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Mating changes the genital microbiome in both sexes of the common bedbug Cimex lectularius across populations

Many bacteria live on host surfaces, in cells and in specific organ systems. In comparison with gut microbiomes, the bacterial communities of reproductive organs (genital microbiomes) have received little attention. During mating, male and female genitalia interact and copulatory wounds occur, provi...

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Autores principales: Bellinvia, Sara, Johnston, Paul R., Mbedi, Susan, Otti, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282915/
https://www.ncbi.nlm.nih.gov/pubmed/32345169
http://dx.doi.org/10.1098/rspb.2020.0302
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author Bellinvia, Sara
Johnston, Paul R.
Mbedi, Susan
Otti, Oliver
author_facet Bellinvia, Sara
Johnston, Paul R.
Mbedi, Susan
Otti, Oliver
author_sort Bellinvia, Sara
collection PubMed
description Many bacteria live on host surfaces, in cells and in specific organ systems. In comparison with gut microbiomes, the bacterial communities of reproductive organs (genital microbiomes) have received little attention. During mating, male and female genitalia interact and copulatory wounds occur, providing an entrance for sexually transmitted microbes. Besides being potentially harmful to the host, invading microbes might interact with resident genital microbes and affect immunity. Apart from the investigation of sexually transmitted symbionts, few studies have addressed how mating changes genital microbiomes. We dissected reproductive organs from virgin and mated common bedbugs, Cimex lectularius L., and sequenced their microbiomes to investigate composition and mating-induced changes. We show that mating changes the genital microbiomes, suggesting bacteria are sexually transmitted. Also, genital microbiomes varied between populations and the sexes. This provides evidence for local and sex-specific adaptation of bacteria and hosts, suggesting bacteria might play an important role in shaping the evolution of reproductive traits. Coadaptation of genital microbiomes and reproductive traits might further lead to reproductive isolation between populations, giving reproductive ecology an important role in speciation. Future studies should investigate the transmission dynamics between the sexes and populations to uncover potential reproductive barriers.
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spelling pubmed-72829152020-06-25 Mating changes the genital microbiome in both sexes of the common bedbug Cimex lectularius across populations Bellinvia, Sara Johnston, Paul R. Mbedi, Susan Otti, Oliver Proc Biol Sci Evolution Many bacteria live on host surfaces, in cells and in specific organ systems. In comparison with gut microbiomes, the bacterial communities of reproductive organs (genital microbiomes) have received little attention. During mating, male and female genitalia interact and copulatory wounds occur, providing an entrance for sexually transmitted microbes. Besides being potentially harmful to the host, invading microbes might interact with resident genital microbes and affect immunity. Apart from the investigation of sexually transmitted symbionts, few studies have addressed how mating changes genital microbiomes. We dissected reproductive organs from virgin and mated common bedbugs, Cimex lectularius L., and sequenced their microbiomes to investigate composition and mating-induced changes. We show that mating changes the genital microbiomes, suggesting bacteria are sexually transmitted. Also, genital microbiomes varied between populations and the sexes. This provides evidence for local and sex-specific adaptation of bacteria and hosts, suggesting bacteria might play an important role in shaping the evolution of reproductive traits. Coadaptation of genital microbiomes and reproductive traits might further lead to reproductive isolation between populations, giving reproductive ecology an important role in speciation. Future studies should investigate the transmission dynamics between the sexes and populations to uncover potential reproductive barriers. The Royal Society 2020-05-13 2020-04-29 /pmc/articles/PMC7282915/ /pubmed/32345169 http://dx.doi.org/10.1098/rspb.2020.0302 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 Evolution
Bellinvia, Sara
Johnston, Paul R.
Mbedi, Susan
Otti, Oliver
Mating changes the genital microbiome in both sexes of the common bedbug Cimex lectularius across populations
title Mating changes the genital microbiome in both sexes of the common bedbug Cimex lectularius across populations
title_full Mating changes the genital microbiome in both sexes of the common bedbug Cimex lectularius across populations
title_fullStr Mating changes the genital microbiome in both sexes of the common bedbug Cimex lectularius across populations
title_full_unstemmed Mating changes the genital microbiome in both sexes of the common bedbug Cimex lectularius across populations
title_short Mating changes the genital microbiome in both sexes of the common bedbug Cimex lectularius across populations
title_sort mating changes the genital microbiome in both sexes of the common bedbug cimex lectularius across populations
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282915/
https://www.ncbi.nlm.nih.gov/pubmed/32345169
http://dx.doi.org/10.1098/rspb.2020.0302
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