TY - JOUR
AU - de Almeida, Sandro Rogério
AB - Introduction Chromoblastomycosis is a chronic fungal infection primarily affecting the skin and subcutaneous tissues. It is caused by several species of dematiaceous fungi such as Cladophialophora, Exophiala, Fonsecaea, Phialophora, and Rhinocladiella. F. pedrosoi, F. monophora, and F. nubica represent three cryptic entities that could induce the same disease [1–4]. Fonsecaea pedrosoi and F. nubica are associated with muriform cell formation in chromoblastomycosis, whereas F. monophora could be involved in dissemination to the brain and other organs with hyphae in tissue [5]. Recently, some cases have been confirmed caused by Fonsecaea monophora [6,7]. These fungi are found in soil, decaying vegetation, and wood, particularly in tropical and subtropical regions. The infection typically begins following traumatic inoculation of fungal spores into the skin, often through minor injuries like cuts, scratches, or thorn pricks. Once inoculated, the fungi establish a chronic infection characterized by the formation of verrucous or nodular lesions on exposed areas of the body, most commonly the lower extremities. [8,9]. The severity of disease is graded according to number, extension, and dissemination of the lesions as described by Queiro-Telles et al. [10]. In general, the treatment of chromoblastomycosis is a therapeutic challenge because various methods and antimicrobials are used in attempts to cure or control the disease, but most of them fail. There are many cases of relapse and few reports of ultimate cures [4,11]. The immune response to chromoblastomycosis involves both innate and adaptive components. Our laboratory showed that PBMC from patients with severe forms of chromoblastomycosis failed to proliferate in vitro after induction with chromoAg and produced high levels of IL-10 and low levels of IFN-γ [12]. In contrast, cells from patients with mild forms of the disease efficiently induced T-cell proliferation and IFN-γ production. These results suggest that the Th1 response is essential to induce protective immunity during chromoblastomycosis. The recognition of pathogens is a severe challenge to the innate immune system due to the enormous variability and characteristically high rate of mutation of microorganisms. However, the innate immune system has evolved receptors, which target molecular structures common to large groups of pathogens or produced by pathogens, not the host. These structures are called pathogen-associated molecular patterns (PAMPs). The PAMPs are recognized by receptors called pattern recognition receptors (PRRs). Members of several family proteins function as PRRs and are expressed in cells responsible for the first line of defense of the body, such as macrophages and dendritic cells [13]. Caspase-1 is produced as a zymogen, called pro-caspase-1, cleaved into two subunits of 20-kDa (p20) and 10 kDa (p10). This event transforms the zymogen into an active enzyme that can cleave proteins at specific regions, such as the IL-1β and IL-18 cytokines [14,15]. Interleukin-18 (IL-18) is a pro-inflammatory cytokine that plays a crucial role in regulating immune responses, particularly those involving T cells and natural killer (NK) cells. It is a member of the interleukin-1 (IL-1) superfamily and is produced by various cell types, including macrophages, dendritic cells, epithelial cells, and endothelial cells, in response to microbial products, inflammatory stimuli, or other cytokines. IL-18 is synthesized as an inactive precursor protein (pro-IL-18) and requires proteolytic processing by caspase-1, which is activated by multiprotein complexes known as inflammasomes, to become biologically active [16]. The primary function of IL-18 is to induce the production of interferon-gamma (IFNγ), another important pro-inflammatory cytokine, mainly from T cells and NK cells. This makes IL-18 a potent inducer of Th1 responses, which are characterized by the activation of CD4+ T cells to produce IFNγ and promote cell-mediated immunity against intracellular pathogens, including bacteria, viruses, and fungi. Our laboratory [17] showed that macrophages infected by F. pedrosoi and R. aquaspersa, the etiological agents of chromoblastomycosis, induced the production of inflammatory cytokines such as IL-1β and TNF-α. De Castro et al. 2017, showed that F. pedrosoi hyphae, induce IL-1β secretion in bone marrow-derived dendritic cells and macrophages. IL-1β production was NLRP3-dependent inflammasome activation, which required potassium efflux, reactive oxygen species production, phagolysosomal acidification, and cathepsin B release as triggers. However, there is no data on the importance of IL-18 in activating Th cells during chromoblastomycosis. Our results indicate that F. pedrosoi is sensed by the NLRP3 inflammasome, which induces caspase-1 activation and a proinflammatory response. Moreover, we showed that IL-18 is required to activate the Th1 response and control fungal loads during chromoblastomycosis. Materials & methods Microorganism The isolate of F. pedrosoi (CBS125763) was used for the present investigation. Stock cultures were maintained on Sabouraud-dextrose-agar (SDA), under oil at 4oC, with transfer every six months. Conidia of F. pedrosoi To obtain large numbers of conidia, fungal fragments from the Sabouraud medium were scraped off the agar and incubated in Potato-broth medium, which consisted of 50 g of potatoes, 5 g of glucose (MERCK – Germany), and 500 mL of distilled water at 25°C under constant rotation for four days. The fungal suspension was then filtered through a sterile Whatman #1 filter to remove hyphal fragments but not microconidia. The conidia were washed with PBS and counted in a hemocytometer. Animals Wild-type male C57BL/6 mice, 8–12 weeks old, were provided from the Faculty of Pharmaceutical Sciences, University of São Paulo (USP) animal facilities. Male C57BL/6 mice, 8–12 weeks old, knocked out individually for NLRP3, IFN-γ, Caspase-1/-11, or IL-18 were obtained from the animal facilities at the School of Medicine of Ribeirão Preto (University of São Paulo). The Institutional Ethics Committee previously approved the experimental protocols involving animals for Animal Care and Research at the Faculty of Pharmaceutical Sciences (Protocols no: 057). The in vivo experiments were carried out following the recommendations of the ARRIVE Guidelines and the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The animals were maintained in an SPF environment and housed in temperature-controlled rooms at 23–25 °C with food and water ad-libitum throughout the experiments. The euthanasia procedure was performed according to the American Veterinary Medical Association Guidelines for the Euthanasia of Animals (2020), using the overdose of ketamine and xylazine method. Bone Marrow-Derived Macrophages (BMDMs) BMDMs were obtained as described [18]. Briefly, bone marrow from the femurs of C57BL/6 mice was collected and cultured in R20/30 media, which is RPMI-1640 medium supplemented with 20% FBS, 30% L929-cell conditioned medium (LCCM) and gentamicin (40 mg/L), at 37°C in a 5% CO2 atmosphere. After four days, the cells were supplemented with the same medium and incubated for three more days. Macrophages were collected and incubated in R10/5 media, RPMI-1640 medium supplemented with 10% FBS, 5% LCCM and gentamicin (40 mg/L), at 37°C in a 5% CO2 atmosphere. To validate the participation of K+ efflux or ROS production on the activation of the inflammasome, the BMDMs were treated for 2 h before the infection with 130 mM potassium chloride or 5 mM N-acetylcysteine (NAC) or 100 µM APDC (2R,4R)-4 aminopyrrolidine-2,4-dicarboxylic acid. To evaluate the importance of endosomal acidification on the activation of inflammasomes, the BMDMs were treated for 2 h before the infection with 50 µM of cathepsin B inhibitor CA-074Me or 250 nM of inhibitor bafilomycin. Interaction between BMDMs and F. pedrosoi in vitro BMDMs were plated over glass slides in 24-wells plates and kept overnight at 37°C and 5% CO2 to allow cell adhesion. F. pedrosoi conidia produced as described above were diluted in fresh R10/5 media and incubated with the BMDMs at a MOI of 1:5. The systems were maintained at 37°C and 5% CO2 for 12 hours. After 12 h, the supernatants were collected and centrifuged at 3000 rpm for 10 minutes and stored for cytokine measurements. Infection assays In this work we used the murine chronic model of chromoblastomycosis described by Cardona-Castro et al. 1999 [19]. The C57BL/6 mice, received an intraperitoneal (i.p.) injection of 1 ml of PBS (the control) or 2 x 107 conidia of F. pedrosoi. After 14 days post-infection, the animals were sacrificed, and the spleen and liver were removed for fungal quantification and measurement of cytokines in the organs’ supernatants. Colony Forming Units (CFUs) To evaluate the in vivo survival of fungal infections, the spleen and liver were macerated in PBS surface seeded onto plates containing Sabouraud agar. It incubated at 37 ° C for 14 days to count the colony-forming units (CFUs). Quantification of cytokines All cytokines were measured by ELISA using monoclonal antibody capture and detection against cytokine concentrations recommended by the manufacturer (R & D Systems). Flow cytometry The cells from the spleen and liver were stained with Abs specific for the surface molecules CD3 and CD4 and for the intracellular cytokine IFN-γ. For the intracellular cytokine staining, the cells were previously permeabilized using 1× PBS containing 1% FBS, 0.1% sodium azide, and 0.2% saponin. The cellular data were acquired using a FACSCanto II flow cytometer, and data were analyzed using FlowJo software (Tree Star, Ashland, OR). Statistical analysis Data were expressed as mean+s.e.m. and analyzed in the software GraphPad Prism (version 5.00 for Windows, GraphPad Software, San Diego California USA, www.graphpad.com). For data analysis, the following statistical tests were used: Two-way ANOVA and Bonferroni post test, and Paired t-test. Differences were considered statistically significant at p<0.05. Microorganism The isolate of F. pedrosoi (CBS125763) was used for the present investigation. Stock cultures were maintained on Sabouraud-dextrose-agar (SDA), under oil at 4oC, with transfer every six months. Conidia of F. pedrosoi To obtain large numbers of conidia, fungal fragments from the Sabouraud medium were scraped off the agar and incubated in Potato-broth medium, which consisted of 50 g of potatoes, 5 g of glucose (MERCK – Germany), and 500 mL of distilled water at 25°C under constant rotation for four days. The fungal suspension was then filtered through a sterile Whatman #1 filter to remove hyphal fragments but not microconidia. The conidia were washed with PBS and counted in a hemocytometer. Animals Wild-type male C57BL/6 mice, 8–12 weeks old, were provided from the Faculty of Pharmaceutical Sciences, University of São Paulo (USP) animal facilities. Male C57BL/6 mice, 8–12 weeks old, knocked out individually for NLRP3, IFN-γ, Caspase-1/-11, or IL-18 were obtained from the animal facilities at the School of Medicine of Ribeirão Preto (University of São Paulo). The Institutional Ethics Committee previously approved the experimental protocols involving animals for Animal Care and Research at the Faculty of Pharmaceutical Sciences (Protocols no: 057). The in vivo experiments were carried out following the recommendations of the ARRIVE Guidelines and the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The animals were maintained in an SPF environment and housed in temperature-controlled rooms at 23–25 °C with food and water ad-libitum throughout the experiments. The euthanasia procedure was performed according to the American Veterinary Medical Association Guidelines for the Euthanasia of Animals (2020), using the overdose of ketamine and xylazine method. Bone Marrow-Derived Macrophages (BMDMs) BMDMs were obtained as described [18]. Briefly, bone marrow from the femurs of C57BL/6 mice was collected and cultured in R20/30 media, which is RPMI-1640 medium supplemented with 20% FBS, 30% L929-cell conditioned medium (LCCM) and gentamicin (40 mg/L), at 37°C in a 5% CO2 atmosphere. After four days, the cells were supplemented with the same medium and incubated for three more days. Macrophages were collected and incubated in R10/5 media, RPMI-1640 medium supplemented with 10% FBS, 5% LCCM and gentamicin (40 mg/L), at 37°C in a 5% CO2 atmosphere. To validate the participation of K+ efflux or ROS production on the activation of the inflammasome, the BMDMs were treated for 2 h before the infection with 130 mM potassium chloride or 5 mM N-acetylcysteine (NAC) or 100 µM APDC (2R,4R)-4 aminopyrrolidine-2,4-dicarboxylic acid. To evaluate the importance of endosomal acidification on the activation of inflammasomes, the BMDMs were treated for 2 h before the infection with 50 µM of cathepsin B inhibitor CA-074Me or 250 nM of inhibitor bafilomycin. Interaction between BMDMs and F. pedrosoi in vitro BMDMs were plated over glass slides in 24-wells plates and kept overnight at 37°C and 5% CO2 to allow cell adhesion. F. pedrosoi conidia produced as described above were diluted in fresh R10/5 media and incubated with the BMDMs at a MOI of 1:5. The systems were maintained at 37°C and 5% CO2 for 12 hours. After 12 h, the supernatants were collected and centrifuged at 3000 rpm for 10 minutes and stored for cytokine measurements. Infection assays In this work we used the murine chronic model of chromoblastomycosis described by Cardona-Castro et al. 1999 [19]. The C57BL/6 mice, received an intraperitoneal (i.p.) injection of 1 ml of PBS (the control) or 2 x 107 conidia of F. pedrosoi. After 14 days post-infection, the animals were sacrificed, and the spleen and liver were removed for fungal quantification and measurement of cytokines in the organs’ supernatants. Colony Forming Units (CFUs) To evaluate the in vivo survival of fungal infections, the spleen and liver were macerated in PBS surface seeded onto plates containing Sabouraud agar. It incubated at 37 ° C for 14 days to count the colony-forming units (CFUs). Quantification of cytokines All cytokines were measured by ELISA using monoclonal antibody capture and detection against cytokine concentrations recommended by the manufacturer (R & D Systems). Flow cytometry The cells from the spleen and liver were stained with Abs specific for the surface molecules CD3 and CD4 and for the intracellular cytokine IFN-γ. For the intracellular cytokine staining, the cells were previously permeabilized using 1× PBS containing 1% FBS, 0.1% sodium azide, and 0.2% saponin. The cellular data were acquired using a FACSCanto II flow cytometer, and data were analyzed using FlowJo software (Tree Star, Ashland, OR). Statistical analysis Data were expressed as mean+s.e.m. and analyzed in the software GraphPad Prism (version 5.00 for Windows, GraphPad Software, San Diego California USA, www.graphpad.com). For data analysis, the following statistical tests were used: Two-way ANOVA and Bonferroni post test, and Paired t-test. Differences were considered statistically significant at p<0.05. Results IL-18 production by macrophages in the presence of F. pedrosoi is dependent on NLRP3 and Caspase-1 First, we evaluated the production of anti and proinflammatory cytokines by BMDM in the presence of F. pedrosoi. The results showed that F. pedrosoi induces the production of TNF-α, IL-1-β and IL-18 by macrophages from C57BL/6 mice. No significant differences were observed in the secretion of IL-10 and IL-12 (Fig 1A). The next step was to evaluate the participation of caspase-1 and NLRP3 in IL-18 secretion by macrophages in the presence of F. pedrosoi. For this, the macrophages from wild-type C57BL/6 mice and caspase-1 and NLRP3 knockouts C57BL/6 mice were infected for 12 hours, and IL-18 production was monitored. The activation of caspase-1 in response to F. pedrosoi was dependent on NLRP3 because the secretion of IL-18 from macrophages of NLRP3 and caspase-1 KO animals was significantly lower when compared with that of wild-type macrophages (Fig 1B). As expected, TNF-α production by macrophages infected by F. pedrosoi is independent of caspase-1 and NLRP3, because no difference in TNF-α production was observed between WT and KO macrophages (Fig 1C). Our results showed that K+ efflux, lysosomal acidification, cathepsin B activity, and ROS production interfere with IL-18 secretion, but not with TNF-α production (Fig 1D and 1E). Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 1. NLRP3 and Caspase-1 deficiency reduces IL-18 secretion by BMDMs, but not TNF-α. BMDMs from C57BL/6 mice were incubated with F. pedrosoi conidia for 12 h, and MOI 1:5, and TNF-α, IL-1β, IL-12, IL-10, and IL-18 were detected by ELISA (A). BMDMs from NLRP3-/- or Caspase-1/11-/- C57BL/6 mice were incubated with F. pedrosoi conidia for 12 h and MOI 1:5. (B) IL-18 production by BMDMs from NLRP3-/- or Caspase-1/11-/- C57BL/6 mice (C) TNF-α. NLRP3 inflammasome activation by F. pedrosoi requires lysosomal acidification, K+ efflux, and the release of cathepsin B. BMDMs from C57BL/6 mice were incubated with KCL 130 mM (block of K+ efflux), NAC 5 mM or APDC 100μM (ROS depletion), or Bafilomycin A 250 nM or CA-074 50 μM (lysosomal acidification), or without inhibitor (control) for 2 hours before the infection with F. pedrosoi and IL-18 (D) and TNF-α (E) determined. Results are expressed as mean ± SEM. Two-way ANOVA and Bonferroni post test: * p<0.05 when compared with control. Cytokine data pooled from three independent experiments performed in triplicate wells each are shown. https://doi.org/10.1371/journal.pone.0322127.g001 The control of chromoblastomycosis is dependent on IFN-γ Our laboratory showed that patients with a severe form of chromoblastomycosis presented a low level of IFN-γ, but on the other hand, patients with a mild form presented a high level of IFN-γ [12]. This result suggests that IFN-γ is essential to control the disease. To confirm the importance of IFN-γ in the control of infection, we conducted experiments using C57BL/6 mice KO to IFN-γ. As expected, our results showed that animals deficient in IFNγ production had a high fungal burden when compared with control animals (Fig 2). Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 2. Systemic chromoblastomycosis in mice deficient to IFN-γ. Animals IFN-γ KO were infected i.p. with 2 x107 conidia of F. pedrosoi, and after 14 days post-infection, the spleen and liver were removed, and fungal burden was determined by CFU. Data expressed as mean ± SEM. CFU data were pooled from three independent experiments performed. * p<0.05 when compared with WT mice (C57Bl6). https://doi.org/10.1371/journal.pone.0322127.g002 IL-18 is essential for the control of chromoblastomycosis The next step was to evaluate the participation of IL-18 in the control of infection by F. pedrosoi. Then, we analyzed F. pedrosoi infections in C57BL/6 mice KO mice lacking functional IL-18 genes. Our results showed that IL-18 is essential for the control of infection because the absence of this cytokine results in a severe infection (Fig 3A). When we analyzed the cytokine production, it was possible to observe a significant decrease in IFN-γ output in the organs of KO mice when compared with normal mice (Fig 3B). Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 3. A-Chromoblastomycosis in mice deficient in IL-18. Animals were infected i.p. with 2 x107 conidia of F. pedrosoi, and after 14 days post-infection, the spleen and liver were removed, and fungal burden was determined by CFU. Data expressed as mean ± SEM. CFU data were pooled from three independent experiments performed. * p<0.05 when compared with WT mice (C57Bl6). Fig 3 B- Mice deficient in IL-18 show decreased production of IFN-γ in response to F. pedrosoi. Animals were infected i.p. with F. pedrosoi conidia, and cytokines levels (IFN-γ; IL-10 and IL-17) were determined in spleen and liver homogenates 14 days post-infection. https://doi.org/10.1371/journal.pone.0322127.g003 Animals deficient in IL-18 presented decreased Th1 cells Several papers have shown that IL-12 and IL-18 are essential for inducing a vigorous Th-1 response [20–23]. In order to evaluate the importance of IL-18 in inducing Th1 cells, we analyzed the percentage of IFNγ–CD4+ T cells in the organs of infected animals and deficient to IL-18. Our results show a significant decrease of Th1 cells in the organs of C57BL/6 KO mice suggests that IL-18 is implicated in the induction of a Th1 response and control of chromoblastomycosis (Fig 4). Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 4. Mice deficient in IL-18 show decreased IFN-γ-CD4 T cells in response to F. pedrosoi. After infection, the cells from the spleen and liver were stained with Abs specific for the surface molecules CD3 and CD4 and the intracellular cytokine IFN-γ. The cellular data were acquired using a FACSCanto II flow cytometer, and data were analyzed using FlowJo software. Two-way ANOVA and Bonferroni posttest: * p<0.05 compared to WT mice. https://doi.org/10.1371/journal.pone.0322127.g004 IL-18 production by macrophages in the presence of F. pedrosoi is dependent on NLRP3 and Caspase-1 First, we evaluated the production of anti and proinflammatory cytokines by BMDM in the presence of F. pedrosoi. The results showed that F. pedrosoi induces the production of TNF-α, IL-1-β and IL-18 by macrophages from C57BL/6 mice. No significant differences were observed in the secretion of IL-10 and IL-12 (Fig 1A). The next step was to evaluate the participation of caspase-1 and NLRP3 in IL-18 secretion by macrophages in the presence of F. pedrosoi. For this, the macrophages from wild-type C57BL/6 mice and caspase-1 and NLRP3 knockouts C57BL/6 mice were infected for 12 hours, and IL-18 production was monitored. The activation of caspase-1 in response to F. pedrosoi was dependent on NLRP3 because the secretion of IL-18 from macrophages of NLRP3 and caspase-1 KO animals was significantly lower when compared with that of wild-type macrophages (Fig 1B). As expected, TNF-α production by macrophages infected by F. pedrosoi is independent of caspase-1 and NLRP3, because no difference in TNF-α production was observed between WT and KO macrophages (Fig 1C). Our results showed that K+ efflux, lysosomal acidification, cathepsin B activity, and ROS production interfere with IL-18 secretion, but not with TNF-α production (Fig 1D and 1E). Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 1. NLRP3 and Caspase-1 deficiency reduces IL-18 secretion by BMDMs, but not TNF-α. BMDMs from C57BL/6 mice were incubated with F. pedrosoi conidia for 12 h, and MOI 1:5, and TNF-α, IL-1β, IL-12, IL-10, and IL-18 were detected by ELISA (A). BMDMs from NLRP3-/- or Caspase-1/11-/- C57BL/6 mice were incubated with F. pedrosoi conidia for 12 h and MOI 1:5. (B) IL-18 production by BMDMs from NLRP3-/- or Caspase-1/11-/- C57BL/6 mice (C) TNF-α. NLRP3 inflammasome activation by F. pedrosoi requires lysosomal acidification, K+ efflux, and the release of cathepsin B. BMDMs from C57BL/6 mice were incubated with KCL 130 mM (block of K+ efflux), NAC 5 mM or APDC 100μM (ROS depletion), or Bafilomycin A 250 nM or CA-074 50 μM (lysosomal acidification), or without inhibitor (control) for 2 hours before the infection with F. pedrosoi and IL-18 (D) and TNF-α (E) determined. Results are expressed as mean ± SEM. Two-way ANOVA and Bonferroni post test: * p<0.05 when compared with control. Cytokine data pooled from three independent experiments performed in triplicate wells each are shown. https://doi.org/10.1371/journal.pone.0322127.g001 The control of chromoblastomycosis is dependent on IFN-γ Our laboratory showed that patients with a severe form of chromoblastomycosis presented a low level of IFN-γ, but on the other hand, patients with a mild form presented a high level of IFN-γ [12]. This result suggests that IFN-γ is essential to control the disease. To confirm the importance of IFN-γ in the control of infection, we conducted experiments using C57BL/6 mice KO to IFN-γ. As expected, our results showed that animals deficient in IFNγ production had a high fungal burden when compared with control animals (Fig 2). Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 2. Systemic chromoblastomycosis in mice deficient to IFN-γ. Animals IFN-γ KO were infected i.p. with 2 x107 conidia of F. pedrosoi, and after 14 days post-infection, the spleen and liver were removed, and fungal burden was determined by CFU. Data expressed as mean ± SEM. CFU data were pooled from three independent experiments performed. * p<0.05 when compared with WT mice (C57Bl6). https://doi.org/10.1371/journal.pone.0322127.g002 IL-18 is essential for the control of chromoblastomycosis The next step was to evaluate the participation of IL-18 in the control of infection by F. pedrosoi. Then, we analyzed F. pedrosoi infections in C57BL/6 mice KO mice lacking functional IL-18 genes. Our results showed that IL-18 is essential for the control of infection because the absence of this cytokine results in a severe infection (Fig 3A). When we analyzed the cytokine production, it was possible to observe a significant decrease in IFN-γ output in the organs of KO mice when compared with normal mice (Fig 3B). Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 3. A-Chromoblastomycosis in mice deficient in IL-18. Animals were infected i.p. with 2 x107 conidia of F. pedrosoi, and after 14 days post-infection, the spleen and liver were removed, and fungal burden was determined by CFU. Data expressed as mean ± SEM. CFU data were pooled from three independent experiments performed. * p<0.05 when compared with WT mice (C57Bl6). Fig 3 B- Mice deficient in IL-18 show decreased production of IFN-γ in response to F. pedrosoi. Animals were infected i.p. with F. pedrosoi conidia, and cytokines levels (IFN-γ; IL-10 and IL-17) were determined in spleen and liver homogenates 14 days post-infection. https://doi.org/10.1371/journal.pone.0322127.g003 Animals deficient in IL-18 presented decreased Th1 cells Several papers have shown that IL-12 and IL-18 are essential for inducing a vigorous Th-1 response [20–23]. In order to evaluate the importance of IL-18 in inducing Th1 cells, we analyzed the percentage of IFNγ–CD4+ T cells in the organs of infected animals and deficient to IL-18. Our results show a significant decrease of Th1 cells in the organs of C57BL/6 KO mice suggests that IL-18 is implicated in the induction of a Th1 response and control of chromoblastomycosis (Fig 4). Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 4. Mice deficient in IL-18 show decreased IFN-γ-CD4 T cells in response to F. pedrosoi. After infection, the cells from the spleen and liver were stained with Abs specific for the surface molecules CD3 and CD4 and the intracellular cytokine IFN-γ. The cellular data were acquired using a FACSCanto II flow cytometer, and data were analyzed using FlowJo software. Two-way ANOVA and Bonferroni posttest: * p<0.05 compared to WT mice. https://doi.org/10.1371/journal.pone.0322127.g004 Discussion The expansion of a subpopulation of T-cells (Th1, Th2, and Th17) for infection control is significant, as specific pathogens are more effectively controlled by Th1 and Th17 cells and others more effectively by a Th2 response. Recent studies have shown that cellular Th1 and Th17 responses induced by Candida albicans prevent the spread of disease [24–27]. In our study, we found that F. pedrosoi triggered the activation of caspase-1 and the production of IL-18 in vitro. Additionally, we observed that IL-18 secretion was reduced in the absence of NLRP3. NLRP3 has been associated with the response against other fungal pathogens, such as Candida albicans [28], Aspergillus fumigatus [29], Paracoccidioides brasiliensis [30] and dermatophytes such as Trichophyton rubrum [18] and Microsporum canis [31]. In accordance with recent publications, our results show that F. pedrosoi also induces IL-18 through this inflammasome and support the notion that NLRP3 may be a critical fungal sensor. Different processes associated with intracellular perturbations have been implicated in NLRP3 inflammasome activation, including K+ cation efflux, ROS generation, lysosomal acidification, and the release of cathepsin B into the cytosol. When the macrophages were treated with NAC or APDC a significant decrease in cytokine production was observed, demonstrating that neither K+ efflux blockade nor ROS depletion interferes with IL-18 secretion. In the same way, when BMDMs were treated with bafilomycin, which inhibits the vacuolar H+ ATPase, or CA-074, which inhibits cathepsin B activity, was observed a significant decrease of IL-18 secretion. It is essential to point out here that the systemic mouse model of chromoblastomycosis used in this work is not an accurate representation of the human subcutaneous infection, but it is thought to be the best model for studying the chronic nature of this disease [19]. Moreover, the systemic infection is chronic in mice, and the pathogen persists for many weeks in the organs of untreated animals. Therefore, this model becomes essential for studying humoral and cellular immunological mechanisms during the disease’s and host’s evolution. Some studies have shown that caspase–1–dependent cytokines exert essential effects on the initiation of the adaptive Th1 and Th17 cellular responses to fungal infection [32]. Previously, our group showed that IFN-γ is an important cytokine involved in immune defenses during chromoblastomycosis [33–35]; therefore, we speculated that IFN-γ could play a role in the central mechanism regulated by caspase-1 after F. pedrosoi infection. Confirming this hypothesis, the Th1 response, mainly IFN-γ-T-CD4+ cells, was lower in infected Il-18-/− mice compared with the wild-type. Therefore, we suggest that the IL-18−/− mice were susceptible to chromoblastomycosis because they exhibited reduced Th1 (and not Th17) immunity. In the context of Th-1 differentiation, caspase-1, via the NLRP3 inflammasome, is required to produce IL-18, which then induces IFN-γ and promotes the efficient killing of the pathogen. Recent studies have shown the importance of IL-18 for the resistance to infection by many pathogens, including Paracoccidioides brasiliensis [36], Burkholderia pseudomallei [37] and Streptococcus pneumoniae [38]. Ketelut-Carneiro et al. [36] showed that Il18−/− mice were profoundly vulnerable to paracoccidioidomycosis (PCM), but that, surprisingly, Il1r1−/− mice had mortality rates similar to wild-type mice. Thus, the role of IL-18 during PCM is related to its ability to induce IFN-γ. Our data showed that Il18−/− mice were more susceptible to infection, which was mediated by the decrease in IFN-γ production. Consistent with our data, IL-18 is upregulated in a caspase–1–dependent manner in response to C. albicans and to mediate the development of protective Th1 immunity [32,39]. Understanding the role of IL-18 in the immune response to fungal infections may have implications for developing novel therapeutic approaches, such as targeting IL-18 signaling pathways to modulate the immune response and improve outcomes in patients with fungal infections. In conclusion, the present data demonstrate, for the first time, that the inflammasome is activated and that NLRP3 and caspase-1 mediated the F. pedrosoi-induced production of IL-18, which promotes the Th-1-mediated immune response during chromoblastomycosis. Acknowledgments We thank Maira Cristina Nakamura and Dario Simões Zamboni from the School of Medicine of Ribeirão Preto (University of São Paulo) for providing knockout animals.
TI - IL-18 production is required for the generation of a Th1 response during experimental chromoblastomycosis
JO - PLoS ONE
DO - 10.1371/journal.pone.0322127
DA - 2025-05-02
UR - https://www.deepdyve.com/lp/public-library-of-science-plos-journal/il-18-production-is-required-for-the-generation-of-a-th1-response-6PoBAzgYq3
SP - e0322127
VL - 20
IS - 5
DP - DeepDyve
ER -