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Weevil endosymbiont dynamics is associated with a clamping of immunity
BACKGROUND: Insects subsisting on nutritionally unbalanced diets have evolved long-term mutualistic relationships with intracellular symbiotic bacteria (endosymbionts). The endosymbiont population load undergoes changes along with insect development. In the cereal weevil Sitophilus oryzae, the midgu...
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/PMC4617454/ https://www.ncbi.nlm.nih.gov/pubmed/26482132 http://dx.doi.org/10.1186/s12864-015-2048-5 |
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author | Masson, Florent Moné, Yves Vigneron, Aurélien Vallier, Agnès Parisot, Nicolas Vincent-Monégat, Carole Balmand, Séverine Carpentier, Marie-Christine Zaidman-Rémy, Anna Heddi, Abdelaziz |
author_facet | Masson, Florent Moné, Yves Vigneron, Aurélien Vallier, Agnès Parisot, Nicolas Vincent-Monégat, Carole Balmand, Séverine Carpentier, Marie-Christine Zaidman-Rémy, Anna Heddi, Abdelaziz |
author_sort | Masson, Florent |
collection | PubMed |
description | BACKGROUND: Insects subsisting on nutritionally unbalanced diets have evolved long-term mutualistic relationships with intracellular symbiotic bacteria (endosymbionts). The endosymbiont population load undergoes changes along with insect development. In the cereal weevil Sitophilus oryzae, the midgut endosymbionts Sodalis pierantonius drastically multiply following adult metamorphosis and rapidly decline until total elimination when the insect achieves its cuticle synthesis. Whilst symbiont load was shown to timely meet insect metabolic needs, little is known about the host molecular and immune processes underlying this dynamics. METHODS: We performed RNA sequencing analysis on weevil midguts at three representative phases of the endosymbiont dynamics (i.e. increase, climax and decrease). To screen genes which transcriptional changes are specifically related to symbiont dynamics and not to the intrinsic development of the midgut, we further have monitored by RT-qPCR sixteen gene transcript levels in symbiotic and artificially non-symbiotic (aposymbiotic) weevils. We also localized the endosymbionts during the elimination process by fluorescence microscopy. RESULTS: Functional analysis of the host differentially expressed genes by RNA sequencing showed that the main transcriptional changes occur during endosymbiont growth phase and affect cell proliferation, apoptosis, autophagy, phagocytosis, and metabolism of fatty acids and nucleic acids. We also showed that symbiont dynamics alters the expression of several genes involved in insect development. Our results strengthened the implication of apoptosis and autophagy processes in symbiont elimination and recycling. Remarkably, apart from the coleoptericin A that is known to target endosymbionts and controls their division and location, no gene coding antimicrobial peptide was upregulated during the symbiont growth and elimination phases. CONCLUSION: We show that endosymbiont dynamics parallels numerous transcriptional changes in weevil developing adults and affects several biological processes, including metabolism and development. It also triggers cell apoptosis, autophagy and gut epithelial cell swelling and delamination. Strikingly, immunity is repressed during the whole process, presumably avoiding tissue inflammation and allowing insects to optimize nutrient recovery from recycled endosymbiont. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2048-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4617454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46174542015-10-24 Weevil endosymbiont dynamics is associated with a clamping of immunity Masson, Florent Moné, Yves Vigneron, Aurélien Vallier, Agnès Parisot, Nicolas Vincent-Monégat, Carole Balmand, Séverine Carpentier, Marie-Christine Zaidman-Rémy, Anna Heddi, Abdelaziz BMC Genomics Research Article BACKGROUND: Insects subsisting on nutritionally unbalanced diets have evolved long-term mutualistic relationships with intracellular symbiotic bacteria (endosymbionts). The endosymbiont population load undergoes changes along with insect development. In the cereal weevil Sitophilus oryzae, the midgut endosymbionts Sodalis pierantonius drastically multiply following adult metamorphosis and rapidly decline until total elimination when the insect achieves its cuticle synthesis. Whilst symbiont load was shown to timely meet insect metabolic needs, little is known about the host molecular and immune processes underlying this dynamics. METHODS: We performed RNA sequencing analysis on weevil midguts at three representative phases of the endosymbiont dynamics (i.e. increase, climax and decrease). To screen genes which transcriptional changes are specifically related to symbiont dynamics and not to the intrinsic development of the midgut, we further have monitored by RT-qPCR sixteen gene transcript levels in symbiotic and artificially non-symbiotic (aposymbiotic) weevils. We also localized the endosymbionts during the elimination process by fluorescence microscopy. RESULTS: Functional analysis of the host differentially expressed genes by RNA sequencing showed that the main transcriptional changes occur during endosymbiont growth phase and affect cell proliferation, apoptosis, autophagy, phagocytosis, and metabolism of fatty acids and nucleic acids. We also showed that symbiont dynamics alters the expression of several genes involved in insect development. Our results strengthened the implication of apoptosis and autophagy processes in symbiont elimination and recycling. Remarkably, apart from the coleoptericin A that is known to target endosymbionts and controls their division and location, no gene coding antimicrobial peptide was upregulated during the symbiont growth and elimination phases. CONCLUSION: We show that endosymbiont dynamics parallels numerous transcriptional changes in weevil developing adults and affects several biological processes, including metabolism and development. It also triggers cell apoptosis, autophagy and gut epithelial cell swelling and delamination. Strikingly, immunity is repressed during the whole process, presumably avoiding tissue inflammation and allowing insects to optimize nutrient recovery from recycled endosymbiont. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2048-5) contains supplementary material, which is available to authorized users. BioMed Central 2015-10-19 /pmc/articles/PMC4617454/ /pubmed/26482132 http://dx.doi.org/10.1186/s12864-015-2048-5 Text en © Masson et al. 2015 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 Masson, Florent Moné, Yves Vigneron, Aurélien Vallier, Agnès Parisot, Nicolas Vincent-Monégat, Carole Balmand, Séverine Carpentier, Marie-Christine Zaidman-Rémy, Anna Heddi, Abdelaziz Weevil endosymbiont dynamics is associated with a clamping of immunity |
title | Weevil endosymbiont dynamics is associated with a clamping of immunity |
title_full | Weevil endosymbiont dynamics is associated with a clamping of immunity |
title_fullStr | Weevil endosymbiont dynamics is associated with a clamping of immunity |
title_full_unstemmed | Weevil endosymbiont dynamics is associated with a clamping of immunity |
title_short | Weevil endosymbiont dynamics is associated with a clamping of immunity |
title_sort | weevil endosymbiont dynamics is associated with a clamping of immunity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4617454/ https://www.ncbi.nlm.nih.gov/pubmed/26482132 http://dx.doi.org/10.1186/s12864-015-2048-5 |
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