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Recurrent evolution of host and vector association in bacteria of the Borrelia burgdorferi sensu lato species complex

BACKGROUND: The Borrelia burgdorferi sensu lato (s.l.) species complex consists of tick-transmitted bacteria and currently comprises approximately 20 named and proposed genospecies some of which are known to cause Lyme Borreliosis. Species have been defined via genetic distances and ecological niche...

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Autores principales: Becker, Noémie S., Margos, Gabriele, Blum, Helmut, Krebs, Stefan, Graf, Alexander, Lane, Robert S., Castillo-Ramírez, Santiago, Sing, Andreas, Fingerle, Volker
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025617/
https://www.ncbi.nlm.nih.gov/pubmed/27632983
http://dx.doi.org/10.1186/s12864-016-3016-4
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author Becker, Noémie S.
Margos, Gabriele
Blum, Helmut
Krebs, Stefan
Graf, Alexander
Lane, Robert S.
Castillo-Ramírez, Santiago
Sing, Andreas
Fingerle, Volker
author_facet Becker, Noémie S.
Margos, Gabriele
Blum, Helmut
Krebs, Stefan
Graf, Alexander
Lane, Robert S.
Castillo-Ramírez, Santiago
Sing, Andreas
Fingerle, Volker
author_sort Becker, Noémie S.
collection PubMed
description BACKGROUND: The Borrelia burgdorferi sensu lato (s.l.) species complex consists of tick-transmitted bacteria and currently comprises approximately 20 named and proposed genospecies some of which are known to cause Lyme Borreliosis. Species have been defined via genetic distances and ecological niches they occupy. Understanding the evolutionary relationship of species of the complex is fundamental to explaining patterns of speciation. This in turn forms a crucial basis to frame testable hypotheses concerning the underlying processes including host and vector adaptations. RESULTS: Illumina Technology was used to obtain genome-wide sequence data for 93 strains of 14 named genospecies of the B. burgdorferi species complex and genomic data already published for 18 additional strain (including one new species) was added. Phylogenetic reconstruction based on 114 orthologous single copy genes shows that the genospecies represent clearly distinguishable taxa with recent and still ongoing speciation events apparent in Europe and Asia. The position of Borrelia species in the phylogeny is consistent with host associations constituting a major driver for speciation. Interestingly, the data also demonstrate that vector associations are an additional driver for diversification in this tick-borne species complex. This is particularly obvious in B. bavariensis, a rodent adapted species that has diverged from the bird-associated B. garinii most likely in Asia. It now consists of two populations one of which most probably invaded Europe following adaptation to a new vector (Ixodes ricinus) and currently expands its distribution range. CONCLUSIONS: The results imply that genotypes/species with novel properties regarding host or vector associations have evolved recurrently during the history of the species complex and may emerge at any time. We suggest that the finding of vector associations as a driver for diversification may be a general pattern for tick-borne pathogens. The core genome analysis presented here provides an important source for investigations of the underlying mechanisms of speciation in tick-borne pathogens. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3016-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-50256172016-09-20 Recurrent evolution of host and vector association in bacteria of the Borrelia burgdorferi sensu lato species complex Becker, Noémie S. Margos, Gabriele Blum, Helmut Krebs, Stefan Graf, Alexander Lane, Robert S. Castillo-Ramírez, Santiago Sing, Andreas Fingerle, Volker BMC Genomics Research Article BACKGROUND: The Borrelia burgdorferi sensu lato (s.l.) species complex consists of tick-transmitted bacteria and currently comprises approximately 20 named and proposed genospecies some of which are known to cause Lyme Borreliosis. Species have been defined via genetic distances and ecological niches they occupy. Understanding the evolutionary relationship of species of the complex is fundamental to explaining patterns of speciation. This in turn forms a crucial basis to frame testable hypotheses concerning the underlying processes including host and vector adaptations. RESULTS: Illumina Technology was used to obtain genome-wide sequence data for 93 strains of 14 named genospecies of the B. burgdorferi species complex and genomic data already published for 18 additional strain (including one new species) was added. Phylogenetic reconstruction based on 114 orthologous single copy genes shows that the genospecies represent clearly distinguishable taxa with recent and still ongoing speciation events apparent in Europe and Asia. The position of Borrelia species in the phylogeny is consistent with host associations constituting a major driver for speciation. Interestingly, the data also demonstrate that vector associations are an additional driver for diversification in this tick-borne species complex. This is particularly obvious in B. bavariensis, a rodent adapted species that has diverged from the bird-associated B. garinii most likely in Asia. It now consists of two populations one of which most probably invaded Europe following adaptation to a new vector (Ixodes ricinus) and currently expands its distribution range. CONCLUSIONS: The results imply that genotypes/species with novel properties regarding host or vector associations have evolved recurrently during the history of the species complex and may emerge at any time. We suggest that the finding of vector associations as a driver for diversification may be a general pattern for tick-borne pathogens. The core genome analysis presented here provides an important source for investigations of the underlying mechanisms of speciation in tick-borne pathogens. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3016-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-15 /pmc/articles/PMC5025617/ /pubmed/27632983 http://dx.doi.org/10.1186/s12864-016-3016-4 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Becker, Noémie S.
Margos, Gabriele
Blum, Helmut
Krebs, Stefan
Graf, Alexander
Lane, Robert S.
Castillo-Ramírez, Santiago
Sing, Andreas
Fingerle, Volker
Recurrent evolution of host and vector association in bacteria of the Borrelia burgdorferi sensu lato species complex
title Recurrent evolution of host and vector association in bacteria of the Borrelia burgdorferi sensu lato species complex
title_full Recurrent evolution of host and vector association in bacteria of the Borrelia burgdorferi sensu lato species complex
title_fullStr Recurrent evolution of host and vector association in bacteria of the Borrelia burgdorferi sensu lato species complex
title_full_unstemmed Recurrent evolution of host and vector association in bacteria of the Borrelia burgdorferi sensu lato species complex
title_short Recurrent evolution of host and vector association in bacteria of the Borrelia burgdorferi sensu lato species complex
title_sort recurrent evolution of host and vector association in bacteria of the borrelia burgdorferi sensu lato species complex
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025617/
https://www.ncbi.nlm.nih.gov/pubmed/27632983
http://dx.doi.org/10.1186/s12864-016-3016-4
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