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Mutation Analysis in Regulator DNA-Binding Regions for Antimicrobial Efflux Pumps in 17,000 Pseudomonas aeruginosa Genomes

Mutations leading to upregulation of efflux pumps can produce multiple drug resistance in the pathogen Pseudomonas aeruginosa. Changes in their DNA binding regions, i.e., palindromic operators, can compromise pump depression and subsequently enhance resistance against several antibacterials and bioc...

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Autores principales: Pérez-Vázquez, María, López-Causapé, Carla, Corral-Lugo, Andrés, McConnell, Michael J., Oteo-Iglesias, Jesús, Oliver, Antonio, Martín-Galiano, Antonio J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10609311/
https://www.ncbi.nlm.nih.gov/pubmed/37894144
http://dx.doi.org/10.3390/microorganisms11102486
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author Pérez-Vázquez, María
López-Causapé, Carla
Corral-Lugo, Andrés
McConnell, Michael J.
Oteo-Iglesias, Jesús
Oliver, Antonio
Martín-Galiano, Antonio J.
author_facet Pérez-Vázquez, María
López-Causapé, Carla
Corral-Lugo, Andrés
McConnell, Michael J.
Oteo-Iglesias, Jesús
Oliver, Antonio
Martín-Galiano, Antonio J.
author_sort Pérez-Vázquez, María
collection PubMed
description Mutations leading to upregulation of efflux pumps can produce multiple drug resistance in the pathogen Pseudomonas aeruginosa. Changes in their DNA binding regions, i.e., palindromic operators, can compromise pump depression and subsequently enhance resistance against several antibacterials and biocides. Here, we have identified (pseudo)palindromic repeats close to promoters of genes encoding 13 core drug-efflux pumps of P. aeruginosa. This framework was applied to detect mutations in these repeats in 17,292 genomes. Eighty-nine percent of isolates carried at least one mutation. Eight binary genetic properties potentially related to expression were calculated for mutations. These included palindromicity reduction, mutation type, positioning within the repeat and DNA-bending shift. High-risk ST298, ST308 and ST357 clones commonly carried four conserved mutations while ST175 and the cystic fibrosis-linked ST649 clones showed none. Remarkably, a T-to-C transition in the fourth position of the upstream repeat for mexEF-oprN was nearly exclusive of the high-risk ST111 clone. Other mutations were associated with high-risk sublineages using sample geotemporal metadata. Moreover, 1.5% of isolates carried five or more mutations suggesting they undergo an alternative program for regulation of their effluxome. Overall, P. aeruginosa shows a wide range of operator mutations with a potential effect on efflux pump expression and antibiotic resistance.
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spelling pubmed-106093112023-10-28 Mutation Analysis in Regulator DNA-Binding Regions for Antimicrobial Efflux Pumps in 17,000 Pseudomonas aeruginosa Genomes Pérez-Vázquez, María López-Causapé, Carla Corral-Lugo, Andrés McConnell, Michael J. Oteo-Iglesias, Jesús Oliver, Antonio Martín-Galiano, Antonio J. Microorganisms Article Mutations leading to upregulation of efflux pumps can produce multiple drug resistance in the pathogen Pseudomonas aeruginosa. Changes in their DNA binding regions, i.e., palindromic operators, can compromise pump depression and subsequently enhance resistance against several antibacterials and biocides. Here, we have identified (pseudo)palindromic repeats close to promoters of genes encoding 13 core drug-efflux pumps of P. aeruginosa. This framework was applied to detect mutations in these repeats in 17,292 genomes. Eighty-nine percent of isolates carried at least one mutation. Eight binary genetic properties potentially related to expression were calculated for mutations. These included palindromicity reduction, mutation type, positioning within the repeat and DNA-bending shift. High-risk ST298, ST308 and ST357 clones commonly carried four conserved mutations while ST175 and the cystic fibrosis-linked ST649 clones showed none. Remarkably, a T-to-C transition in the fourth position of the upstream repeat for mexEF-oprN was nearly exclusive of the high-risk ST111 clone. Other mutations were associated with high-risk sublineages using sample geotemporal metadata. Moreover, 1.5% of isolates carried five or more mutations suggesting they undergo an alternative program for regulation of their effluxome. Overall, P. aeruginosa shows a wide range of operator mutations with a potential effect on efflux pump expression and antibiotic resistance. MDPI 2023-10-04 /pmc/articles/PMC10609311/ /pubmed/37894144 http://dx.doi.org/10.3390/microorganisms11102486 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pérez-Vázquez, María
López-Causapé, Carla
Corral-Lugo, Andrés
McConnell, Michael J.
Oteo-Iglesias, Jesús
Oliver, Antonio
Martín-Galiano, Antonio J.
Mutation Analysis in Regulator DNA-Binding Regions for Antimicrobial Efflux Pumps in 17,000 Pseudomonas aeruginosa Genomes
title Mutation Analysis in Regulator DNA-Binding Regions for Antimicrobial Efflux Pumps in 17,000 Pseudomonas aeruginosa Genomes
title_full Mutation Analysis in Regulator DNA-Binding Regions for Antimicrobial Efflux Pumps in 17,000 Pseudomonas aeruginosa Genomes
title_fullStr Mutation Analysis in Regulator DNA-Binding Regions for Antimicrobial Efflux Pumps in 17,000 Pseudomonas aeruginosa Genomes
title_full_unstemmed Mutation Analysis in Regulator DNA-Binding Regions for Antimicrobial Efflux Pumps in 17,000 Pseudomonas aeruginosa Genomes
title_short Mutation Analysis in Regulator DNA-Binding Regions for Antimicrobial Efflux Pumps in 17,000 Pseudomonas aeruginosa Genomes
title_sort mutation analysis in regulator dna-binding regions for antimicrobial efflux pumps in 17,000 pseudomonas aeruginosa genomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10609311/
https://www.ncbi.nlm.nih.gov/pubmed/37894144
http://dx.doi.org/10.3390/microorganisms11102486
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