» Articles » PMID: 37533761

Endemicity of Producing IMP-18 And/or VIM-2 MBLs from the High-risk Clone ST111 in Central America

Overview
Date 2023 Aug 3
PMID 37533761
Authors
Affiliations
Soon will be listed here.
Abstract

Background: is an important cause of serious nosocomial infections. Despite the overall genetic diversity of this species, highly conserved clonal complexes (CCs) have been observed among MDR isolates. Many of these CCs are associated with MBL-producing isolates.

Objectives: To evaluate five isolates from Central America that carried IMP-18- and/or VIM-2-encoding genes from the SENTRY Antimicrobial Surveillance Program (2017-2018).

Methods: Susceptibility testing was performed by broth microdilution (CLSI). WGS was performed using MiSeq (Illumina) and MinION (Oxford Nanopore). Assembled contigs from short and long reads were combined for screening of resistance genes, MLST, core genome (cg)MLST and SNP analysis.

Results: The isolates were collected in Panama and Mexico from patients with urinary tract infections or pneumonia. Isolates were categorized as XDR (CLSI/EUCAST). All isolates belonged to ST111 but carried different combinations of resistance-encoding genes. Transposon-associated MBL genes, and/or , were chromosomally located. was detected in an In integron whereas was embedded in an In-like integron. Isolates were closely related based on cgMLST (average allele distance 2-34) and SNP analysis (5-423 different SNPs).

Conclusions: MBL-producing ST111 have become endemic in Panama and may have spread to Mexico via clonal dissemination. Recombination events are apparent in the evolution of this CC. Surveillance is warranted to track the expansion and movement of this clone.

Citing Articles

High-risk clones harboring β-lactamases: 2024 update.

Flores-Vega V, Partida-Sanchez S, Ares M, Ortiz-Navarrete V, Rosales-Reyes R Heliyon. 2025; 11(1):e41540.

PMID: 39850428 PMC: 11754179. DOI: 10.1016/j.heliyon.2024.e41540.

References
1.
Barrio-Tofino E, Lopez-Causape C, Oliver A . Pseudomonas aeruginosa epidemic high-risk clones and their association with horizontally-acquired β-lactamases: 2020 update. Int J Antimicrob Agents. 2020; 56(6):106196. DOI: 10.1016/j.ijantimicag.2020.106196. View

2.
Magiorakos A, Srinivasan A, Carey R, Carmeli Y, Falagas M, Giske C . Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect. 2011; 18(3):268-81. DOI: 10.1111/j.1469-0691.2011.03570.x. View

3.
Molina-Mora J, Garcia F . Molecular Determinants of Antibiotic Resistance in the Costa Rican AG1 by a Multi-omics Approach: A Review of 10 Years of Study. Phenomics. 2022; 1(3):129-142. PMC: 8210740. DOI: 10.1007/s43657-021-00016-z. View

4.
Miyoshi-Akiyama T, Tada T, Ohmagari N, Hung N, Tharavichitkul P, Pokhrel B . Emergence and Spread of Epidemic Multidrug-Resistant Pseudomonas aeruginosa. Genome Biol Evol. 2017; 9(12):3238-3245. PMC: 5726472. DOI: 10.1093/gbe/evx243. View

5.
Pournaras S, Maniati M, Petinaki E, Tzouvelekis L, Tsakris A, Legakis N . Hospital outbreak of multiple clones of Pseudomonas aeruginosa carrying the unrelated metallo-beta-lactamase gene variants blaVIM-2 and blaVIM-4. J Antimicrob Chemother. 2003; 51(6):1409-14. DOI: 10.1093/jac/dkg239. View