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Identification of candidate mimicry proteins involved in parasite-driven phenotypic changes
BACKGROUND: Endoparasites with complex life cycles are faced with several biological challenges, as they need to occupy various ecological niches throughout their development. Host phenotypes that increase the parasite’s transmission rate to the next host have been extensively described, but few mec...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4407394/ https://www.ncbi.nlm.nih.gov/pubmed/25888917 http://dx.doi.org/10.1186/s13071-015-0834-1 |
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author | Hebert, Francois Olivier Phelps, Luke Samonte, Irene Panchal, Mahesh Grambauer, Stephan Barber, Iain Kalbe, Martin Landry, Christian R Aubin-Horth, Nadia |
author_facet | Hebert, Francois Olivier Phelps, Luke Samonte, Irene Panchal, Mahesh Grambauer, Stephan Barber, Iain Kalbe, Martin Landry, Christian R Aubin-Horth, Nadia |
author_sort | Hebert, Francois Olivier |
collection | PubMed |
description | BACKGROUND: Endoparasites with complex life cycles are faced with several biological challenges, as they need to occupy various ecological niches throughout their development. Host phenotypes that increase the parasite’s transmission rate to the next host have been extensively described, but few mechanistic explanations have been proposed to describe their proximate causes. In this study we explore the possibility that host phenotypic changes are triggered by the production of mimicry proteins from the parasite by using an ecological model system consisting of the infection of the threespine stickleback (Gasterosteus aculeatus) by the cestode Schistocephalus solidus. METHOD: Using RNA-seq data, we assembled 9,093 protein-coding genes from which ORFs were predicted to generate a reference proteome. Based on a previously published method, we built two complementary analysis pipelines to i) establish a general classification of protein similarity among various species (pipeline A) and ii) identify candidate mimicry proteins showing specific host-parasite similarities (pipeline B), a key feature underlying the possibility of molecular mimicry. RESULTS: Ninety-four tapeworm proteins showed high local sequence homology with stickleback proteins. Four of these candidates correspond to secreted or membrane proteins that could be produced by the parasite and eventually be released in or be in contact with the host to modulate physiological pathways involved in various phenotypes (e.g. behaviors). One of these candidates belongs to the Wnt family, a large group of signaling molecules involved in cell-to-cell interactions and various developmental pathways. The three other candidates are involved in ion transport and post-translational protein modifications. We further confirmed that these four candidates are expressed in three different developmental stages of the cestode by RT-PCR, including the stages found in the host. CONCLUSION: In this study, we identified mimicry candidate peptides from a behavior-altering cestode showing specific sequence similarity with host proteins. Despite their potential role in modulating host pathways that could lead to parasite-induced phenotypic changes and despite our confirmation that they are expressed in the developmental stage corresponding to the altered host behavior, further investigations will be needed to confirm their mechanistic role in the molecular cross-talk taking place between S. solidus and the threespine stickleback. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-015-0834-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4407394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44073942015-04-24 Identification of candidate mimicry proteins involved in parasite-driven phenotypic changes Hebert, Francois Olivier Phelps, Luke Samonte, Irene Panchal, Mahesh Grambauer, Stephan Barber, Iain Kalbe, Martin Landry, Christian R Aubin-Horth, Nadia Parasit Vectors Research BACKGROUND: Endoparasites with complex life cycles are faced with several biological challenges, as they need to occupy various ecological niches throughout their development. Host phenotypes that increase the parasite’s transmission rate to the next host have been extensively described, but few mechanistic explanations have been proposed to describe their proximate causes. In this study we explore the possibility that host phenotypic changes are triggered by the production of mimicry proteins from the parasite by using an ecological model system consisting of the infection of the threespine stickleback (Gasterosteus aculeatus) by the cestode Schistocephalus solidus. METHOD: Using RNA-seq data, we assembled 9,093 protein-coding genes from which ORFs were predicted to generate a reference proteome. Based on a previously published method, we built two complementary analysis pipelines to i) establish a general classification of protein similarity among various species (pipeline A) and ii) identify candidate mimicry proteins showing specific host-parasite similarities (pipeline B), a key feature underlying the possibility of molecular mimicry. RESULTS: Ninety-four tapeworm proteins showed high local sequence homology with stickleback proteins. Four of these candidates correspond to secreted or membrane proteins that could be produced by the parasite and eventually be released in or be in contact with the host to modulate physiological pathways involved in various phenotypes (e.g. behaviors). One of these candidates belongs to the Wnt family, a large group of signaling molecules involved in cell-to-cell interactions and various developmental pathways. The three other candidates are involved in ion transport and post-translational protein modifications. We further confirmed that these four candidates are expressed in three different developmental stages of the cestode by RT-PCR, including the stages found in the host. CONCLUSION: In this study, we identified mimicry candidate peptides from a behavior-altering cestode showing specific sequence similarity with host proteins. Despite their potential role in modulating host pathways that could lead to parasite-induced phenotypic changes and despite our confirmation that they are expressed in the developmental stage corresponding to the altered host behavior, further investigations will be needed to confirm their mechanistic role in the molecular cross-talk taking place between S. solidus and the threespine stickleback. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-015-0834-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-15 /pmc/articles/PMC4407394/ /pubmed/25888917 http://dx.doi.org/10.1186/s13071-015-0834-1 Text en © Hebert et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Hebert, Francois Olivier Phelps, Luke Samonte, Irene Panchal, Mahesh Grambauer, Stephan Barber, Iain Kalbe, Martin Landry, Christian R Aubin-Horth, Nadia Identification of candidate mimicry proteins involved in parasite-driven phenotypic changes |
title | Identification of candidate mimicry proteins involved in parasite-driven phenotypic changes |
title_full | Identification of candidate mimicry proteins involved in parasite-driven phenotypic changes |
title_fullStr | Identification of candidate mimicry proteins involved in parasite-driven phenotypic changes |
title_full_unstemmed | Identification of candidate mimicry proteins involved in parasite-driven phenotypic changes |
title_short | Identification of candidate mimicry proteins involved in parasite-driven phenotypic changes |
title_sort | identification of candidate mimicry proteins involved in parasite-driven phenotypic changes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4407394/ https://www.ncbi.nlm.nih.gov/pubmed/25888917 http://dx.doi.org/10.1186/s13071-015-0834-1 |
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