Justin Maire, Bessem Chouaia, Anna Zaidman-Rémy, Abdelaziz Heddi
{"title":"象鼻虫变态过程中的内共生形态重组存在分歧。","authors":"Justin Maire, Bessem Chouaia, Anna Zaidman-Rémy, Abdelaziz Heddi","doi":"10.1080/19420889.2020.1840707","DOIUrl":null,"url":null,"abstract":"<p><p>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, <i>Sitophilus oryzae</i>. In this model, the bacteriome, a specialized organ that houses the intracellular bacterium <i>Sodalis pierantonius</i>, 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 <i>Rhynchophorus ferrugineus</i>, which is associated with the ancestral endosymbiont <i>Nardonella</i>. 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 <i>S. oryzae</i>. These findings highlight the complexity and divergence of host-symbiont interactions and their intertwining with host development, even in closely-related species. <b>Abbreviations</b>: DAPI: 4',6-diamidino-2-phenylindole; FISH: Fluorescence <i>in situ</i> hybridization; T3SS: Type III secretion system.</p>","PeriodicalId":39647,"journal":{"name":"Communicative and Integrative Biology","volume":" ","pages":"184-188"},"PeriodicalIF":0.0000,"publicationDate":"2020-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/19420889.2020.1840707","citationCount":"7","resultStr":"{\"title\":\"Endosymbiosis morphological reorganization during metamorphosis diverges in weevils.\",\"authors\":\"Justin Maire, Bessem Chouaia, Anna Zaidman-Rémy, Abdelaziz Heddi\",\"doi\":\"10.1080/19420889.2020.1840707\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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, <i>Sitophilus oryzae</i>. In this model, the bacteriome, a specialized organ that houses the intracellular bacterium <i>Sodalis pierantonius</i>, 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 <i>Rhynchophorus ferrugineus</i>, which is associated with the ancestral endosymbiont <i>Nardonella</i>. 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 <i>S. oryzae</i>. These findings highlight the complexity and divergence of host-symbiont interactions and their intertwining with host development, even in closely-related species. <b>Abbreviations</b>: DAPI: 4',6-diamidino-2-phenylindole; FISH: Fluorescence <i>in situ</i> hybridization; T3SS: Type III secretion system.</p>\",\"PeriodicalId\":39647,\"journal\":{\"name\":\"Communicative and Integrative Biology\",\"volume\":\" \",\"pages\":\"184-188\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-11-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1080/19420889.2020.1840707\",\"citationCount\":\"7\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Communicative and Integrative Biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/19420889.2020.1840707\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Agricultural and Biological Sciences\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Communicative and Integrative Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/19420889.2020.1840707","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Agricultural and Biological Sciences","Score":null,"Total":0}
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 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.