Cargando…
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...
Autores principales: | , , , |
---|---|
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 |
_version_ | 1783606402626879488 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7644162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT mairejustin endosymbiosismorphologicalreorganizationduringmetamorphosisdivergesinweevils AT chouaiabessem endosymbiosismorphologicalreorganizationduringmetamorphosisdivergesinweevils AT zaidmanremyanna endosymbiosismorphologicalreorganizationduringmetamorphosisdivergesinweevils AT heddiabdelaziz endosymbiosismorphologicalreorganizationduringmetamorphosisdivergesinweevils |