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Serotype IV Streptococcus agalactiae ST-452 has arisen from large genomic recombination events between CC23 and the hypervirulent CC17 lineages

Streptococcus agalactiae (Group B Streptococcus, GBS) causes life-threatening infections in newborns and adults with chronic medical conditions. Serotype IV strains are emerging both among carriers and as cause of invasive disease and recent studies revealed two main Sequence Types (STs), ST-452 and...

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Autores principales: Campisi, Edmondo, Rinaudo, C. Daniela, Donati, Claudio, Barucco, Mara, Torricelli, Giulia, Edwards, Morven S., Baker, Carol J., Margarit, Imma, Rosini, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4944191/
https://www.ncbi.nlm.nih.gov/pubmed/27411639
http://dx.doi.org/10.1038/srep29799
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author Campisi, Edmondo
Rinaudo, C. Daniela
Donati, Claudio
Barucco, Mara
Torricelli, Giulia
Edwards, Morven S.
Baker, Carol J.
Margarit, Imma
Rosini, Roberto
author_facet Campisi, Edmondo
Rinaudo, C. Daniela
Donati, Claudio
Barucco, Mara
Torricelli, Giulia
Edwards, Morven S.
Baker, Carol J.
Margarit, Imma
Rosini, Roberto
author_sort Campisi, Edmondo
collection PubMed
description Streptococcus agalactiae (Group B Streptococcus, GBS) causes life-threatening infections in newborns and adults with chronic medical conditions. Serotype IV strains are emerging both among carriers and as cause of invasive disease and recent studies revealed two main Sequence Types (STs), ST-452 and ST-459 assigned to Clonal Complexes CC23 and CC1, respectively. Whole genome sequencing of 70 type IV GBS and subsequent phylogenetic analysis elucidated the localization of type IV isolates in a SNP-based phylogenetic tree and suggested that ST-452 could have originated through genetic recombination. SNPs density analysis of the core genome confirmed that the founder strain of this lineage originated from a single large horizontal gene transfer event between CC23 and the hypervirulent CC17. Indeed, ST-452 genomes are composed by two parts that are nearly identical to corresponding regions in ST-24 (CC23) and ST-291 (CC17). Chromosome mapping of the major GBS virulence factors showed that ST-452 strains have an intermediate yet unique profile among CC23 and CC17 strains. We described unreported large recombination events, involving the cps IV operon and resulting in the expansion of serotype IV to CC23. This work sheds further light on the evolution of GBS providing new insights on the recent emergence of serotype IV.
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spelling pubmed-49441912016-07-26 Serotype IV Streptococcus agalactiae ST-452 has arisen from large genomic recombination events between CC23 and the hypervirulent CC17 lineages Campisi, Edmondo Rinaudo, C. Daniela Donati, Claudio Barucco, Mara Torricelli, Giulia Edwards, Morven S. Baker, Carol J. Margarit, Imma Rosini, Roberto Sci Rep Article Streptococcus agalactiae (Group B Streptococcus, GBS) causes life-threatening infections in newborns and adults with chronic medical conditions. Serotype IV strains are emerging both among carriers and as cause of invasive disease and recent studies revealed two main Sequence Types (STs), ST-452 and ST-459 assigned to Clonal Complexes CC23 and CC1, respectively. Whole genome sequencing of 70 type IV GBS and subsequent phylogenetic analysis elucidated the localization of type IV isolates in a SNP-based phylogenetic tree and suggested that ST-452 could have originated through genetic recombination. SNPs density analysis of the core genome confirmed that the founder strain of this lineage originated from a single large horizontal gene transfer event between CC23 and the hypervirulent CC17. Indeed, ST-452 genomes are composed by two parts that are nearly identical to corresponding regions in ST-24 (CC23) and ST-291 (CC17). Chromosome mapping of the major GBS virulence factors showed that ST-452 strains have an intermediate yet unique profile among CC23 and CC17 strains. We described unreported large recombination events, involving the cps IV operon and resulting in the expansion of serotype IV to CC23. This work sheds further light on the evolution of GBS providing new insights on the recent emergence of serotype IV. Nature Publishing Group 2016-07-14 /pmc/articles/PMC4944191/ /pubmed/27411639 http://dx.doi.org/10.1038/srep29799 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Campisi, Edmondo
Rinaudo, C. Daniela
Donati, Claudio
Barucco, Mara
Torricelli, Giulia
Edwards, Morven S.
Baker, Carol J.
Margarit, Imma
Rosini, Roberto
Serotype IV Streptococcus agalactiae ST-452 has arisen from large genomic recombination events between CC23 and the hypervirulent CC17 lineages
title Serotype IV Streptococcus agalactiae ST-452 has arisen from large genomic recombination events between CC23 and the hypervirulent CC17 lineages
title_full Serotype IV Streptococcus agalactiae ST-452 has arisen from large genomic recombination events between CC23 and the hypervirulent CC17 lineages
title_fullStr Serotype IV Streptococcus agalactiae ST-452 has arisen from large genomic recombination events between CC23 and the hypervirulent CC17 lineages
title_full_unstemmed Serotype IV Streptococcus agalactiae ST-452 has arisen from large genomic recombination events between CC23 and the hypervirulent CC17 lineages
title_short Serotype IV Streptococcus agalactiae ST-452 has arisen from large genomic recombination events between CC23 and the hypervirulent CC17 lineages
title_sort serotype iv streptococcus agalactiae st-452 has arisen from large genomic recombination events between cc23 and the hypervirulent cc17 lineages
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4944191/
https://www.ncbi.nlm.nih.gov/pubmed/27411639
http://dx.doi.org/10.1038/srep29799
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