Epidemiological investigation of Pseudomonas aeruginosa isolates including multidrug-resistant serogroup O12 isolates, by use of a rapid and simplified multiple-locus variable-number of tandem repeats analysis and whole genome sequencing.


Journal

The Journal of hospital infection
ISSN: 1532-2939
Titre abrégé: J Hosp Infect
Pays: England
ID NLM: 8007166

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 26 07 2022
revised: 05 09 2022
accepted: 12 09 2022
pubmed: 2 10 2022
medline: 16 11 2022
entrez: 1 10 2022
Statut: ppublish

Résumé

Clustered cases of Pseudomonas aeruginosa infection in immunocompromised patients' wards require rapid characterization of a potential epidemic to guide investigations and identify the potential source of contamination. To design and evaluate a rapid and simple typing method for P. aeruginosa in comparison to whole genome sequencing (WGS). A simplified polymerase chain reaction based on multiple-locus variable-number of tandem repeats analysis (MLVA) was designed and used to investigate cases of P. aeruginosa infection and colonization in a paediatric haematology department. The method was compared to WGS by using the Illumina method. On the 17 isolates recovered from 15 children (eight from blood cultures, three from urinary tract infections, one from sputum and five stool isolates), MLVA distinguished 10 different profiles, and seven isolates from six children shared the same profile. Analysis by WGS revealed that these seven isolates belonged to sequence type ST111 and serotype O12, allowing at least three different genotypes to be distinguished among them. Five environmental strains had three MLVA profiles; one was shared with a clinical isolate but WGS excluded any relationship. The simplified and inexpensive MLVA method enabled the exclusion, in less than 5 h, of most of the unrelated isolates and thus to focus investigations on a small number of cases, whereas WGS, taking several days of work, drew definitive conclusions concerning the outbreak and the genetic relationships of the ST111 isolates circulating in the department. We conclude that sequential use of both methods is the optimal strategy to investigate clustered cases of P. aeruginosa infections.

Sections du résumé

BACKGROUND BACKGROUND
Clustered cases of Pseudomonas aeruginosa infection in immunocompromised patients' wards require rapid characterization of a potential epidemic to guide investigations and identify the potential source of contamination.
AIM OBJECTIVE
To design and evaluate a rapid and simple typing method for P. aeruginosa in comparison to whole genome sequencing (WGS).
METHODS METHODS
A simplified polymerase chain reaction based on multiple-locus variable-number of tandem repeats analysis (MLVA) was designed and used to investigate cases of P. aeruginosa infection and colonization in a paediatric haematology department. The method was compared to WGS by using the Illumina method.
FINDINGS RESULTS
On the 17 isolates recovered from 15 children (eight from blood cultures, three from urinary tract infections, one from sputum and five stool isolates), MLVA distinguished 10 different profiles, and seven isolates from six children shared the same profile. Analysis by WGS revealed that these seven isolates belonged to sequence type ST111 and serotype O12, allowing at least three different genotypes to be distinguished among them. Five environmental strains had three MLVA profiles; one was shared with a clinical isolate but WGS excluded any relationship.
CONCLUSION CONCLUSIONS
The simplified and inexpensive MLVA method enabled the exclusion, in less than 5 h, of most of the unrelated isolates and thus to focus investigations on a small number of cases, whereas WGS, taking several days of work, drew definitive conclusions concerning the outbreak and the genetic relationships of the ST111 isolates circulating in the department. We conclude that sequential use of both methods is the optimal strategy to investigate clustered cases of P. aeruginosa infections.

Identifiants

pubmed: 36181986
pii: S0195-6701(22)00307-3
doi: 10.1016/j.jhin.2022.09.012
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

56-62

Informations de copyright

Copyright © 2022 The Healthcare Infection Society. Published by Elsevier Ltd. All rights reserved.

Auteurs

P Bidet (P)

Université Paris Cité, IAME, INSERM, Paris, France; Service de Microbiologie, Hôpital Robert-Debré, AP-HP, Paris, France. Electronic address: philippe.bidet@aphp.fr.

A Birgy (A)

Université Paris Cité, IAME, INSERM, Paris, France; Service de Microbiologie, Hôpital Robert-Debré, AP-HP, Paris, France.

B Brethon (B)

Service d'Hémato-immunologie, Hôpital Robert-Debré, AP-HP, Paris, France.

J H Dalle (JH)

Service d'Hémato-immunologie, Hôpital Robert-Debré, AP-HP, Paris, France.

P Mariani-Kurkdjian (P)

Université Paris Cité, IAME, INSERM, Paris, France; Service de Microbiologie, Hôpital Robert-Debré, AP-HP, Paris, France.

C Courroux (C)

Service de Microbiologie, Hôpital Robert-Debré, AP-HP, Paris, France.

A Monjault (A)

Service de Microbiologie, Hôpital Robert-Debré, AP-HP, Paris, France.

M Gits-Muselli (M)

Service de Microbiologie, Hôpital Robert-Debré, AP-HP, Paris, France.

S Bonacorsi (S)

Université Paris Cité, IAME, INSERM, Paris, France; Service de Microbiologie, Hôpital Robert-Debré, AP-HP, Paris, France.

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Classifications MeSH