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Random Genetic Drift and Selective Pressures Shaping the Blattabacterium Genome

Estimates suggest that at least half of all extant insect genera harbor obligate bacterial mutualists. Whereas an endosymbiotic relationship imparts many benefits upon host and symbiont alike, the intracellular lifestyle has profound effects on the bacterial genome. The obligate endosymbiont genome...

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Autores principales: Alleman, Austin, Hertweck, Kate L., Kambhampati, Srini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128925/
https://www.ncbi.nlm.nih.gov/pubmed/30194350
http://dx.doi.org/10.1038/s41598-018-31796-6
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author Alleman, Austin
Hertweck, Kate L.
Kambhampati, Srini
author_facet Alleman, Austin
Hertweck, Kate L.
Kambhampati, Srini
author_sort Alleman, Austin
collection PubMed
description Estimates suggest that at least half of all extant insect genera harbor obligate bacterial mutualists. Whereas an endosymbiotic relationship imparts many benefits upon host and symbiont alike, the intracellular lifestyle has profound effects on the bacterial genome. The obligate endosymbiont genome is a product of opposing forces: genes important to host survival are maintained through physiological constraint, contrasted by the fixation of deleterious mutations and genome erosion through random genetic drift. The obligate cockroach endosymbiont, Blattabacterium – providing nutritional augmentation to its host in the form of amino acid synthesis – displays radical genome alterations when compared to its most recent free-living relative Flavobacterium. To date, eight Blattabacterium genomes have been published, affording an unparalleled opportunity to examine the direction and magnitude of selective forces acting upon this group of symbionts. Here, we find that the Blattabacterium genome is experiencing a 10-fold increase in selection rate compared to Flavobacteria. Additionally, the proportion of selection events is largely negative in direction, with only a handful of loci exhibiting signatures of positive selection. These findings suggest that the Blattabacterium genome will continue to erode, potentially resulting in an endosymbiont with an even further reduced genome, as seen in other insect groups such as Hemiptera.
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spelling pubmed-61289252018-09-10 Random Genetic Drift and Selective Pressures Shaping the Blattabacterium Genome Alleman, Austin Hertweck, Kate L. Kambhampati, Srini Sci Rep Article Estimates suggest that at least half of all extant insect genera harbor obligate bacterial mutualists. Whereas an endosymbiotic relationship imparts many benefits upon host and symbiont alike, the intracellular lifestyle has profound effects on the bacterial genome. The obligate endosymbiont genome is a product of opposing forces: genes important to host survival are maintained through physiological constraint, contrasted by the fixation of deleterious mutations and genome erosion through random genetic drift. The obligate cockroach endosymbiont, Blattabacterium – providing nutritional augmentation to its host in the form of amino acid synthesis – displays radical genome alterations when compared to its most recent free-living relative Flavobacterium. To date, eight Blattabacterium genomes have been published, affording an unparalleled opportunity to examine the direction and magnitude of selective forces acting upon this group of symbionts. Here, we find that the Blattabacterium genome is experiencing a 10-fold increase in selection rate compared to Flavobacteria. Additionally, the proportion of selection events is largely negative in direction, with only a handful of loci exhibiting signatures of positive selection. These findings suggest that the Blattabacterium genome will continue to erode, potentially resulting in an endosymbiont with an even further reduced genome, as seen in other insect groups such as Hemiptera. Nature Publishing Group UK 2018-09-07 /pmc/articles/PMC6128925/ /pubmed/30194350 http://dx.doi.org/10.1038/s41598-018-31796-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Alleman, Austin
Hertweck, Kate L.
Kambhampati, Srini
Random Genetic Drift and Selective Pressures Shaping the Blattabacterium Genome
title Random Genetic Drift and Selective Pressures Shaping the Blattabacterium Genome
title_full Random Genetic Drift and Selective Pressures Shaping the Blattabacterium Genome
title_fullStr Random Genetic Drift and Selective Pressures Shaping the Blattabacterium Genome
title_full_unstemmed Random Genetic Drift and Selective Pressures Shaping the Blattabacterium Genome
title_short Random Genetic Drift and Selective Pressures Shaping the Blattabacterium Genome
title_sort random genetic drift and selective pressures shaping the blattabacterium genome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128925/
https://www.ncbi.nlm.nih.gov/pubmed/30194350
http://dx.doi.org/10.1038/s41598-018-31796-6
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