Cargando…

RNAseq Analysis of the Parasitic Nematode Strongyloides stercoralis Reveals Divergent Regulation of Canonical Dauer Pathways

The infectious form of many parasitic nematodes, which afflict over one billion people globally, is a developmentally arrested third-stage larva (L3i). The parasitic nematode Strongyloides stercoralis differs from other nematode species that infect humans, in that its life cycle includes both parasi...

Descripción completa

Detalles Bibliográficos
Autores principales: Stoltzfus, Jonathan D., Minot, Samuel, Berriman, Matthew, Nolan, Thomas J., Lok, James B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493385/
https://www.ncbi.nlm.nih.gov/pubmed/23145190
http://dx.doi.org/10.1371/journal.pntd.0001854
_version_ 1782249257321889792
author Stoltzfus, Jonathan D.
Minot, Samuel
Berriman, Matthew
Nolan, Thomas J.
Lok, James B.
author_facet Stoltzfus, Jonathan D.
Minot, Samuel
Berriman, Matthew
Nolan, Thomas J.
Lok, James B.
author_sort Stoltzfus, Jonathan D.
collection PubMed
description The infectious form of many parasitic nematodes, which afflict over one billion people globally, is a developmentally arrested third-stage larva (L3i). The parasitic nematode Strongyloides stercoralis differs from other nematode species that infect humans, in that its life cycle includes both parasitic and free-living forms, which can be leveraged to investigate the mechanisms of L3i arrest and activation. The free-living nematode Caenorhabditis elegans has a similar developmentally arrested larval form, the dauer, whose formation is controlled by four pathways: cyclic GMP (cGMP) signaling, insulin/IGF-1-like signaling (IIS), transforming growth factor β (TGFβ) signaling, and biosynthesis of dafachronic acid (DA) ligands that regulate a nuclear hormone receptor. We hypothesized that homologous pathways are present in S. stercoralis, have similar developmental regulation, and are involved in L3i arrest and activation. To test this, we undertook a deep-sequencing study of the polyadenylated transcriptome, generating over 2.3 billion paired-end reads from seven developmental stages. We constructed developmental expression profiles for S. stercoralis homologs of C. elegans dauer genes identified by BLAST searches of the S. stercoralis genome as well as de novo assembled transcripts. Intriguingly, genes encoding cGMP pathway components were coordinately up-regulated in L3i. In comparison to C. elegans, S. stercoralis has a paucity of genes encoding IIS ligands, several of which have abundance profiles suggesting involvement in L3i development. We also identified seven S. stercoralis genes encoding homologs of the single C. elegans dauer regulatory TGFβ ligand, three of which are only expressed in L3i. Putative DA biosynthetic genes did not appear to be coordinately regulated in L3i development. Our data suggest that while dauer pathway genes are present in S. stercoralis and may play a role in L3i development, there are significant differences between the two species. Understanding the mechanisms governing L3i development may lead to novel treatment and control strategies.
format Online
Article
Text
id pubmed-3493385
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-34933852012-11-09 RNAseq Analysis of the Parasitic Nematode Strongyloides stercoralis Reveals Divergent Regulation of Canonical Dauer Pathways Stoltzfus, Jonathan D. Minot, Samuel Berriman, Matthew Nolan, Thomas J. Lok, James B. PLoS Negl Trop Dis Research Article The infectious form of many parasitic nematodes, which afflict over one billion people globally, is a developmentally arrested third-stage larva (L3i). The parasitic nematode Strongyloides stercoralis differs from other nematode species that infect humans, in that its life cycle includes both parasitic and free-living forms, which can be leveraged to investigate the mechanisms of L3i arrest and activation. The free-living nematode Caenorhabditis elegans has a similar developmentally arrested larval form, the dauer, whose formation is controlled by four pathways: cyclic GMP (cGMP) signaling, insulin/IGF-1-like signaling (IIS), transforming growth factor β (TGFβ) signaling, and biosynthesis of dafachronic acid (DA) ligands that regulate a nuclear hormone receptor. We hypothesized that homologous pathways are present in S. stercoralis, have similar developmental regulation, and are involved in L3i arrest and activation. To test this, we undertook a deep-sequencing study of the polyadenylated transcriptome, generating over 2.3 billion paired-end reads from seven developmental stages. We constructed developmental expression profiles for S. stercoralis homologs of C. elegans dauer genes identified by BLAST searches of the S. stercoralis genome as well as de novo assembled transcripts. Intriguingly, genes encoding cGMP pathway components were coordinately up-regulated in L3i. In comparison to C. elegans, S. stercoralis has a paucity of genes encoding IIS ligands, several of which have abundance profiles suggesting involvement in L3i development. We also identified seven S. stercoralis genes encoding homologs of the single C. elegans dauer regulatory TGFβ ligand, three of which are only expressed in L3i. Putative DA biosynthetic genes did not appear to be coordinately regulated in L3i development. Our data suggest that while dauer pathway genes are present in S. stercoralis and may play a role in L3i development, there are significant differences between the two species. Understanding the mechanisms governing L3i development may lead to novel treatment and control strategies. Public Library of Science 2012-10-25 /pmc/articles/PMC3493385/ /pubmed/23145190 http://dx.doi.org/10.1371/journal.pntd.0001854 Text en © 2012 Stoltzfus et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Stoltzfus, Jonathan D.
Minot, Samuel
Berriman, Matthew
Nolan, Thomas J.
Lok, James B.
RNAseq Analysis of the Parasitic Nematode Strongyloides stercoralis Reveals Divergent Regulation of Canonical Dauer Pathways
title RNAseq Analysis of the Parasitic Nematode Strongyloides stercoralis Reveals Divergent Regulation of Canonical Dauer Pathways
title_full RNAseq Analysis of the Parasitic Nematode Strongyloides stercoralis Reveals Divergent Regulation of Canonical Dauer Pathways
title_fullStr RNAseq Analysis of the Parasitic Nematode Strongyloides stercoralis Reveals Divergent Regulation of Canonical Dauer Pathways
title_full_unstemmed RNAseq Analysis of the Parasitic Nematode Strongyloides stercoralis Reveals Divergent Regulation of Canonical Dauer Pathways
title_short RNAseq Analysis of the Parasitic Nematode Strongyloides stercoralis Reveals Divergent Regulation of Canonical Dauer Pathways
title_sort rnaseq analysis of the parasitic nematode strongyloides stercoralis reveals divergent regulation of canonical dauer pathways
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493385/
https://www.ncbi.nlm.nih.gov/pubmed/23145190
http://dx.doi.org/10.1371/journal.pntd.0001854
work_keys_str_mv AT stoltzfusjonathand rnaseqanalysisoftheparasiticnematodestrongyloidesstercoralisrevealsdivergentregulationofcanonicaldauerpathways
AT minotsamuel rnaseqanalysisoftheparasiticnematodestrongyloidesstercoralisrevealsdivergentregulationofcanonicaldauerpathways
AT berrimanmatthew rnaseqanalysisoftheparasiticnematodestrongyloidesstercoralisrevealsdivergentregulationofcanonicaldauerpathways
AT nolanthomasj rnaseqanalysisoftheparasiticnematodestrongyloidesstercoralisrevealsdivergentregulationofcanonicaldauerpathways
AT lokjamesb rnaseqanalysisoftheparasiticnematodestrongyloidesstercoralisrevealsdivergentregulationofcanonicaldauerpathways