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Experimental evidence of Wolbachia introgressive acquisition between terrestrial isopod subspecies
Wolbachia are the most widespread endosymbiotic bacteria in animals. In many arthropod host species, they manipulate reproduction via several mechanisms that favor their maternal transmission to offspring. Among them, cytoplasmic incompatibility (CI) promotes the spread of the symbiont by specifical...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489008/ https://www.ncbi.nlm.nih.gov/pubmed/34616942 http://dx.doi.org/10.1093/cz/zoaa078 |
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author | Bech, Nicolas Beltran-Bech, Sophie Chupeau, Cassandre Peccoud, Jean Thierry, Magali Raimond, Roland Caubet, Yves Sicard, Mathieu Grève, Pierre |
author_facet | Bech, Nicolas Beltran-Bech, Sophie Chupeau, Cassandre Peccoud, Jean Thierry, Magali Raimond, Roland Caubet, Yves Sicard, Mathieu Grève, Pierre |
author_sort | Bech, Nicolas |
collection | PubMed |
description | Wolbachia are the most widespread endosymbiotic bacteria in animals. In many arthropod host species, they manipulate reproduction via several mechanisms that favor their maternal transmission to offspring. Among them, cytoplasmic incompatibility (CI) promotes the spread of the symbiont by specifically decreasing the fertility of crosses involving infected males and uninfected females, via embryo mortality. These differences in reproductive efficiency may select for the avoidance of incompatible mating, a process called reinforcement, and thus contribute to population divergence. In the terrestrial isopod Porcellio dilatatus, the Wolbachia wPet strain infecting the subspecies P. d. petiti induces unidirectional CI with uninfected individuals of the subspecies P. d. dilatatus. To study the consequences of CI on P. d. dilatatus and P. d. petiti hybridization, mitochondrial haplotypes and Wolbachia infection dynamics, we used population cages seeded with different proportions of the 2 subspecies in which we monitored these genetic parameters 5 and 7 years after the initial setup. Analysis of microsatellite markers allowed evaluating the degree of hybridization between individuals of the 2 subspecies. These markers revealed an increase in P. d. dilatatus nuclear genetic signature in all mixed cages, reflecting an asymmetry in hybridization. Hybridization led to the introgressive acquisition of Wolbachia and mitochondrial haplotype from P. d. petiti into nuclear genomes dominated by alleles of P. d. dilatatus. We discuss these results with regards to Wolbachia effects on their host (CI and putative fitness cost), and to a possible reinforcement that may have led to assortative mating, as possible factors contributing to the observed results. |
format | Online Article Text |
id | pubmed-8489008 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-84890082021-10-05 Experimental evidence of Wolbachia introgressive acquisition between terrestrial isopod subspecies Bech, Nicolas Beltran-Bech, Sophie Chupeau, Cassandre Peccoud, Jean Thierry, Magali Raimond, Roland Caubet, Yves Sicard, Mathieu Grève, Pierre Curr Zool Articles Wolbachia are the most widespread endosymbiotic bacteria in animals. In many arthropod host species, they manipulate reproduction via several mechanisms that favor their maternal transmission to offspring. Among them, cytoplasmic incompatibility (CI) promotes the spread of the symbiont by specifically decreasing the fertility of crosses involving infected males and uninfected females, via embryo mortality. These differences in reproductive efficiency may select for the avoidance of incompatible mating, a process called reinforcement, and thus contribute to population divergence. In the terrestrial isopod Porcellio dilatatus, the Wolbachia wPet strain infecting the subspecies P. d. petiti induces unidirectional CI with uninfected individuals of the subspecies P. d. dilatatus. To study the consequences of CI on P. d. dilatatus and P. d. petiti hybridization, mitochondrial haplotypes and Wolbachia infection dynamics, we used population cages seeded with different proportions of the 2 subspecies in which we monitored these genetic parameters 5 and 7 years after the initial setup. Analysis of microsatellite markers allowed evaluating the degree of hybridization between individuals of the 2 subspecies. These markers revealed an increase in P. d. dilatatus nuclear genetic signature in all mixed cages, reflecting an asymmetry in hybridization. Hybridization led to the introgressive acquisition of Wolbachia and mitochondrial haplotype from P. d. petiti into nuclear genomes dominated by alleles of P. d. dilatatus. We discuss these results with regards to Wolbachia effects on their host (CI and putative fitness cost), and to a possible reinforcement that may have led to assortative mating, as possible factors contributing to the observed results. Oxford University Press 2020-12-26 /pmc/articles/PMC8489008/ /pubmed/34616942 http://dx.doi.org/10.1093/cz/zoaa078 Text en © The Author(s) (2020). Published by Oxford University Press on behalf of Editorial Office, Current Zoology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Articles Bech, Nicolas Beltran-Bech, Sophie Chupeau, Cassandre Peccoud, Jean Thierry, Magali Raimond, Roland Caubet, Yves Sicard, Mathieu Grève, Pierre Experimental evidence of Wolbachia introgressive acquisition between terrestrial isopod subspecies |
title | Experimental evidence of Wolbachia introgressive acquisition between terrestrial isopod subspecies |
title_full | Experimental evidence of Wolbachia introgressive acquisition between terrestrial isopod subspecies |
title_fullStr | Experimental evidence of Wolbachia introgressive acquisition between terrestrial isopod subspecies |
title_full_unstemmed | Experimental evidence of Wolbachia introgressive acquisition between terrestrial isopod subspecies |
title_short | Experimental evidence of Wolbachia introgressive acquisition between terrestrial isopod subspecies |
title_sort | experimental evidence of wolbachia introgressive acquisition between terrestrial isopod subspecies |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489008/ https://www.ncbi.nlm.nih.gov/pubmed/34616942 http://dx.doi.org/10.1093/cz/zoaa078 |
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