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A comparative analysis of Wolbachia‐induced host reproductive phenotypes reveals transition rate heterogeneity

The endosymbiotic bacterium Wolbachia infects a wide range of arthropods and their relatives. It is an intracellular parasite transmitted through the egg from mother to offspring. Wolbachia can spread and persist through various means of host reproductive manipulation. How these different mechanisms...

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Autores principales: zu Dohna, Heinrich, Houry, Carine, Kambris, Zakaria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817148/
https://www.ncbi.nlm.nih.gov/pubmed/29468014
http://dx.doi.org/10.1002/ece3.3789
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author zu Dohna, Heinrich
Houry, Carine
Kambris, Zakaria
author_facet zu Dohna, Heinrich
Houry, Carine
Kambris, Zakaria
author_sort zu Dohna, Heinrich
collection PubMed
description The endosymbiotic bacterium Wolbachia infects a wide range of arthropods and their relatives. It is an intracellular parasite transmitted through the egg from mother to offspring. Wolbachia can spread and persist through various means of host reproductive manipulation. How these different mechanisms of host manipulation evolved in Wolbachia is unclear. Which host reproductive phenotype is most likely to be ancestral and whether evolutionary transitions between some host phenotypes are more common than others remain unanswered questions. Recent studies have revealed multiple cases where the same Wolbachia strain can induce different reproductive phenotypes in different hosts, raising the question to what degree the induced host phenotype should be regarded as a trait of Wolbachia. In this study, we constructed a phylogenetic tree of Wolbachia and analyzed the patterns of host phenotypes along that tree. We were able to detect a phylogenetic signal of host phenotypes on the Wolbachia tree, indicating that the induced host phenotype can be regarded as a Wolbachia trait. However, we found no clear support for the previously stated hypothesis that cytoplasmic incompatibility is ancestral to Wolbachia in arthropods. Our analysis provides evidence for heterogeneous transition rates between host phenotypes.
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spelling pubmed-58171482018-02-21 A comparative analysis of Wolbachia‐induced host reproductive phenotypes reveals transition rate heterogeneity zu Dohna, Heinrich Houry, Carine Kambris, Zakaria Ecol Evol Original Research The endosymbiotic bacterium Wolbachia infects a wide range of arthropods and their relatives. It is an intracellular parasite transmitted through the egg from mother to offspring. Wolbachia can spread and persist through various means of host reproductive manipulation. How these different mechanisms of host manipulation evolved in Wolbachia is unclear. Which host reproductive phenotype is most likely to be ancestral and whether evolutionary transitions between some host phenotypes are more common than others remain unanswered questions. Recent studies have revealed multiple cases where the same Wolbachia strain can induce different reproductive phenotypes in different hosts, raising the question to what degree the induced host phenotype should be regarded as a trait of Wolbachia. In this study, we constructed a phylogenetic tree of Wolbachia and analyzed the patterns of host phenotypes along that tree. We were able to detect a phylogenetic signal of host phenotypes on the Wolbachia tree, indicating that the induced host phenotype can be regarded as a Wolbachia trait. However, we found no clear support for the previously stated hypothesis that cytoplasmic incompatibility is ancestral to Wolbachia in arthropods. Our analysis provides evidence for heterogeneous transition rates between host phenotypes. John Wiley and Sons Inc. 2018-01-15 /pmc/articles/PMC5817148/ /pubmed/29468014 http://dx.doi.org/10.1002/ece3.3789 Text en © 2018 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
zu Dohna, Heinrich
Houry, Carine
Kambris, Zakaria
A comparative analysis of Wolbachia‐induced host reproductive phenotypes reveals transition rate heterogeneity
title A comparative analysis of Wolbachia‐induced host reproductive phenotypes reveals transition rate heterogeneity
title_full A comparative analysis of Wolbachia‐induced host reproductive phenotypes reveals transition rate heterogeneity
title_fullStr A comparative analysis of Wolbachia‐induced host reproductive phenotypes reveals transition rate heterogeneity
title_full_unstemmed A comparative analysis of Wolbachia‐induced host reproductive phenotypes reveals transition rate heterogeneity
title_short A comparative analysis of Wolbachia‐induced host reproductive phenotypes reveals transition rate heterogeneity
title_sort comparative analysis of wolbachia‐induced host reproductive phenotypes reveals transition rate heterogeneity
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817148/
https://www.ncbi.nlm.nih.gov/pubmed/29468014
http://dx.doi.org/10.1002/ece3.3789
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