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Identification of candidate infection genes from the model entomopathogenic nematode Heterorhabditis bacteriophora

BACKGROUND: Despite important progress in the field of innate immunity, our understanding of host immune responses to parasitic nematode infections lags behind that of responses to microbes. A limiting factor has been the obligate requirement for a vertebrate host which has hindered investigation of...

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Autores principales: Vadnal, Jonathan, Ratnappan, Ramesh, Keaney, Melissa, Kenney, Eric, Eleftherianos, Ioannis, O’Halloran, Damien, Hawdon, John M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5209865/
https://www.ncbi.nlm.nih.gov/pubmed/28049427
http://dx.doi.org/10.1186/s12864-016-3468-6
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author Vadnal, Jonathan
Ratnappan, Ramesh
Keaney, Melissa
Kenney, Eric
Eleftherianos, Ioannis
O’Halloran, Damien
Hawdon, John M.
author_facet Vadnal, Jonathan
Ratnappan, Ramesh
Keaney, Melissa
Kenney, Eric
Eleftherianos, Ioannis
O’Halloran, Damien
Hawdon, John M.
author_sort Vadnal, Jonathan
collection PubMed
description BACKGROUND: Despite important progress in the field of innate immunity, our understanding of host immune responses to parasitic nematode infections lags behind that of responses to microbes. A limiting factor has been the obligate requirement for a vertebrate host which has hindered investigation of the parasitic nematode infective process. The nematode parasite Heterorhabditis bacteriophora offers great potential as a model to genetically dissect the process of infection. With its mutualistic Photorhabdus luminescens bacteria, H. bacteriophora invades multiple species of insects, which it kills and exploits as a food source for the development of several nematode generations. The ability to culture the life cycle of H. bacteriophora on plates growing the bacterial symbiont makes it a very exciting model of parasitic infection that can be used to unlock the molecular events occurring during infection of a host that are inaccessible using vertebrate hosts. RESULTS: To profile the transcriptional response of an infective nematode during the early stage of infection, we performed next generation RNA sequencing on H. bacteriophora IJs incubated in Manduca sexta hemolymph plasma for 9 h. A subset of up-regulated and down-regulated genes were validated using qRT-PCR. Comparative analysis of the transcriptome with untreated controls found a number of differentially expressed genes (DEGs) which cover a number of different functional categories. A subset of DEGs is conserved across Clade V parasitic nematodes revealing an array of candidate parasitic genes. CONCLUSIONS: Our analysis reveals transcriptional changes in the regulation of a large number of genes, most of which have not been shown previously to play a role in the process of infection. A significant proportion of these genes are unique to parasitic nematodes, suggesting the identification of a group of parasitism factors within nematodes. Future studies using these candidates may provide functional insight into the process of nematode parasitism and also the molecular evolution of parasitism within nematodes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3468-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-52098652017-01-04 Identification of candidate infection genes from the model entomopathogenic nematode Heterorhabditis bacteriophora Vadnal, Jonathan Ratnappan, Ramesh Keaney, Melissa Kenney, Eric Eleftherianos, Ioannis O’Halloran, Damien Hawdon, John M. BMC Genomics Research Article BACKGROUND: Despite important progress in the field of innate immunity, our understanding of host immune responses to parasitic nematode infections lags behind that of responses to microbes. A limiting factor has been the obligate requirement for a vertebrate host which has hindered investigation of the parasitic nematode infective process. The nematode parasite Heterorhabditis bacteriophora offers great potential as a model to genetically dissect the process of infection. With its mutualistic Photorhabdus luminescens bacteria, H. bacteriophora invades multiple species of insects, which it kills and exploits as a food source for the development of several nematode generations. The ability to culture the life cycle of H. bacteriophora on plates growing the bacterial symbiont makes it a very exciting model of parasitic infection that can be used to unlock the molecular events occurring during infection of a host that are inaccessible using vertebrate hosts. RESULTS: To profile the transcriptional response of an infective nematode during the early stage of infection, we performed next generation RNA sequencing on H. bacteriophora IJs incubated in Manduca sexta hemolymph plasma for 9 h. A subset of up-regulated and down-regulated genes were validated using qRT-PCR. Comparative analysis of the transcriptome with untreated controls found a number of differentially expressed genes (DEGs) which cover a number of different functional categories. A subset of DEGs is conserved across Clade V parasitic nematodes revealing an array of candidate parasitic genes. CONCLUSIONS: Our analysis reveals transcriptional changes in the regulation of a large number of genes, most of which have not been shown previously to play a role in the process of infection. A significant proportion of these genes are unique to parasitic nematodes, suggesting the identification of a group of parasitism factors within nematodes. Future studies using these candidates may provide functional insight into the process of nematode parasitism and also the molecular evolution of parasitism within nematodes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3468-6) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-03 /pmc/articles/PMC5209865/ /pubmed/28049427 http://dx.doi.org/10.1186/s12864-016-3468-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Article
Vadnal, Jonathan
Ratnappan, Ramesh
Keaney, Melissa
Kenney, Eric
Eleftherianos, Ioannis
O’Halloran, Damien
Hawdon, John M.
Identification of candidate infection genes from the model entomopathogenic nematode Heterorhabditis bacteriophora
title Identification of candidate infection genes from the model entomopathogenic nematode Heterorhabditis bacteriophora
title_full Identification of candidate infection genes from the model entomopathogenic nematode Heterorhabditis bacteriophora
title_fullStr Identification of candidate infection genes from the model entomopathogenic nematode Heterorhabditis bacteriophora
title_full_unstemmed Identification of candidate infection genes from the model entomopathogenic nematode Heterorhabditis bacteriophora
title_short Identification of candidate infection genes from the model entomopathogenic nematode Heterorhabditis bacteriophora
title_sort identification of candidate infection genes from the model entomopathogenic nematode heterorhabditis bacteriophora
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5209865/
https://www.ncbi.nlm.nih.gov/pubmed/28049427
http://dx.doi.org/10.1186/s12864-016-3468-6
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