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Host gene response to endosymbiont and pathogen in the cereal weevil Sitophilus oryzae

BACKGROUND: Insects thriving on nutritionally poor habitats have integrated mutualistic intracellular symbiotic bacteria (endosymbionts) in a bacteria-bearing tissue (the bacteriome) that isolates the endosymbionts and protects them against a host systemic immune response. Whilst the metabolic and p...

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Autores principales: Vigneron, Aurélien, Charif, Delphine, Vincent-Monégat, Carole, Vallier, Agnès, Gavory, Frédérick, Wincker, Patrick, Heddi, Abdelaziz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287511/
https://www.ncbi.nlm.nih.gov/pubmed/22375912
http://dx.doi.org/10.1186/1471-2180-12-S1-S14
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author Vigneron, Aurélien
Charif, Delphine
Vincent-Monégat, Carole
Vallier, Agnès
Gavory, Frédérick
Wincker, Patrick
Heddi, Abdelaziz
author_facet Vigneron, Aurélien
Charif, Delphine
Vincent-Monégat, Carole
Vallier, Agnès
Gavory, Frédérick
Wincker, Patrick
Heddi, Abdelaziz
author_sort Vigneron, Aurélien
collection PubMed
description BACKGROUND: Insects thriving on nutritionally poor habitats have integrated mutualistic intracellular symbiotic bacteria (endosymbionts) in a bacteria-bearing tissue (the bacteriome) that isolates the endosymbionts and protects them against a host systemic immune response. Whilst the metabolic and physiological features of long-term insect associations have been investigated in detail over the past decades, cellular and immune regulations that determine the host response to endosymbionts and pathogens have attracted interest more recently. RESULTS: To investigate bacteriome cellular specificities and weevil immune responses to bacteria, we have constructed and sequenced 7 cDNA libraries from Sitophilus oryzae whole larvae and bacteriomes. Bioinformatic analysis of 26,886 ESTs led to the generation of 8,941 weevil unigenes. Based on in silico analysis and on the examination of genes involved in the cellular pathways of potential interest to intracellular symbiosis (i.e. cell growth and apoptosis, autophagy, immunity), we have selected and analyzed 29 genes using qRT-PCR, taking into consideration bacteriome specificity and symbiosis impact on the host response to pathogens. We show that the bacteriome tissue accumulates transcripts from genes involved in cellular development and survival, such as the apoptotic inhibitors iap2 and iap3, and endosomal fusion and trafficking, such as Rab7, Hrs, and SNARE. As regards our investigation into immunity, we first strengthen the bacteriome immunomodulation previously reported in S. zeamais. We show that the sarcotoxin, the c-type lysozyme, and the wpgrp2 genes are downregulated in the S. oryzae bacteriome, when compared to aposymbiotic insects and insects challenged with E. coli. Secondly, transcript level comparison between symbiotic and aposymbiotic larvae provides evidence that the immune systemic response to pathogens is decreased in symbiotic insects, as shown by the relatively high expression of wpgrp2, wpgrp3, coleoptericin-B, diptericin, and sarcotoxin genes in aposymbiotic insects. CONCLUSIONS: Library sequencing significantly increased the number of unigenes, allowing for improved functional and genetic investigations in the cereal weevil S. oryzae. Transcriptomic analyses support selective and local immune gene expression in the bacteriome tissue and uncover cellular pathways that are of potential interest to bacteriocyte survival and homeostasis. Bacterial challenge experiments have revealed that the systemic immune response would be less induced in a symbiotic insect, thus highlighting new perspectives on host immunity in long-term invertebrate co-evolutionary associations.
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spelling pubmed-32875112012-02-28 Host gene response to endosymbiont and pathogen in the cereal weevil Sitophilus oryzae Vigneron, Aurélien Charif, Delphine Vincent-Monégat, Carole Vallier, Agnès Gavory, Frédérick Wincker, Patrick Heddi, Abdelaziz BMC Microbiol Research BACKGROUND: Insects thriving on nutritionally poor habitats have integrated mutualistic intracellular symbiotic bacteria (endosymbionts) in a bacteria-bearing tissue (the bacteriome) that isolates the endosymbionts and protects them against a host systemic immune response. Whilst the metabolic and physiological features of long-term insect associations have been investigated in detail over the past decades, cellular and immune regulations that determine the host response to endosymbionts and pathogens have attracted interest more recently. RESULTS: To investigate bacteriome cellular specificities and weevil immune responses to bacteria, we have constructed and sequenced 7 cDNA libraries from Sitophilus oryzae whole larvae and bacteriomes. Bioinformatic analysis of 26,886 ESTs led to the generation of 8,941 weevil unigenes. Based on in silico analysis and on the examination of genes involved in the cellular pathways of potential interest to intracellular symbiosis (i.e. cell growth and apoptosis, autophagy, immunity), we have selected and analyzed 29 genes using qRT-PCR, taking into consideration bacteriome specificity and symbiosis impact on the host response to pathogens. We show that the bacteriome tissue accumulates transcripts from genes involved in cellular development and survival, such as the apoptotic inhibitors iap2 and iap3, and endosomal fusion and trafficking, such as Rab7, Hrs, and SNARE. As regards our investigation into immunity, we first strengthen the bacteriome immunomodulation previously reported in S. zeamais. We show that the sarcotoxin, the c-type lysozyme, and the wpgrp2 genes are downregulated in the S. oryzae bacteriome, when compared to aposymbiotic insects and insects challenged with E. coli. Secondly, transcript level comparison between symbiotic and aposymbiotic larvae provides evidence that the immune systemic response to pathogens is decreased in symbiotic insects, as shown by the relatively high expression of wpgrp2, wpgrp3, coleoptericin-B, diptericin, and sarcotoxin genes in aposymbiotic insects. CONCLUSIONS: Library sequencing significantly increased the number of unigenes, allowing for improved functional and genetic investigations in the cereal weevil S. oryzae. Transcriptomic analyses support selective and local immune gene expression in the bacteriome tissue and uncover cellular pathways that are of potential interest to bacteriocyte survival and homeostasis. Bacterial challenge experiments have revealed that the systemic immune response would be less induced in a symbiotic insect, thus highlighting new perspectives on host immunity in long-term invertebrate co-evolutionary associations. BioMed Central 2012-01-18 /pmc/articles/PMC3287511/ /pubmed/22375912 http://dx.doi.org/10.1186/1471-2180-12-S1-S14 Text en Copyright ©2012 Vigneron et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Vigneron, Aurélien
Charif, Delphine
Vincent-Monégat, Carole
Vallier, Agnès
Gavory, Frédérick
Wincker, Patrick
Heddi, Abdelaziz
Host gene response to endosymbiont and pathogen in the cereal weevil Sitophilus oryzae
title Host gene response to endosymbiont and pathogen in the cereal weevil Sitophilus oryzae
title_full Host gene response to endosymbiont and pathogen in the cereal weevil Sitophilus oryzae
title_fullStr Host gene response to endosymbiont and pathogen in the cereal weevil Sitophilus oryzae
title_full_unstemmed Host gene response to endosymbiont and pathogen in the cereal weevil Sitophilus oryzae
title_short Host gene response to endosymbiont and pathogen in the cereal weevil Sitophilus oryzae
title_sort host gene response to endosymbiont and pathogen in the cereal weevil sitophilus oryzae
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287511/
https://www.ncbi.nlm.nih.gov/pubmed/22375912
http://dx.doi.org/10.1186/1471-2180-12-S1-S14
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