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A genome-wide study of recombination rate variation in Bartonella henselae
BACKGROUND: Rates of recombination vary by three orders of magnitude in bacteria but the reasons for this variation is unclear. We performed a genome-wide study of recombination rate variation among genes in the intracellular bacterium Bartonella henselae, which has among the lowest estimated ratio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3483213/ https://www.ncbi.nlm.nih.gov/pubmed/22577862 http://dx.doi.org/10.1186/1471-2148-12-65 |
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author | Guy, Lionel Nystedt, Björn Sun, Yu Näslund, Kristina Berglund, Eva C Andersson, Siv GE |
author_facet | Guy, Lionel Nystedt, Björn Sun, Yu Näslund, Kristina Berglund, Eva C Andersson, Siv GE |
author_sort | Guy, Lionel |
collection | PubMed |
description | BACKGROUND: Rates of recombination vary by three orders of magnitude in bacteria but the reasons for this variation is unclear. We performed a genome-wide study of recombination rate variation among genes in the intracellular bacterium Bartonella henselae, which has among the lowest estimated ratio of recombination relative to mutation in prokaryotes. RESULTS: The 1.9 Mb genomes of B. henselae strains IC11, UGA10 and Houston-1 genomes showed only minor gene content variation. Nucleotide sequence divergence levels were less than 1% and the relative rate of recombination to mutation was estimated to 1.1 for the genome overall. Four to eight segments per genome presented significantly enhanced divergences, the most pronounced of which were the virB and trw gene clusters for type IV secretion systems that play essential roles in the infection process. Consistently, multiple recombination events were identified inside these gene clusters. High recombination frequencies were also observed for a gene putatively involved in iron metabolism. A phylogenetic study of this gene in 80 strains of Bartonella quintana, B. henselae and B. grahamii indicated different population structures for each species and revealed horizontal gene transfers across Bartonella species with different host preferences. CONCLUSIONS: Our analysis has shown little novel gene acquisition in B. henselae, indicative of a closed pan-genome, but higher recombination frequencies within the population than previously estimated. We propose that the dramatically increased fixation rate for recombination events at gene clusters for type IV secretion systems is driven by selection for sequence variability. |
format | Online Article Text |
id | pubmed-3483213 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34832132012-10-30 A genome-wide study of recombination rate variation in Bartonella henselae Guy, Lionel Nystedt, Björn Sun, Yu Näslund, Kristina Berglund, Eva C Andersson, Siv GE BMC Evol Biol Research Article BACKGROUND: Rates of recombination vary by three orders of magnitude in bacteria but the reasons for this variation is unclear. We performed a genome-wide study of recombination rate variation among genes in the intracellular bacterium Bartonella henselae, which has among the lowest estimated ratio of recombination relative to mutation in prokaryotes. RESULTS: The 1.9 Mb genomes of B. henselae strains IC11, UGA10 and Houston-1 genomes showed only minor gene content variation. Nucleotide sequence divergence levels were less than 1% and the relative rate of recombination to mutation was estimated to 1.1 for the genome overall. Four to eight segments per genome presented significantly enhanced divergences, the most pronounced of which were the virB and trw gene clusters for type IV secretion systems that play essential roles in the infection process. Consistently, multiple recombination events were identified inside these gene clusters. High recombination frequencies were also observed for a gene putatively involved in iron metabolism. A phylogenetic study of this gene in 80 strains of Bartonella quintana, B. henselae and B. grahamii indicated different population structures for each species and revealed horizontal gene transfers across Bartonella species with different host preferences. CONCLUSIONS: Our analysis has shown little novel gene acquisition in B. henselae, indicative of a closed pan-genome, but higher recombination frequencies within the population than previously estimated. We propose that the dramatically increased fixation rate for recombination events at gene clusters for type IV secretion systems is driven by selection for sequence variability. BioMed Central 2012-05-11 /pmc/articles/PMC3483213/ /pubmed/22577862 http://dx.doi.org/10.1186/1471-2148-12-65 Text en Copyright ©2012 Guy et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Guy, Lionel Nystedt, Björn Sun, Yu Näslund, Kristina Berglund, Eva C Andersson, Siv GE A genome-wide study of recombination rate variation in Bartonella henselae |
title | A genome-wide study of recombination rate variation in Bartonella henselae |
title_full | A genome-wide study of recombination rate variation in Bartonella henselae |
title_fullStr | A genome-wide study of recombination rate variation in Bartonella henselae |
title_full_unstemmed | A genome-wide study of recombination rate variation in Bartonella henselae |
title_short | A genome-wide study of recombination rate variation in Bartonella henselae |
title_sort | genome-wide study of recombination rate variation in bartonella henselae |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3483213/ https://www.ncbi.nlm.nih.gov/pubmed/22577862 http://dx.doi.org/10.1186/1471-2148-12-65 |
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