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Endosymbiosis morphological reorganization during metamorphosis diverges in weevils

Virtually all animals associate with beneficial symbiotic bacteria. Whether and how these associations are modulated across a host’s lifecycle is an important question in disentangling animal-bacteria interactions. We recently reported a case of complete morphological reorganization of symbiosis dur...

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Autores principales: Maire, Justin, Chouaia, Bessem, Zaidman-Rémy, Anna, Heddi, Abdelaziz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644162/
https://www.ncbi.nlm.nih.gov/pubmed/33193996
http://dx.doi.org/10.1080/19420889.2020.1840707
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author Maire, Justin
Chouaia, Bessem
Zaidman-Rémy, Anna
Heddi, Abdelaziz
author_facet Maire, Justin
Chouaia, Bessem
Zaidman-Rémy, Anna
Heddi, Abdelaziz
author_sort Maire, Justin
collection PubMed
description Virtually all animals associate with beneficial symbiotic bacteria. Whether and how these associations are modulated across a host’s lifecycle is an important question in disentangling animal-bacteria interactions. We recently reported a case of complete morphological reorganization of symbiosis during metamorphosis of the cereal weevil, Sitophilus oryzae. In this model, the bacteriome, a specialized organ that houses the intracellular bacterium Sodalis pierantonius, undergoes a two-phase remodeling program synchronously driven by host and endosymbiont, resulting in a localization shift and the formation of multiple new bacteriomes. Here, we provide comparative data in a closely-related coleopteran, the red palm weevil Rhynchophorus ferrugineus, which is associated with the ancestral endosymbiont Nardonella. Using cell imaging experiments, we show that the red pal weevil bacteriome remains unchanged during metamorphosis, hence contrasting with what we reported in the cereal weevil S. oryzae. These findings highlight the complexity and divergence of host-symbiont interactions and their intertwining with host development, even in closely-related species. Abbreviations: DAPI: 4′,6-diamidino-2-phenylindole; FISH: Fluorescence in situ hybridization; T3SS: Type III secretion system.
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spelling pubmed-76441622020-11-13 Endosymbiosis morphological reorganization during metamorphosis diverges in weevils Maire, Justin Chouaia, Bessem Zaidman-Rémy, Anna Heddi, Abdelaziz Commun Integr Biol Short Communication Virtually all animals associate with beneficial symbiotic bacteria. Whether and how these associations are modulated across a host’s lifecycle is an important question in disentangling animal-bacteria interactions. We recently reported a case of complete morphological reorganization of symbiosis during metamorphosis of the cereal weevil, Sitophilus oryzae. In this model, the bacteriome, a specialized organ that houses the intracellular bacterium Sodalis pierantonius, undergoes a two-phase remodeling program synchronously driven by host and endosymbiont, resulting in a localization shift and the formation of multiple new bacteriomes. Here, we provide comparative data in a closely-related coleopteran, the red palm weevil Rhynchophorus ferrugineus, which is associated with the ancestral endosymbiont Nardonella. Using cell imaging experiments, we show that the red pal weevil bacteriome remains unchanged during metamorphosis, hence contrasting with what we reported in the cereal weevil S. oryzae. These findings highlight the complexity and divergence of host-symbiont interactions and their intertwining with host development, even in closely-related species. Abbreviations: DAPI: 4′,6-diamidino-2-phenylindole; FISH: Fluorescence in situ hybridization; T3SS: Type III secretion system. Taylor & Francis 2020-11-02 /pmc/articles/PMC7644162/ /pubmed/33193996 http://dx.doi.org/10.1080/19420889.2020.1840707 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Maire, Justin
Chouaia, Bessem
Zaidman-Rémy, Anna
Heddi, Abdelaziz
Endosymbiosis morphological reorganization during metamorphosis diverges in weevils
title Endosymbiosis morphological reorganization during metamorphosis diverges in weevils
title_full Endosymbiosis morphological reorganization during metamorphosis diverges in weevils
title_fullStr Endosymbiosis morphological reorganization during metamorphosis diverges in weevils
title_full_unstemmed Endosymbiosis morphological reorganization during metamorphosis diverges in weevils
title_short Endosymbiosis morphological reorganization during metamorphosis diverges in weevils
title_sort endosymbiosis morphological reorganization during metamorphosis diverges in weevils
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644162/
https://www.ncbi.nlm.nih.gov/pubmed/33193996
http://dx.doi.org/10.1080/19420889.2020.1840707
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