Abstract

BackgroundIatrogenic infection of humans with Trichuris suis (a parasitic nematode of swine) is being evaluated or promoted as a biological, curative treatment of immune diseases, such as inflammatory bowel disease (IBD) and ulcerative colitis, in humans. Although it is understood that short-term T. suis infection in people with such diseases usually induces a modified Th2-immune response, nothing is known about the molecules in the parasite that induce this response.Methodology/Principal FindingsAs a first step toward filling the gaps in our knowledge of the molecular biology of T. suis, we characterised the transcriptome of the adult stage of this nematode employing next-generation sequencing and bioinformatic techniques. A total of ∼65,000,000 reads were generated and assembled into ∼20,000 contiguous sequences ( = contigs); ∼17,000 peptides were predicted and classified based on homology searches, protein motifs and gene ontology and biological pathway mapping.ConclusionsThese analyses provided interesting insights into a number of molecular groups, particularly predicted excreted/secreted molecules (n = 1,288), likely to be involved in the parasite-host interactions, and also various molecules (n = 120) linked to chemokine, T-cell receptor and TGF-β signalling as well as leukocyte transendothelial migration and natural killer cell-mediated cytotoxicity, which are likely to be immuno-regulatory or -modulatory in the infected host. This information provides a conceptual framework within which to test the immunobiological basis for the curative effect of T. suis infection in humans against some immune diseases. Importantly, the T. suis transcriptome characterised herein provides a curated resource for detailed studies of the immuno-molecular biology of this parasite, and will underpin future genomic and proteomic explorations.

Highlights

  • Parasitic nematodes that infect the gastrointestinal tracts of humans are of major socioeconomic significance worldwide [1,2]

  • Raw reads Contigs GC content (%) Raw reads mapped to contigs (%) Containing an Open Reading frame (%) With homologues in Caenorhabditis elegans (%) Trichinella spiralis Homo sapiens Sus scrofa other parasitic nematodes (%) other organisms (%) Returning InterProScan results (%) Number of InterPro terms Gene Ontology (%) Number of Biological process terms Cellular component Molecular function Returning a KOBAS result (%) Number of predicted biological pathways (KEGG) Predicted proteins with signal peptides (%) with transmembrane domains (%) Homologous to proteins in the SPD database (%) Predicted excretory/secretory proteins*

  • *Inferred based on the presence of a signal peptide and homology to known proteins in the SPD database. doi:10.1371/journal.pone.0023590.t001 (Table 1); 10,324 of them (58.5%) had highest homology to proteins predicted for T. spiralis, followed by those from C. elegans (n = 8,754; 49.6%), M. hapla (n = 7,575; 49.9%) and P. pacificus (n = 8,232; 46.6%) (Figure 1)

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Summary

Introduction

Parasitic nematodes that infect the gastrointestinal tracts of humans are of major socioeconomic significance worldwide [1,2]. There is an increasing body of evidence suggesting that, STHs can a have major adverse impact on human health, people in endemic countries tend to suffer significantly less from (chronic) immunopathological diseases [7] This situation contrasts published evidence [8,9,10,11] for developed countries, where people who are not exposed to STHs (and/or other parasites; cf [12]) suffer significantly more from these diseases, such as inflammatory bowel diseases (IBD; including Crohn’s disease and ulcerative colitis [9]) and asthma [8,10,11]. It is understood that short-term T. suis infection in people with such diseases usually induces a modified Th2-immune response, nothing is known about the molecules in the parasite that induce this response

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