TY - JOUR
AB - Introduction Soil-transmitted helminthiasis (STH) affects up to one in four individuals in the world, disproportionately impacting impoverished populations with less access to clean water, sanitation, and opportunities for socioeconomic development [1]. Strongyloidiasis is one of the most neglected tropical diseases [2,3]. Estimates of the number of people infected with the causative agent Strongyloides stercoralis vary and go up to 370 million worldwide [2,4,5]. The local prevalence can reach more than 40% in some tropical and subtropical countries [3,6]. Factors such as high temperature, high moisture, poor sanitation and sharing premises with domestic animals may contribute to high prevalence of S. stercoralis [3,7,8]. S. stercoralis is the major causative agent of human strongyloidiasis [9] but there are also reports of people infected with Strongyloides fuelleborni and Strongyloides fuelleborni kellyi, in Africa and in Papua New Guinea [9]. Based on molecular data, S. fuelleborni kellyi should probably be considered an independent species rather than a subspecies of S. fuelleborni, [10]. Although S. stercoralis infection frequently remains asymptomatic, immuno-compromised patients can develop a systemic infection, which may lead to fatal forms of strongyloidiasis. The medical relevance of this parasite has probably been grossly underestimated due to difficulty of diagnosis [4,5,11]. Also, it should be noted that Strongyloides is not limited to tropical and underdeveloped areas, and the presence of S. stercoralis and fatal cases caused by it have also been reported from well-developed regions with temperate climates such as the European Union and North America [12–18]. S. stercoralis has a complex, rather unique life cycle (Fig 1) consisting of parasitic and free-living generations [19–21]. In brief: infective third stage larvae (L3i), which are all females, invade a new host by skin penetration and, after migrating through the blood and the lungs, are coughed up and swallowed and eventually establish in the small intestine of the host. The parasitic adult females reproduce by parthenogenesis. The progeny of the parasitic females have four developmental options: 1) Firstly, they may become female, and develop into infective third stage larvae (iL3) within the host and re-infect the same host individual (autoinfective cycle); 2) Secondly, they may become female, but this time leave the host as first-stage larvae, develop into iL3 and search for a new host (direct/homogonic development); 3) Thirdly, they may become female and leave the host, but this time develop into free-living, non-infective third stage larvae and subsequently into adult females (indirect/heterogonic development); 4) Or fourthly, they become male and leave the host and develop into free-living adult males (indirect/heterogonic cycle). The free-living adults mate and reproduce in the environment and all their progeny are females and develop to iL3s. No male iL3s have been reported in any Strongyloides species. For two species of Strongyloides (Strongyloides ratti and Strongyloides papillosus), it has been shown that the reproduction in the free-living generation is sexual, in spite of some earlier literature that had described it as pseudogamic (by sperm dependent parthenogenesis) [22–24]. For S. stercoralis prior to this report no genetic analysis of the mode of reproduction had been conducted and non-sexual (pseudogamic) reproduction as proposed based on cytological observations remained an option [25,26]. Whilst all species of Strongyloides may undergo homogonic or heterogonic development, the autoinfective cycle (option 1) appears to be specific for S. stercoralis and maybe a few other less well-investigated species [19]. This autoinfective cycle allows the parasite to persist in a particular host individual for many years, much longer than the life expectancy of an individual worm. Usually, healthy individuals tolerate such long lasting infections well and control them at very low levels [5]. These people have no clinical symptoms and the infection is unlikely to be detected. However, if such a chronically infected person becomes immunodeficient due to disease or immunosuppressive treatment (i.e. cancer chemotherapy or organ transplantation), this may lead to failure to control the infection and consequentially to self-enhancing progression of strongyloidiasis (hyperinfection syndrome and disseminated strongyloidiasis), which is lethal if not treated [5]. Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 1. The life cycle of S. stercoralis. The life cycle of Strongyloides stercoralis. The numbers refer to the numbers of the developmental options in the description of the life cycle in the text. https://doi.org/10.1371/journal.pntd.0005752.g001 Parts of the 18S rDNA (small Subunit, SSU) sequence, in particular the hypervariable regions (HVR) I and IV, are widely used as nuclear markers for molecular taxonomy of nematodes in general (e.g. [27–33]) and Strongyloides spp. in particular [8,34–36]. Whilst some sequence variation in HVR I within S. stercoralis was reported [35,37], HVR IV appears virtually invariable within this species. To our knowledge, there is only one report to date of a single nucleotide difference within this region [38](accession number M84229). Whilst humans are their natural hosts, dogs, cats, and non-human primates have also been proposed to be suitable hosts for S. stercoralis [39–42]. To what extent strongyloidiasis is a zoonotic disease has been the subject of controversy in the literature for several decades. Originally Brumpt (1922) [43], later supported by Augustine (1940) [44] split the Strongyloides of dogs from S. stercoralis and described it as a separate species, called Strongyloides canis. Recent comparative analyses of the mitochondrial locus cytochrome c oxidase subunit 1 (cox1) [6,36,38,45] and the whole genome sequence of 33 individual S. stercoralis from Japan and Myanmar [46] indicated that there is substantial genetic diversity among S. stercoralis isolated from human hosts and [38] suggested that there might exist human- and dog-specialized subpopulations. On the other hand, dogs have long been known to be suitable experimental hosts for human derived S. stercoralis [39,41], and many authors consider Strongyloides in dogs and humans to belong to the same species, i.e. S. stercoralis. While the more recent literature appears to favor separation, it remains unclear whether S. stercoralis naturally infecting dogs and humans belong to the same populations or not, and correspondingly, what the potential is for dogs to serve as a source for human S. stercoralis infections (recently reviewed by Thamsborg and colleagues [42]). In order to address this question, we compared individual Strongyloides isolated at the same time and location from humans and dogs, which, to our knowledge, had never been done. In our study area, rural communities in Northern Cambodia, people share their premises closely with their dogs, and the prevalence of strongyloidiasis is high [3]. We compared the sequences of the nuclear SSU HVR I and HVR IV and, for a selected subset of worms, the mitochondrial cox1 gene and whole genome sequences. Further, we characterized reproduction in the free-living generations of wild and laboratory isolates of S. stercoralis. Our results show that dogs carry S. stercoralis genetically indistinguishable from the ones in humans in addition to a dog specific population. Further, we demonstrate that reproduction in the free-living generation of both wild and laboratory isolates of S. stercoralis is sexual and not pseudogamic. Overall, our observations strongly support the hypothesis that dogs are a potential source for human S. stercoralis infection and suggest that in order to reduce the exposure of people to infective Strongyloides larvae, dogs should be treated along with their owners in settings where people are exposed to dog excrement. Materials and methods Study area Fecal samples were collected from humans and dogs of the same households in the villages Anlong Svay (AS) and Chom Long (CL) in May 2013 and in Damnak Chin (DC) and Kampot (KP) in June 2016. All villages are in the Rovieng District (13°21′N 105°07′E) in Preah Vihear province in Northern Cambodia. Stool sample collection and S. stercoralis isolation Human stool samples were collected and S. stercoralis larvae were isolated according to established methods [47]. In brief, stool samples were collected for two consecutive days from each member of the household who agreed to participate in this study. In May 2013 all the fecal samples collected from humans were analyzed within 3 hours after collection using Baermann and Kato-Katz methods. The sediments of positive Baermann funnels were preserved and transported to our laboratory in Tübingen in 70% ethanol at ambient temperature. In June 2016 the fecal samples were mixed with an approximately equal volume of sawdust, moisturized and cultured at ambient temperature for 24–48 hours and analyzed using the Baermann method. From positive Baermann funnels a portion of the worms were transferred individually into 10 μl of water or, for those intended for whole genome sequencing, 10 μl of Tissue and Cell Lysis Solution (component of the MasterPure DNA Purification Kit, Epicenter MC85201) and the remaining worms were preserved as batches in 70% ethanol. While the work was ongoing the samples were stored in the hotel freezer. For transport to our laboratory the samples were refrigerated using wet ice but not frozen. In the majority of cases, worms from the 2016 sample come from those that had been picked individually whilst alive into water or Tissue and Cell Lysis Solution. If any ethanol preserved specimen from 2016 was used, this is explicitly stated. Fecal samples were also collected from dogs found in the proximity of S. stercoralis positive households. The samples were taken directly from the rectum of the animals with the help of the owners and the field assistants. The samples were further processed like the human samples except that for some samples, 3 g of feces were placed on NGM agar plates [48] and incubated for 24–48 hours at ambient temperature and emerging S. stercoralis were picked directly from the plates instead of setting up saw dust cultures followed by baermanization. Single worm DNA preparation for PCR and whole genome sequencing For ethanol fixed samples, single worms were picked and washed twice with Phosphate-buffered saline (PBS) and then incubated in 20 μl 1X lysis buffer (20 mM Tris-HCl pH 8. 3, 100 mM KCl, 5 mM MgCl2, 0.9% NP-40, 0.9% Tween 20, 0.02% Gelatine, 240 μg/ml Proteinase K) at 65°C for 2h, followed by incubation at 95°C for 15 min. 2 μl (for SSU) or 4 μl (or single copy loci) of this lysate were used as template for PCR amplification. For worms stored in 10 μl water, 10 μl 2x lysis buffer were added, after which the samples were treated as described above. For samples preserved in Tissue and Cell Lysis Solution, single worm DNA was prepared using the MasterPure DNA Purification Kit (Epicenter MC85201) according to the manufacturer’s protocol, and the DNA was stored frozen in 10 μl of TE buffer. 1 μl was used for SSU amplification, and the reminder for sequencing library construction. PCR for SSU, cox1 and single copy locus genotyping PCR reactions were done in a total volume of 25 μl (up to 25 μl nuclease-free water, 2.5 μl 10X ThermoPol Reaction buffer (New England BioLabs), 0.5 μl dNTP’s (2mM each), 0.5 μl 10 mM forward primer (Table 1, Fig 2), 0.5 μl 10 mM reverse primer (Table 1, Fig 2), 0.3 μl Taq DNA polymerase (New England BioLabs), 1 μl to 4 μl template as specified above). Thermocycling program: 94 °C for 2 min, followed by 35 cycles of denaturing (94 °C for 30 sec), annealing (temperature given in Table 1 for 15 sec), extension (72 °C for time given in Table 1), and a post amplification final extension (72°C for 10 min) and cooling to 4 °C. Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 2. The different SSU HVR variants found. The sequence of the portion of the SSU amplified for genotyping of the two HVRs. Arrows indicate the positions of the primers used for amplification, from top to bottom SSU18A, 18SP4F, SSU26R, 18SPCR (c.f. Table 1). Note that forward primers are above the sequence while reverse primers are below the sequence. HVR I and HVR IV as defined by Hasegawa and colleagues [35] are boxed. For sequencing results for both SSU HVR and cox1 for each individual worm see S1 Table. https://doi.org/10.1371/journal.pntd.0005752.g002 Download: PPT PowerPoint slide PNG larger image TIFF original image Table 1. Primers and PCR conditions. https://doi.org/10.1371/journal.pntd.0005752.t001 Sequencing of PCR products and sequence analysis 1 μl of the PCR reaction and either one of the PCR primers or, in the case of SSU HVR I, a designated sequencing primer were used in sequencing reactions using the BigDye Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems,) according to the manufacture’s protocol. The reactions were submitted to the in-house sequencing facility at the Max Planck Institute for Developmental Biology at Tübingen for electrophoresis and base calling. Sequences were analyzed with SeqMan Pro version 12 (Lasergene package; DNAStar, Inc., Madison, WI USA). Chromatograms were visually inspected to detect ambiguous signals indicating mixed sequences (heterozygous worms). For comparison with published sequences, we used BLAST against the NCBI nucleotide database (http://blast.ncbi.nlm.nih.gov/Blast.cgi). For the SSU, we used the GenBank entry AF279916 as reference sequence. All position numbers refer to this entry. For S. stercoralis cox1, we used the sequence LC050212 as reference. 552 base pairs, of which 63 were polymorphic, were considered (for the full sequences of the different haplotypes see S1 Text). For ytPxxx markers, position 1 is the first base of the (non-nested) forward primer (for the sequences of the markers see S1 Text). Phylogenetic analysis of the cox1 sequences was done using MEGA7 [49] with default settings. As an outgroup species we used Necator americanus (AJ417719). The Maximum Likelihood tree is shown in Fig 3. For comparison we also reconstructed Maximum Parsimony and Neighbor Joining trees, which resulted in the same tree topology as far as well-supported nodes are concerned. Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 3. Gene tree of the mitochondrial gene cox1. Maximum likelihood tree of the 17 different cox1 sequences we found and representative previously published sequences. The numbers are bootstrap values based on 1000 bootstraps. For haplotypes isolated in this study the labels have the following format: Haplotype number (accession number) host country (number of individuals this haplotype was found in). 1For sequences previously published by Hasegawa and colleagues [36] the label starts with Hasegawa. 2For sequences previously published by Laymanifong and colleagues [6] the label starts with the cox1 clade this reference assigned the particular sequence to. This is followed by: (accession number) host country (CAR = Central African Republic). The hosts are also highlighted by red circles (human) and blue squares (dog). Entries to the right of the tree indicate for each cox1 haplotype the SSU haplotypes it was found together in the same individual. If a given cox1 haplotype existed in the context of multiple SSU haplotypes, the number of worms with this particular combination is given in parentheses. Note: the cox1 haplotypes 2 and 3 were found in both hosts and are included twice in this tree. For the sequencing results for both SSU HVR and cox1 for each individual worm see S1 Table. https://doi.org/10.1371/journal.pntd.0005752.g003 Whole genome sequencing and analysis DNA of 23 single free-living males S. stercoralis from different hosts (11 males from 9 different humans and 12 males from 10 different dogs) was prepared as described above. Whole-genome sequencing libraries were prepared with Clontech Low Input Library Prep Kits (Takara Bio, USA) following the manufacturer's protocol. Samples were submitted to in-house sequencing on an Illumina HiSeq 3000 instrument (150 bp paired-end). An approach similar to a previous S. stercoralis population study [46] was used to analyze the whole genome data. In brief, raw reads were trimmed with skewer [50] (version 0.1.123; -q 30 -Q30 -l 60). Trimmed reads were mapped to the S. stercoralis reference genome (GCA_000947215.1) and the small subunit ribosomal RNA (SSU rRNA; AF279916) using bwa mem [51] (version 0.7.12; MEM algorithm with defaults). Duplicate reads were marked with Picard tools (http://broadinstitute.github.io/picard) (version 2.2.1; MarkDuplicates with defaults). Variants were called with GATK [52] (build 2016-09-27-g026f7e8; HaplotypeCaller and GenotypeGVCFs both with defaults) after Indel realignment (GATK IndelRealigner with defaults) and freebayes [53] (version 1.0.2-6-g3ce827d, defaults). The intersection of both variant calls was imported into GNU R using SNPRelate [54] (version 1.8.0; method = "biallelic.only"). Single-nucleotide polymorphism (SNPs) were recursively removed using a sliding window approach and a Linkage Disequilibrium (LD) threshold of 0.05 and or a minimum allele frequency (MAF) of 0.05. The resulting SNP set was used to calculate the fraction of identity by state (IBS) for each pair of samples. Results were stored in a genomic identity-by-state relationship matrix and used to estimate a phylogeny with the BIONJ algorithm implemented in ape [55] (version 4.1; defaults). A second phylogeny was estimated with a reference-free approach. Trimmed short reads were used to generate a k-mer count graph with khmer (version 0.2.0; load-into-counting.py with a k-mer size of 19 otherwise defaults). k-mer counts were used to calculate pairwise distances between samples using kWIP [56]. The resulting distance matrix was imported into GNU R to estimate a phylogeny; again using the BIONJ algorithm. Analysis of free-living females and their progeny Free-living females were isolated after two days of culture as described above and placed individually onto NGM plates seeded with E. coli OP50 [48]. The plates were inspected daily. Females that had produced progeny but presumably had ceased reproduction because they no longer contained embryos in their uterus were picked and prepared for genotyping as described above. One day later, larvae from these females were also isolated and processed. For 17 of these families the mothers and the progeny were picked individually and alive into 10 μl of water and processed as described above. Five more families (Females 7, 8, 14, 15, 16) were preserved in Ethanol (one tube per family) and the individuals were only separated when they were genotyped. The mothers and the progeny were genotyped at ytP289 and ytP290 as described above. ytP289 contains single nucleotide polymorphisms at positions 308 (A/G), 359 (A/G), 416 (C/T) and 566 (C/T). Three different combinations (alleles) existed in our samples. Allele 1 has the combination G+A+C+C, allele 2 A+G+T+T, and allele 3 A+A+C+C. ytP290 contains single nucleotide polymorphisms at positions 291 (A/C) and 310 (A/G). Two different combinations (alleles) existed in our samples. Allele 1 has the combination A+A and allele 2 C+G. For the full sequences see S1 Text. Crossing free-living stages of S. stercoralis (laboratory strain) The UPD strain and PV001 line of S. stercoralis were maintained in immuno-suppressed dogs and cultured in fecal cultures with charcoal as previously described [41]. Free-living L4 larvae and young adults (males and virgin females) were isolated from 1-day fecal cultures at 22 °C using Baermann funnels as described [41]. Single virgin females and males were handpicked and transferred in male-female pairs onto NGM plates spotted with 30 μl of OP50 [48] and 20 μl of water from a Baermann funnel and incubated at 22 oC for 24 hrs. On the next day, from pairs where the female contained developing embryos in the uterus, the males were transferred into PCR tubes containing 10 μl of lysis buffer (see above) and frozen for later use. Once the females contained no embryos any longer (after three days) they were processed like the males. After all the eggs had hatched, all the L1/L2 were transferred individually into PCR tubes as described for the parents. Single worm lysis was performed as described above for ethanol fixed specimens without the PBS washing step. The parents and eight progeny per cross were genotyped at the marker ytP274 as described above. ytP274 has a single SNP (T/C) at position 236. For the full sequence of ytP274 see S1 Text. Ethics statements The sampling of material in Cambodia was approved by the National Ethics Committee for Health Research (NECHR), Ministry of Health, Cambodia and the ethics committee of the cantons of Basel-Stadt and Basel-Land (EKBB), Switzerland. All participants were informed of the study procedures and provided written informed consent prior to enrolment. All data handled were strictly confidential. All individuals infected with S. stercoralis were treated with Ivermectin (single oral dose of 200 μg/kg BW). Co-infections with other intestinal helminths were treated according the Cambodian treatment guidelines. The experiments requiring culture of S. stercoralis in host animals were all done at the University of Pennsylvania with the approval of the University of Pennsylvania Institutional Animal Care and Use Committee (IACUC). The S. stercoralis UPD strain and PV001 isolate were maintained in prednisolone-treated dogs according to IACUC protocols 702342, 801905, and 802593. All IACUC protocols, as well as routine husbandry care of the animals, were conducted in strict accordance with the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. No human subjects were used in this part of the study. Accession numbers The sequences obtained from this study are available from GenBank (accession numbers KU724124-KU724129 and KX226367-KX226384 and KY548505). The whole genome data are available permanently from the FTP server of the Max Planck Institute for Developmental Biology (ftp://ftp.tuebingen.mpg.de/pub/PLOS_NTD_Jaleta_2017_whole_genome_data). They have also been submitted to the European Nucleotide Archive (accession number PRJEB20999). Study area Fecal samples were collected from humans and dogs of the same households in the villages Anlong Svay (AS) and Chom Long (CL) in May 2013 and in Damnak Chin (DC) and Kampot (KP) in June 2016. All villages are in the Rovieng District (13°21′N 105°07′E) in Preah Vihear province in Northern Cambodia. Stool sample collection and S. stercoralis isolation Human stool samples were collected and S. stercoralis larvae were isolated according to established methods [47]. In brief, stool samples were collected for two consecutive days from each member of the household who agreed to participate in this study. In May 2013 all the fecal samples collected from humans were analyzed within 3 hours after collection using Baermann and Kato-Katz methods. The sediments of positive Baermann funnels were preserved and transported to our laboratory in Tübingen in 70% ethanol at ambient temperature. In June 2016 the fecal samples were mixed with an approximately equal volume of sawdust, moisturized and cultured at ambient temperature for 24–48 hours and analyzed using the Baermann method. From positive Baermann funnels a portion of the worms were transferred individually into 10 μl of water or, for those intended for whole genome sequencing, 10 μl of Tissue and Cell Lysis Solution (component of the MasterPure DNA Purification Kit, Epicenter MC85201) and the remaining worms were preserved as batches in 70% ethanol. While the work was ongoing the samples were stored in the hotel freezer. For transport to our laboratory the samples were refrigerated using wet ice but not frozen. In the majority of cases, worms from the 2016 sample come from those that had been picked individually whilst alive into water or Tissue and Cell Lysis Solution. If any ethanol preserved specimen from 2016 was used, this is explicitly stated. Fecal samples were also collected from dogs found in the proximity of S. stercoralis positive households. The samples were taken directly from the rectum of the animals with the help of the owners and the field assistants. The samples were further processed like the human samples except that for some samples, 3 g of feces were placed on NGM agar plates [48] and incubated for 24–48 hours at ambient temperature and emerging S. stercoralis were picked directly from the plates instead of setting up saw dust cultures followed by baermanization. Single worm DNA preparation for PCR and whole genome sequencing For ethanol fixed samples, single worms were picked and washed twice with Phosphate-buffered saline (PBS) and then incubated in 20 μl 1X lysis buffer (20 mM Tris-HCl pH 8. 3, 100 mM KCl, 5 mM MgCl2, 0.9% NP-40, 0.9% Tween 20, 0.02% Gelatine, 240 μg/ml Proteinase K) at 65°C for 2h, followed by incubation at 95°C for 15 min. 2 μl (for SSU) or 4 μl (or single copy loci) of this lysate were used as template for PCR amplification. For worms stored in 10 μl water, 10 μl 2x lysis buffer were added, after which the samples were treated as described above. For samples preserved in Tissue and Cell Lysis Solution, single worm DNA was prepared using the MasterPure DNA Purification Kit (Epicenter MC85201) according to the manufacturer’s protocol, and the DNA was stored frozen in 10 μl of TE buffer. 1 μl was used for SSU amplification, and the reminder for sequencing library construction. PCR for SSU, cox1 and single copy locus genotyping PCR reactions were done in a total volume of 25 μl (up to 25 μl nuclease-free water, 2.5 μl 10X ThermoPol Reaction buffer (New England BioLabs), 0.5 μl dNTP’s (2mM each), 0.5 μl 10 mM forward primer (Table 1, Fig 2), 0.5 μl 10 mM reverse primer (Table 1, Fig 2), 0.3 μl Taq DNA polymerase (New England BioLabs), 1 μl to 4 μl template as specified above). Thermocycling program: 94 °C for 2 min, followed by 35 cycles of denaturing (94 °C for 30 sec), annealing (temperature given in Table 1 for 15 sec), extension (72 °C for time given in Table 1), and a post amplification final extension (72°C for 10 min) and cooling to 4 °C. Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 2. The different SSU HVR variants found. The sequence of the portion of the SSU amplified for genotyping of the two HVRs. Arrows indicate the positions of the primers used for amplification, from top to bottom SSU18A, 18SP4F, SSU26R, 18SPCR (c.f. Table 1). Note that forward primers are above the sequence while reverse primers are below the sequence. HVR I and HVR IV as defined by Hasegawa and colleagues [35] are boxed. For sequencing results for both SSU HVR and cox1 for each individual worm see S1 Table. https://doi.org/10.1371/journal.pntd.0005752.g002 Download: PPT PowerPoint slide PNG larger image TIFF original image Table 1. Primers and PCR conditions. https://doi.org/10.1371/journal.pntd.0005752.t001 Sequencing of PCR products and sequence analysis 1 μl of the PCR reaction and either one of the PCR primers or, in the case of SSU HVR I, a designated sequencing primer were used in sequencing reactions using the BigDye Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems,) according to the manufacture’s protocol. The reactions were submitted to the in-house sequencing facility at the Max Planck Institute for Developmental Biology at Tübingen for electrophoresis and base calling. Sequences were analyzed with SeqMan Pro version 12 (Lasergene package; DNAStar, Inc., Madison, WI USA). Chromatograms were visually inspected to detect ambiguous signals indicating mixed sequences (heterozygous worms). For comparison with published sequences, we used BLAST against the NCBI nucleotide database (http://blast.ncbi.nlm.nih.gov/Blast.cgi). For the SSU, we used the GenBank entry AF279916 as reference sequence. All position numbers refer to this entry. For S. stercoralis cox1, we used the sequence LC050212 as reference. 552 base pairs, of which 63 were polymorphic, were considered (for the full sequences of the different haplotypes see S1 Text). For ytPxxx markers, position 1 is the first base of the (non-nested) forward primer (for the sequences of the markers see S1 Text). Phylogenetic analysis of the cox1 sequences was done using MEGA7 [49] with default settings. As an outgroup species we used Necator americanus (AJ417719). The Maximum Likelihood tree is shown in Fig 3. For comparison we also reconstructed Maximum Parsimony and Neighbor Joining trees, which resulted in the same tree topology as far as well-supported nodes are concerned. Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 3. Gene tree of the mitochondrial gene cox1. Maximum likelihood tree of the 17 different cox1 sequences we found and representative previously published sequences. The numbers are bootstrap values based on 1000 bootstraps. For haplotypes isolated in this study the labels have the following format: Haplotype number (accession number) host country (number of individuals this haplotype was found in). 1For sequences previously published by Hasegawa and colleagues [36] the label starts with Hasegawa. 2For sequences previously published by Laymanifong and colleagues [6] the label starts with the cox1 clade this reference assigned the particular sequence to. This is followed by: (accession number) host country (CAR = Central African Republic). The hosts are also highlighted by red circles (human) and blue squares (dog). Entries to the right of the tree indicate for each cox1 haplotype the SSU haplotypes it was found together in the same individual. If a given cox1 haplotype existed in the context of multiple SSU haplotypes, the number of worms with this particular combination is given in parentheses. Note: the cox1 haplotypes 2 and 3 were found in both hosts and are included twice in this tree. For the sequencing results for both SSU HVR and cox1 for each individual worm see S1 Table. https://doi.org/10.1371/journal.pntd.0005752.g003 Whole genome sequencing and analysis DNA of 23 single free-living males S. stercoralis from different hosts (11 males from 9 different humans and 12 males from 10 different dogs) was prepared as described above. Whole-genome sequencing libraries were prepared with Clontech Low Input Library Prep Kits (Takara Bio, USA) following the manufacturer's protocol. Samples were submitted to in-house sequencing on an Illumina HiSeq 3000 instrument (150 bp paired-end). An approach similar to a previous S. stercoralis population study [46] was used to analyze the whole genome data. In brief, raw reads were trimmed with skewer [50] (version 0.1.123; -q 30 -Q30 -l 60). Trimmed reads were mapped to the S. stercoralis reference genome (GCA_000947215.1) and the small subunit ribosomal RNA (SSU rRNA; AF279916) using bwa mem [51] (version 0.7.12; MEM algorithm with defaults). Duplicate reads were marked with Picard tools (http://broadinstitute.github.io/picard) (version 2.2.1; MarkDuplicates with defaults). Variants were called with GATK [52] (build 2016-09-27-g026f7e8; HaplotypeCaller and GenotypeGVCFs both with defaults) after Indel realignment (GATK IndelRealigner with defaults) and freebayes [53] (version 1.0.2-6-g3ce827d, defaults). The intersection of both variant calls was imported into GNU R using SNPRelate [54] (version 1.8.0; method = "biallelic.only"). Single-nucleotide polymorphism (SNPs) were recursively removed using a sliding window approach and a Linkage Disequilibrium (LD) threshold of 0.05 and or a minimum allele frequency (MAF) of 0.05. The resulting SNP set was used to calculate the fraction of identity by state (IBS) for each pair of samples. Results were stored in a genomic identity-by-state relationship matrix and used to estimate a phylogeny with the BIONJ algorithm implemented in ape [55] (version 4.1; defaults). A second phylogeny was estimated with a reference-free approach. Trimmed short reads were used to generate a k-mer count graph with khmer (version 0.2.0; load-into-counting.py with a k-mer size of 19 otherwise defaults). k-mer counts were used to calculate pairwise distances between samples using kWIP [56]. The resulting distance matrix was imported into GNU R to estimate a phylogeny; again using the BIONJ algorithm. Analysis of free-living females and their progeny Free-living females were isolated after two days of culture as described above and placed individually onto NGM plates seeded with E. coli OP50 [48]. The plates were inspected daily. Females that had produced progeny but presumably had ceased reproduction because they no longer contained embryos in their uterus were picked and prepared for genotyping as described above. One day later, larvae from these females were also isolated and processed. For 17 of these families the mothers and the progeny were picked individually and alive into 10 μl of water and processed as described above. Five more families (Females 7, 8, 14, 15, 16) were preserved in Ethanol (one tube per family) and the individuals were only separated when they were genotyped. The mothers and the progeny were genotyped at ytP289 and ytP290 as described above. ytP289 contains single nucleotide polymorphisms at positions 308 (A/G), 359 (A/G), 416 (C/T) and 566 (C/T). Three different combinations (alleles) existed in our samples. Allele 1 has the combination G+A+C+C, allele 2 A+G+T+T, and allele 3 A+A+C+C. ytP290 contains single nucleotide polymorphisms at positions 291 (A/C) and 310 (A/G). Two different combinations (alleles) existed in our samples. Allele 1 has the combination A+A and allele 2 C+G. For the full sequences see S1 Text. Crossing free-living stages of S. stercoralis (laboratory strain) The UPD strain and PV001 line of S. stercoralis were maintained in immuno-suppressed dogs and cultured in fecal cultures with charcoal as previously described [41]. Free-living L4 larvae and young adults (males and virgin females) were isolated from 1-day fecal cultures at 22 °C using Baermann funnels as described [41]. Single virgin females and males were handpicked and transferred in male-female pairs onto NGM plates spotted with 30 μl of OP50 [48] and 20 μl of water from a Baermann funnel and incubated at 22 oC for 24 hrs. On the next day, from pairs where the female contained developing embryos in the uterus, the males were transferred into PCR tubes containing 10 μl of lysis buffer (see above) and frozen for later use. Once the females contained no embryos any longer (after three days) they were processed like the males. After all the eggs had hatched, all the L1/L2 were transferred individually into PCR tubes as described for the parents. Single worm lysis was performed as described above for ethanol fixed specimens without the PBS washing step. The parents and eight progeny per cross were genotyped at the marker ytP274 as described above. ytP274 has a single SNP (T/C) at position 236. For the full sequence of ytP274 see S1 Text. Ethics statements The sampling of material in Cambodia was approved by the National Ethics Committee for Health Research (NECHR), Ministry of Health, Cambodia and the ethics committee of the cantons of Basel-Stadt and Basel-Land (EKBB), Switzerland. All participants were informed of the study procedures and provided written informed consent prior to enrolment. All data handled were strictly confidential. All individuals infected with S. stercoralis were treated with Ivermectin (single oral dose of 200 μg/kg BW). Co-infections with other intestinal helminths were treated according the Cambodian treatment guidelines. The experiments requiring culture of S. stercoralis in host animals were all done at the University of Pennsylvania with the approval of the University of Pennsylvania Institutional Animal Care and Use Committee (IACUC). The S. stercoralis UPD strain and PV001 isolate were maintained in prednisolone-treated dogs according to IACUC protocols 702342, 801905, and 802593. All IACUC protocols, as well as routine husbandry care of the animals, were conducted in strict accordance with the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. No human subjects were used in this part of the study. Accession numbers The sequences obtained from this study are available from GenBank (accession numbers KU724124-KU724129 and KX226367-KX226384 and KY548505). The whole genome data are available permanently from the FTP server of the Max Planck Institute for Developmental Biology (ftp://ftp.tuebingen.mpg.de/pub/PLOS_NTD_Jaleta_2017_whole_genome_data). They have also been submitted to the European Nucleotide Archive (accession number PRJEB20999). Results Prevalence of S. stercoralis in humans and dogs In May 2013, we collected stool samples from a total of 537 persons from 128 households. Of these, 177 individuals (32.96%) living in 95 different households were positive for S. stercoralis. From positive households we obtained rectal fecal samples from a total of 88 dogs. Of these, 78 (88.63%) originating from 44 different households were positive. In June 2016, 20 of 169 (11.8%) people from 17 out of 62 households tested positive for S. stercoralis. Of the 29 dogs from 14 households tested, 22 (75.9%) living in 12 different households were positive. It should be noted that the prevalence in the two hosts cannot be compared directly because of the biased sampling of dogs. Multiple SSU HVR I haplotypes among S. stercoralis Firstly, we sequenced the region around the HVR I of the SSU from individual S. stercoralis isolated from humans and dogs [10,34–36,27–33]. Overall, we found the five different haplotypes described in Fig 2. The two most dissimilar haplotypes (III and IV) show four differences (2 indels and 2 SNPs). Earlier studies [27–30,35,36] found this fragment to be largely invariable within species and two or more differences to be fairly reliable indicators of different species. Therefore, a within species variability as we observed was rather unexpected but not entirely implausible. In order to obtain additional information, we next sequenced the SSU HVR IV[35,36]. Dogs carry two different populations of S. stercoralis identifiable by the SSU HVR IV sequence Among all Strongyloides individuals from dogs, we found two sequence variants in the SSU HVR IV as defined in [35]. The two haplotypes differed at three positions (two indels, one base substitution, Fig 2). One of these variants, from now on referred to as HVR IV haplotype A, is the one previously described as the HVR IV sequence of S. stercoralis [35], and was found (Table 2) in 11 (11.5%) out of 96 dog derived worms in the 2013 sample and 39 (31%) out of 126 dog derived worms in the 2016 sample (in total 50 (22.5%) out of 222). This variant was also found in all human derived worms of both samples (in total 521 worms from a total of 85 host individuals, S1 Table). The other variant, referred to hereafter as HVR IV haplotype B, has, to our knowledge, not been described previously and was present in 85/96 (88.5%) dog derived worms in the 2013 sample, and in 87/126 (69%) dog derived worms in the 2016 sample. Notably, this haplotype was not found in any of the 521 human derived worms. If the two haplotypes indeed indicate two reproductively isolated groups, which have been separated for some time in evolution, this should also be reflected in their mitochondrial and nuclear genomes. Therefore, from the 2013 sample we sequenced a portion of the mitochondrial cox1 gene of 21 dog-derived worms (17 with SSU HVR IV haplotype B and 4 with SSU HVR IV haplotype A) and 57 human derived worms (all with SSU HVR IV haplotype A) [6,36,38]. In total we identified 17 different cox1 haplotypes. Seven were associated with SSU HVR IV haplotype A and 10 with SSU HVR IV haplotype B (Fig 3, S1 Table). No haplotypes were shared between worms with the two SSU HVR IV haplotypes. In a phylogenetic analysis, the cox1 haplotypes associated with the two HVR IV haplotypes were well separated from each other. From the 2016 sample we selected 23 worms for whole genome sequencing and compared them over their entire genome using two different approaches (Fig 4). Both methods robustly separated the worms with SSU HVR IV haplotype B form all worms with SSU HVR IV haplotype A. The two methods yielded different results on the exact topology of the tree within the two SSU HVR IV defined groups but provided no indication that the dog derived worms with SSU HVR IV haplotype A form a group different from the human derived worms. From this we conclude that dogs in our study area carry two populations of S. stercoralis, which are distinguishable by their SSU HVR IV haplotype. One population, to which the majority of the Strongyloides belong, was not found humans. The other population, however, is shared with humans, strongly indicating that S. stercoralis with SSU HVR IV haplotype A can shuttle between the two vertebrate host species. Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 4. Sample relatedness analysis on whole genome data. A) Neighbor joining tree based on a genomic identity-by-state relationship matrix in cooperating 1326 SNPs (thresholds: LD = 0.05, MAF = 0.05). B) Neighbor joining tree based on pairwise similarities of the 23 individual genomes estimated using kWIP. The same samples in the two trees are connected with dotted lines colored in red for human derived worms and in blue for dog derived worms. ERX044031 indicates the reference genome short read data set [57], which has HVR I haplotype I and HVR IV haplotype A. The labels contain: [identifier of the worm] | [identifier of the host individual] | [HVR I haplotype, HVR IV haplotype], with each attribute separated by vertical lines. https://doi.org/10.1371/journal.pntd.0005752.g004 Download: PPT PowerPoint slide PNG larger image TIFF original image Table 2. SSU HVR IV haplotype distribution in S. stercoralis from humans and dogs. https://doi.org/10.1371/journal.pntd.0005752.t002 Different HVR I haplotypes appear not to reflect genetically separated populations When we analyzed the region around HVR I of S. stercoralis with HVR IV haplotype A, we found the same three variants (haplotypes I, II, III c.f. Fig 2) as described by Schär, Guo and colleagues [37] at various frequencies (Table 3). In combination with HVR IV haplotype B, which occurs only in dogs, we also found three variants of HVR I (haplotypes I, IV, V c.f. Fig 2). It is noteworthy that only HVR I haplotype I occurred in combination with both HVR IV haplotypes (c.f. Fig 2) [37]. If the different HVR I haplotypes reflect at least partially separated populations this should be reflected in the whole nuclear genome and the separation should also be visible in the mitochondrial genome. However, the mitochondrial cox1 phylogeny is not correlated with the HVR I differences (Fig 3), indicating that there is mixing of the nuclear genome between the different mitochondrial matrilinages. In addition, data from whole genome sequencing (Fig 4) are not consistent with the null hypothesis that worms with the same HVR I haplotype are more closely related to each other than to individuals with a different HVR I haplotype. The two methods lead to different tree topologies, none of which correlates with the HVR I haplotypes. Therefore this analysis provides no evidence for the existence of genetically isolated subpopulations within the worms with HVR IV haplotype A. The same is true for the worms with HVR IV haplotype B and different HVR I haplotypes. These results show that among the worms analyzed, other than SSU HVR IV haplotypes, not every SSU HVR I haplotype appears to represent its own separate genetically isolated population. Download: PPT PowerPoint slide PNG larger image TIFF original image Table 3. SSU HVR I haplotypes of S. stercoralis with HVR IV haplotype A isolated from humans and dogs, 2013 and 2016. https://doi.org/10.1371/journal.pntd.0005752.t003 S. stercoralis free-living adults reproduce sexually As a possible explanation for the absence of hybrids, Schär, Guo and colleagues [37] proposed that S. stercoralis might not reproduce sexually, either because the free-living generation undergoes pseudogamy (sperm dependent parthenogenesis) as proposed earlier [25], or because in the study area the population propagates only through the non-sexual homogonic cycle. We showed above that the nuclear genome and the mitochondrial genomes, which are normally maternally inherited, do not evolve in parallel. This argues strongly for at least occasional sexual reproduction. Large numbers of free-living S. stercoralis of both sexes were present in our field and laboratory isolates and males were clearly required for reproduction in the free-living generation. Of a total of 480 females (96 from field isolates and 384 from a laboratory isolate) placed individually on plates before they had a chance to mate, none produced progeny. This result indicates that female autonomous reproduction by parthenogenesis or self-fertilization occurs rarely or not at all. However, the result is not an argument against pseudogamy, because, although they do not contribute genetic material to the progeny, males and their sperm are required to activate embryogenesis in this mode of reproduction. Further, although mitochondria are normally inherited only from the mother, in other nematodes male derived mitochondria occasionally fail to be degraded and are incorporated in zygotes [58,59]. This could also happen upon pseudogamic interaction between oocyte and sperm and lead to a recombination of nuclear and mitochondrial genomes. Therefore, we sought to demonstrate sexual reproduction more directly. To this end we genotyped 22 individual mothers (all derived from humans) and several of their progeny at two single-copy loci (Table 4). These results demonstrate clearly that the progeny were not the product of clonal reproduction because we found larvae with genetic material absent from the mother but presumably derived from the male and/or larvae that did not have alleles present in the mother, indicating that the mother passed on only half of its genetic material as expected for sexual but not for clonal reproduction. Download: PPT PowerPoint slide PNG larger image TIFF original image Table 4. Genotypes of free-living mothers and their progeny. https://doi.org/10.1371/journal.pntd.0005752.t004 We sought to further solidify this in a fully controlled experiment with known males and a larger number of progeny. To this end, we set up crosses with single females and males using a laboratory isolate of S. stercoralis. The results (Table 5) were fully consistent with Mendelian inheritance with equal genetic contribution by males and females but not with clonal reproduction. Download: PPT PowerPoint slide PNG larger image TIFF original image Table 5. Genotypes of free-living parents and their progeny at ytP274. https://doi.org/10.1371/journal.pntd.0005752.t005 Are there hybrids between SSU haplotypes? Given the results above, one would expect to observe animals that are hybrids between the different SSU HVR I haplotypes. However, like in an earlier study [37], we failed to find any hybrids among the 436 larvae from 97 different host individuals (68 humans 29 dogs) isolated in 2013. The SSU locus is on the X chromosome in S. stercoralis (information extracted from a previously published dataset [57]). Therefore, hybrid males could not be detected because they only contain one X chromosome. However, for [37] and in our 2013 sampling, young larvae that were the progeny of parasitic worms were analyzed. The sex of these larvae was unknown but given that the field isolates produced both sexes, it is very likely that a substantial number of females were among them. In 2016 we tested adult worms and used predominantly males because, unlike females, they may not contain genetic material from other individuals (sperm, embryos). Only 30 of the 307 worms from 2016 listed in Table 2 were pre-reproductive females. None of them was a hybrid. However, of the gravid females described in Table 4 one (Female 17) and one of its progeny showed a mixture of HVR I haplotypes II and III. While the mixed signal in the female might have been caused by sperm and embryos derived from a male with a different haplotype than the mother, the larva was most likely a true hybrid. This prompted us to test fully mature females that had been isolated from cultures, after they had a chance to mate, preserved in ethanol and separated by host individuals. We analyzed 9 to 23 worms from each of six host individuals (four humans, two dogs), from which we had already isolated S. stercoralis of different HVR I haplotypes. In five of the cases we found worms with mixed haplotypes, along with individuals with only one SSU haplotype (Table 6). Two observations are noteworthy. Firstly, both dogs had worms with HVR IV haplotypes A and B. In total, 11 out of 21 worms had mixed HVR I haplotypes but only a single one showed a mixture between the two HVR IV haplotypes, which might indicate that males and females with different HVR IV haplotypes tend to avoid each other. Secondly, from host individual KP57 (human), 9 of 14 worms had mixed haplotypes. From the same host individual we had also genotyped 12 pre-reproductive females, none of which was a hybrid. This finding suggests that the females genotyped in this experiment were not true hybrids but contained sperm and developing embryos derived from males of the other haplotype detected. Download: PPT PowerPoint slide PNG larger image TIFF original image Table 6. SSU haplotypes found in individual gravid females. https://doi.org/10.1371/journal.pntd.0005752.t006 Prevalence of S. stercoralis in humans and dogs In May 2013, we collected stool samples from a total of 537 persons from 128 households. Of these, 177 individuals (32.96%) living in 95 different households were positive for S. stercoralis. From positive households we obtained rectal fecal samples from a total of 88 dogs. Of these, 78 (88.63%) originating from 44 different households were positive. In June 2016, 20 of 169 (11.8%) people from 17 out of 62 households tested positive for S. stercoralis. Of the 29 dogs from 14 households tested, 22 (75.9%) living in 12 different households were positive. It should be noted that the prevalence in the two hosts cannot be compared directly because of the biased sampling of dogs. Multiple SSU HVR I haplotypes among S. stercoralis Firstly, we sequenced the region around the HVR I of the SSU from individual S. stercoralis isolated from humans and dogs [10,34–36,27–33]. Overall, we found the five different haplotypes described in Fig 2. The two most dissimilar haplotypes (III and IV) show four differences (2 indels and 2 SNPs). Earlier studies [27–30,35,36] found this fragment to be largely invariable within species and two or more differences to be fairly reliable indicators of different species. Therefore, a within species variability as we observed was rather unexpected but not entirely implausible. In order to obtain additional information, we next sequenced the SSU HVR IV[35,36]. Dogs carry two different populations of S. stercoralis identifiable by the SSU HVR IV sequence Among all Strongyloides individuals from dogs, we found two sequence variants in the SSU HVR IV as defined in [35]. The two haplotypes differed at three positions (two indels, one base substitution, Fig 2). One of these variants, from now on referred to as HVR IV haplotype A, is the one previously described as the HVR IV sequence of S. stercoralis [35], and was found (Table 2) in 11 (11.5%) out of 96 dog derived worms in the 2013 sample and 39 (31%) out of 126 dog derived worms in the 2016 sample (in total 50 (22.5%) out of 222). This variant was also found in all human derived worms of both samples (in total 521 worms from a total of 85 host individuals, S1 Table). The other variant, referred to hereafter as HVR IV haplotype B, has, to our knowledge, not been described previously and was present in 85/96 (88.5%) dog derived worms in the 2013 sample, and in 87/126 (69%) dog derived worms in the 2016 sample. Notably, this haplotype was not found in any of the 521 human derived worms. If the two haplotypes indeed indicate two reproductively isolated groups, which have been separated for some time in evolution, this should also be reflected in their mitochondrial and nuclear genomes. Therefore, from the 2013 sample we sequenced a portion of the mitochondrial cox1 gene of 21 dog-derived worms (17 with SSU HVR IV haplotype B and 4 with SSU HVR IV haplotype A) and 57 human derived worms (all with SSU HVR IV haplotype A) [6,36,38]. In total we identified 17 different cox1 haplotypes. Seven were associated with SSU HVR IV haplotype A and 10 with SSU HVR IV haplotype B (Fig 3, S1 Table). No haplotypes were shared between worms with the two SSU HVR IV haplotypes. In a phylogenetic analysis, the cox1 haplotypes associated with the two HVR IV haplotypes were well separated from each other. From the 2016 sample we selected 23 worms for whole genome sequencing and compared them over their entire genome using two different approaches (Fig 4). Both methods robustly separated the worms with SSU HVR IV haplotype B form all worms with SSU HVR IV haplotype A. The two methods yielded different results on the exact topology of the tree within the two SSU HVR IV defined groups but provided no indication that the dog derived worms with SSU HVR IV haplotype A form a group different from the human derived worms. From this we conclude that dogs in our study area carry two populations of S. stercoralis, which are distinguishable by their SSU HVR IV haplotype. One population, to which the majority of the Strongyloides belong, was not found humans. The other population, however, is shared with humans, strongly indicating that S. stercoralis with SSU HVR IV haplotype A can shuttle between the two vertebrate host species. Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 4. Sample relatedness analysis on whole genome data. A) Neighbor joining tree based on a genomic identity-by-state relationship matrix in cooperating 1326 SNPs (thresholds: LD = 0.05, MAF = 0.05). B) Neighbor joining tree based on pairwise similarities of the 23 individual genomes estimated using kWIP. The same samples in the two trees are connected with dotted lines colored in red for human derived worms and in blue for dog derived worms. ERX044031 indicates the reference genome short read data set [57], which has HVR I haplotype I and HVR IV haplotype A. The labels contain: [identifier of the worm] | [identifier of the host individual] | [HVR I haplotype, HVR IV haplotype], with each attribute separated by vertical lines. https://doi.org/10.1371/journal.pntd.0005752.g004 Download: PPT PowerPoint slide PNG larger image TIFF original image Table 2. SSU HVR IV haplotype distribution in S. stercoralis from humans and dogs. https://doi.org/10.1371/journal.pntd.0005752.t002 Different HVR I haplotypes appear not to reflect genetically separated populations When we analyzed the region around HVR I of S. stercoralis with HVR IV haplotype A, we found the same three variants (haplotypes I, II, III c.f. Fig 2) as described by Schär, Guo and colleagues [37] at various frequencies (Table 3). In combination with HVR IV haplotype B, which occurs only in dogs, we also found three variants of HVR I (haplotypes I, IV, V c.f. Fig 2). It is noteworthy that only HVR I haplotype I occurred in combination with both HVR IV haplotypes (c.f. Fig 2) [37]. If the different HVR I haplotypes reflect at least partially separated populations this should be reflected in the whole nuclear genome and the separation should also be visible in the mitochondrial genome. However, the mitochondrial cox1 phylogeny is not correlated with the HVR I differences (Fig 3), indicating that there is mixing of the nuclear genome between the different mitochondrial matrilinages. In addition, data from whole genome sequencing (Fig 4) are not consistent with the null hypothesis that worms with the same HVR I haplotype are more closely related to each other than to individuals with a different HVR I haplotype. The two methods lead to different tree topologies, none of which correlates with the HVR I haplotypes. Therefore this analysis provides no evidence for the existence of genetically isolated subpopulations within the worms with HVR IV haplotype A. The same is true for the worms with HVR IV haplotype B and different HVR I haplotypes. These results show that among the worms analyzed, other than SSU HVR IV haplotypes, not every SSU HVR I haplotype appears to represent its own separate genetically isolated population. Download: PPT PowerPoint slide PNG larger image TIFF original image Table 3. SSU HVR I haplotypes of S. stercoralis with HVR IV haplotype A isolated from humans and dogs, 2013 and 2016. https://doi.org/10.1371/journal.pntd.0005752.t003 S. stercoralis free-living adults reproduce sexually As a possible explanation for the absence of hybrids, Schär, Guo and colleagues [37] proposed that S. stercoralis might not reproduce sexually, either because the free-living generation undergoes pseudogamy (sperm dependent parthenogenesis) as proposed earlier [25], or because in the study area the population propagates only through the non-sexual homogonic cycle. We showed above that the nuclear genome and the mitochondrial genomes, which are normally maternally inherited, do not evolve in parallel. This argues strongly for at least occasional sexual reproduction. Large numbers of free-living S. stercoralis of both sexes were present in our field and laboratory isolates and males were clearly required for reproduction in the free-living generation. Of a total of 480 females (96 from field isolates and 384 from a laboratory isolate) placed individually on plates before they had a chance to mate, none produced progeny. This result indicates that female autonomous reproduction by parthenogenesis or self-fertilization occurs rarely or not at all. However, the result is not an argument against pseudogamy, because, although they do not contribute genetic material to the progeny, males and their sperm are required to activate embryogenesis in this mode of reproduction. Further, although mitochondria are normally inherited only from the mother, in other nematodes male derived mitochondria occasionally fail to be degraded and are incorporated in zygotes [58,59]. This could also happen upon pseudogamic interaction between oocyte and sperm and lead to a recombination of nuclear and mitochondrial genomes. Therefore, we sought to demonstrate sexual reproduction more directly. To this end we genotyped 22 individual mothers (all derived from humans) and several of their progeny at two single-copy loci (Table 4). These results demonstrate clearly that the progeny were not the product of clonal reproduction because we found larvae with genetic material absent from the mother but presumably derived from the male and/or larvae that did not have alleles present in the mother, indicating that the mother passed on only half of its genetic material as expected for sexual but not for clonal reproduction. Download: PPT PowerPoint slide PNG larger image TIFF original image Table 4. Genotypes of free-living mothers and their progeny. https://doi.org/10.1371/journal.pntd.0005752.t004 We sought to further solidify this in a fully controlled experiment with known males and a larger number of progeny. To this end, we set up crosses with single females and males using a laboratory isolate of S. stercoralis. The results (Table 5) were fully consistent with Mendelian inheritance with equal genetic contribution by males and females but not with clonal reproduction. Download: PPT PowerPoint slide PNG larger image TIFF original image Table 5. Genotypes of free-living parents and their progeny at ytP274. https://doi.org/10.1371/journal.pntd.0005752.t005 Are there hybrids between SSU haplotypes? Given the results above, one would expect to observe animals that are hybrids between the different SSU HVR I haplotypes. However, like in an earlier study [37], we failed to find any hybrids among the 436 larvae from 97 different host individuals (68 humans 29 dogs) isolated in 2013. The SSU locus is on the X chromosome in S. stercoralis (information extracted from a previously published dataset [57]). Therefore, hybrid males could not be detected because they only contain one X chromosome. However, for [37] and in our 2013 sampling, young larvae that were the progeny of parasitic worms were analyzed. The sex of these larvae was unknown but given that the field isolates produced both sexes, it is very likely that a substantial number of females were among them. In 2016 we tested adult worms and used predominantly males because, unlike females, they may not contain genetic material from other individuals (sperm, embryos). Only 30 of the 307 worms from 2016 listed in Table 2 were pre-reproductive females. None of them was a hybrid. However, of the gravid females described in Table 4 one (Female 17) and one of its progeny showed a mixture of HVR I haplotypes II and III. While the mixed signal in the female might have been caused by sperm and embryos derived from a male with a different haplotype than the mother, the larva was most likely a true hybrid. This prompted us to test fully mature females that had been isolated from cultures, after they had a chance to mate, preserved in ethanol and separated by host individuals. We analyzed 9 to 23 worms from each of six host individuals (four humans, two dogs), from which we had already isolated S. stercoralis of different HVR I haplotypes. In five of the cases we found worms with mixed haplotypes, along with individuals with only one SSU haplotype (Table 6). Two observations are noteworthy. Firstly, both dogs had worms with HVR IV haplotypes A and B. In total, 11 out of 21 worms had mixed HVR I haplotypes but only a single one showed a mixture between the two HVR IV haplotypes, which might indicate that males and females with different HVR IV haplotypes tend to avoid each other. Secondly, from host individual KP57 (human), 9 of 14 worms had mixed haplotypes. From the same host individual we had also genotyped 12 pre-reproductive females, none of which was a hybrid. This finding suggests that the females genotyped in this experiment were not true hybrids but contained sperm and developing embryos derived from males of the other haplotype detected. Download: PPT PowerPoint slide PNG larger image TIFF original image Table 6. SSU haplotypes found in individual gravid females. https://doi.org/10.1371/journal.pntd.0005752.t006 Discussion In rural communities in Cambodia, many people share their premises with domestic animals and the general hygenic, water and sanitation infrastructures are precarious [60,61]. Therefore, the conditions appear very favorable for human to animal and animal to human transmission of STH including S. stercoralis [3]. In order to find evidence for or against zoonotic transmission of S. stercoralis under such circumstances, we isolated large numbers of S. stercoralis from humans and dogs at the same time and in the same households and analyzed individual worms using molecular genetic markers. To our knowledge there had been no such study of S. stercoralis of comparable scale undertaken anywhere. It should be noted that our experimental strategy aimed to sample individuals with a large potential for transfer of Strongyloides spp. between the two hosts (e.g., only dogs found close to households with positive people were sampled). Therefore our study was not designed to yield accurate estimates of haplotype frequencies in the entire population. We also point out that we did not directly demonstrate transmission from dogs to humans and therefore cannot exclude that the transmission is mostly or exclusively from human to dog. Nevertheless, our results strongly suggest that there is a considerable risk for dog to human transmission. This would not be in agreement with conclusions by Takano and colleagues [62] who found that humans in households with Strongyloides-infected dogs were not more likely to be parasitized by S. stercoralis than those with parasite free dogs and concluded that natural transmission does not occur between humans and dogs. However, this study was conducted in Japan, in areas with presumably much better sanitary conditions than in the Cambodian villages where the present study was conducted. Consequently, only five Strongyloides positive dogs were found and none of their owners was infected. Likewise, a study conducted in Southern China, in a setting probably more comparable to our study area [47], did not identify the presence of animals as a statistically significant risk factor for human strongyloidiasis. However, this conclusion was based on only 21 infected individuals (11.7% of the tested), and no details about the exposure to dogs are given. In rural settings dogs are usually semi-domesticated and roam freely such that the risk of exposure to contamination by canine feces among people who do not own a dog themselves might be approximately equal to the risk among people who do. Therefore, the lack of statistical significance cannot be taken as evidence against zoonotic transmission. Interestingly, a later study in a similar setting [63] revealed that anthelmintic treatment of people alone was not sufficient to significantly reduce the prevalence of S. stercoralis. Overall, the present findings strongly suggest that dogs must be seriously considered as sources for human strongyloidiasis. Whether dogs are the only non-human carrier of concern or if other animals also have the same potential remains to be determined. However, our results also show that at least in our study area, the majority of the Strongyloides present in dogs is of a genotype that we never found humans. Therefore, the number of Strongyloides spp. detected in dogs by coproscopic diagnosis might be an inaccurate index of the risk of exposure to S. stercoralis that dogs pose to humans. The 18S rDNA HVR IV appears to be diagnostic for the two separate Strongyloides populations in dogs. This agrees with the findings of Hasegawa and colleagues [35] who found this region to be invariable within S. stercoralis. Both, the mitochondrial cox1 and whole genome sequence analyses confirmed that the two HVR IV variants represent separate phylogenetic groups. Therefore, our results support the proposal by Brumpt and Augustine [43,44] of a separate species, Strongyloides canis. Consistent with [37] we found three different 18S rDNA HVR-I genotypes in human derived S. stercoralis. Worms of different haplotypes sometimes co-existed in the same host individual. In comparison with other nematodes [27–33] it is unusual that such differences in this region of the SSU occur within one species. However, species status can never be inferred from sequence information alone. Nevertheless, in those examples in nematodes where the same fragment around the HVR I was used and more rigorous criteria for species separation (e.g. mating experiments) could be applied, a sequence difference of more than one position was a safe indicator of a distinct species [28–33]. Most of the time, this region appears completely invariable within a species and there are several examples where even separate species do not differ in their HVR I. However, our comparative analyses of the mitochondrial cox1 locus and of whole genome data suggest that in S. stercoralis, different HVR I genotypes do not indicate separate species, but rather that in S. stercoralis the HVR I is more variable than in other nematodes. It should be noted that all the well-studied cases mentioned above involve obligate sexual nematode species, some of which are capable of self-fertilization. Asexual reproduction through the homogonic cycle, which may be a frequent mode of reproduction in S. stercoralis, might contribute to a higher variability within the species. Nevertheless, although we show that the different HVR I genotypes are not diagnostic for different species, our results do not exclude the existence of cryptic species among S. stercoralis. It is striking that, like Schar et al. [37], we failed to detect hybrids between different HVR I haplotypes among all worms that were the progeny of parasitic mothers and that were definitely unmated. However, in mature free-living females and in their progeny, we frequently found mixed signals. While, for reasons described above, we doubt that these females were true hybrids, their offspring presumably were. We think that this indicates that adults of different HVR I haplotype do mate, at least in laboratory fecal cultures, and that at least some of the progeny develop to larval stages. We can only speculate about why such hybrids are not found in the progeny of the parasitic generation. It might be that the hybrids, or even the progeny of the free-living generation in general, are sub-viable and only rarely develop into successful fertile parasitic females. In this case genetic mixing between subpopulations would occur only rarely. Over long periods of time, even rare exchange might be significant and cause enough mixing of the genomes that we were not able to detect genetic differentiation between subpopulations. Alternatively, in the S. stercoralis populations in our study area there might be very high inbreeding (brother sister mating) under natural conditions. This would lead to a very high degree of homozygosity in the population. Both scenarios described above would lead to a very low number of SSU haplotype heterozygotes in the population, and we may have simply missed the rare hybrids. In order to address this, controlled crosses and experimental infections are required. In the context of this study we had no opportunity to do such experiments because, for logistic and for legal reasons, we were not able to bring live worms into our laboratory. Our results demonstrate, however, that such crossing experiments are possible. We demonstrate that in contrast to earlier claims [25], sexual reproduction in the free-living generation of S. stercoralis does occur and is likely the predominant, if not the only the mode of reproduction in this generation. With this, the number of species of Strongyloides for which genetic analyses demonstrated that the reproduction in the free-living generation is sexual rises to four out of four tested (S. ratti [23,24], S. papillosus [22], S. vituli [64], S. stecoralis, this study). Sexual reproduction by S. stercoralis has also been confirmed recently by experimental crossing of free-living male and female worms harboring discrete reporter transgenes[65]. Although these findings do not exclude that asexual species or strains might exist, even within what is currently referred to as S. stercoralis, they do suggest strongly that sexual reproduction rather than pseudogamy is the prevailing mode of reproduction in free-living Strongyloides spp. Conclusions and outlook Our results provide a compelling solution for the long-standing controversy about whether the Strongyloides sp. of dogs is identical to the S. stercoralis of humans or not. In fact, both scenarios appear to be true. Dogs, at least in our study area, host two different populations. These either represent separate species or well-separated sub-species of Strongyloides spp, and only one of them is shared with humans. It remains to be determined if the different types of Strongyloides we observed in humans and dogs also occur in other regions of the world. Among S. stercoralis in humans there is variability in the rDNA sequence. While we did not find further genomic evidence supporting multiple genetically separate populations in humans the absence of hybrids between the different SSU HVR I haplotypes is striking. It will be most interesting to ascertain whether different SSU HVR I types indeed interbreed and, even more importantly, if they might be associated with different clinical outcomes. Therefore, we suggest using molecular diagnostics for Strongyloides spp. wherever possible. In order to generate comparable data, we propose following the lead of Hasegawa and colleagues [35,38], and using the SSU HVRs I and IV and the mitochondrial cox1 locus as primary markers as was done in this study. With respect to strongyloidiasis control and prevention, this study suggests that dogs should be seriously considered as a source for human S. stercoralis infection at least in settings similar to our study area. Prevention of human contact with dog feces and of dog contact with human excrement as well as anthelmintic treatment of dogs are likely to reduce the exposure of humans to infective S. stercoralis larvae. Supporting information S1 Text. Sequences of the cox1 haplotypes and the molecular markers. The sequences of the mitochondrial cox1 haplotypes and the sequences of the nuclear molecular markers are given. GenBank accession numbers are in (KX226367-KX226384). For the nuclear markers the polymorphic positions are indicated by red boxes. https://doi.org/10.1371/journal.pntd.0005752.s001 (DOCX) S1 Table. SSU HVR I and IV and cox 1 haplotypes of all individuals analyzed. Sheet 1: worms collected 2016 from humans. Sheet 2: worms collected 2016 from dogs. Sheet 3: worms collected 2013 from humans. Sheet 4: worms collected 2013 from dogs. https://doi.org/10.1371/journal.pntd.0005752.s002 (XLSX) Acknowledgments We thank Christa Lanz, Julia Hildebrandt and Mireille Belkacemi from the MPI for Developmental Biology Genome Center for sequencing service and Dorothee Harbecke for technical assistance. We are indebted to all the participants of this study and the field assistants. We thank Alex Dulovic for critically reading the manuscript.
TI - Different but overlapping populations of Strongyloides stercoralis in dogs and humans—Dogs as a possible source for zoonotic strongyloidiasis
JF - PLoS Neglected Tropical Diseases
DO - 10.1371/journal.pntd.0005752
DA - 2017-08-09
UR - https://www.deepdyve.com/lp/public-library-of-science-plos-journal/different-but-overlapping-populations-of-strongyloides-stercoralis-in-LMqV7Rm8h9
SP - e0005752
VL - 11
IS - 8
DP - DeepDyve
ER -