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  4. Ceftazidime/avibactam resistance is associated with PER-3-producing ST309 lineage in Chilean clinical isolates of non-carbapenemase producing Pseudomonas aeruginosa
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Ceftazidime/avibactam resistance is associated with PER-3-producing ST309 lineage in Chilean clinical isolates of non-carbapenemase producing Pseudomonas aeruginosa

Journal
Frontiers in Cellular and Infection Microbiology
ISSN
2235-2988
Date Issued
2024
Author(s)
Katherine D. Soto
ALCALDE RICO, MANUEL  
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
UGALDE, JUAN ANTONIO
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Jorge Olivares Pacheco
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Valeria Quiroz
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Bárbara Brito
RIVAS JIMENEZ, LINA MARIA  
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
MUNITA SEPULVEDA, JOSE MANUEL  
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
GARCÍA CEBALLOS, PATRICIA
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Aniela Wozniak
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Type
journal-article
Scopus ID
2-s2.0-85196292950
WoS ID
WOS:001250656000001
DOI
10.3389/fcimb.2024.1410834
URL
https://investigadores.udd.cl/handle/123456789/10020
Abstract
<jats:sec><jats:title>Introduction</jats:title><jats:p>Ceftazidime/avibactam (CZA) is indicated against multidrug-resistant <jats:italic>Pseudomonas aeruginosa</jats:italic>, particularly those that are carbapenem resistant. CZA resistance in <jats:italic>P. aeruginosa</jats:italic> producing PER, a class A extended-spectrum β-lactamase, has been well documented <jats:italic>in vitro</jats:italic>. However, data regarding clinical isolates are scarce. Our aim was to analyze the contribution of PER to CZA resistance in non-carbapenemase-producing <jats:italic>P. aeruginosa</jats:italic> clinical isolates that were ceftazidime and/or carbapenem non-susceptible.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Antimicrobial susceptibility was determined through agar dilution and broth microdilution, while <jats:italic>bla</jats:italic><jats:sub>PER</jats:sub> gene was screened through PCR. All PER-positive isolates and five PER-negative isolates were analyzed through Whole Genome Sequencing. The mutational resistome associated to CZA resistance was determined through sequence analysis of genes coding for PBPs 1b, 3 and 4, MexAB-OprM regulators MexZ, MexR, NalC and NalD, AmpC regulators AmpD and AmpR, and OprD porin. Loss of <jats:italic>bla</jats:italic><jats:sub>PER-3</jats:sub> gene was induced in a PER-positive isolate by successive passages at 43°C without antibiotics. </jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Twenty-six of 287 isolates studied (9.1%) were CZA-resistant. Thirteen of 26 CZA-resistant isolates (50%) carried <jats:italic>bla</jats:italic><jats:sub>PER</jats:sub>. One isolate carried <jats:italic>bla</jats:italic><jats:sub>PER</jats:sub> but was CZA-susceptible. PER-producing isolates had significantly higher MICs for CZA, amikacin, gentamicin, ceftazidime, meropenem and ciprofloxacin than non-PER-producing isolates. All PER-producing isolates were ST309 and their <jats:italic>bla</jats:italic><jats:sub>PER-3</jats:sub> gene was associated to ISCR1, an insertion sequence known to mobilize adjacent DNA. PER-negative isolates were classified as ST41, ST235 (two isolates), ST395 and ST253. PER-negative isolates carried genes for narrow-spectrum β-lactamases and the mutational resistome showed that all isolates had one major alteration in at least one of the genes analyzed. Loss of <jats:italic>bla</jats:italic><jats:sub>PER-3</jats:sub> gene restored susceptibility to CZA, ceftolozane/tazobactam and other β-lactamsin the <jats:italic>in vitro</jats:italic> evolved isolate. </jats:p></jats:sec><jats:sec><jats:title>Discussion</jats:title><jats:p>PER-3-producing ST309 <jats:italic>P. aeruginosa</jats:italic> is a successful multidrug-resistant clone with <jats:italic>bla<jats:sub>PER-3</jats:sub></jats:italic> gene implicated in resistance to CZA and other β-lactams.</jats:p></jats:sec>
Cite this document
Soto, K. D., Alcalde-Rico, M., Ugalde, J. A., Olivares-Pacheco, J., Quiroz, V., Brito, B., Rivas, L. M., Munita, J. M., García, P. C., & Wozniak, A. (2024). Ceftazidime/avibactam resistance is associated with PER-3-producing ST309 lineage in Chilean clinical isolates of non-carbapenemase producing Pseudomonas aeruginosa. Frontiers in Cellular and Infection Microbiology, 14, 1410834. https://doi.org/10.3389/fcimb.2024.1410834
Project(s)
Establishing a long-term observatory of the urban microbiome and antimicrobial resistance in Chile  
GENomic Epidemiology in Emergent Diseases (GENE2DIS)  
Dataset(s)
Ceftazidime/avibactam resistance is associated with PER-3-producing ST309 lineage in Chilean clinical isolates of non-carbapenemase producing Pseudomonas aeruginosa  
Dataset - Ceftazidime/avibactam resistance is associated with PER-3-producing ST309 lineage in Chilean clinical isolates of non-carbapenemase producing Pseudomonas aeruginosa  
Subjects
pseudomonas aeruginosa

; 

blaper-3 gene

; 

per-3 extended-spectrum beta-lactamase

; 

ceftazidime/avibactam resistance

; 

mutations conferring cza resistance
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