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Gut Bacteriome Analysis of Anastrepha fraterculus sp. 1 During the Early Steps of Laboratory Colonization

Microbial communities associated to insect species are involved in essential biological functions such as host nutrition, reproduction and survivability. Main factors have been described as modulators of gut bacterial community, such as diet, habit, developmental stage and taxonomy of the host. The...

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Autores principales: Salgueiro, Julieta, Pimper, Lida E., Segura, Diego F., Milla, Fabián H., Russo, Romina M., Asimakis, Elias, Stathopoulou, Panagiota, Bourtzis, Kostas, Cladera, Jorge L., Tsiamis, George, Lanzavecchia, Silvia B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7606190/
https://www.ncbi.nlm.nih.gov/pubmed/33193166
http://dx.doi.org/10.3389/fmicb.2020.570960
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author Salgueiro, Julieta
Pimper, Lida E.
Segura, Diego F.
Milla, Fabián H.
Russo, Romina M.
Asimakis, Elias
Stathopoulou, Panagiota
Bourtzis, Kostas
Cladera, Jorge L.
Tsiamis, George
Lanzavecchia, Silvia B.
author_facet Salgueiro, Julieta
Pimper, Lida E.
Segura, Diego F.
Milla, Fabián H.
Russo, Romina M.
Asimakis, Elias
Stathopoulou, Panagiota
Bourtzis, Kostas
Cladera, Jorge L.
Tsiamis, George
Lanzavecchia, Silvia B.
author_sort Salgueiro, Julieta
collection PubMed
description Microbial communities associated to insect species are involved in essential biological functions such as host nutrition, reproduction and survivability. Main factors have been described as modulators of gut bacterial community, such as diet, habit, developmental stage and taxonomy of the host. The present work focuses on the complex changes that gut microbial communities go through when wild insects are introduced to artificial rearing conditions. Specifically, we analyzed the effect of the laboratory colonization on the richness and diversity of the gut bacteriome hosted by the fruit fly pest Anastrepha fraterculus sp. 1. Bacterial profiles were studied by amplicon sequencing of the 16S rRNA V3–V4 hypervariable region in gut samples of males and females, in teneral (1-day-old, unfed) and post-teneral (15-day-old, fed) flies. A total of 3,147,665 sequence reads were obtained and 32 bacterial operational taxonomic units (OTUs) were identified. Proteobacteria was the most abundant phylum (93.3% of the total reads) and, Wolbachia and Enterobacter were the most represented taxa at the genus level (29.9% and 27.7%, respectively, of the total read counts). Wild and laboratory flies showed highly significant differences in the relative abundances of bacteria. The analysis of the core bacteriome showed the presence of five OTUs in all samples grouped by origin, while nine and five OTUs were exclusively detected in laboratory and wild flies, respectively. Irrespective of fly origin or sex, a dominant presence of Wolbachia was observed in teneral flies, whereas Enterobacter was highly abundant in post-teneral individuals. We evidenced significant differences in bacterial richness and diversity among generations under laboratory colonization (F0, F1, F3 and F6) and compared to laboratory and wild flies, displaying also differential patterns between teneral and post-teneral flies. Laboratory and wild A. fraterculus sp. 1 harbor different gut bacterial communities. Laboratory colonization has an important effect on the microbiota, most likely associated to the combined effects of insect physiology and environmental conditions (e.g., diet and colony management).
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spelling pubmed-76061902020-11-13 Gut Bacteriome Analysis of Anastrepha fraterculus sp. 1 During the Early Steps of Laboratory Colonization Salgueiro, Julieta Pimper, Lida E. Segura, Diego F. Milla, Fabián H. Russo, Romina M. Asimakis, Elias Stathopoulou, Panagiota Bourtzis, Kostas Cladera, Jorge L. Tsiamis, George Lanzavecchia, Silvia B. Front Microbiol Microbiology Microbial communities associated to insect species are involved in essential biological functions such as host nutrition, reproduction and survivability. Main factors have been described as modulators of gut bacterial community, such as diet, habit, developmental stage and taxonomy of the host. The present work focuses on the complex changes that gut microbial communities go through when wild insects are introduced to artificial rearing conditions. Specifically, we analyzed the effect of the laboratory colonization on the richness and diversity of the gut bacteriome hosted by the fruit fly pest Anastrepha fraterculus sp. 1. Bacterial profiles were studied by amplicon sequencing of the 16S rRNA V3–V4 hypervariable region in gut samples of males and females, in teneral (1-day-old, unfed) and post-teneral (15-day-old, fed) flies. A total of 3,147,665 sequence reads were obtained and 32 bacterial operational taxonomic units (OTUs) were identified. Proteobacteria was the most abundant phylum (93.3% of the total reads) and, Wolbachia and Enterobacter were the most represented taxa at the genus level (29.9% and 27.7%, respectively, of the total read counts). Wild and laboratory flies showed highly significant differences in the relative abundances of bacteria. The analysis of the core bacteriome showed the presence of five OTUs in all samples grouped by origin, while nine and five OTUs were exclusively detected in laboratory and wild flies, respectively. Irrespective of fly origin or sex, a dominant presence of Wolbachia was observed in teneral flies, whereas Enterobacter was highly abundant in post-teneral individuals. We evidenced significant differences in bacterial richness and diversity among generations under laboratory colonization (F0, F1, F3 and F6) and compared to laboratory and wild flies, displaying also differential patterns between teneral and post-teneral flies. Laboratory and wild A. fraterculus sp. 1 harbor different gut bacterial communities. Laboratory colonization has an important effect on the microbiota, most likely associated to the combined effects of insect physiology and environmental conditions (e.g., diet and colony management). Frontiers Media S.A. 2020-10-20 /pmc/articles/PMC7606190/ /pubmed/33193166 http://dx.doi.org/10.3389/fmicb.2020.570960 Text en Copyright © 2020 Salgueiro, Pimper, Segura, Milla, Russo, Asimakis, Stathopoulou, Bourtzis, Cladera, Tsiamis and Lanzavecchia. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Salgueiro, Julieta
Pimper, Lida E.
Segura, Diego F.
Milla, Fabián H.
Russo, Romina M.
Asimakis, Elias
Stathopoulou, Panagiota
Bourtzis, Kostas
Cladera, Jorge L.
Tsiamis, George
Lanzavecchia, Silvia B.
Gut Bacteriome Analysis of Anastrepha fraterculus sp. 1 During the Early Steps of Laboratory Colonization
title Gut Bacteriome Analysis of Anastrepha fraterculus sp. 1 During the Early Steps of Laboratory Colonization
title_full Gut Bacteriome Analysis of Anastrepha fraterculus sp. 1 During the Early Steps of Laboratory Colonization
title_fullStr Gut Bacteriome Analysis of Anastrepha fraterculus sp. 1 During the Early Steps of Laboratory Colonization
title_full_unstemmed Gut Bacteriome Analysis of Anastrepha fraterculus sp. 1 During the Early Steps of Laboratory Colonization
title_short Gut Bacteriome Analysis of Anastrepha fraterculus sp. 1 During the Early Steps of Laboratory Colonization
title_sort gut bacteriome analysis of anastrepha fraterculus sp. 1 during the early steps of laboratory colonization
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7606190/
https://www.ncbi.nlm.nih.gov/pubmed/33193166
http://dx.doi.org/10.3389/fmicb.2020.570960
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