Sex-Biased Transcriptome of Schistosoma mansoni: Host-Parasite Interaction, Genetic Determinants and Epigenetic Regulators Are Associated with Sexual Differentiation

Background Among more than 20,000 species of hermaphroditic trematodes, Schistosomatidae are unusual since they have evolved gonochorism. In schistosomes, sex is determined by a female heterogametic system, but phenotypic sexual dimorphism appears only after infection of the vertebrate definitive host. The completion of gonad maturation occurs even later, after pairing. To date, the molecular mechanisms that trigger the sexual differentiation in these species remain unknown, and in vivo studies on the developing schistosomulum stages are lacking. To study the molecular basis of sex determination and sexual differentiation in schistosomes, we investigated the whole transcriptome of the human parasite Schistosoma mansoni in a stage-and sex-comparative manner. Methodology/Principal Findings We performed a RNA-seq on males and females for five developmental stages: cercariae larvae, three in vivo schistosomulum stages and adults. We detected 7,168 genes differentially expressed between sexes in at least one of the developmental stages, and 4,065 of them were functionally annotated. Transcriptome data were completed with H3K27me3 histone modification analysis using ChIP-Seq before (in cercariae) and after (in adults) the phenotypic sexual dimorphism appearance. In this paper we present (i) candidate determinants of the sexual differentiation, (ii) sex-biased players of the interaction with the vertebrate host, and (iii) different dynamic of the H3K27me3 histone mark between sexes as an illustration of sex-biased epigenetic landscapes. Conclusions/Significance Our work presents evidence that sexual differentiation in S. mansoni is accompanied by distinct male and female transcriptional landscapes of known players of the host-parasite crosstalk, genetic determinants and epigenetic regulators. Our results suggest that such combination could lead to the optimized sexual dimorphism of this parasitic species. As S. mansoni is pathogenic for humans, this study represents a promising source of therapeutic targets, providing not only data on the parasite development in interaction with its vertebrate host, but also new insights on its reproductive function.

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S1 Protocol. Sorting criteria of in vivo schistosomulum stages.
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S1 Supporting information. Bioinformatic workflow and quality of the metrics.
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S2 Supporting information. RT-qPCR experiments.
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S1 Table. PCR/qPCR primers.
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S2 Table. De novo functional annotation and structural analysis of the 100 best adjusted P-values.
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S3 Table. Gene Ontology.
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S4 Table. Functional analysis.
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S5 Table. Global data: Sequences of unique transcripts (TCONS), functional annotation of the de novo transcriptome, cross-references between XLOC and Smp_ID, Blast results for miRNA precursors and...
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S6 Table. Gene annotation and expression levels of clustered genes (Corresponding to Fig 3).
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S7 Table. Micro-exon gene structures.
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How to cite
Picard Marion A. L., Boissier Jerome, Roquis David, Grunau Christoph, Allienne Jean-Francois, Duval David, Toulza Eve, Arancibia Nathalie, Caffrey Conor R., Long Thavy, Nidelet Sabine, Rohmer Marine, Cosseau Celine (2016). Sex-Biased Transcriptome of Schistosoma mansoni: Host-Parasite Interaction, Genetic Determinants and Epigenetic Regulators Are Associated with Sexual Differentiation. Plos Neglected Tropical Diseases. 10 (9). 582 (11p.). https://doi.org/10.1371/journal.pntd.0004930, https://archimer.ifremer.fr/doc/00358/46876/

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