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Transmission efficiency drives host–microbe associations

Sequencing technologies have fuelled a rapid rise in descriptions of microbial communities associated with hosts, but what is often harder to ascertain is the evolutionary significance of these symbioses. Here, we review the role of vertical (VT), horizontal (HT), environmental acquisition and mixed...

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Autores principales: Leftwich, Philip T., Edgington, Matthew P., Chapman, Tracey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542779/
https://www.ncbi.nlm.nih.gov/pubmed/32873208
http://dx.doi.org/10.1098/rspb.2020.0820
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author Leftwich, Philip T.
Edgington, Matthew P.
Chapman, Tracey
author_facet Leftwich, Philip T.
Edgington, Matthew P.
Chapman, Tracey
author_sort Leftwich, Philip T.
collection PubMed
description Sequencing technologies have fuelled a rapid rise in descriptions of microbial communities associated with hosts, but what is often harder to ascertain is the evolutionary significance of these symbioses. Here, we review the role of vertical (VT), horizontal (HT), environmental acquisition and mixed modes of transmission (MMT), in the establishment of animal host–microbe associations. We then model four properties of gut microbiota proposed as key to promoting animal host–microbe relationships: modes of transmission, host reproductive mode, host mate choice and host fitness. We found that: (i) MMT led to the highest frequencies of host–microbe associations, and that some environmental acquisition or HT of microbes was required for persistent associations to form unless VT was perfect; (ii) host reproductive mode (sexual versus asexual) and host mate choice (for microbe carriers versus non-carriers) had little impact on the establishment of host–microbe associations; (iii) host mate choice did not itself lead to reproductive isolation, but could reinforce it; and (iv) changes in host fitness due to host–microbe associations had a minimal impact upon the formation of co-associations. When we introduced a second population, into which host–microbe carriers could disperse but in which environmental acquisition did not occur, highly efficient VT was required for host–microbe co-associations to persist. Our study reveals that transmission mode is of key importance in establishing host–microbe associations.
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spelling pubmed-75427792020-10-11 Transmission efficiency drives host–microbe associations Leftwich, Philip T. Edgington, Matthew P. Chapman, Tracey Proc Biol Sci Special Feature Sequencing technologies have fuelled a rapid rise in descriptions of microbial communities associated with hosts, but what is often harder to ascertain is the evolutionary significance of these symbioses. Here, we review the role of vertical (VT), horizontal (HT), environmental acquisition and mixed modes of transmission (MMT), in the establishment of animal host–microbe associations. We then model four properties of gut microbiota proposed as key to promoting animal host–microbe relationships: modes of transmission, host reproductive mode, host mate choice and host fitness. We found that: (i) MMT led to the highest frequencies of host–microbe associations, and that some environmental acquisition or HT of microbes was required for persistent associations to form unless VT was perfect; (ii) host reproductive mode (sexual versus asexual) and host mate choice (for microbe carriers versus non-carriers) had little impact on the establishment of host–microbe associations; (iii) host mate choice did not itself lead to reproductive isolation, but could reinforce it; and (iv) changes in host fitness due to host–microbe associations had a minimal impact upon the formation of co-associations. When we introduced a second population, into which host–microbe carriers could disperse but in which environmental acquisition did not occur, highly efficient VT was required for host–microbe co-associations to persist. Our study reveals that transmission mode is of key importance in establishing host–microbe associations. The Royal Society 2020-09-09 2020-09-02 /pmc/articles/PMC7542779/ /pubmed/32873208 http://dx.doi.org/10.1098/rspb.2020.0820 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Special Feature
Leftwich, Philip T.
Edgington, Matthew P.
Chapman, Tracey
Transmission efficiency drives host–microbe associations
title Transmission efficiency drives host–microbe associations
title_full Transmission efficiency drives host–microbe associations
title_fullStr Transmission efficiency drives host–microbe associations
title_full_unstemmed Transmission efficiency drives host–microbe associations
title_short Transmission efficiency drives host–microbe associations
title_sort transmission efficiency drives host–microbe associations
topic Special Feature
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542779/
https://www.ncbi.nlm.nih.gov/pubmed/32873208
http://dx.doi.org/10.1098/rspb.2020.0820
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