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High frequency of the exoU+/exoS+ genotype associated with multidrug-resistant “high-risk clones” of Pseudomonas aeruginosa clinical isolates from Peruvian hospitals

  • Gertrudis Horna
    ,
  • Catherine Amaro
    ,
  • Aida Palacios
    ,
  • Humberto Guerra
    ,
  • Universitat de Barcelona
    ,
  • Universidad Peruana Cayetano Heredia, Instituto de Medicina Tropical Alexander von Humboldt
    ,
  • Universidad Católica los Ángeles de Chimbote
    ,
  • Hospital Nacional Cayetano Heredia
    ,
  • ,
  • Universidad Continental, Huancayo
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Article number

10874

Journal (Volume, Issue Number)

Scientific Reports (Volume 9, Issue 1)

Publication milestones

  • Published - 01/12/2019

Publication status

Published - 01/12/2019

Publication IDs

  • Scopus: 85069750063
  • PubMed: 31350412

Abstract

The type III secretion system of Pseudomonas aeruginosa is an important virulence factor contributing to the cytotoxicity and the invasion process of this microorganism. The current study aimed to determine the presence of the exoU+/exoS+ genotype in P. aeruginosa clinical isolates. The presence of exoS, exoT, exoU and exoY was determined in 189 P. aeruginosa by PCR, and the presence/absence of exoU was analysed according to source infection, clonal relationships, biofilm formation, motility and antimicrobial susceptibility. The gyrA, parC, oprD, efflux pump regulators and β-lactamases genes were also analysed by PCR/sequencing. The exoS, exoT and exoY genes were found in 100% of the isolates. Meanwhile, exoU was present in 43/189 (22.8%) of the isolates, being significantly associated with multidrug resistance, extensively drug resistance as well as with higher level quinolone resistance. However, the presence of β-lactamases, mutations in gyrA and parC, and relevant modifications in efflux pumps and OprD were not significantly associated with exoU+ isolates. MLST analysis of a subset of 25 isolates showed 8 different STs displaying the exoU+/exoS+ genotype. The MDR basis of the exoU+ isolates remain to be elucidated. Furthermore, the clinical implications and spread of exoU+/exoS+ P. aeruginosa isolates need to be established.

Funding Details

GH has a personal fellowship from the Schlumberger Foundation - Faculty for The Future Program. JR was supported by a fellowship from the I3SNS program (2012–2016), of the ISCIII (grant number: CES11/012). We thank to Angel Sacha for his technical support in the development of microbiological techniques. We thank to Donna Pringle for idiomatic correction. “ISGlobal is a member of the CERCA Programme, Generalitat de Catalunya”.
FundersFunding numbers
Schlumberger Foundation
-
ISCIII
CES11/012