First nationwide survey on <i>Pseudomonas aeruginosa</i> in Bolivia: susceptibility profiles, resistome, and genomic epidemiology

dc.contributor.authorNeisa Alvarado-Orosco
dc.contributor.authorMaría A. Gomis-Font
dc.contributor.authorMiquel Àngel Sastre-Femenía
dc.contributor.authorSantiago Ortiz
dc.contributor.authorMarcos Miguel Medina Arce
dc.contributor.authorMaría José Barba
dc.contributor.authorM. Duran
dc.contributor.authorSandra Grisel Vargas Nattez
dc.contributor.authorGabriela Cabellos Astorga
dc.contributor.authorPedro Alonso Slon Rodríguez
dc.coverage.spatialBolivia
dc.date.accessioned2026-03-22T14:29:36Z
dc.date.available2026-03-22T14:29:36Z
dc.date.issued2025
dc.descriptionCitaciones: 1
dc.description.abstractInformation on the molecular epidemiology of <i>Pseudomonas aeruginosa</i> and antimicrobial resistance mechanisms is still limited in some South American countries. This study aims to decipher the population structure of 111 extensive drug-resistant <i>P. aeruginosa</i> isolates from a national study conducted in Bolivia during 2023-2024. The antibiotic susceptibility profiles were determined for 15 antipseudomonal agents. All isolates were subjected to whole-genome sequencing (WGS), and, through bioinformatics analysis, sequence types (ST), clonal relatedness, and acquired mutation-driven and transferable resistance mechanisms were elucidated. The most active antipseudomonal agents were colistin (98.2% intermediate, MIC<sub>50/90</sub>=1/2 mg/L) and cefiderocol (92.7% susceptible, MIC<sub>50/90</sub>=0.25/4 mg/L) according to the Clinical and Laboratory Standards Institute (CLSI). High resistance rates to ceftazidime/avibactam (79.3%), ceftolozane/tazobactam (82.9%), and imipenem/relebactam (71.2%) were documented. Carbapenemases were found in 60.3%, particularly including metallo-β-lactamases (MBL), such as SPM-1 (35%), VIM-2 (9%), the co-production of NDM-1 and DIM-1 (4%), or the new IMP variant IMP-111. Extended-spectrum β-lactamases (ESBLs) were detected in 12% of the isolates, including OXA-17 (7%), PER-1 (3%), and some GES variants. The most commonly detected clone was ST277 (35%) associated with SPM-1, followed by the ST309 (25%) producer of OXA-2 and various GES, and ST235 (20%) related with OXA-17 and new IMP-111. These clones harbored other acquired resistance genes, including emerging 16S rRNA methyltransferases, RmtD and RmtG. The high resistance rates for novel beta-lactams linked to an alarming spread of high-risk clones ST277 and ST235 and the very high prevalence of MBLs and ESBLs raise significant concern. This underscores the urgent need for establishing epidemiological surveillance and infection control strategies.
dc.identifier.doi10.1128/aac.01163-25
dc.identifier.urihttps://doi.org/10.1128/aac.01163-25
dc.identifier.urihttps://andeanlibrary.org/handle/123456789/46832
dc.language.isoen
dc.publisherAmerican Society for Microbiology
dc.relation.ispartofAntimicrobial Agents and Chemotherapy
dc.sourceCentro Nacional de Enfermedades Tropicales
dc.subjectColistin
dc.subjectBiology
dc.subjectEpidemiology
dc.subjectMolecular epidemiology
dc.subjectAntibiotic resistance
dc.subjectPopulation
dc.subjectDrug resistance
dc.subjectclone (Java method)
dc.subjectAntimicrobial
dc.subjectMicrobiology
dc.titleFirst nationwide survey on <i>Pseudomonas aeruginosa</i> in Bolivia: susceptibility profiles, resistome, and genomic epidemiology
dc.typearticle

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