiuB LiuJ SunH , et al. Autoimmune encephalitis after Japanese encephalitis in children: a prospective study. J Neurol Sci 2021; 424: 117394.33773410)
LiuB LiuJ SunH , et al. Autoimmune encephalitis after Japanese encephalitis in children: a prospective study. J Neurol Sci 2021; 424: 117394.33773410LiuB LiuJ SunH , et al. Autoimmune encephalitis after Japanese encephalitis in children: a prospective study. J Neurol Sci 2021; 424: 117394.33773410, LiuB LiuJ SunH , et al. Autoimmune encephalitis after Japanese encephalitis in children: a prospective study. J Neurol Sci 2021; 424: 117394.33773410
( GermanAC MyintKS MaiNT , et al. A preliminary neuropathological study of Japanese encephalitis in humans and a mouse model. Trans R Soc Trop Med Hyg 2006; 100: 1135–1145.16814333)
GermanAC MyintKS MaiNT , et al. A preliminary neuropathological study of Japanese encephalitis in humans and a mouse model. Trans R Soc Trop Med Hyg 2006; 100: 1135–1145.16814333GermanAC MyintKS MaiNT , et al. A preliminary neuropathological study of Japanese encephalitis in humans and a mouse model. Trans R Soc Trop Med Hyg 2006; 100: 1135–1145.16814333, GermanAC MyintKS MaiNT , et al. A preliminary neuropathological study of Japanese encephalitis in humans and a mouse model. Trans R Soc Trop Med Hyg 2006; 100: 1135–1145.16814333
M. Iwamoto, D. Jernigan, A. Guasch, M. Trepka, C. Blackmore, W. Hellinger, S. Pham, S. Zaki, R. Lanciotti, S. Lance-Parker, C. Diazgranados, A. Winquist, C. Perlino, S. Wiersma, K. Hillyer, J. Goodman, A. Marfin, M. Chamberland, L. Petersen (2003)
Transmission of West Nile virus from an organ donor to four transplant recipients.The New England journal of medicine, 348 22
R. Kaiser (2012)
Tick-borne Encephalitis—still a serious disease?Wiener Medizinische Wochenschrift, 162
( FigueiredoCP Barros-AragãoFGQ NerisRLS , et al. Zika virus replicates in adult human brain tissue and impairs synapses and memory in mice. Nat Commun 2019; 10: 3890.31488835)
FigueiredoCP Barros-AragãoFGQ NerisRLS , et al. Zika virus replicates in adult human brain tissue and impairs synapses and memory in mice. Nat Commun 2019; 10: 3890.31488835FigueiredoCP Barros-AragãoFGQ NerisRLS , et al. Zika virus replicates in adult human brain tissue and impairs synapses and memory in mice. Nat Commun 2019; 10: 3890.31488835, FigueiredoCP Barros-AragãoFGQ NerisRLS , et al. Zika virus replicates in adult human brain tissue and impairs synapses and memory in mice. Nat Commun 2019; 10: 3890.31488835
Fang Li, Yueyun Wang, Lan Yu, S. Cao, Ke Wang, Jiaolong Yuan, Chong Wang, Kunlun Wang, Min Cui, Z. Fu (2015)
Viral Infection of the Central Nervous System and Neuroinflammation Precede Blood-Brain Barrier Disruption during Japanese Encephalitis Virus InfectionJournal of Virology, 89
( ChanceyC GrinevA VolkovaE , et al. The global ecology and epidemiology of West Nile virus. Biomed Res Int 2015; 2015: 376230.25866777)
ChanceyC GrinevA VolkovaE , et al. The global ecology and epidemiology of West Nile virus. Biomed Res Int 2015; 2015: 376230.25866777ChanceyC GrinevA VolkovaE , et al. The global ecology and epidemiology of West Nile virus. Biomed Res Int 2015; 2015: 376230.25866777, ChanceyC GrinevA VolkovaE , et al. The global ecology and epidemiology of West Nile virus. Biomed Res Int 2015; 2015: 376230.25866777
C. Chancey, A. Grinev, Evgeniya Volkova, M. Rios (2015)
The Global Ecology and Epidemiology of West Nile VirusBioMed Research International, 2015
Bruce Thompson, B. Moesker, J. Smit, J. Wilschut, M. Diamond, D. Fremont (2009)
A Therapeutic Antibody against West Nile Virus Neutralizes Infection by Blocking Fusion within EndosomesPLoS Pathogens, 5
( ShivesKD TylerKL BeckhamJD . Molecular mechanisms of neuroinflammation and injury during acute viral encephalitis. J Neuroimmunol 2017; 308: 102–111.28291542)
ShivesKD TylerKL BeckhamJD . Molecular mechanisms of neuroinflammation and injury during acute viral encephalitis. J Neuroimmunol 2017; 308: 102–111.28291542ShivesKD TylerKL BeckhamJD . Molecular mechanisms of neuroinflammation and injury during acute viral encephalitis. J Neuroimmunol 2017; 308: 102–111.28291542, ShivesKD TylerKL BeckhamJD . Molecular mechanisms of neuroinflammation and injury during acute viral encephalitis. J Neuroimmunol 2017; 308: 102–111.28291542
( HaslwanterD BlaasD HeinzFX , et al. A novel mechanism of antibody-mediated enhancement of flavivirus infection. PLoS Pathog 2017; 13: e1006643.28915259)
HaslwanterD BlaasD HeinzFX , et al. A novel mechanism of antibody-mediated enhancement of flavivirus infection. PLoS Pathog 2017; 13: e1006643.28915259HaslwanterD BlaasD HeinzFX , et al. A novel mechanism of antibody-mediated enhancement of flavivirus infection. PLoS Pathog 2017; 13: e1006643.28915259, HaslwanterD BlaasD HeinzFX , et al. A novel mechanism of antibody-mediated enhancement of flavivirus infection. PLoS Pathog 2017; 13: e1006643.28915259
( TarbeM DongW HuG , et al. Japanese encephalitis virus vaccination elicits cross-reactive HLA-class I-restricted CD8 T cell response against Zika virus infection. Front Immunol 2020; 11: 577546.33101303)
TarbeM DongW HuG , et al. Japanese encephalitis virus vaccination elicits cross-reactive HLA-class I-restricted CD8 T cell response against Zika virus infection. Front Immunol 2020; 11: 577546.33101303TarbeM DongW HuG , et al. Japanese encephalitis virus vaccination elicits cross-reactive HLA-class I-restricted CD8 T cell response against Zika virus infection. Front Immunol 2020; 11: 577546.33101303, TarbeM DongW HuG , et al. Japanese encephalitis virus vaccination elicits cross-reactive HLA-class I-restricted CD8 T cell response against Zika virus infection. Front Immunol 2020; 11: 577546.33101303
( Ngwe TunMM MuthugalaR NabeshimaT , et al. Unusual, neurological and severe dengue manifestations during the outbreak in Sri Lanka, 2017. J Clin Virol Off Publ Pan Am Soc Clin Virol 2020; 125: 104304.)
Ngwe TunMM MuthugalaR NabeshimaT , et al. Unusual, neurological and severe dengue manifestations during the outbreak in Sri Lanka, 2017. J Clin Virol Off Publ Pan Am Soc Clin Virol 2020; 125: 104304.Ngwe TunMM MuthugalaR NabeshimaT , et al. Unusual, neurological and severe dengue manifestations during the outbreak in Sri Lanka, 2017. J Clin Virol Off Publ Pan Am Soc Clin Virol 2020; 125: 104304., Ngwe TunMM MuthugalaR NabeshimaT , et al. Unusual, neurological and severe dengue manifestations during the outbreak in Sri Lanka, 2017. J Clin Virol Off Publ Pan Am Soc Clin Virol 2020; 125: 104304.
D. Ireland, Mohanraj Manangeeswaran, Aaron Lewkowicz, Kaliroi Engel, S. Clark, Adelle Laniyan, Jacob Sykes, Ha-Na Lee, Ian McWilliams, Logan Kelley-Baker, L. Tonelli, D. Verthelyi (2020)
Long-term persistence of infectious Zika virus: Inflammation and behavioral sequela in micePLoS Pathogens, 16
( LeonhardSE HalsteadS LantSB , et al. Guillain-Barré syndrome during the Zika virus outbreak in Northeast Brazil: an observational cohort study. J Neurol Sci 2021; 420: 117272.33360425)
LeonhardSE HalsteadS LantSB , et al. Guillain-Barré syndrome during the Zika virus outbreak in Northeast Brazil: an observational cohort study. J Neurol Sci 2021; 420: 117272.33360425LeonhardSE HalsteadS LantSB , et al. Guillain-Barré syndrome during the Zika virus outbreak in Northeast Brazil: an observational cohort study. J Neurol Sci 2021; 420: 117272.33360425, LeonhardSE HalsteadS LantSB , et al. Guillain-Barré syndrome during the Zika virus outbreak in Northeast Brazil: an observational cohort study. J Neurol Sci 2021; 420: 117272.33360425
( MehtaR SoaresCN Medialdea-CarreraR , et al. The spectrum of neurological disease associated with Zika and chikungunya viruses in adults in Rio de Janeiro, Brazil: a case series. PLoS Negl Trop Dis 2018; 12:e0006212.29432457)
MehtaR SoaresCN Medialdea-CarreraR , et al. The spectrum of neurological disease associated with Zika and chikungunya viruses in adults in Rio de Janeiro, Brazil: a case series. PLoS Negl Trop Dis 2018; 12:e0006212.29432457MehtaR SoaresCN Medialdea-CarreraR , et al. The spectrum of neurological disease associated with Zika and chikungunya viruses in adults in Rio de Janeiro, Brazil: a case series. PLoS Negl Trop Dis 2018; 12:e0006212.29432457, MehtaR SoaresCN Medialdea-CarreraR , et al. The spectrum of neurological disease associated with Zika and chikungunya viruses in adults in Rio de Janeiro, Brazil: a case series. PLoS Negl Trop Dis 2018; 12:e0006212.29432457
( SadekJR PergamSA HarringtonJA , et al. Persistent neuropsychological impairment associated with West Nile virus infection. J Clin Exp Neuropsychol 2010; 32: 81–87.19513920)
SadekJR PergamSA HarringtonJA , et al. Persistent neuropsychological impairment associated with West Nile virus infection. J Clin Exp Neuropsychol 2010; 32: 81–87.19513920SadekJR PergamSA HarringtonJA , et al. Persistent neuropsychological impairment associated with West Nile virus infection. J Clin Exp Neuropsychol 2010; 32: 81–87.19513920, SadekJR PergamSA HarringtonJA , et al. Persistent neuropsychological impairment associated with West Nile virus infection. J Clin Exp Neuropsychol 2010; 32: 81–87.19513920
Ammar Alli, J. Ortíz, A. Atoot, Ali Atoot, Paul Millhouse (2021)
Management of West Nile Encephalitis: An Uncommon Complication of West Nile VirusCureus, 13
( CarsonPJ BorchardtSM CusterB , et al. Neuroinvasive disease and West Nile virus infection, North Dakota, USA, 1999–2008. Emerg Infect Dis 2012; 18: 684–686.22469465)
CarsonPJ BorchardtSM CusterB , et al. Neuroinvasive disease and West Nile virus infection, North Dakota, USA, 1999–2008. Emerg Infect Dis 2012; 18: 684–686.22469465CarsonPJ BorchardtSM CusterB , et al. Neuroinvasive disease and West Nile virus infection, North Dakota, USA, 1999–2008. Emerg Infect Dis 2012; 18: 684–686.22469465, CarsonPJ BorchardtSM CusterB , et al. Neuroinvasive disease and West Nile virus infection, North Dakota, USA, 1999–2008. Emerg Infect Dis 2012; 18: 684–686.22469465
( MussoD KoAI BaudD . Zika virus infection – after the pandemic. N Engl J Med 2019; 381: 1444–1457.31597021)
MussoD KoAI BaudD . Zika virus infection – after the pandemic. N Engl J Med 2019; 381: 1444–1457.31597021MussoD KoAI BaudD . Zika virus infection – after the pandemic. N Engl J Med 2019; 381: 1444–1457.31597021, MussoD KoAI BaudD . Zika virus infection – after the pandemic. N Engl J Med 2019; 381: 1444–1457.31597021
( LandryML St. GeorgeK . Laboratory diagnosis of Zika virus infection. Arch Pathol Lab Med 2016; 141: 60–67.27763787)
LandryML St. GeorgeK . Laboratory diagnosis of Zika virus infection. Arch Pathol Lab Med 2016; 141: 60–67.27763787LandryML St. GeorgeK . Laboratory diagnosis of Zika virus infection. Arch Pathol Lab Med 2016; 141: 60–67.27763787, LandryML St. GeorgeK . Laboratory diagnosis of Zika virus infection. Arch Pathol Lab Med 2016; 141: 60–67.27763787
Kalaimani Sivamani, V. Dhir, Surjit Singh, Aman Sharma (2017)
Diagnostic dilemma—dengue or Japanese encephalitis?Neurology India, 65
( AnayaJ-M Ramirez-SantanaC Salgado-CastanedaI , et al. Zika virus and neurologic autoimmunity: the putative role of gangliosides. BMC Med 2016; 14: 49.27001187)
AnayaJ-M Ramirez-SantanaC Salgado-CastanedaI , et al. Zika virus and neurologic autoimmunity: the putative role of gangliosides. BMC Med 2016; 14: 49.27001187AnayaJ-M Ramirez-SantanaC Salgado-CastanedaI , et al. Zika virus and neurologic autoimmunity: the putative role of gangliosides. BMC Med 2016; 14: 49.27001187, AnayaJ-M Ramirez-SantanaC Salgado-CastanedaI , et al. Zika virus and neurologic autoimmunity: the putative role of gangliosides. BMC Med 2016; 14: 49.27001187
( ZhangL WeiL WangZ , et al. COVID-19: neuroinvasiveness, neurotropism and neurovirulence. J Neurol Exp Neurosci 2020; 6: S24–S31.)
ZhangL WeiL WangZ , et al. COVID-19: neuroinvasiveness, neurotropism and neurovirulence. J Neurol Exp Neurosci 2020; 6: S24–S31.ZhangL WeiL WangZ , et al. COVID-19: neuroinvasiveness, neurotropism and neurovirulence. J Neurol Exp Neurosci 2020; 6: S24–S31., ZhangL WeiL WangZ , et al. COVID-19: neuroinvasiveness, neurotropism and neurovirulence. J Neurol Exp Neurosci 2020; 6: S24–S31.
( LindquistL VapalahtiO . Tick-borne encephalitis. The Lancet 2008; 371: 1861–1871.)
LindquistL VapalahtiO . Tick-borne encephalitis. The Lancet 2008; 371: 1861–1871.LindquistL VapalahtiO . Tick-borne encephalitis. The Lancet 2008; 371: 1861–1871., LindquistL VapalahtiO . Tick-borne encephalitis. The Lancet 2008; 371: 1861–1871.
A. Budak (1975)
[Japanese encephalitis].Fel'dsher i akusherka, 40 9
( DesforgesM Le CoupanecA BrisonE , et al. Neuroinvasive and neurotropic human respiratory coronaviruses: potential neurovirulent agents in humans. Adv Exp Med Biol 2014; 807: 75–96.24619619)
DesforgesM Le CoupanecA BrisonE , et al. Neuroinvasive and neurotropic human respiratory coronaviruses: potential neurovirulent agents in humans. Adv Exp Med Biol 2014; 807: 75–96.24619619DesforgesM Le CoupanecA BrisonE , et al. Neuroinvasive and neurotropic human respiratory coronaviruses: potential neurovirulent agents in humans. Adv Exp Med Biol 2014; 807: 75–96.24619619, DesforgesM Le CoupanecA BrisonE , et al. Neuroinvasive and neurotropic human respiratory coronaviruses: potential neurovirulent agents in humans. Adv Exp Med Biol 2014; 807: 75–96.24619619
J. Gnann, A. Agrawal, J. Hart, Martha Buitrago, P. Carson, Diane Hanfelt-Goade, K. Tyler, J. Spotkov, A. Freifeld, T. Moore, J. Reyno, H. Masur, P. Jester, Ilet Dale, Yufeng Li, I. Aban, F. Lakeman, R. Whitley (2019)
Lack of Efficacy of High-Titered Immunoglobulin in Patients with West Nile Virus Central Nervous System DiseaseEmerging Infectious Diseases, 25
Who Publication (2011)
Vaccines against tick-borne encephalitis: WHO position paper--recommendations.Vaccine, 29 48
( BirgeJ SonnesynS . Powassan virus encephalitis, Minnesota, USA. Emerg Infect Dis 2012; 18: 1669–1671.23017222)
BirgeJ SonnesynS . Powassan virus encephalitis, Minnesota, USA. Emerg Infect Dis 2012; 18: 1669–1671.23017222BirgeJ SonnesynS . Powassan virus encephalitis, Minnesota, USA. Emerg Infect Dis 2012; 18: 1669–1671.23017222, BirgeJ SonnesynS . Powassan virus encephalitis, Minnesota, USA. Emerg Infect Dis 2012; 18: 1669–1671.23017222
P. Carson, S. Borchardt, B. Custer, H. Prince, Joan Dunn-Williams, V. Winkelman, L. Tobler, B. Biggerstaff, R. Lanciotti, L. Petersen, M. Busch (2012)
Neuroinvasive Disease and West Nile Virus Infection, North Dakota, USA, 1999–2008Emerging Infectious Diseases, 18
Marcio Leyser, O. Nascimento (2017)
Congenital Zika Virus Infection: Beyond Neonatal Microcephaly.JAMA neurology, 74 5
( da SilvaIRF FronteraJA Bispode FilippisAM , et al. Neurologic complications associated with the Zika virus in Brazilian adults. JAMA Neurol 2017; 74: 1190–1198.28806453)
da SilvaIRF FronteraJA Bispode FilippisAM , et al. Neurologic complications associated with the Zika virus in Brazilian adults. JAMA Neurol 2017; 74: 1190–1198.28806453da SilvaIRF FronteraJA Bispode FilippisAM , et al. Neurologic complications associated with the Zika virus in Brazilian adults. JAMA Neurol 2017; 74: 1190–1198.28806453, da SilvaIRF FronteraJA Bispode FilippisAM , et al. Neurologic complications associated with the Zika virus in Brazilian adults. JAMA Neurol 2017; 74: 1190–1198.28806453
T. Araújo, R. Ximenes, D. Miranda-Filho, W. Souza, U. Montarroyos, Ana Melo, Sandra Valongueiro, M. Albuquerque, C. Braga, S. Filho, M. Cordeiro, Enrique Vazquez, Danielle Cruz, C. Henriques, L. Bezerra, Priscila Castanha, R. Dhalia, Ernesto Marques-Júnior, C. Martelli, L. Rodrigues (2017)
Association between microcephaly, Zika virus infection, and other risk factors in Brazil: final report of a case-control study.The Lancet. Infectious diseases, 18 3
R. Hughes (1990)
Clinical Features of Guillain-Barré Syndrome
R. Kaiser (2008)
Tick-borne encephalitis.Infectious disease clinics of North America, 22 3
( UpretiSR JanuszKB SchluterWW , et al. Estimation of the impact of a Japanese encephalitis immunization program with live, attenuated SA 14-14-2 vaccine in Nepal. Am J Trop Med Hyg 2013; 88: 464–468.23358643)
UpretiSR JanuszKB SchluterWW , et al. Estimation of the impact of a Japanese encephalitis immunization program with live, attenuated SA 14-14-2 vaccine in Nepal. Am J Trop Med Hyg 2013; 88: 464–468.23358643UpretiSR JanuszKB SchluterWW , et al. Estimation of the impact of a Japanese encephalitis immunization program with live, attenuated SA 14-14-2 vaccine in Nepal. Am J Trop Med Hyg 2013; 88: 464–468.23358643, UpretiSR JanuszKB SchluterWW , et al. Estimation of the impact of a Japanese encephalitis immunization program with live, attenuated SA 14-14-2 vaccine in Nepal. Am J Trop Med Hyg 2013; 88: 464–468.23358643
(2011)
World Health Organization. Asia Pacific strategy for emerging diseases. Geneva: World Health Organization
M. Hawkes, I. Carabenciov, Eelco Wijdicks, A. Rabinstein (2018)
Outcomes in Patients With Severe West Nile Neuroinvasive DiseaseCritical Care Medicine, 46
Wang H (2009)
10.7883/yoken.JJID.2009.270Jpn J Infect Dis, 62
( ChenC-J OuY-C LinS-Y , et al. Glial activation involvement in neuronal death by Japanese encephalitis virus infection. J Gen Virol 2010; 91: 1028–1037.20007359)
ChenC-J OuY-C LinS-Y , et al. Glial activation involvement in neuronal death by Japanese encephalitis virus infection. J Gen Virol 2010; 91: 1028–1037.20007359ChenC-J OuY-C LinS-Y , et al. Glial activation involvement in neuronal death by Japanese encephalitis virus infection. J Gen Virol 2010; 91: 1028–1037.20007359, ChenC-J OuY-C LinS-Y , et al. Glial activation involvement in neuronal death by Japanese encephalitis virus infection. J Gen Virol 2010; 91: 1028–1037.20007359
( MulkeySB Arroyave-WesselM PeytonC , et al. Neurodevelopmental abnormalities in children with in utero Zika virus exposure without congenital Zika syndrome. JAMA Pediatr 2020; 174: 269–276.31904798)
MulkeySB Arroyave-WesselM PeytonC , et al. Neurodevelopmental abnormalities in children with in utero Zika virus exposure without congenital Zika syndrome. JAMA Pediatr 2020; 174: 269–276.31904798MulkeySB Arroyave-WesselM PeytonC , et al. Neurodevelopmental abnormalities in children with in utero Zika virus exposure without congenital Zika syndrome. JAMA Pediatr 2020; 174: 269–276.31904798, MulkeySB Arroyave-WesselM PeytonC , et al. Neurodevelopmental abnormalities in children with in utero Zika virus exposure without congenital Zika syndrome. JAMA Pediatr 2020; 174: 269–276.31904798
( WHO. Sexual transmission of Zika Virus: Current status challenges and research priorities. Geneva: WHO, http://www.who.int/reproductivehealth/zika/sexual-transmission-experts-meeting/en/ (accessed 18 August 2022).)
WHO. Sexual transmission of Zika Virus: Current status challenges and research priorities. Geneva: WHO, http://www.who.int/reproductivehealth/zika/sexual-transmission-experts-meeting/en/ (accessed 18 August 2022).WHO. Sexual transmission of Zika Virus: Current status challenges and research priorities. Geneva: WHO, http://www.who.int/reproductivehealth/zika/sexual-transmission-experts-meeting/en/ (accessed 18 August 2022)., WHO. Sexual transmission of Zika Virus: Current status challenges and research priorities. Geneva: WHO, http://www.who.int/reproductivehealth/zika/sexual-transmission-experts-meeting/en/ (accessed 18 August 2022).
Emily Curren, J. Lehman, Jonathan Kolsin, W. Walker, Stacey Martin, J. Staples, S. Hills, Carolyn Gould, I. Rabe, M. Fischer, N. Lindsey (2018)
West Nile Virus and Other Nationally Notifiable Arboviral Diseases — United States, 2017Morbidity and Mortality Weekly Report, 67
Xiao-yan Gao, Hong Liu, Xiaolong Li, S. Fu, Lei Cao, Nan Shao, Weijia Zhang, Qianying Wang, Zhi Lu, W. Lei, Ying He, Yu-xi Cao, Huanyu Wang, G. Liang (2019)
Changing Geographic Distribution of Japanese Encephalitis Virus Genotypes, 1935-2017.Vector borne and zoonotic diseases, 19 1
Maoqiang Tian, Juan Li, Wenting Lei, Xiao-mei Shu (2019)
Japanese Encephalitis Virus-Induced Anti-N-Methyl-D-Aspartate Receptor Encephalitis: A Case Report and Review of LiteratureNeuropediatrics, 50
L. Petersen, A. Brault, R. Nasci (2013)
West Nile virus: review of the literature.JAMA, 310 3
( FamiliarI BoivinM MagenJ , et al. Neurodevelopment outcomes in infants born to women with Zika virus infection during pregnancy in Mexico. Child Care Health Dev 2021; 47: 311–318.33332632)
FamiliarI BoivinM MagenJ , et al. Neurodevelopment outcomes in infants born to women with Zika virus infection during pregnancy in Mexico. Child Care Health Dev 2021; 47: 311–318.33332632FamiliarI BoivinM MagenJ , et al. Neurodevelopment outcomes in infants born to women with Zika virus infection during pregnancy in Mexico. Child Care Health Dev 2021; 47: 311–318.33332632, FamiliarI BoivinM MagenJ , et al. Neurodevelopment outcomes in infants born to women with Zika virus infection during pregnancy in Mexico. Child Care Health Dev 2021; 47: 311–318.33332632
( Prevention| Dengue| CDC, 2021, https://www.cdc.gov/dengue/healthcare-providers/hc-providers-prevention.html (accessed 9 January 2022).)
Prevention| Dengue| CDC, 2021, https://www.cdc.gov/dengue/healthcare-providers/hc-providers-prevention.html (accessed 9 January 2022).Prevention| Dengue| CDC, 2021, https://www.cdc.gov/dengue/healthcare-providers/hc-providers-prevention.html (accessed 9 January 2022)., Prevention| Dengue| CDC, 2021, https://www.cdc.gov/dengue/healthcare-providers/hc-providers-prevention.html (accessed 9 January 2022).
Chun-juan Wang, Z. Zeng, Fu-sheng Zhang, Shou-gang Guo (2020)
Clinical features of adult anti-N-methyl-d-aspartate receptor encephalitis after Japanese encephalitisJournal of the Neurological Sciences, 417
( GnannJWJr AgrawalA HartJ , et al. Lack of efficacy of high-titered immunoglobulin in patients with West Nile virus central nervous system disease. Emerg Infect Dis 2019; 25: 2064–2073.31625835)
GnannJWJr AgrawalA HartJ , et al. Lack of efficacy of high-titered immunoglobulin in patients with West Nile virus central nervous system disease. Emerg Infect Dis 2019; 25: 2064–2073.31625835GnannJWJr AgrawalA HartJ , et al. Lack of efficacy of high-titered immunoglobulin in patients with West Nile virus central nervous system disease. Emerg Infect Dis 2019; 25: 2064–2073.31625835, GnannJWJr AgrawalA HartJ , et al. Lack of efficacy of high-titered immunoglobulin in patients with West Nile virus central nervous system disease. Emerg Infect Dis 2019; 25: 2064–2073.31625835
( PimentelR KhoslaS RondonJ , et al. Birth defects and long- term neurodevelopmental abnormalities in infants born during the Zika virus epidemic in the Dominican Republic. Ann Glob Health 2021; 87: 4.33505863)
PimentelR KhoslaS RondonJ , et al. Birth defects and long- term neurodevelopmental abnormalities in infants born during the Zika virus epidemic in the Dominican Republic. Ann Glob Health 2021; 87: 4.33505863PimentelR KhoslaS RondonJ , et al. Birth defects and long- term neurodevelopmental abnormalities in infants born during the Zika virus epidemic in the Dominican Republic. Ann Glob Health 2021; 87: 4.33505863, PimentelR KhoslaS RondonJ , et al. Birth defects and long- term neurodevelopmental abnormalities in infants born during the Zika virus epidemic in the Dominican Republic. Ann Glob Health 2021; 87: 4.33505863
Anne Piantadosi, I. Solomon (2022)
Powassan Virus Encephalitis.Infectious disease clinics of North America, 36 3
K. Shives, K. Tyler, J. Beckham (2017)
Molecular mechanisms of neuroinflammation and injury during acute viral encephalitisJournal of Neuroimmunology, 308
H. Yadav, Parthopratim Majumder, J. Biswas (2017)
Dengue associated choroiditis: a rare entityJournal of Ophthalmic Inflammation and Infection, 7
A. German, K. Myint, N. Mai, I. Pomeroy, N. Phu, J. Tzartos, P. Winter, J. Collett, J. Farrar, A. Barrett, A. Kipar, M. Esiri, T. Solomon (2006)
A preliminary neuropathological study of Japanese encephalitis in humans and a mouse model.Transactions of the Royal Society of Tropical Medicine and Hygiene, 100 12
( LannesN SummerfieldA FilgueiraL . Regulation of inflammation in Japanese encephalitis. J Neuroinflammation 2017; 14: 158.28807053)
LannesN SummerfieldA FilgueiraL . Regulation of inflammation in Japanese encephalitis. J Neuroinflammation 2017; 14: 158.28807053LannesN SummerfieldA FilgueiraL . Regulation of inflammation in Japanese encephalitis. J Neuroinflammation 2017; 14: 158.28807053, LannesN SummerfieldA FilgueiraL . Regulation of inflammation in Japanese encephalitis. J Neuroinflammation 2017; 14: 158.28807053
C. Mathers, M. Ezzati, Alan Lopez (2007)
Measuring the Burden of Neglected Tropical Diseases: The Global Burden of Disease FrameworkPLoS Neglected Tropical Diseases, 1
( KuhnJH CharrelRN . Arthropod-Borne and Rodent-Borne virus infections. In: JamesonJL FauciAS KasperDL , et al. (eds) Harrison’s principles of internal medicine. 20th ed. New York: McGraw-Hill Education, 2018, accessmedicine.mhmedical.com/content.aspx?aid=1155971053 (accessed 17 July 2021).)
KuhnJH CharrelRN . Arthropod-Borne and Rodent-Borne virus infections. In: JamesonJL FauciAS KasperDL , et al. (eds) Harrison’s principles of internal medicine. 20th ed. New York: McGraw-Hill Education, 2018, accessmedicine.mhmedical.com/content.aspx?aid=1155971053 (accessed 17 July 2021).KuhnJH CharrelRN . Arthropod-Borne and Rodent-Borne virus infections. In: JamesonJL FauciAS KasperDL , et al. (eds) Harrison’s principles of internal medicine. 20th ed. New York: McGraw-Hill Education, 2018, accessmedicine.mhmedical.com/content.aspx?aid=1155971053 (accessed 17 July 2021)., KuhnJH CharrelRN . Arthropod-Borne and Rodent-Borne virus infections. In: JamesonJL FauciAS KasperDL , et al. (eds) Harrison’s principles of internal medicine. 20th ed. New York: McGraw-Hill Education, 2018, accessmedicine.mhmedical.com/content.aspx?aid=1155971053 (accessed 17 July 2021).
( Carod-ArtalFJ . [Neurological complications associated with dengue virus infection]. Rev Neurol 2019; 69: 113–122.31310001)
Carod-ArtalFJ . [Neurological complications associated with dengue virus infection]. Rev Neurol 2019; 69: 113–122.31310001Carod-ArtalFJ . [Neurological complications associated with dengue virus infection]. Rev Neurol 2019; 69: 113–122.31310001, Carod-ArtalFJ . [Neurological complications associated with dengue virus infection]. Rev Neurol 2019; 69: 113–122.31310001
( YunSI KimSY ChoiWY , et al. Molecular characterization of the full-length genome of the Japanese encephalitis viral strain K87P39. Virus Res 2003; 96: 129–140.12951273)
YunSI KimSY ChoiWY , et al. Molecular characterization of the full-length genome of the Japanese encephalitis viral strain K87P39. Virus Res 2003; 96: 129–140.12951273YunSI KimSY ChoiWY , et al. Molecular characterization of the full-length genome of the Japanese encephalitis viral strain K87P39. Virus Res 2003; 96: 129–140.12951273, YunSI KimSY ChoiWY , et al. Molecular characterization of the full-length genome of the Japanese encephalitis viral strain K87P39. Virus Res 2003; 96: 129–140.12951273
Viral hemorrhagic fevers (VHFs)
S. Pradhan, Rakesh Gupta, Mamta Singh, A. Mathur (2001)
Biphasic illness pattern due to early relapse in Japanese-B virus encephalitisJournal of the Neurological Sciences, 183
Laura Muñoz, P. Barreras, C. Pardo (2016)
Zika Virus–Associated Neurological Disease in the Adult: Guillain–Barré Syndrome, Encephalitis, and MyelitisSeminars in Reproductive Medicine, 34
( FauciAS MorensDM . Zika virus in the Americas – yet another arbovirus threat. N Engl J Med 2016; 374: 601–604.26761185)
FauciAS MorensDM . Zika virus in the Americas – yet another arbovirus threat. N Engl J Med 2016; 374: 601–604.26761185FauciAS MorensDM . Zika virus in the Americas – yet another arbovirus threat. N Engl J Med 2016; 374: 601–604.26761185, FauciAS MorensDM . Zika virus in the Americas – yet another arbovirus threat. N Engl J Med 2016; 374: 601–604.26761185
( AlvesLV HazinAN AlvesJGB . Neuroimaging in children born with congenital Zika syndrome: a cohort study. J Child Neurol 2021; 36: 1066–1070.34315277)
AlvesLV HazinAN AlvesJGB . Neuroimaging in children born with congenital Zika syndrome: a cohort study. J Child Neurol 2021; 36: 1066–1070.34315277AlvesLV HazinAN AlvesJGB . Neuroimaging in children born with congenital Zika syndrome: a cohort study. J Child Neurol 2021; 36: 1066–1070.34315277, AlvesLV HazinAN AlvesJGB . Neuroimaging in children born with congenital Zika syndrome: a cohort study. J Child Neurol 2021; 36: 1066–1070.34315277
( KimH ChaGW JeongYE , et al. Detection of Japanese encephalitis Virus genotype V in Culex orientalis and Culex pipiens (Diptera: Culicidae) in Korea. PLoS ONE 2015; 10: e0116547.25658839)
KimH ChaGW JeongYE , et al. Detection of Japanese encephalitis Virus genotype V in Culex orientalis and Culex pipiens (Diptera: Culicidae) in Korea. PLoS ONE 2015; 10: e0116547.25658839KimH ChaGW JeongYE , et al. Detection of Japanese encephalitis Virus genotype V in Culex orientalis and Culex pipiens (Diptera: Culicidae) in Korea. PLoS ONE 2015; 10: e0116547.25658839, KimH ChaGW JeongYE , et al. Detection of Japanese encephalitis Virus genotype V in Culex orientalis and Culex pipiens (Diptera: Culicidae) in Korea. PLoS ONE 2015; 10: e0116547.25658839
( ThompsonBS MoeskerB SmitJM , et al. A therapeutic antibody against West Nile virus neutralizes infection by blocking fusion within endosomes. PLoS Pathog 2009; 5: e1000453.19478866)
ThompsonBS MoeskerB SmitJM , et al. A therapeutic antibody against West Nile virus neutralizes infection by blocking fusion within endosomes. PLoS Pathog 2009; 5: e1000453.19478866ThompsonBS MoeskerB SmitJM , et al. A therapeutic antibody against West Nile virus neutralizes infection by blocking fusion within endosomes. PLoS Pathog 2009; 5: e1000453.19478866, ThompsonBS MoeskerB SmitJM , et al. A therapeutic antibody against West Nile virus neutralizes infection by blocking fusion within endosomes. PLoS Pathog 2009; 5: e1000453.19478866
L. Pealer, A. Marfin, L. Petersen, R. Lanciotti, P. Page, S. Stramer, M. Stobierski, K. Signs, B. Newman, H. Kapoor, J. Goodman, M. Chamberland (2003)
Transmission of West Nile virus through blood transfusion in the United States in 2002.The New England journal of medicine, 349 13
A. Fauci, D. Morens (2016)
Zika Virus in the Americas — Yet Another Arbovirus Threat
A. Act, P. Brasil, J. Pereira, C. Gabaglia, L. Damasceno, M. Wakimoto, R. Nogueira, P. Sequeira, A. Siqueira, L. Carvalho, D. Cunha, G. Calvet, E. Neves, M. Moreira, A. Baião, Paulo Carvalho, C. Janzen, S. Valderramos, J. Cherry, A. Filippis, K. Nielsen‐Saines (2016)
Zika Virus Infection in Pregnant Women in Rio de Janeiro - Preliminary Report.The New England Journal of Medicine, 375
J. Bigby (1988)
Harrison's Principles of Internal MedicineArchives of Dermatology, 124
Chun-Jung Chen, Y. Ou, Shih-Yi Lin, S. Raung, Su-Lan Liao, Ching-Yi Lai, Shih-Yun Chen, Jian-hong Chen (2010)
Glial activation involvement in neuronal death by Japanese encephalitis virus infection.The Journal of general virology, 91 Pt 4
( RiceME . Vital signs: Zika-associated birth defects and neurodevelopmental abnormalities possibly associated with congenital Zika virus infection – U.S. territories and freely associated states, 2018. MMWR Morb Mortal Wkly Rep 2018; 67: 858–867.30091967)
RiceME . Vital signs: Zika-associated birth defects and neurodevelopmental abnormalities possibly associated with congenital Zika virus infection – U.S. territories and freely associated states, 2018. MMWR Morb Mortal Wkly Rep 2018; 67: 858–867.30091967RiceME . Vital signs: Zika-associated birth defects and neurodevelopmental abnormalities possibly associated with congenital Zika virus infection – U.S. territories and freely associated states, 2018. MMWR Morb Mortal Wkly Rep 2018; 67: 858–867.30091967, RiceME . Vital signs: Zika-associated birth defects and neurodevelopmental abnormalities possibly associated with congenital Zika virus infection – U.S. territories and freely associated states, 2018. MMWR Morb Mortal Wkly Rep 2018; 67: 858–867.30091967
Y. Mustafá, L. Meuren, S. Coelho, L. Arruda (2019)
Pathways Exploited by Flaviviruses to Counteract the Blood-Brain Barrier and Invade the Central Nervous SystemFrontiers in Microbiology, 10
L. Pomar, G. Malinger, G. Benoist, G. Carles, Y. Ville, D. Rousset, N. Hcini, C. Pomar, A. Jolivet, V. Lambert (2017)
Association between Zika virus and fetopathy: a prospective cohort study in French GuianaUltrasound in Obstetrics & Gynecology, 49
P. Tilley, J. Fox, G. Jayaraman, J. Preiksaitis (2006)
Nucleic acid testing for west nile virus RNA in plasma enhances rapid diagnosis of acute infection in symptomatic patients.The Journal of infectious diseases, 193 10
( FloridisJ McGuinnessSL KuruczN , et al. Murray valley encephalitis virus: an ongoing cause of encephalitis in Australia’s North. Trop Med Infect Dis 2018; 3: 49.)
FloridisJ McGuinnessSL KuruczN , et al. Murray valley encephalitis virus: an ongoing cause of encephalitis in Australia’s North. Trop Med Infect Dis 2018; 3: 49.FloridisJ McGuinnessSL KuruczN , et al. Murray valley encephalitis virus: an ongoing cause of encephalitis in Australia’s North. Trop Med Infect Dis 2018; 3: 49., FloridisJ McGuinnessSL KuruczN , et al. Murray valley encephalitis virus: an ongoing cause of encephalitis in Australia’s North. Trop Med Infect Dis 2018; 3: 49.
Mya Tun, R. Muthugala, T. Nabeshima, Lakmali Rajamanthri, Dulani Jayawardana, Shanthi Attanayake, Aung Soe, S. Dumre, Tsuyoshi Ando, D. Hayasaka, S. Inoue, C. Buerano, K. Morita (2020)
Unusual, neurological and severe dengue manifestations during the outbreak in Sri Lanka, 2017.Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology, 125
Jonathan Soverow, G. Wellenius, D. Fisman, M. Mittleman (2009)
Infectious Disease in a Warming World: How Weather Influenced West Nile Virus in the United States (2001–2005)Environmental Health Perspectives, 117
( Dengue vaccines: WHO and position paper, September 2018, https://www.who.int/publications-detail-redirect/WER9335-457-476 (accessed 9 January 2022).)
Dengue vaccines: WHO and position paper, September 2018, https://www.who.int/publications-detail-redirect/WER9335-457-476 (accessed 9 January 2022).Dengue vaccines: WHO and position paper, September 2018, https://www.who.int/publications-detail-redirect/WER9335-457-476 (accessed 9 January 2022)., Dengue vaccines: WHO and position paper, September 2018, https://www.who.int/publications-detail-redirect/WER9335-457-476 (accessed 9 January 2022).
( PomarL MalingerG BenoistG , et al. Association between Zika virus and fetopathy: a prospective cohort study in French Guiana. Ultrasound Obstet Gynecol 2017; 49: 729–736.28078779)
PomarL MalingerG BenoistG , et al. Association between Zika virus and fetopathy: a prospective cohort study in French Guiana. Ultrasound Obstet Gynecol 2017; 49: 729–736.28078779PomarL MalingerG BenoistG , et al. Association between Zika virus and fetopathy: a prospective cohort study in French Guiana. Ultrasound Obstet Gynecol 2017; 49: 729–736.28078779, PomarL MalingerG BenoistG , et al. Association between Zika virus and fetopathy: a prospective cohort study in French Guiana. Ultrasound Obstet Gynecol 2017; 49: 729–736.28078779
C. Figueiredo, Fernanda Barros-Aragão, Rômulo Neris, Paula Frost, C. Soares, Isis Souza, J. Zeidler, Daniele Zamberlan, Virginia Sousa, Amanda Souza, André Guimarães, M. Bellio, J. Souza, S. Alves‐Leon, G. Neves, H. Paula-Neto, N. Castro, F. Felice, I. Assunção-Miranda, J. Clarke, A. Poian, S. Ferreira (2019)
Zika virus replicates in adult human brain tissue and impairs synapses and memory in miceNature Communications, 10
Harsh Pastel, B. Chakrabarty, L. Saini, Atin Kumar, S. Gulati (2017)
A case of anti- N-methyl-D-aspartate (NMDA) receptor encephalitis possibly triggered by an episode of Japanese B encephalitisNeurology India, 65
( SuQ XieZ-X HeF , et al. Adults with severe Japanese encephalitis: a retrospective analysis of 9 cases in Linyi, China. Neurol Sci. Epub ahead of print 9 November 2020. DOI: 10.1007/s10072-020-04867-8.)
SuQ XieZ-X HeF , et al. Adults with severe Japanese encephalitis: a retrospective analysis of 9 cases in Linyi, China. Neurol Sci. Epub ahead of print 9 November 2020. DOI: 10.1007/s10072-020-04867-8.SuQ XieZ-X HeF , et al. Adults with severe Japanese encephalitis: a retrospective analysis of 9 cases in Linyi, China. Neurol Sci. Epub ahead of print 9 November 2020. DOI: 10.1007/s10072-020-04867-8., SuQ XieZ-X HeF , et al. Adults with severe Japanese encephalitis: a retrospective analysis of 9 cases in Linyi, China. Neurol Sci. Epub ahead of print 9 November 2020. DOI: 10.1007/s10072-020-04867-8.
T. Dahm, Henriette Rudolph, C. Schwerk, H. Schroten, T. Tenenbaum (2016)
Neuroinvasion and Inflammation in Viral Central Nervous System InfectionsMediators of Inflammation, 2016
( SivamaniK DhirV SinghS , et al. Diagnostic dilemma – dengue or Japanese encephalitis? Neurol India 2017; 65: 105.28084251)
SivamaniK DhirV SinghS , et al. Diagnostic dilemma – dengue or Japanese encephalitis? Neurol India 2017; 65: 105.28084251SivamaniK DhirV SinghS , et al. Diagnostic dilemma – dengue or Japanese encephalitis? Neurol India 2017; 65: 105.28084251, SivamaniK DhirV SinghS , et al. Diagnostic dilemma – dengue or Japanese encephalitis? Neurol India 2017; 65: 105.28084251
M. Lauréti, D. Narayanan, Julio Rodriguez-Andres, J. Fazakerley, L. Kedzierski (2018)
Flavivirus Receptors: Diversity, Identity, and Cell EntryFrontiers in Immunology, 9
( PatabendigeA MichaelBD CraigAG , et al. Brain microvascular endothelial-astrocyte cell responses following Japanese encephalitis virus infection in an in vitro human blood-brain barrier model. Mol Cell Neurosci 2018; 89: 60–70.29635016)
PatabendigeA MichaelBD CraigAG , et al. Brain microvascular endothelial-astrocyte cell responses following Japanese encephalitis virus infection in an in vitro human blood-brain barrier model. Mol Cell Neurosci 2018; 89: 60–70.29635016PatabendigeA MichaelBD CraigAG , et al. Brain microvascular endothelial-astrocyte cell responses following Japanese encephalitis virus infection in an in vitro human blood-brain barrier model. Mol Cell Neurosci 2018; 89: 60–70.29635016, PatabendigeA MichaelBD CraigAG , et al. Brain microvascular endothelial-astrocyte cell responses following Japanese encephalitis virus infection in an in vitro human blood-brain barrier model. Mol Cell Neurosci 2018; 89: 60–70.29635016
( Ben-NathanD Gershoni-YahalomO SaminaI , et al. Using high titer West Nile intravenous immunoglobulin from selected Israeli donors for treatment of West Nile virus infection. BMC Infect Dis 2009; 9: 18.19222853)
Ben-NathanD Gershoni-YahalomO SaminaI , et al. Using high titer West Nile intravenous immunoglobulin from selected Israeli donors for treatment of West Nile virus infection. BMC Infect Dis 2009; 9: 18.19222853Ben-NathanD Gershoni-YahalomO SaminaI , et al. Using high titer West Nile intravenous immunoglobulin from selected Israeli donors for treatment of West Nile virus infection. BMC Infect Dis 2009; 9: 18.19222853, Ben-NathanD Gershoni-YahalomO SaminaI , et al. Using high titer West Nile intravenous immunoglobulin from selected Israeli donors for treatment of West Nile virus infection. BMC Infect Dis 2009; 9: 18.19222853
L. Alves, A. Hazin, J. Alves (2021)
Neuroimaging in Children Born With Congenital Zika Syndrome: A Cohort StudyJournal of Child Neurology, 36
T. Pierson, M. Diamond (2020)
The continued threat of emerging flavivirusesNature Microbiology, 5
M. White, Hassen Wollebo, J. Beckham, K. Tyler, K. Khalili (2016)
Zika virus: An emergent neuropathological agentAnnals of Neurology, 80
( JehaLE SilaCA LedermanRJ , et al. West Nile virus infection: a new acute paralytic illness. Neurology 2003; 61: 55–59.12847156)
JehaLE SilaCA LedermanRJ , et al. West Nile virus infection: a new acute paralytic illness. Neurology 2003; 61: 55–59.12847156JehaLE SilaCA LedermanRJ , et al. West Nile virus infection: a new acute paralytic illness. Neurology 2003; 61: 55–59.12847156, JehaLE SilaCA LedermanRJ , et al. West Nile virus infection: a new acute paralytic illness. Neurology 2003; 61: 55–59.12847156
( Dengue severe dengue, https://www.who.int/news-room/fact-sheets/detail/dengue-and-severe-dengue (accessed 4 January 2022).)
Dengue severe dengue, https://www.who.int/news-room/fact-sheets/detail/dengue-and-severe-dengue (accessed 4 January 2022).Dengue severe dengue, https://www.who.int/news-room/fact-sheets/detail/dengue-and-severe-dengue (accessed 4 January 2022)., Dengue severe dengue, https://www.who.int/news-room/fact-sheets/detail/dengue-and-severe-dengue (accessed 4 January 2022).
( WhiteMK WolleboHS David BeckhamJ , et al. Zika virus: an emergent neuropathological agent. Ann Neurol 2016; 80: 479–489.27464346)
WhiteMK WolleboHS David BeckhamJ , et al. Zika virus: an emergent neuropathological agent. Ann Neurol 2016; 80: 479–489.27464346WhiteMK WolleboHS David BeckhamJ , et al. Zika virus: an emergent neuropathological agent. Ann Neurol 2016; 80: 479–489.27464346, WhiteMK WolleboHS David BeckhamJ , et al. Zika virus: an emergent neuropathological agent. Ann Neurol 2016; 80: 479–489.27464346
( RuzekD Avšicˇ ŽupancT BordeJ , et al. Tick-borne encephalitis in Europe and Russia: review of pathogenesis, clinical features, therapy, and vaccines. Antiviral Res 2019; 164: 23–51.30710567)
RuzekD Avšicˇ ŽupancT BordeJ , et al. Tick-borne encephalitis in Europe and Russia: review of pathogenesis, clinical features, therapy, and vaccines. Antiviral Res 2019; 164: 23–51.30710567RuzekD Avšicˇ ŽupancT BordeJ , et al. Tick-borne encephalitis in Europe and Russia: review of pathogenesis, clinical features, therapy, and vaccines. Antiviral Res 2019; 164: 23–51.30710567, RuzekD Avšicˇ ŽupancT BordeJ , et al. Tick-borne encephalitis in Europe and Russia: review of pathogenesis, clinical features, therapy, and vaccines. Antiviral Res 2019; 164: 23–51.30710567
Q. Su, Zhong Xie, Feng He, Zhen-Chuan Liu, Xiao-jie Song, Fu-Chun Zhao, Dibin Li, F. Che (2020)
Adults with severe Japanese encephalitis: a retrospective analysis of 9 cases in Linyi, ChinaNeurological Sciences, 42
Karen Hussmann, Melanie Samuel, K. Kim, M. Diamond, B. Fredericksen (2012)
Differential Replication of Pathogenic and Nonpathogenic Strains of West Nile Virus within AstrocytesJournal of Virology, 87
B. Migdalska-Kassurowa (1973)
[Japanese B encephalitis].Przeglad epidemiologiczny, 27 2
( MathersCD EzzatiM LopezAD . Measuring the burden of neglected tropical diseases: the global burden of disease framework. PLoS Negl Trop Dis 2007; 1: e114.18060077)
MathersCD EzzatiM LopezAD . Measuring the burden of neglected tropical diseases: the global burden of disease framework. PLoS Negl Trop Dis 2007; 1: e114.18060077MathersCD EzzatiM LopezAD . Measuring the burden of neglected tropical diseases: the global burden of disease framework. PLoS Negl Trop Dis 2007; 1: e114.18060077, MathersCD EzzatiM LopezAD . Measuring the burden of neglected tropical diseases: the global burden of disease framework. PLoS Negl Trop Dis 2007; 1: e114.18060077
( PealerLN MarfinAA PetersenLR , et al. Transmission of West Nile virus through blood transfusion in the United States in 2002. N Eng J Med 2003; 349: 1236–1245.)
PealerLN MarfinAA PetersenLR , et al. Transmission of West Nile virus through blood transfusion in the United States in 2002. N Eng J Med 2003; 349: 1236–1245.PealerLN MarfinAA PetersenLR , et al. Transmission of West Nile virus through blood transfusion in the United States in 2002. N Eng J Med 2003; 349: 1236–1245., PealerLN MarfinAA PetersenLR , et al. Transmission of West Nile virus through blood transfusion in the United States in 2002. N Eng J Med 2003; 349: 1236–1245.
S. Montgomery, Jennifer Brown, M. Kuehnert, Theresa Smith, Nicholas Crall, R. Lanciotti, A. Oliveira, Thomas Boo, A. Marfin (2006)
Transfusion‐associated transmission of West Nile virus, United States 2003 through 2005Transfusion, 46
(2022)
Current status challenges and research priorities
( DirlikovE MajorCG MedinaNA , et al. Clinical features of Guillain-Barré syndrome with vs without Zika virus infection, Puerto Rico, 2016. JAMA Neurol 2018; 75: 1089–1097.29799940)
DirlikovE MajorCG MedinaNA , et al. Clinical features of Guillain-Barré syndrome with vs without Zika virus infection, Puerto Rico, 2016. JAMA Neurol 2018; 75: 1089–1097.29799940DirlikovE MajorCG MedinaNA , et al. Clinical features of Guillain-Barré syndrome with vs without Zika virus infection, Puerto Rico, 2016. JAMA Neurol 2018; 75: 1089–1097.29799940, DirlikovE MajorCG MedinaNA , et al. Clinical features of Guillain-Barré syndrome with vs without Zika virus infection, Puerto Rico, 2016. JAMA Neurol 2018; 75: 1089–1097.29799940
( HinckleyAF O’LearyDR HayesEB . Transmission of West Nile virus through human breast milk seems to be rare. Pediatrics 2007; 119: e666–e671.17332186)
HinckleyAF O’LearyDR HayesEB . Transmission of West Nile virus through human breast milk seems to be rare. Pediatrics 2007; 119: e666–e671.17332186HinckleyAF O’LearyDR HayesEB . Transmission of West Nile virus through human breast milk seems to be rare. Pediatrics 2007; 119: e666–e671.17332186, HinckleyAF O’LearyDR HayesEB . Transmission of West Nile virus through human breast milk seems to be rare. Pediatrics 2007; 119: e666–e671.17332186
T. Chouin-Carneiro, M. David, F. Nogueira, F. Santos, R. Lourenço-de-Oliveira (2020)
Zika virus transmission by Brazilian Aedes aegypti and Aedes albopictus is virus dose and temperature-dependentPLoS Neglected Tropical Diseases, 14
Chris Goates, S. Tsuha, Selene Working, J. Carey, E. Spivak (2017)
Seronegative West Nile Virus Infection in a Patient Treated with Rituximab for Rheumatoid Arthritis.The American journal of medicine, 130 6
( Simon-LoriereE FayeO ProtM , et al. Autochthonous Japanese encephalitis with yellow fever coinfection in Africa. N Engl J Med 2017; 376: 1483–1485.28402771)
Simon-LoriereE FayeO ProtM , et al. Autochthonous Japanese encephalitis with yellow fever coinfection in Africa. N Engl J Med 2017; 376: 1483–1485.28402771Simon-LoriereE FayeO ProtM , et al. Autochthonous Japanese encephalitis with yellow fever coinfection in Africa. N Engl J Med 2017; 376: 1483–1485.28402771, Simon-LoriereE FayeO ProtM , et al. Autochthonous Japanese encephalitis with yellow fever coinfection in Africa. N Engl J Med 2017; 376: 1483–1485.28402771
Nils Lannes, A. Summerfield, L. Filgueira (2017)
Regulation of inflammation in Japanese encephalitisJournal of Neuroinflammation, 14
(2009)
Dengue: guidelines for diagnosis, treatment, prevention and control. Geneva: World Health Organization
N. Lindsey, E. Hayes, J. Staples, Marc Fischer (2009)
West Nile Virus Disease in Children, United States, 1999–2007Pediatrics, 123
( OspinaML TongVT GonzalezM , et al. Zika virus disease and pregnancy outcomes in Colombia. N Engl J Med 2020; 383: 537–545.32757522)
OspinaML TongVT GonzalezM , et al. Zika virus disease and pregnancy outcomes in Colombia. N Engl J Med 2020; 383: 537–545.32757522OspinaML TongVT GonzalezM , et al. Zika virus disease and pregnancy outcomes in Colombia. N Engl J Med 2020; 383: 537–545.32757522, OspinaML TongVT GonzalezM , et al. Zika virus disease and pregnancy outcomes in Colombia. N Engl J Med 2020; 383: 537–545.32757522
D. Ben‐Nathan, O. Gershoni-Yahalom, I. Samina, Y. Khinich, I. Nur, O. Laub, A. Gottreich, Michael Simanov, A. Porgador, B. Rager-Zisman, Nadav Orr (2009)
Using high titer West Nile intravenous immunoglobulin from selected Israeli donors for treatment of West Nile virus infectionBMC Infectious Diseases, 9
T. Solomon, N. Dung, R. Kneen, M. Gainsborough, D. Vaughn, V. Khanh (2000)
NEUROLOGICAL ASPECTS OF TROPICAL DISEASE: Japanese encephalitisJournal of Neurology, Neurosurgery, and Psychiatry, 68
( ChanV MinalyanA OttmanP , et al. Falling for a diagnosis: West Nile myelitis without encephalitis. Cureus 2019; 11: e5838.31754573)
ChanV MinalyanA OttmanP , et al. Falling for a diagnosis: West Nile myelitis without encephalitis. Cureus 2019; 11: e5838.31754573ChanV MinalyanA OttmanP , et al. Falling for a diagnosis: West Nile myelitis without encephalitis. Cureus 2019; 11: e5838.31754573, ChanV MinalyanA OttmanP , et al. Falling for a diagnosis: West Nile myelitis without encephalitis. Cureus 2019; 11: e5838.31754573
( LiG-H NingZ-J LiuY-M , et al. Neurological manifestations of dengue infection. Front Cell Infect Microbiol 2017; 7: 449.29119088)
LiG-H NingZ-J LiuY-M , et al. Neurological manifestations of dengue infection. Front Cell Infect Microbiol 2017; 7: 449.29119088LiG-H NingZ-J LiuY-M , et al. Neurological manifestations of dengue infection. Front Cell Infect Microbiol 2017; 7: 449.29119088, LiG-H NingZ-J LiuY-M , et al. Neurological manifestations of dengue infection. Front Cell Infect Microbiol 2017; 7: 449.29119088
S. Mulkey, Margarita Arroyave-Wessel, C. Peyton, D. Bulas, Y. Fourzali, Jiji Jiang, S. Russo, R. McCarter, M. Msall, A. Plessis, R. DeBiasi, C. Cure (2020)
Neurodevelopmental Abnormalities in Children With In Utero Zika Virus Exposure Without Congenital Zika Syndrome.JAMA pediatrics
( SomkijrungrojT KongwattananonW . Ocular manifestations of dengue. Curr Opin Ophthalmol 2019; 30: 500–505.31503074)
SomkijrungrojT KongwattananonW . Ocular manifestations of dengue. Curr Opin Ophthalmol 2019; 30: 500–505.31503074SomkijrungrojT KongwattananonW . Ocular manifestations of dengue. Curr Opin Ophthalmol 2019; 30: 500–505.31503074, SomkijrungrojT KongwattananonW . Ocular manifestations of dengue. Curr Opin Ophthalmol 2019; 30: 500–505.31503074
( LauretiM NarayananD Rodriguez-AndresJ , et al. Flavivirus receptors: diversity, identity, and cell entry. Front Immunol 2018; 9: 2180.30319635)
LauretiM NarayananD Rodriguez-AndresJ , et al. Flavivirus receptors: diversity, identity, and cell entry. Front Immunol 2018; 9: 2180.30319635LauretiM NarayananD Rodriguez-AndresJ , et al. Flavivirus receptors: diversity, identity, and cell entry. Front Immunol 2018; 9: 2180.30319635, LauretiM NarayananD Rodriguez-AndresJ , et al. Flavivirus receptors: diversity, identity, and cell entry. Front Immunol 2018; 9: 2180.30319635
James Versalovic (2000)
Viral infections of the nervous systemArchives of pathology & laboratory medicine, 124 12
( WangC ZengZ ZhangF , et al. Clinical features of adult anti-N-methyl-d-aspartate receptor encephalitis after Japanese encephalitis. J Neurol Sci 2020; 417: 117080.32777576)
WangC ZengZ ZhangF , et al. Clinical features of adult anti-N-methyl-d-aspartate receptor encephalitis after Japanese encephalitis. J Neurol Sci 2020; 417: 117080.32777576WangC ZengZ ZhangF , et al. Clinical features of adult anti-N-methyl-d-aspartate receptor encephalitis after Japanese encephalitis. J Neurol Sci 2020; 417: 117080.32777576, WangC ZengZ ZhangF , et al. Clinical features of adult anti-N-methyl-d-aspartate receptor encephalitis after Japanese encephalitis. J Neurol Sci 2020; 417: 117080.32777576
G. Fall, Nicholas Paola, Martin Faye, M. Dia, Caio Freire, C. Loucoubar, P. Zanotto, O. Faye, A. Sall (2017)
Biological and phylogenetic characteristics of West African lineages of West Nile virusPLoS Neglected Tropical Diseases, 11
( SejvarJJ BodeAV MarfinAA , et al. West Nile virus–associated flaccid paralysis. Emerg Infect Dis 2005; 11: 1021–1027.16022775)
SejvarJJ BodeAV MarfinAA , et al. West Nile virus–associated flaccid paralysis. Emerg Infect Dis 2005; 11: 1021–1027.16022775SejvarJJ BodeAV MarfinAA , et al. West Nile virus–associated flaccid paralysis. Emerg Infect Dis 2005; 11: 1021–1027.16022775, SejvarJJ BodeAV MarfinAA , et al. West Nile virus–associated flaccid paralysis. Emerg Infect Dis 2005; 11: 1021–1027.16022775
( MontgomerySP BrownJA KuehnertM , et al. Transfusion-associated transmission of West Nile virus, United States 2003 through 2005. Transfusion 2006; 46: 2038–2046.17176314)
MontgomerySP BrownJA KuehnertM , et al. Transfusion-associated transmission of West Nile virus, United States 2003 through 2005. Transfusion 2006; 46: 2038–2046.17176314MontgomerySP BrownJA KuehnertM , et al. Transfusion-associated transmission of West Nile virus, United States 2003 through 2005. Transfusion 2006; 46: 2038–2046.17176314, MontgomerySP BrownJA KuehnertM , et al. Transfusion-associated transmission of West Nile virus, United States 2003 through 2005. Transfusion 2006; 46: 2038–2046.17176314
Hsiuying Wang (2017)
Anti-NMDA Receptor Encephalitis and VaccinationInternational Journal of Molecular Sciences, 18
A. Vittor, M. Long, Paramita Chakrabarty, Lauren Aycock, V. Kollu, S. DeKosky (2020)
West Nile Virus-Induced Neurologic Sequelae—Relationship to Neurodegenerative Cascades and DementiasCurrent Tropical Medicine Reports, 7
( West Nile virus. CDC, 2020, https://www.cdc.gov/westnile/index.html (accessed 21 July 2021).)
West Nile virus. CDC, 2020, https://www.cdc.gov/westnile/index.html (accessed 21 July 2021).West Nile virus. CDC, 2020, https://www.cdc.gov/westnile/index.html (accessed 21 July 2021)., West Nile virus. CDC, 2020, https://www.cdc.gov/westnile/index.html (accessed 21 July 2021).
Almerinda Agrelli, R. Moura, S. Crovella, L. Brandão (2019)
ZIKA virus entry mechanisms in human cells.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases, 69
C. Khoo (2018)
Dengue Cerebellitis: A Case Report and Literature ReviewThe American Journal of Case Reports, 19
L. Jeha, C. Sila, R. Lederman, R. Prayson, C. Isada, S. Gordon (2003)
West Nile virus infectionNeurology, 61
Martha Ospina, Van Tong, Maritza Gonzalez, D. Valencia, M. Mercado, S. Gilboa, Andrea Rodriguez, Sarah Tinker, A. Rico, Christina Winfield, L. Pardo, J. Thomas, Greace Avila, J. Villanueva, Sara Gómez, D. Jamieson, Franklyn Prieto, D. Meaney-Delman, Óscar Pacheco, M. Honein (2020)
Zika Virus Disease and Pregnancy Outcomes in Colombia.The New England journal of medicine, 383 6
( WilliamsDT MacKenzieJS BinghamJ . Flaviviruses. In: ZimmermanJJ KarrikerL RamirezA , et al. (eds) Diseases of swine. 11th ed. Hoboken, NJ: John Wiley & Sons, 2019, pp. 530–543.)
WilliamsDT MacKenzieJS BinghamJ . Flaviviruses. In: ZimmermanJJ KarrikerL RamirezA , et al. (eds) Diseases of swine. 11th ed. Hoboken, NJ: John Wiley & Sons, 2019, pp. 530–543.WilliamsDT MacKenzieJS BinghamJ . Flaviviruses. In: ZimmermanJJ KarrikerL RamirezA , et al. (eds) Diseases of swine. 11th ed. Hoboken, NJ: John Wiley & Sons, 2019, pp. 530–543., WilliamsDT MacKenzieJS BinghamJ . Flaviviruses. In: ZimmermanJJ KarrikerL RamirezA , et al. (eds) Diseases of swine. 11th ed. Hoboken, NJ: John Wiley & Sons, 2019, pp. 530–543.
W. Organization (1985)
Arthropod-borne and rodent-borne viral diseases. Report of a WHO Scientific Group.World Health Organization technical report series, 719
N. Hcini, Y. Kugbe, Z. Rafalimanana, V. Lambert, Mérédith Mathieu, G. Carles, D. Baud, A. Panchaud, L. Pomar (2021)
Association between confirmed congenital Zika infection at birth and outcomes up to 3 years of lifeNature Communications, 12
Marion Rice, R. Galang, Nicole Roth, S. Ellington, C. Moore, Miguel Valencia-Prado, Esther Ellis, A. Tufa, Livinson Taulung, Julia Alfred, J. Pérez-Padilla, Camille Delgado-López, S. Zaki, Sarah Reagan‐Steiner, J. Bhatnagar, John Nahabedian, Megan Reynolds, M. Yeargin-Allsopp, Laura Viens, Samantha Olson, Abbey Jones, Madelyn Baez-Santiago, Philip Oppong-Twene, Kelley VanMaldeghem, E. Simon, Jazmyn Moore, K. Polen, Braeanna Hillman, Ruta Ropeti, L. Nieves-Ferrer, Mariam Marcano-Huertas, Carolee Masao, Edlen Anzures, R. Hansen, Stephany Pérez-Gonzalez, Carla Espinet-Crespo, Mildred Luciano-Román, C. Shapiro-Mendoza, S. Gilboa, M. Honein (2018)
Vital Signs: Zika-Associated Birth Defects and Neurodevelopmental Abnormalities Possibly Associated with Congenital Zika Virus Infection — U.S. Territories and Freely Associated States, 2018Morbidity and Mortality Weekly Report, 67
M. Landry, K. George (2017)
Laboratory Diagnosis of Zika Virus Infection.Archives of pathology & laboratory medicine, 141 1
R. Shaik, M. Netravathi, L. Nitish, Reeta Mani, P. Shah, T. Damodar, M. Anita, P. Pal (2018)
A rare case of Japanese encephalitis-induced anti-N-methyl-d-aspartate receptor encephalitisNeurology India, 66
E. Dirlikov, Chelsea Major, Nicole Medina, Roberta Lugo-Robles, D. Matos, J. Muñoz-Jordán, Candimar Colón-Sánchez, Myriam Garcia, Marangely Olivero-Segarra, Graciela Malave, G. Rodríguez-Vega, Dana Thomas, S. Waterman, J. Sejvar, C. Luciano, Tyler Sharp, Brenda Rivera-García (2018)
Clinical Features of Guillain-Barré Syndrome With vs Without Zika Virus Infection, Puerto Rico, 2016JAMA Neurology, 75
( WalterosDM SoaresJ StyczynskiAR , et al. Long-term outcomes of Guillain-Barré syndrome possibly associated with Zika virus infection. PLoS ONE 2019; 14: e0220049.31369576)
WalterosDM SoaresJ StyczynskiAR , et al. Long-term outcomes of Guillain-Barré syndrome possibly associated with Zika virus infection. PLoS ONE 2019; 14: e0220049.31369576WalterosDM SoaresJ StyczynskiAR , et al. Long-term outcomes of Guillain-Barré syndrome possibly associated with Zika virus infection. PLoS ONE 2019; 14: e0220049.31369576, WalterosDM SoaresJ StyczynskiAR , et al. Long-term outcomes of Guillain-Barré syndrome possibly associated with Zika virus infection. PLoS ONE 2019; 14: e0220049.31369576
Van-Mai Cao-Lormeau, A. Blake, S. Mons, S. Lastère, C. Roche, J. Vanhomwegen, T. Dub, Laure Baudouin, A. Teissier, P. Larre, Anne-Laure Vial, C. Decam, V. Choumet, S. Halstead, H. Willison, L. Musset, J. Manuguerra, P. Desprès, E. Fournier, H. Mallet, D. Musso, A. Fontanet, J. Neil, F. Ghawché (2016)
Guillain-Barré Syndrome outbreak associated with Zika virus infection in French Polynesia: a case-control studyThe Lancet, 387
Thanapong Somkijrungroj, W. Kongwattananon (2019)
Ocular manifestations of dengue.Current Opinion in Ophthalmology
( FarrarF . West Nile virus: an infectious viral agent to the central nervous system. Crit Care Nurs Clin North Am 2013; 25: 191–203.23692938)
FarrarF . West Nile virus: an infectious viral agent to the central nervous system. Crit Care Nurs Clin North Am 2013; 25: 191–203.23692938FarrarF . West Nile virus: an infectious viral agent to the central nervous system. Crit Care Nurs Clin North Am 2013; 25: 191–203.23692938, FarrarF . West Nile virus: an infectious viral agent to the central nervous system. Crit Care Nurs Clin North Am 2013; 25: 191–203.23692938
( Chouin-CarneiroT DavidMR de Bruycker NogueiraF , et al. Zika virus transmission by Brazilian Aedes aegypti and Aedes albopictus is virus dose and temperature-dependent. PLoS Negl Trop Dis 2020; 14: e0008527.32898136)
Chouin-CarneiroT DavidMR de Bruycker NogueiraF , et al. Zika virus transmission by Brazilian Aedes aegypti and Aedes albopictus is virus dose and temperature-dependent. PLoS Negl Trop Dis 2020; 14: e0008527.32898136Chouin-CarneiroT DavidMR de Bruycker NogueiraF , et al. Zika virus transmission by Brazilian Aedes aegypti and Aedes albopictus is virus dose and temperature-dependent. PLoS Negl Trop Dis 2020; 14: e0008527.32898136, Chouin-CarneiroT DavidMR de Bruycker NogueiraF , et al. Zika virus transmission by Brazilian Aedes aegypti and Aedes albopictus is virus dose and temperature-dependent. PLoS Negl Trop Dis 2020; 14: e0008527.32898136
A. Thompson, S. Kutz (2019)
Introduction to the Special Issue on ‘Emerging Zoonoses and Wildlife’International Journal for Parasitology: Parasites and Wildlife, 9
N. Dung, L. Turtle, L. Turtle, W. Chong, N. Mai, T. Thao, T. Thuy, R. Kneen, N. Phu, B. Wills, J. Farrar, K. Das, T. Solomon, T. Solomon (2009)
An evaluation of the usefulness of neuroimaging for the diagnosis of Japanese encephalitisJournal of Neurology, 256
( KaragianniP AlexopoulosH SourdiA , et al. West Nile Virus infection triggering autoimmune encephalitis: pathophysiological and therapeutic implications. Clin Immunol 2019; 207: 97–99.31454696)
KaragianniP AlexopoulosH SourdiA , et al. West Nile Virus infection triggering autoimmune encephalitis: pathophysiological and therapeutic implications. Clin Immunol 2019; 207: 97–99.31454696KaragianniP AlexopoulosH SourdiA , et al. West Nile Virus infection triggering autoimmune encephalitis: pathophysiological and therapeutic implications. Clin Immunol 2019; 207: 97–99.31454696, KaragianniP AlexopoulosH SourdiA , et al. West Nile Virus infection triggering autoimmune encephalitis: pathophysiological and therapeutic implications. Clin Immunol 2019; 207: 97–99.31454696
( IrelandDDC ManangeeswaranM LewkowiczAP , et al. Long-term persistence of infectious Zika virus: inflammation and behavioral sequela in mice. PLoS Pathog 2020; 16: e1008689.33301527)
IrelandDDC ManangeeswaranM LewkowiczAP , et al. Long-term persistence of infectious Zika virus: inflammation and behavioral sequela in mice. PLoS Pathog 2020; 16: e1008689.33301527IrelandDDC ManangeeswaranM LewkowiczAP , et al. Long-term persistence of infectious Zika virus: inflammation and behavioral sequela in mice. PLoS Pathog 2020; 16: e1008689.33301527, IrelandDDC ManangeeswaranM LewkowiczAP , et al. Long-term persistence of infectious Zika virus: inflammation and behavioral sequela in mice. PLoS Pathog 2020; 16: e1008689.33301527
Alex Wessel, M. Doyle, Taylor Engdahl, Jessica Rodriguez, J. Crowe, M. Diamond (2021)
Human Monoclonal Antibodies against NS1 Protein Protect against Lethal West Nile Virus InfectionmBio, 12
Xiaoyi Dai, Guobao Shang, Shan Lu, Jing Yang, Jianguo Xu (2018)
A new subtype of eastern tick-borne encephalitis virus discovered in Qinghai-Tibet Plateau, ChinaEmerging Microbes & Infections, 7
S. Leonhard, S. Halstead, S. Lant, M. Albuquerque, C. Brito, L. Albuquerque, M. Ellul, R. Franca, Dawn Gourlay, M. Griffiths, A. Henriques-Souza, M. Machado, R. Medialdea-Carrera, Ravi Mehta, Roberta Melo, S. Mesquita, Álvaro Moreira, L. Pena, M. Santos, L. Turtle, T. Solomon, H. Willison, B. Jacobs, M. Ferreira (2020)
Guillain-Barré syndrome during the Zika virus outbreak in Northeast Brazil: An observational cohort studyJournal of the Neurological Sciences, 420
( KhooCS . Dengue cerebellitis: a case report and literature review. Am J Case Rep 2018; 19: 864–867.30038209)
KhooCS . Dengue cerebellitis: a case report and literature review. Am J Case Rep 2018; 19: 864–867.30038209KhooCS . Dengue cerebellitis: a case report and literature review. Am J Case Rep 2018; 19: 864–867.30038209, KhooCS . Dengue cerebellitis: a case report and literature review. Am J Case Rep 2018; 19: 864–867.30038209
Hyunwoo Kim, G. Cha, Y. Jeong, Wook-Gyo Lee, Kyu‐Sik Chang, J. Roh, S. Yang, Mi-yeoun Park, C. Park, E. Shin (2015)
Detection of Japanese Encephalitis Virus Genotype V in Culex orientalis and Culex pipiens (Diptera: Culicidae) in KoreaPLoS ONE, 10
( ThakurK NobleJM . Viral infections of the nervous system. In: BrustJCM (ed.) CURRENT diagnosis & treatment: neurology. 3rd ed. New York: McGraw-Hill Education, 2019, accessmedicine.mhmedical.com/content.aspx?aid=1159972608 (accessed 17 June 2021).)
ThakurK NobleJM . Viral infections of the nervous system. In: BrustJCM (ed.) CURRENT diagnosis & treatment: neurology. 3rd ed. New York: McGraw-Hill Education, 2019, accessmedicine.mhmedical.com/content.aspx?aid=1159972608 (accessed 17 June 2021).ThakurK NobleJM . Viral infections of the nervous system. In: BrustJCM (ed.) CURRENT diagnosis & treatment: neurology. 3rd ed. New York: McGraw-Hill Education, 2019, accessmedicine.mhmedical.com/content.aspx?aid=1159972608 (accessed 17 June 2021)., ThakurK NobleJM . Viral infections of the nervous system. In: BrustJCM (ed.) CURRENT diagnosis & treatment: neurology. 3rd ed. New York: McGraw-Hill Education, 2019, accessmedicine.mhmedical.com/content.aspx?aid=1159972608 (accessed 17 June 2021).
( MeloAS deO AguiarRS , et al. Congenital Zika virus infection: beyond neonatal microcephaly. JAMA Neurol 2016; 73: 1407–1416.27695855)
MeloAS deO AguiarRS , et al. Congenital Zika virus infection: beyond neonatal microcephaly. JAMA Neurol 2016; 73: 1407–1416.27695855MeloAS deO AguiarRS , et al. Congenital Zika virus infection: beyond neonatal microcephaly. JAMA Neurol 2016; 73: 1407–1416.27695855, MeloAS deO AguiarRS , et al. Congenital Zika virus infection: beyond neonatal microcephaly. JAMA Neurol 2016; 73: 1407–1416.27695855
( TianM LiJ LeiW , et al. Japanese encephalitis virus-induced anti-N-methyl-D-aspartate receptor encephalitis: a case report and review of literature. Neuropediatrics 2019; 50: 111–115.30620950)
TianM LiJ LeiW , et al. Japanese encephalitis virus-induced anti-N-methyl-D-aspartate receptor encephalitis: a case report and review of literature. Neuropediatrics 2019; 50: 111–115.30620950TianM LiJ LeiW , et al. Japanese encephalitis virus-induced anti-N-methyl-D-aspartate receptor encephalitis: a case report and review of literature. Neuropediatrics 2019; 50: 111–115.30620950, TianM LiJ LeiW , et al. Japanese encephalitis virus-induced anti-N-methyl-D-aspartate receptor encephalitis: a case report and review of literature. Neuropediatrics 2019; 50: 111–115.30620950
( MorensDM FauciAS . Emerging pandemic diseases: how we got to COVID-19. Cell 2020; 182: 1077–1092.32846157)
MorensDM FauciAS . Emerging pandemic diseases: how we got to COVID-19. Cell 2020; 182: 1077–1092.32846157MorensDM FauciAS . Emerging pandemic diseases: how we got to COVID-19. Cell 2020; 182: 1077–1092.32846157, MorensDM FauciAS . Emerging pandemic diseases: how we got to COVID-19. Cell 2020; 182: 1077–1092.32846157
( Flaviviridae. Viral hemorrhagic fevers (VHFs). CDC, 2021, https://www.cdc.gov/vhf/virus-families/flaviviridae.html (accessed 18 January 2022).)
Flaviviridae. Viral hemorrhagic fevers (VHFs). CDC, 2021, https://www.cdc.gov/vhf/virus-families/flaviviridae.html (accessed 18 January 2022).Flaviviridae. Viral hemorrhagic fevers (VHFs). CDC, 2021, https://www.cdc.gov/vhf/virus-families/flaviviridae.html (accessed 18 January 2022)., Flaviviridae. Viral hemorrhagic fevers (VHFs). CDC, 2021, https://www.cdc.gov/vhf/virus-families/flaviviridae.html (accessed 18 January 2022).
Ben-ke Liu, Jiehua Liu, Hong Sun, Mingdan Xie, Chen Yang, Yanan Pan, D. Huang, Li Cheng, Heng-sheng Chen, Jiannan Ma, Li Jiang (2021)
Autoimmune encephalitis after Japanese encephalitis in children: A prospective studyJournal of the Neurological Sciences, 424
L. Lima, S. Vianello, Sérgio Pimentel, Gabriel Andrade, C. Zett, Léo Muller, M. Farah, R. Belfort (2018)
Dengue Fever Presenting as Purtscher-like RetinopathyOcular Immunology and Inflammation, 26
( MayxayM DouangdalaP VilayhongC , et al. Outcome of Japanese encephalitis virus (JEV) infection in pediatric and adult patients at Mahosot Hospital, Vientiane, Lao PDR. Am J Trop Med Hyg 2021; 104: 567–575.)
MayxayM DouangdalaP VilayhongC , et al. Outcome of Japanese encephalitis virus (JEV) infection in pediatric and adult patients at Mahosot Hospital, Vientiane, Lao PDR. Am J Trop Med Hyg 2021; 104: 567–575.MayxayM DouangdalaP VilayhongC , et al. Outcome of Japanese encephalitis virus (JEV) infection in pediatric and adult patients at Mahosot Hospital, Vientiane, Lao PDR. Am J Trop Med Hyg 2021; 104: 567–575., MayxayM DouangdalaP VilayhongC , et al. Outcome of Japanese encephalitis virus (JEV) infection in pediatric and adult patients at Mahosot Hospital, Vientiane, Lao PDR. Am J Trop Med Hyg 2021; 104: 567–575.
( Zika virus, https://www.who.int/news-room/fact-sheets/detail/zika-virus (accessed 22 June 2021).)
Zika virus, https://www.who.int/news-room/fact-sheets/detail/zika-virus (accessed 22 June 2021).Zika virus, https://www.who.int/news-room/fact-sheets/detail/zika-virus (accessed 22 June 2021)., Zika virus, https://www.who.int/news-room/fact-sheets/detail/zika-virus (accessed 22 June 2021).
J. Sadek, S. Pergam, J. Harrington, L. Echevarria, L. Davis, D. Goade, JoAnn Harnar, R. Nofchissey, C. Sewell, P. Ettestad, K. Haaland (2010)
Persistent neuropsychological impairment associated with West Nile virus infectionJournal of Clinical and Experimental Neuropsychology, 32
Denise Haslwanter, D. Blaas, F. Heinz, K. Stiasny (2017)
A novel mechanism of antibody-mediated enhancement of flavivirus infectionPLoS Pathogens, 13
L. Lindquist, O. Vapalahti (2008)
Tick-borne encephalitisThe Lancet, 371
The Brazilian Journal of INFECTIOUS DISEASES Japanese encephalitis: a review of the Indian perspective
( SchultzV BarrieJA DonaldCL , et al. Oligodendrocytes are susceptible to Zika virus infection in a mouse model of perinatal exposure: implications for CNS complications. Glia 2021; 69: 2023–2036.33942402)
SchultzV BarrieJA DonaldCL , et al. Oligodendrocytes are susceptible to Zika virus infection in a mouse model of perinatal exposure: implications for CNS complications. Glia 2021; 69: 2023–2036.33942402SchultzV BarrieJA DonaldCL , et al. Oligodendrocytes are susceptible to Zika virus infection in a mouse model of perinatal exposure: implications for CNS complications. Glia 2021; 69: 2023–2036.33942402, SchultzV BarrieJA DonaldCL , et al. Oligodendrocytes are susceptible to Zika virus infection in a mouse model of perinatal exposure: implications for CNS complications. Glia 2021; 69: 2023–2036.33942402
D. Walteros, Jesus Soares, A. Styczynski, Joseph Abrams, Jose Galindo-Buitrago, J. Acosta-Reyes, Elsa Bravo-Ribero, Zuleima Arteta, Alma Solano-Sanchez, Franklyn Prieto, Maritza González‐Duarte, Edgar Navarro-Lechuga, Jorge Salinas, E. Belay, L. Schonberger, I. Damon, Martha Ospina, J. Sejvar (2019)
Long-term outcomes of Guillain-Barré syndrome possibly associated with Zika virus infectionPLoS ONE, 14
( WangH LiY LiangX , et al. Japanese Encephalitis in Mainland China. Jpn J Infect Dis 2009; 62: 331–336.19762980)
WangH LiY LiangX , et al. Japanese Encephalitis in Mainland China. Jpn J Infect Dis 2009; 62: 331–336.19762980WangH LiY LiangX , et al. Japanese Encephalitis in Mainland China. Jpn J Infect Dis 2009; 62: 331–336.19762980, WangH LiY LiangX , et al. Japanese Encephalitis in Mainland China. Jpn J Infect Dis 2009; 62: 331–336.19762980
( WesselAW DoyleMP EngdahlTB , et al. Human monoclonal antibodies against NS1 protein protect against Lethal West Nile virus infection. Mbio 2021; 12: e02440.)
WesselAW DoyleMP EngdahlTB , et al. Human monoclonal antibodies against NS1 protein protect against Lethal West Nile virus infection. Mbio 2021; 12: e02440.WesselAW DoyleMP EngdahlTB , et al. Human monoclonal antibodies against NS1 protein protect against Lethal West Nile virus infection. Mbio 2021; 12: e02440., WesselAW DoyleMP EngdahlTB , et al. Human monoclonal antibodies against NS1 protein protect against Lethal West Nile virus infection. Mbio 2021; 12: e02440.
( LimaLH VianelloS PimentelS , et al. Dengue fever presenting as purtscher-like retinopathy. Ocul Immunol Inflamm 2018; 26: 660–665.28323496)
LimaLH VianelloS PimentelS , et al. Dengue fever presenting as purtscher-like retinopathy. Ocul Immunol Inflamm 2018; 26: 660–665.28323496LimaLH VianelloS PimentelS , et al. Dengue fever presenting as purtscher-like retinopathy. Ocul Immunol Inflamm 2018; 26: 660–665.28323496, LimaLH VianelloS PimentelS , et al. Dengue fever presenting as purtscher-like retinopathy. Ocul Immunol Inflamm 2018; 26: 660–665.28323496
V. Schultz, J. Barrie, Claire Donald, C. Crawford, M. Mullin, T. Anderson, T. Solomon, S. Barnett, C. Linington, A. Kohl, H. Willison, J. Edgar (2021)
Oligodendrocytes are susceptible to Zika virus infection in a mouse model of perinatal exposure: Implications for CNS complicationsGlia, 69
V. Lee, X. Aguilera, David Heymann, A. Wilder-Smith, Vernon Br, V. Lee, X. Aguilera, D. Heymann, A. Wilder-Smith, D. Bausch, S. Briand, C. Bruschke, E. Carmo, S. Cleghorn, L. Dandona, C. Donnelly, I. Fall, J. Halton, Richard Hatchett, Felicia Hong, P. Horby, C. Ihekweazu, Michael Jacobs, K. Khan, Yijun Lin, G. Leung, C. Low, Bethan McDonald, Z. Memish, R. Morhard, Deborah Ng, J. Nkengasong, J. Pang, S. Redd, Karen Tan, Wen Yeo (2019)
Preparedness for emerging epidemic threats: a Lancet Infectious Diseases CommissionThe Lancet. Infectious Diseases, 20
( KojomLP SinghV . A review on emerging infectious diseases prioritized under the 2018 WHO research and development blueprint: lessons from the Indian context. Vector Borne Zoonotic Dis 2021; 21: 149–159.33316200)
KojomLP SinghV . A review on emerging infectious diseases prioritized under the 2018 WHO research and development blueprint: lessons from the Indian context. Vector Borne Zoonotic Dis 2021; 21: 149–159.33316200KojomLP SinghV . A review on emerging infectious diseases prioritized under the 2018 WHO research and development blueprint: lessons from the Indian context. Vector Borne Zoonotic Dis 2021; 21: 149–159.33316200, KojomLP SinghV . A review on emerging infectious diseases prioritized under the 2018 WHO research and development blueprint: lessons from the Indian context. Vector Borne Zoonotic Dis 2021; 21: 149–159.33316200
Saguna Verma, Yeung Lo, M. Chapagain, S. Lum, Mukesh Kumar, Ulziijargal Gurjav, H. Luo, Austin Nakatsuka, V. Nerurkar (2009)
West Nile virus infection modulates human brain microvascular endothelial cells tight junction proteins and cell adhesion molecules: Transmigration across the in vitro blood-brain barrier.Virology, 385 2
( LindseyNP SejvarJJ BodeAV , et al. Delayed mortality in a cohort of persons hospitalized with West Nile virus disease in Colorado in 2003. Vector Borne Zoonotic Dis 2012; 12: 230–235.22022816)
LindseyNP SejvarJJ BodeAV , et al. Delayed mortality in a cohort of persons hospitalized with West Nile virus disease in Colorado in 2003. Vector Borne Zoonotic Dis 2012; 12: 230–235.22022816LindseyNP SejvarJJ BodeAV , et al. Delayed mortality in a cohort of persons hospitalized with West Nile virus disease in Colorado in 2003. Vector Borne Zoonotic Dis 2012; 12: 230–235.22022816, LindseyNP SejvarJJ BodeAV , et al. Delayed mortality in a cohort of persons hospitalized with West Nile virus disease in Colorado in 2003. Vector Borne Zoonotic Dis 2012; 12: 230–235.22022816
D. Musso, A. Ko, D. Baud (2019)
Zika Virus Infection - After the Pandemic.The New England journal of medicine, 381 15
( FallG Di PaolaN FayeM , et al. Biological and phylogenetic characteristics of West African lineages of West Nile virus. Plos Negl Trop Dis 2017; 11: e0006078.29117195)
FallG Di PaolaN FayeM , et al. Biological and phylogenetic characteristics of West African lineages of West Nile virus. Plos Negl Trop Dis 2017; 11: e0006078.29117195FallG Di PaolaN FayeM , et al. Biological and phylogenetic characteristics of West African lineages of West Nile virus. Plos Negl Trop Dis 2017; 11: e0006078.29117195, FallG Di PaolaN FayeM , et al. Biological and phylogenetic characteristics of West African lineages of West Nile virus. Plos Negl Trop Dis 2017; 11: e0006078.29117195
( VittorAY LongM ChakrabartyP , et al. West Nile virus-induced neurologic sequelae – relationship to neurodegenerative cascades and dementias. Curr Trop Med Rep 2020; 7: 25–36.32775145)
VittorAY LongM ChakrabartyP , et al. West Nile virus-induced neurologic sequelae – relationship to neurodegenerative cascades and dementias. Curr Trop Med Rep 2020; 7: 25–36.32775145VittorAY LongM ChakrabartyP , et al. West Nile virus-induced neurologic sequelae – relationship to neurodegenerative cascades and dementias. Curr Trop Med Rep 2020; 7: 25–36.32775145, VittorAY LongM ChakrabartyP , et al. West Nile virus-induced neurologic sequelae – relationship to neurodegenerative cascades and dementias. Curr Trop Med Rep 2020; 7: 25–36.32775145
( BogovicP StrleF . Tick-borne encephalitis: a review of epidemiology, clinical characteristics, and management. World J Clin Cases 2015; 3: 430–441.25984517)
BogovicP StrleF . Tick-borne encephalitis: a review of epidemiology, clinical characteristics, and management. World J Clin Cases 2015; 3: 430–441.25984517BogovicP StrleF . Tick-borne encephalitis: a review of epidemiology, clinical characteristics, and management. World J Clin Cases 2015; 3: 430–441.25984517, BogovicP StrleF . Tick-borne encephalitis: a review of epidemiology, clinical characteristics, and management. World J Clin Cases 2015; 3: 430–441.25984517
( BrasilP PereiraJP MoreiraME , et al. Zika virus infection in pregnant women in Rio de Janeiro. N Engl J Med 2016; 375: 2321–2334.26943629)
BrasilP PereiraJP MoreiraME , et al. Zika virus infection in pregnant women in Rio de Janeiro. N Engl J Med 2016; 375: 2321–2334.26943629BrasilP PereiraJP MoreiraME , et al. Zika virus infection in pregnant women in Rio de Janeiro. N Engl J Med 2016; 375: 2321–2334.26943629, BrasilP PereiraJP MoreiraME , et al. Zika virus infection in pregnant women in Rio de Janeiro. N Engl J Med 2016; 375: 2321–2334.26943629
D. Růžek, T. Županc, J. Borde, A. Chrdle, L. Eyer, G. Karganova, I. Kholodilov, N. Knap, L. Kozlovskaya, A. Matveev, Andrew Miller, D. Osolodkin, Anna Överby, N. Tikunova, S. Tkachev, J. Zajkowska (2019)
Tick-borne encephalitis in Europe and Russia: Review of pathogenesis, clinical features, therapy, and vaccines.Antiviral research, 164
M. Desforges, Alain Coupanec, É. Brison, Mathieu Meessen-Pinard, P. Talbot (2014)
Neuroinvasive and Neurotropic Human Respiratory Coronaviruses: Potential Neurovirulent Agents in HumansInfectious Diseases and Nanomedicine I, 807
Takashi Kimura, M. Sasaki, M. Okumura, Eunmi Kim, H. Sawa (2010)
Flavivirus EncephalitisVeterinary Pathology, 47
( DahmT RudolphH SchwerkC , et al. Neuroinvasion and inflammation in viral central nervous system infections. Mediators Inflamm 2016; 2016: 8562805.27313404)
DahmT RudolphH SchwerkC , et al. Neuroinvasion and inflammation in viral central nervous system infections. Mediators Inflamm 2016; 2016: 8562805.27313404DahmT RudolphH SchwerkC , et al. Neuroinvasion and inflammation in viral central nervous system infections. Mediators Inflamm 2016; 2016: 8562805.27313404, DahmT RudolphH SchwerkC , et al. Neuroinvasion and inflammation in viral central nervous system infections. Mediators Inflamm 2016; 2016: 8562805.27313404
John Floridis, Sarah McGuinness, N. Kurucz, J. Burrow, R. Baird, Josh Francis (2018)
Murray Valley Encephalitis Virus: An Ongoing Cause of Encephalitis in Australia’s NorthTropical Medicine and Infectious Disease, 3
M. Patrick, J. Johnston, C. Power (2002)
Lentiviral Neuropathogenesis: Comparative Neuroinvasion, Neurotropism, Neurovirulence, and Host NeurosusceptibilityJournal of Virology, 76
Harpreet Singh, A. Pannu, A. Bhalla, V. Suri, S. Kumari (2019)
Dengue: Uncommon Neurological Presentations of a Common Tropical IllnessIndian Journal of Critical Care Medicine : Peer-reviewed, Official Publication of Indian Society of Critical Care Medicine, 23
E. Simon-Lorière, O. Faye, M. Prot, I. Casadémont, G. Fall, M. Fernandez-Garcia, M. Diagne, J. Kipela, I. Fall, E. Holmes, A. Sakuntabhai, A. Sall (2017)
Autochthonous Japanese Encephalitis with Yellow Fever Coinfection in Africa.The New England journal of medicine, 376 15
J. Birge, S. Sonnesyn (2012)
Powassan Virus Encephalitis, Minnesota, USAEmerging Infectious Diseases, 18
( HussmannKL SamuelMA KimKS , et al. Differential replication of pathogenic and nonpathogenic strains of West Nile virus within astrocytes. J Virol 2013; 87: 2814–2822.23269784)
HussmannKL SamuelMA KimKS , et al. Differential replication of pathogenic and nonpathogenic strains of West Nile virus within astrocytes. J Virol 2013; 87: 2814–2822.23269784HussmannKL SamuelMA KimKS , et al. Differential replication of pathogenic and nonpathogenic strains of West Nile virus within astrocytes. J Virol 2013; 87: 2814–2822.23269784, HussmannKL SamuelMA KimKS , et al. Differential replication of pathogenic and nonpathogenic strains of West Nile virus within astrocytes. J Virol 2013; 87: 2814–2822.23269784
I. Kozlova, T. Demina, S. Tkachev, E. Doroshchenko, O. Lisak, M. Verkhozina, L. Karan, Y. Dzhioev, A. Paramonov, O. Suntsova, Y. Savinova, O. Chernoivanova, D. Růžek, N. Tikunova, V. Zlobin (2018)
CHARACTERISTICS OF THE BAIKAL SUBTYPE OF TICK-BORNE ENCEPHALITIS VIRUS CIRCULATING IN EASTERN SIBERIAActa Biomedica Scientifica (East Siberian Biomedical Journal)
C. Jani, Alexander Walker, O. Omari, D. Patel, Alejandro Heffess, Edward Wolpow, S. Page, Daniel Bourque (2021)
Acute transverse myelitis in West Nile Virus, a rare neurological presentationIDCases, 24
( MehtaA SinghR ManiVE , et al. Japanese B encephalitis. Indian J Crit Care Med 2021; 25(Suppl 2.): S171–S174.34345134)
MehtaA SinghR ManiVE , et al. Japanese B encephalitis. Indian J Crit Care Med 2021; 25(Suppl 2.): S171–S174.34345134MehtaA SinghR ManiVE , et al. Japanese B encephalitis. Indian J Crit Care Med 2021; 25(Suppl 2.): S171–S174.34345134, MehtaA SinghR ManiVE , et al. Japanese B encephalitis. Indian J Crit Care Med 2021; 25(Suppl 2.): S171–S174.34345134
L. Illis (1982)
Viral Infections of the Nervous SystemJournal of Neurology, Neurosurgery & Psychiatry, 45
(2021)
Jameson JL, Fauci AS, Kasper DL, et al
( IwamotoM JerniganDB GuaschA , et al. Transmission of West Nile virus from an organ donor to four transplant recipients. N Eng J Med 2003; 348: 2196–2203.)
IwamotoM JerniganDB GuaschA , et al. Transmission of West Nile virus from an organ donor to four transplant recipients. N Eng J Med 2003; 348: 2196–2203.IwamotoM JerniganDB GuaschA , et al. Transmission of West Nile virus from an organ donor to four transplant recipients. N Eng J Med 2003; 348: 2196–2203., IwamotoM JerniganDB GuaschA , et al. Transmission of West Nile virus from an organ donor to four transplant recipients. N Eng J Med 2003; 348: 2196–2203.
( DaiX ShangG LuS , et al. A new subtype of eastern tick-borne encephalitis virus discovered in Qinghai-Tibet Plateau, China. Emerg Microbes Infect 2018; 7: 1–9.29323102)
DaiX ShangG LuS , et al. A new subtype of eastern tick-borne encephalitis virus discovered in Qinghai-Tibet Plateau, China. Emerg Microbes Infect 2018; 7: 1–9.29323102DaiX ShangG LuS , et al. A new subtype of eastern tick-borne encephalitis virus discovered in Qinghai-Tibet Plateau, China. Emerg Microbes Infect 2018; 7: 1–9.29323102, DaiX ShangG LuS , et al. A new subtype of eastern tick-borne encephalitis virus discovered in Qinghai-Tibet Plateau, China. Emerg Microbes Infect 2018; 7: 1–9.29323102
( AgrelliA de MouraRR CrovellaS , et al. ZIKA virus entry mechanisms in human cells. Infect Genet Evol 2019; 69: 22–29.30658214)
AgrelliA de MouraRR CrovellaS , et al. ZIKA virus entry mechanisms in human cells. Infect Genet Evol 2019; 69: 22–29.30658214AgrelliA de MouraRR CrovellaS , et al. ZIKA virus entry mechanisms in human cells. Infect Genet Evol 2019; 69: 22–29.30658214, AgrelliA de MouraRR CrovellaS , et al. ZIKA virus entry mechanisms in human cells. Infect Genet Evol 2019; 69: 22–29.30658214
( PradhanS GuptaRK SinghMB , et al. Biphasic illness pattern due to early relapse in Japanese-B virus encephalitis. J Neurol Sci 2001; 183: 13–18.11166788)
PradhanS GuptaRK SinghMB , et al. Biphasic illness pattern due to early relapse in Japanese-B virus encephalitis. J Neurol Sci 2001; 183: 13–18.11166788PradhanS GuptaRK SinghMB , et al. Biphasic illness pattern due to early relapse in Japanese-B virus encephalitis. J Neurol Sci 2001; 183: 13–18.11166788, PradhanS GuptaRK SinghMB , et al. Biphasic illness pattern due to early relapse in Japanese-B virus encephalitis. J Neurol Sci 2001; 183: 13–18.11166788
( Japanese encephalitis, https://www.who.int/news-room/fact-sheets/detail/japanese-encephalitis (accessed 18 January 2022).)
Japanese encephalitis, https://www.who.int/news-room/fact-sheets/detail/japanese-encephalitis (accessed 18 January 2022).Japanese encephalitis, https://www.who.int/news-room/fact-sheets/detail/japanese-encephalitis (accessed 18 January 2022)., Japanese encephalitis, https://www.who.int/news-room/fact-sheets/detail/japanese-encephalitis (accessed 18 January 2022).
D. Freitas, R. Souza-Santos, L. Carvalho, W. Barros, L. Neves, P. Brasil, M. Wakimoto (2020)
Congenital Zika syndrome: A systematic reviewPLoS ONE, 15
( MuñozLS BarrerasP PardoCA . Zika virus–associated neurological disease in the adult: Guillain–Barré syndrome, encephalitis, and myelitis. Semin Reprod Med 2016; 34: 273–279.27612158)
MuñozLS BarrerasP PardoCA . Zika virus–associated neurological disease in the adult: Guillain–Barré syndrome, encephalitis, and myelitis. Semin Reprod Med 2016; 34: 273–279.27612158MuñozLS BarrerasP PardoCA . Zika virus–associated neurological disease in the adult: Guillain–Barré syndrome, encephalitis, and myelitis. Semin Reprod Med 2016; 34: 273–279.27612158, MuñozLS BarrerasP PardoCA . Zika virus–associated neurological disease in the adult: Guillain–Barré syndrome, encephalitis, and myelitis. Semin Reprod Med 2016; 34: 273–279.27612158
( DungNM TurtleL ChongWK , et al. An evaluation of the usefulness of neuroimaging for the diagnosis of Japanese encephalitis. J Neurol 2009; 256: 2052–2060.19633907)
DungNM TurtleL ChongWK , et al. An evaluation of the usefulness of neuroimaging for the diagnosis of Japanese encephalitis. J Neurol 2009; 256: 2052–2060.19633907DungNM TurtleL ChongWK , et al. An evaluation of the usefulness of neuroimaging for the diagnosis of Japanese encephalitis. J Neurol 2009; 256: 2052–2060.19633907, DungNM TurtleL ChongWK , et al. An evaluation of the usefulness of neuroimaging for the diagnosis of Japanese encephalitis. J Neurol 2009; 256: 2052–2060.19633907
Ashutosh Singh, A. Mehta, K. Kushwaha, A. Pandey, M. Mittal, B. Sharma, J. Pandey (2016)
Minocycline trial in japanese encephalitis: a double blind, randomized placebo studyPediatric Review: International Journal of Pediatric Research, 3
( Cao-LormeauV-M BlakeA MonsS , et al. Guillain-Barré Syndrome outbreak associated with Zika virus infection in French Polynesia: a case-control study. The Lancet 2016; 387: 1531–1539.)
Cao-LormeauV-M BlakeA MonsS , et al. Guillain-Barré Syndrome outbreak associated with Zika virus infection in French Polynesia: a case-control study. The Lancet 2016; 387: 1531–1539.Cao-LormeauV-M BlakeA MonsS , et al. Guillain-Barré Syndrome outbreak associated with Zika virus infection in French Polynesia: a case-control study. The Lancet 2016; 387: 1531–1539., Cao-LormeauV-M BlakeA MonsS , et al. Guillain-Barré Syndrome outbreak associated with Zika virus infection in French Polynesia: a case-control study. The Lancet 2016; 387: 1531–1539.
Leslie Goo, Kari Debbink, Nurgun Kose, G. Sapparapu, M. Doyle, Alex Wessel, Justin Richner, Katherine Burgomaster, Bridget Larman, Kimberly Dowd, M. Diamond, J. Crowe, T. Pierson (2018)
A potently neutralizing human monoclonal antibody targeting an epitope in the West Nile virus E protein preferentially recognizes mature virionsNature microbiology, 4
Who Publication (2011)
Vaccines against tick-borne encephalitis: WHO position paper.Releve epidemiologique hebdomadaire, 86 24
( HciniN KugbeY RafalimananaZHL , et al. Association between confirmed congenital Zika infection at birth and outcomes up to 3 years of life. Nat Commun 2021; 12: 3270.34075035)
HciniN KugbeY RafalimananaZHL , et al. Association between confirmed congenital Zika infection at birth and outcomes up to 3 years of life. Nat Commun 2021; 12: 3270.34075035HciniN KugbeY RafalimananaZHL , et al. Association between confirmed congenital Zika infection at birth and outcomes up to 3 years of life. Nat Commun 2021; 12: 3270.34075035, HciniN KugbeY RafalimananaZHL , et al. Association between confirmed congenital Zika infection at birth and outcomes up to 3 years of life. Nat Commun 2021; 12: 3270.34075035
( KaiserR . Tick-borne Encephalitis – still a serious disease? Wien Med Wochenschr 2012; 162: 229–229.22695812)
KaiserR . Tick-borne Encephalitis – still a serious disease? Wien Med Wochenschr 2012; 162: 229–229.22695812KaiserR . Tick-borne Encephalitis – still a serious disease? Wien Med Wochenschr 2012; 162: 229–229.22695812, KaiserR . Tick-borne Encephalitis – still a serious disease? Wien Med Wochenschr 2012; 162: 229–229.22695812
The COVID-19 pandemic has shed light on the challenges we face as a global society in preventing and containing emerging and re-emerging pathogens. Multiple intersecting factors, including environmental changes, host immunological factors, and pathogen dynamics, are intimately connected to the emergence and re-emergence of communicable diseases. There is a large and expanding list of communicable diseases that can cause neurological damage, either through direct or indirect routes. Novel pathogens of neurotropic potential have been identified through advanced diagnostic techniques, including metagenomic next-generation sequencing, but there are also known pathogens which have expanded their geographic distribution to infect non-immune individuals. Factors including population growth, climate change, the increase in animal and human interface, and an increase in international travel and trade are contributing to the expansion of emerging and re-emerging pathogens. Challenges exist around antimicrobial misuse giving rise to antimicrobial-resistant infectious neurotropic organisms and increased susceptibility to infection related to the expanded use of immunomodulatory treatments. In this article, we will review key concepts around emerging and re-emerging pathogens and discuss factors associated with neurotropism and neuroinvasion. We highlight several neurotropic pathogens of interest, including West Nile virus (WNV), Zika Virus, Japanese Encephalitis Virus (JEV), and Tick-Borne Encephalitis Virus (TBEV). We emphasize neuroinfectious diseases which impact the central nervous system (CNS) and focus on flaviviruses, a group of vector-borne pathogens that have expanded globally in recent years and have proven capable of widespread outbreak.
Therapeutic Advances in Infectious Disease – SAGE
Published: Jun 1, 2022
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