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Acquisition and loss of virulence-associated factors during genome evolution and speciation in three clades of Bordetella species

BACKGROUND: The genus Bordetella consists of nine species that include important respiratory pathogens such as the ‘classical’ species B. bronchiseptica, B. pertussis and B. parapertussis and six more distantly related and less extensively studied species. Here we analyze sequence diversity and gene...

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Autores principales: Linz, Bodo, Ivanov, Yury V., Preston, Andrew, Brinkac, Lauren, Parkhill, Julian, Kim, Maria, Harris, Simon R., Goodfield, Laura L., Fry, Norman K., Gorringe, Andrew R., Nicholson, Tracy L., Register, Karen B., Losada, Liliana, Harvill, Eric T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045587/
https://www.ncbi.nlm.nih.gov/pubmed/27716057
http://dx.doi.org/10.1186/s12864-016-3112-5
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author Linz, Bodo
Ivanov, Yury V.
Preston, Andrew
Brinkac, Lauren
Parkhill, Julian
Kim, Maria
Harris, Simon R.
Goodfield, Laura L.
Fry, Norman K.
Gorringe, Andrew R.
Nicholson, Tracy L.
Register, Karen B.
Losada, Liliana
Harvill, Eric T.
author_facet Linz, Bodo
Ivanov, Yury V.
Preston, Andrew
Brinkac, Lauren
Parkhill, Julian
Kim, Maria
Harris, Simon R.
Goodfield, Laura L.
Fry, Norman K.
Gorringe, Andrew R.
Nicholson, Tracy L.
Register, Karen B.
Losada, Liliana
Harvill, Eric T.
author_sort Linz, Bodo
collection PubMed
description BACKGROUND: The genus Bordetella consists of nine species that include important respiratory pathogens such as the ‘classical’ species B. bronchiseptica, B. pertussis and B. parapertussis and six more distantly related and less extensively studied species. Here we analyze sequence diversity and gene content of 128 genome sequences from all nine species with focus on the evolution of virulence-associated factors. RESULTS: Both genome-wide sequence-based and gene content-based phylogenetic trees divide the genus into three species clades. The phylogenies are congruent between species suggesting genus-wide co-evolution of sequence diversity and gene content, but less correlated within species, mainly because of strain-specific presence of many different prophages. We compared the genomes with focus on virulence-associated genes and identified multiple clade-specific, species-specific and strain-specific events of gene acquisition and gene loss, including genes encoding O-antigens, protein secretion systems and bacterial toxins. Gene loss was more frequent than gene gain throughout the evolution, and loss of hundreds of genes was associated with the origin of several species, including the recently evolved human-restricted B. pertussis and B. holmesii, B. parapertussis and the avian pathogen B. avium. CONCLUSIONS: Acquisition and loss of multiple genes drive the evolution and speciation in the genus Bordetella, including large scale gene loss associated with the origin of several species. Recent loss and functional inactivation of genes, including those encoding pertussis vaccine components and bacterial toxins, in individual strains emphasize ongoing evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3112-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-50455872016-10-12 Acquisition and loss of virulence-associated factors during genome evolution and speciation in three clades of Bordetella species Linz, Bodo Ivanov, Yury V. Preston, Andrew Brinkac, Lauren Parkhill, Julian Kim, Maria Harris, Simon R. Goodfield, Laura L. Fry, Norman K. Gorringe, Andrew R. Nicholson, Tracy L. Register, Karen B. Losada, Liliana Harvill, Eric T. BMC Genomics Research Article BACKGROUND: The genus Bordetella consists of nine species that include important respiratory pathogens such as the ‘classical’ species B. bronchiseptica, B. pertussis and B. parapertussis and six more distantly related and less extensively studied species. Here we analyze sequence diversity and gene content of 128 genome sequences from all nine species with focus on the evolution of virulence-associated factors. RESULTS: Both genome-wide sequence-based and gene content-based phylogenetic trees divide the genus into three species clades. The phylogenies are congruent between species suggesting genus-wide co-evolution of sequence diversity and gene content, but less correlated within species, mainly because of strain-specific presence of many different prophages. We compared the genomes with focus on virulence-associated genes and identified multiple clade-specific, species-specific and strain-specific events of gene acquisition and gene loss, including genes encoding O-antigens, protein secretion systems and bacterial toxins. Gene loss was more frequent than gene gain throughout the evolution, and loss of hundreds of genes was associated with the origin of several species, including the recently evolved human-restricted B. pertussis and B. holmesii, B. parapertussis and the avian pathogen B. avium. CONCLUSIONS: Acquisition and loss of multiple genes drive the evolution and speciation in the genus Bordetella, including large scale gene loss associated with the origin of several species. Recent loss and functional inactivation of genes, including those encoding pertussis vaccine components and bacterial toxins, in individual strains emphasize ongoing evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3112-5) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-30 /pmc/articles/PMC5045587/ /pubmed/27716057 http://dx.doi.org/10.1186/s12864-016-3112-5 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
Linz, Bodo
Ivanov, Yury V.
Preston, Andrew
Brinkac, Lauren
Parkhill, Julian
Kim, Maria
Harris, Simon R.
Goodfield, Laura L.
Fry, Norman K.
Gorringe, Andrew R.
Nicholson, Tracy L.
Register, Karen B.
Losada, Liliana
Harvill, Eric T.
Acquisition and loss of virulence-associated factors during genome evolution and speciation in three clades of Bordetella species
title Acquisition and loss of virulence-associated factors during genome evolution and speciation in three clades of Bordetella species
title_full Acquisition and loss of virulence-associated factors during genome evolution and speciation in three clades of Bordetella species
title_fullStr Acquisition and loss of virulence-associated factors during genome evolution and speciation in three clades of Bordetella species
title_full_unstemmed Acquisition and loss of virulence-associated factors during genome evolution and speciation in three clades of Bordetella species
title_short Acquisition and loss of virulence-associated factors during genome evolution and speciation in three clades of Bordetella species
title_sort acquisition and loss of virulence-associated factors during genome evolution and speciation in three clades of bordetella species
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045587/
https://www.ncbi.nlm.nih.gov/pubmed/27716057
http://dx.doi.org/10.1186/s12864-016-3112-5
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