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Endemicity of Pseudomonas aeruginosa producing IMP-18 and/or VIM-2 MBLs from the high-risk clone ST111 in Central America

BACKGROUND: Pseudomonas aeruginosa 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: T...

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Autores principales: Deshpande, Lalitagauri M, Vega, Silvio, Tinoco, Juan Carlos, Castanheira, Mariana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10391700/
https://www.ncbi.nlm.nih.gov/pubmed/37533761
http://dx.doi.org/10.1093/jacamr/dlad092
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author Deshpande, Lalitagauri M
Vega, Silvio
Tinoco, Juan Carlos
Castanheira, Mariana
author_facet Deshpande, Lalitagauri M
Vega, Silvio
Tinoco, Juan Carlos
Castanheira, Mariana
author_sort Deshpande, Lalitagauri M
collection PubMed
description BACKGROUND: Pseudomonas aeruginosa 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 P. aeruginosa 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 in silico screening of resistance genes, MLST, core genome (cg)MLST and SNP analysis. RESULTS: The P. aeruginosa 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, bla(IMP-18) and/or bla(VIM-2), were chromosomally located. bla(IMP-18) was detected in an In1666 integron whereas bla(VIM-2) was embedded in an In59-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 P. aeruginosa 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.
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spelling pubmed-103917002023-08-02 Endemicity of Pseudomonas aeruginosa producing IMP-18 and/or VIM-2 MBLs from the high-risk clone ST111 in Central America Deshpande, Lalitagauri M Vega, Silvio Tinoco, Juan Carlos Castanheira, Mariana JAC Antimicrob Resist Original Article BACKGROUND: Pseudomonas aeruginosa 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 P. aeruginosa 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 in silico screening of resistance genes, MLST, core genome (cg)MLST and SNP analysis. RESULTS: The P. aeruginosa 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, bla(IMP-18) and/or bla(VIM-2), were chromosomally located. bla(IMP-18) was detected in an In1666 integron whereas bla(VIM-2) was embedded in an In59-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 P. aeruginosa 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. Oxford University Press 2023-08-01 /pmc/articles/PMC10391700/ /pubmed/37533761 http://dx.doi.org/10.1093/jacamr/dlad092 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Deshpande, Lalitagauri M
Vega, Silvio
Tinoco, Juan Carlos
Castanheira, Mariana
Endemicity of Pseudomonas aeruginosa producing IMP-18 and/or VIM-2 MBLs from the high-risk clone ST111 in Central America
title Endemicity of Pseudomonas aeruginosa producing IMP-18 and/or VIM-2 MBLs from the high-risk clone ST111 in Central America
title_full Endemicity of Pseudomonas aeruginosa producing IMP-18 and/or VIM-2 MBLs from the high-risk clone ST111 in Central America
title_fullStr Endemicity of Pseudomonas aeruginosa producing IMP-18 and/or VIM-2 MBLs from the high-risk clone ST111 in Central America
title_full_unstemmed Endemicity of Pseudomonas aeruginosa producing IMP-18 and/or VIM-2 MBLs from the high-risk clone ST111 in Central America
title_short Endemicity of Pseudomonas aeruginosa producing IMP-18 and/or VIM-2 MBLs from the high-risk clone ST111 in Central America
title_sort endemicity of pseudomonas aeruginosa producing imp-18 and/or vim-2 mbls from the high-risk clone st111 in central america
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10391700/
https://www.ncbi.nlm.nih.gov/pubmed/37533761
http://dx.doi.org/10.1093/jacamr/dlad092
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