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Interplay of recombination and selection in the genomes of Chlamydia trachomatis

BACKGROUND: Chlamydia trachomatis is an obligate intracellular bacterial parasite, which causes several severe and debilitating diseases in humans. This study uses comparative genomic analyses of 12 complete published C. trachomatis genomes to assess the contribution of recombination and selection i...

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Autores principales: Joseph, Sandeep J, Didelot, Xavier, Gandhi, Khanjan, Dean, Deborah, Read, Timothy D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3126793/
https://www.ncbi.nlm.nih.gov/pubmed/21615910
http://dx.doi.org/10.1186/1745-6150-6-28
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author Joseph, Sandeep J
Didelot, Xavier
Gandhi, Khanjan
Dean, Deborah
Read, Timothy D
author_facet Joseph, Sandeep J
Didelot, Xavier
Gandhi, Khanjan
Dean, Deborah
Read, Timothy D
author_sort Joseph, Sandeep J
collection PubMed
description BACKGROUND: Chlamydia trachomatis is an obligate intracellular bacterial parasite, which causes several severe and debilitating diseases in humans. This study uses comparative genomic analyses of 12 complete published C. trachomatis genomes to assess the contribution of recombination and selection in this pathogen and to understand the major evolutionary forces acting on the genome of this bacterium. RESULTS: The conserved core genes of C. trachomatis are a large proportion of the pan-genome: we identified 836 core genes in C. trachomatis out of a range of 874-927 total genes in each genome. The ratio of recombination events compared to mutation (ρ/θ) was 0.07 based on ancestral reconstructions using the ClonalFrame tool, but recombination had a significant effect on genetic diversification (r/m = 0.71). The distance-dependent decay of linkage disequilibrium also indicated that C. trachomatis populations behaved intermediately between sexual and clonal extremes. Fifty-five genes were identified as having a history of recombination and 92 were under positive selection based on statistical tests. Twenty-three genes showed evidence of being under both positive selection and recombination, which included genes with a known role in virulence and pathogencity (e.g., ompA, pmps, tarp). Analysis of inter-clade recombination flux indicated non-uniform currents of recombination between clades, which suggests the possibility of spatial population structure in C. trachomatis infections. CONCLUSIONS: C. trachomatis is the archetype of a bacterial species where recombination is relatively frequent yet gene gains by horizontal gene transfer (HGT) and losses (by deletion) are rare. Gene conversion occurs at sites across the whole C. trachomatis genome but may be more often fixed in genes that are under diversifying selection. Furthermore, genome sequencing will reveal patterns of serotype specific gene exchange and selection that will generate important research questions for understanding C. trachomatis pathogenesis. REVIEWERS: This article was reviewed by Dr. Jeremy Selengut, Dr. Lee S. Katz (nominated by Dr. I. King Jordan) and Dr. Arcady Mushegian.
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spelling pubmed-31267932011-06-30 Interplay of recombination and selection in the genomes of Chlamydia trachomatis Joseph, Sandeep J Didelot, Xavier Gandhi, Khanjan Dean, Deborah Read, Timothy D Biol Direct Research BACKGROUND: Chlamydia trachomatis is an obligate intracellular bacterial parasite, which causes several severe and debilitating diseases in humans. This study uses comparative genomic analyses of 12 complete published C. trachomatis genomes to assess the contribution of recombination and selection in this pathogen and to understand the major evolutionary forces acting on the genome of this bacterium. RESULTS: The conserved core genes of C. trachomatis are a large proportion of the pan-genome: we identified 836 core genes in C. trachomatis out of a range of 874-927 total genes in each genome. The ratio of recombination events compared to mutation (ρ/θ) was 0.07 based on ancestral reconstructions using the ClonalFrame tool, but recombination had a significant effect on genetic diversification (r/m = 0.71). The distance-dependent decay of linkage disequilibrium also indicated that C. trachomatis populations behaved intermediately between sexual and clonal extremes. Fifty-five genes were identified as having a history of recombination and 92 were under positive selection based on statistical tests. Twenty-three genes showed evidence of being under both positive selection and recombination, which included genes with a known role in virulence and pathogencity (e.g., ompA, pmps, tarp). Analysis of inter-clade recombination flux indicated non-uniform currents of recombination between clades, which suggests the possibility of spatial population structure in C. trachomatis infections. CONCLUSIONS: C. trachomatis is the archetype of a bacterial species where recombination is relatively frequent yet gene gains by horizontal gene transfer (HGT) and losses (by deletion) are rare. Gene conversion occurs at sites across the whole C. trachomatis genome but may be more often fixed in genes that are under diversifying selection. Furthermore, genome sequencing will reveal patterns of serotype specific gene exchange and selection that will generate important research questions for understanding C. trachomatis pathogenesis. REVIEWERS: This article was reviewed by Dr. Jeremy Selengut, Dr. Lee S. Katz (nominated by Dr. I. King Jordan) and Dr. Arcady Mushegian. BioMed Central 2011-05-26 /pmc/articles/PMC3126793/ /pubmed/21615910 http://dx.doi.org/10.1186/1745-6150-6-28 Text en Copyright ©2011 Joseph 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
Joseph, Sandeep J
Didelot, Xavier
Gandhi, Khanjan
Dean, Deborah
Read, Timothy D
Interplay of recombination and selection in the genomes of Chlamydia trachomatis
title Interplay of recombination and selection in the genomes of Chlamydia trachomatis
title_full Interplay of recombination and selection in the genomes of Chlamydia trachomatis
title_fullStr Interplay of recombination and selection in the genomes of Chlamydia trachomatis
title_full_unstemmed Interplay of recombination and selection in the genomes of Chlamydia trachomatis
title_short Interplay of recombination and selection in the genomes of Chlamydia trachomatis
title_sort interplay of recombination and selection in the genomes of chlamydia trachomatis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3126793/
https://www.ncbi.nlm.nih.gov/pubmed/21615910
http://dx.doi.org/10.1186/1745-6150-6-28
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