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The red flour beetle Tribolium castaneum: A model for host-microbiome interactions

A large body of ongoing research focuses on understanding the mechanisms and processes underlying host-microbiome interactions, and predicting their ecological and evolutionary outcomes. To draw general conclusions about such interactions and understand how they are established, we must synthesize i...

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Detalles Bibliográficos
Autores principales: Agarwal, Aparna, Agashe, Deepa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7531845/
https://www.ncbi.nlm.nih.gov/pubmed/33006995
http://dx.doi.org/10.1371/journal.pone.0239051
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author Agarwal, Aparna
Agashe, Deepa
author_facet Agarwal, Aparna
Agashe, Deepa
author_sort Agarwal, Aparna
collection PubMed
description A large body of ongoing research focuses on understanding the mechanisms and processes underlying host-microbiome interactions, and predicting their ecological and evolutionary outcomes. To draw general conclusions about such interactions and understand how they are established, we must synthesize information from a diverse set of species. We analysed the microbiome of an important insect model–the red flour beetle Tribolium castaneum–which is a widespread generalist pest of stored cereals. The beetles complete their entire life cycle in flour, which thus serves multiple functions: habitat, food, and a source of microbes. We determined key factors that shape the T. castaneum microbiome, established protocols to manipulate it, and tested its consequences for host fitness. We show that the T. castaneum microbiome is derived from flour-acquired microbes, and varies as a function of (flour) resource and beetle density. Beetles gain multiple fitness benefits from their microbiome, such as higher fecundity, egg survival, and lifespan; and reduced cannibalism. In contrast, the microbiome has a limited effect on development rate, and does not enhance pathogen resistance. Importantly, the benefits are derived only from microbes in the ancestral resource (wheat flour), and not from novel resources such as finger millet, sorghum, and corn. Notably, the microbiome is not essential for beetle survival and development under any of the tested conditions. Thus, the red flour beetle is a tractable model system to understand the ecology, evolution and mechanisms of host-microbiome interactions, while closely mimicking the host species’ natural niche.
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spelling pubmed-75318452020-10-08 The red flour beetle Tribolium castaneum: A model for host-microbiome interactions Agarwal, Aparna Agashe, Deepa PLoS One Research Article A large body of ongoing research focuses on understanding the mechanisms and processes underlying host-microbiome interactions, and predicting their ecological and evolutionary outcomes. To draw general conclusions about such interactions and understand how they are established, we must synthesize information from a diverse set of species. We analysed the microbiome of an important insect model–the red flour beetle Tribolium castaneum–which is a widespread generalist pest of stored cereals. The beetles complete their entire life cycle in flour, which thus serves multiple functions: habitat, food, and a source of microbes. We determined key factors that shape the T. castaneum microbiome, established protocols to manipulate it, and tested its consequences for host fitness. We show that the T. castaneum microbiome is derived from flour-acquired microbes, and varies as a function of (flour) resource and beetle density. Beetles gain multiple fitness benefits from their microbiome, such as higher fecundity, egg survival, and lifespan; and reduced cannibalism. In contrast, the microbiome has a limited effect on development rate, and does not enhance pathogen resistance. Importantly, the benefits are derived only from microbes in the ancestral resource (wheat flour), and not from novel resources such as finger millet, sorghum, and corn. Notably, the microbiome is not essential for beetle survival and development under any of the tested conditions. Thus, the red flour beetle is a tractable model system to understand the ecology, evolution and mechanisms of host-microbiome interactions, while closely mimicking the host species’ natural niche. Public Library of Science 2020-10-02 /pmc/articles/PMC7531845/ /pubmed/33006995 http://dx.doi.org/10.1371/journal.pone.0239051 Text en © 2020 Agarwal, Agashe http://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/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Agarwal, Aparna
Agashe, Deepa
The red flour beetle Tribolium castaneum: A model for host-microbiome interactions
title The red flour beetle Tribolium castaneum: A model for host-microbiome interactions
title_full The red flour beetle Tribolium castaneum: A model for host-microbiome interactions
title_fullStr The red flour beetle Tribolium castaneum: A model for host-microbiome interactions
title_full_unstemmed The red flour beetle Tribolium castaneum: A model for host-microbiome interactions
title_short The red flour beetle Tribolium castaneum: A model for host-microbiome interactions
title_sort red flour beetle tribolium castaneum: a model for host-microbiome interactions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7531845/
https://www.ncbi.nlm.nih.gov/pubmed/33006995
http://dx.doi.org/10.1371/journal.pone.0239051
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