Genome sequencing of strains of the most prevalent clonal group of O1:K1:H7 Escherichia coli that causes neonatal meningitis in France.


Journal

BMC microbiology
ISSN: 1471-2180
Titre abrégé: BMC Microbiol
Pays: England
ID NLM: 100966981

Informations de publication

Date de publication:
17 01 2019
Historique:
received: 26 06 2018
accepted: 18 12 2018
entrez: 19 1 2019
pubmed: 19 1 2019
medline: 24 9 2019
Statut: epublish

Résumé

To describe the temporal dynamics, molecular characterization, clinical and ex vivo virulence of emerging O1:K1 neonatal meningitis Escherichia coli (NMEC) strains of Sequence Type complex (STc) 95 in France. The national reference center collected NMEC strains and performed whole genome sequencing (WGS) of O1:K1 STc95 NMEC strains for phylogenetic and virulence genes content analysis. Data on the clinical and biological features of patients were also collected. Ex vivo virulence was assessed using the Dictyostelium discoideum amoeba model. Among 250 NMEC strains collected between 1998 and 2015, 38 belonged to O1:K1 STc95. This clonal complex was the most frequently collected after 2004, representing up to 25% of NMEC strains in France. Phylogenetic analysis demonstrated that most (74%) belonged to a cluster designated D-1, characterized by the adhesin FimH30. There is no clinical data to suggest that this cluster is more pathogenic than its counterparts, although it is highly predominant and harbors a large repertoire of extraintestinal virulence factors, including a pS88-like plasmid. Ex vivo virulence model showed that this cluster was generally less virulent than STc95 reference strains of O45 The emerging clonal group O1:K1 STc95 of NMEC strains is mainly composed of a cluster with many virulence factors but of only moderate virulence. Whether its emergence is due to its ability to colonize the gut thanks to FimH30 or pS88-like plasmid remains to be determined.

Sections du résumé

BACKGROUND
To describe the temporal dynamics, molecular characterization, clinical and ex vivo virulence of emerging O1:K1 neonatal meningitis Escherichia coli (NMEC) strains of Sequence Type complex (STc) 95 in France. The national reference center collected NMEC strains and performed whole genome sequencing (WGS) of O1:K1 STc95 NMEC strains for phylogenetic and virulence genes content analysis. Data on the clinical and biological features of patients were also collected. Ex vivo virulence was assessed using the Dictyostelium discoideum amoeba model.
RESULTS
Among 250 NMEC strains collected between 1998 and 2015, 38 belonged to O1:K1 STc95. This clonal complex was the most frequently collected after 2004, representing up to 25% of NMEC strains in France. Phylogenetic analysis demonstrated that most (74%) belonged to a cluster designated D-1, characterized by the adhesin FimH30. There is no clinical data to suggest that this cluster is more pathogenic than its counterparts, although it is highly predominant and harbors a large repertoire of extraintestinal virulence factors, including a pS88-like plasmid. Ex vivo virulence model showed that this cluster was generally less virulent than STc95 reference strains of O45
CONCLUSIONS
The emerging clonal group O1:K1 STc95 of NMEC strains is mainly composed of a cluster with many virulence factors but of only moderate virulence. Whether its emergence is due to its ability to colonize the gut thanks to FimH30 or pS88-like plasmid remains to be determined.

Identifiants

pubmed: 30654756
doi: 10.1186/s12866-018-1376-4
pii: 10.1186/s12866-018-1376-4
pmc: PMC6337857
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

17

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Auteurs

Guillaume Geslain (G)

IAME, UMR 1137, INSERM, Université Paris Diderot, Sorbonne Paris Cité, Paris, France.
Service de Microbiologie, Centre National de Référence Escherichia coli, Hôpital Robert-Debré, AP-HP, 48 boulevard Sérurier, 75019, Paris, France.

André Birgy (A)

IAME, UMR 1137, INSERM, Université Paris Diderot, Sorbonne Paris Cité, Paris, France.
Service de Microbiologie, Centre National de Référence Escherichia coli, Hôpital Robert-Debré, AP-HP, 48 boulevard Sérurier, 75019, Paris, France.

Sandrine Adiba (S)

Institut de Biologie de l'Ecole Normale Supérieure, Ecole Normale Supérieure, PSL Research University Paris, Paris, France.

Mélanie Magnan (M)

IAME, UMR 1137, INSERM, Université Paris Diderot, Sorbonne Paris Cité, Paris, France.

Céline Courroux (C)

Service de Microbiologie, Centre National de Référence Escherichia coli, Hôpital Robert-Debré, AP-HP, 48 boulevard Sérurier, 75019, Paris, France.

Corinne Levy (C)

Association Clinique Thérapeutique Infantile du Val de Marne, Saint Maur des Fossés, France.

Robert Cohen (R)

Association Clinique Thérapeutique Infantile du Val de Marne, Saint Maur des Fossés, France.

Philippe Bidet (P)

IAME, UMR 1137, INSERM, Université Paris Diderot, Sorbonne Paris Cité, Paris, France.
Service de Microbiologie, Centre National de Référence Escherichia coli, Hôpital Robert-Debré, AP-HP, 48 boulevard Sérurier, 75019, Paris, France.

Stéphane Bonacorsi (S)

IAME, UMR 1137, INSERM, Université Paris Diderot, Sorbonne Paris Cité, Paris, France. stephane.bonacorsi@aphp.fr.
Service de Microbiologie, Centre National de Référence Escherichia coli, Hôpital Robert-Debré, AP-HP, 48 boulevard Sérurier, 75019, Paris, France. stephane.bonacorsi@aphp.fr.

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