Dépôt numérique
RECHERCHER

High-Throughput Short Sequence Typing Schemes for Pseudomonas aeruginosa and Stenotrophomonas maltophilia Pure Culture and Environmental DNA

Téléchargements

Téléchargements par mois depuis la dernière année

Plus de statistiques...

Bourdin, Thibault; Benoît, Marie-Eve; Bédard, Émilie; Prévost, Michèle; Quach, Caroline; Déziel, Éric ORCID logoORCID: https://orcid.org/0000-0002-4609-0115 et Constant, Philippe ORCID logoORCID: https://orcid.org/0000-0003-2739-2801 (2023). High-Throughput Short Sequence Typing Schemes for Pseudomonas aeruginosa and Stenotrophomonas maltophilia Pure Culture and Environmental DNA Microorganisms , vol. 12 , nº 1. pp. 1-15. DOI: 10.3390/microorganisms12010048.

[thumbnail of High-Throughput Short Sequence Typing Schemes for Pseudomonas aeruginosa and Stenotrophomonas maltophilia Pure Culture and Environmental DNA.pdf]
Prévisualisation
PDF - Version publiée
Disponible sous licence Creative Commons Attribution.

Télécharger (2MB) | Prévisualisation

Résumé


Molecular typing techniques are utilized to determine genetic similarities between bacterial isolates. However, the use of environmental DNA profiling to assess epidemiologic links between patients and their environment has not been fully explored. This work reports the development and validation of two high-throughput short sequence typing (HiSST) schemes targeting the opportunistic pathogens Pseudomonas aeruginosa and Stenotrophomonas maltophilia, along with a modified SM2I selective medium for the specific isolation of S. maltophilia. These HiSST schemes are based on four discriminative loci for each species and demonstrate high discriminating power, comparable to pairwise whole-genome comparisons. Each scheme includes species-specific PCR primers for precise differentiation from closely related taxa, without the need for upstream culture-dependent methods. For example, the primers targeting the bvgS locus make it possible to distinguish P. aeruginosa from the very closely related Pseudomonas paraeruginosa sp. nov. The selected loci included in the schemes are adapted to massive parallel amplicon sequencing technology. An R-based script implemented in the DADA2 pipeline was assembled to facilitate HiSST analyses for efficient and accurate genotyping of P. aeruginosa and S. maltophilia. We demonstrate the performance of both schemes through in silico validations, assessments against reference culture collections, and a case study involving environmental samples.

Type de document: Article
Mots-clés libres: Pseudomonas paraeruginosa; eDNA; genotyping; healthcare-associated infections (HAIs); molecular typing; neonatal intensive care units (NICUs); opportunistic pathogens; opportunistic premise plumbing pathogens (OPPP); selective medium
Centre: Centre INRS-Institut Armand Frappier
Date de dépôt: 28 janv. 2024 15:07
Dernière modification: 28 janv. 2024 15:07
URI: https://espace.inrs.ca/id/eprint/14155

Gestion Actions (Identification requise)

Modifier la notice Modifier la notice