4.3 Article

Carbapenemase-producing Pseudomonas aeruginosa isolates from Turkey: first report of P. aeruginosa high-risk clones with VIM-5-and IMP-7-type carbapenemases in a tertiary hospital

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.diagmicrobio.2020.115174

关键词

Carbapenem resistance; VIM-5; ST308; IMP-7; ST357; crpP; Fluoroquinolone resistance

资金

  1. Assistance Publique - Hopitaux de Paris (AP-HP)
  2. University Paris-Sud
  3. Laboratory of Excellence in Research on Medication and Innovative Therapeutics (LERMIT) - French National Research Agency [ANR-10LABX-33]
  4. Joint Programming Initiative on Antimicrobial Resistance (JPIAMR) DesInMBL [ANR-14-JAMR-002]
  5. DIM Malinf, Ile de France

向作者/读者索取更多资源

In a Turkish hospital, carbapenemases were investigated in carbapenem-resistant Pseudomonas aeruginosa isolates. Two high-risk clones were identified, carrying VIM-5 and IMP-7 carbapenemases along with multiple resistance determinants.
We investigated the presence of carbapenemases in carbapenem-resistant Pseudomonas aeruginosa isolates, which were collected over a 14-month period in a Turkish hospital, with in-depth molecular characterization of carbapenemase-producing isolates. Among 45 study isolates, 2 isolates were identified as carbapenemase producers by both Carba NP and Carbapenem Inactivation Method tests, and only 1 of them gave a positive result in polymerase chain reaction tests for a carbapenemase gene (bla(VIM)). Whole genome sequencing of the 2 isolates revealed the presence of bla(VIM-5) gene in an ST308 isolate, while the other one expressed IMP-7 in an ST357 isolate; both STs are considered high-risk clones. The 2 carbapenemase-producing isolates were multidrug resistant, as they harbored other resistance determinants, including a variant of the recently described plasmid-encoded fluoroquinolone resistance determinant crpP gene, crpP-2. We report for the first time P. aeruginosa high-risk clones carrying VIM-5- and IMP-7-type carbapenemases with multiple resistance determinants in Turkey. (C) 2020 Elsevier Inc. All rights reserved.

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