Pangenome analysis reveals genetic isolation in Campylobacter hyointestinalis subspecies adapted to different mammalian hosts.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
09 02 2021
Historique:
received: 12 02 2018
accepted: 24 01 2021
entrez: 10 2 2021
pubmed: 11 2 2021
medline: 12 11 2021
Statut: epublish

Résumé

Campylobacter hyointestinalis is an emerging pathogen currently divided in two subspecies: C. hyointestinalis subsp. lawsonii which is predominantly recovered from pigs, and C. hyointestinalis subsp. hyointestinalis which can be found in a much wider range of mammalian hosts. Despite C. hyointestinalis being reported as an emerging pathogen, its evolutionary and host-associated diversification patterns are still vastly unexplored. For this reason, we generated whole-genome sequences of 13 C. hyointestinalis subsp. hyointestinalis strains and performed a comprehensive comparative analysis including publicly available C. hyointestinalis subsp. hyointestinalis and C. hyointestinalis subsp. lawsonii genomes, to gain insight into the genomic variation of these differentially-adapted subspecies. Both subspecies are distinct phylogenetic lineages which present an apparent barrier to homologous recombination, suggesting genetic isolation. This is further supported by accessory gene patterns that recapitulate the core genome phylogeny. Additionally, C. hyointestinalis subsp. hyointestinalis presents a bigger and more diverse accessory genome, which probably reflects its capacity to colonize different mammalian hosts unlike C. hyointestinalis subsp. lawsonii that is presumably host-restricted. This greater plasticity in the accessory genome of C. hyointestinalis subsp. hyointestinalis correlates to a higher incidence of genome-wide recombination events, that may be the underlying mechanism driving its diversification. Concordantly, both subspecies present distinct patterns of gene families involved in genome plasticity and DNA repair like CRISPR-associated proteins and restriction-modification systems. Together, our results provide an overview of the genetic mechanisms shaping the genomes of C. hyointestinalis subspecies, contributing to understand the biology of Campylobacter species that are increasingly recognized as emerging pathogens.

Identifiants

pubmed: 33564053
doi: 10.1038/s41598-021-82993-9
pii: 10.1038/s41598-021-82993-9
pmc: PMC7873201
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3431

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Auteurs

Daniela Costa (D)

Microbial Genomics Laboratory, Institut Pasteur Montevideo, 11400, Montevideo, Uruguay.
Sección Genética Evolutiva, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.

Simon Lévesque (S)

Laboratoire de Santé Publique du Québec, Quebec City, Canada.

Nitin Kumar (N)

Wellcome Sanger Institute, Hinxton, Cambridgeshire, UK.

Pablo Fresia (P)

Microbial Genomics Laboratory, Institut Pasteur Montevideo, 11400, Montevideo, Uruguay.
Unidad Mixta UMPI, Institut Pasteur de Montevideo + Instituto Nacional de Investigación Agropecuaria INIA, Montevideo, Uruguay.

Ignacio Ferrés (I)

Microbial Genomics Laboratory, Institut Pasteur Montevideo, 11400, Montevideo, Uruguay.

Trevor D Lawley (TD)

Wellcome Sanger Institute, Hinxton, Cambridgeshire, UK.

Gregorio Iraola (G)

Microbial Genomics Laboratory, Institut Pasteur Montevideo, 11400, Montevideo, Uruguay. giraola@pasteur.edu.uy.
Wellcome Sanger Institute, Hinxton, Cambridgeshire, UK. giraola@pasteur.edu.uy.
Center for Integrative Biology, Universidad Mayor, Santiago de Chile, Chile. giraola@pasteur.edu.uy.

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