Mutational Analysis of Colistin-Resistant <i>Pseudomonas aeruginosa</i> Isolates: From Genomic Background to Antibiotic Resistance

This study analyzed eleven isolates of colistin-resistant <i>Pseudomonas aeruginosa</i>, originating from Portugal and Taiwan, which are associated with various pathologies. The results revealed significant genetic diversity among the isolates, with each exhibiting a distinct genetic pro...

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Main Authors: Telma De Sousa, Hsin-Yao Wang, Ting-Wei Lin, Manuela Caniça, Miguel J. N. Ramos, Daniela Santos, Catarina Silva, Sónia Saraiva, Racha Beyrouthy, Richard Bonnet, Michel Hébraud, Gilberto Igrejas, Patrícia Poeta
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Language:English
Published: MDPI AG 2025-04-01
Series:Pathogens
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Online Access:https://www.mdpi.com/2076-0817/14/4/387
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author Telma De Sousa
Hsin-Yao Wang
Ting-Wei Lin
Manuela Caniça
Miguel J. N. Ramos
Daniela Santos
Catarina Silva
Sónia Saraiva
Racha Beyrouthy
Richard Bonnet
Michel Hébraud
Gilberto Igrejas
Patrícia Poeta
author_facet Telma De Sousa
Hsin-Yao Wang
Ting-Wei Lin
Manuela Caniça
Miguel J. N. Ramos
Daniela Santos
Catarina Silva
Sónia Saraiva
Racha Beyrouthy
Richard Bonnet
Michel Hébraud
Gilberto Igrejas
Patrícia Poeta
author_sort Telma De Sousa
collection DOAJ
description This study analyzed eleven isolates of colistin-resistant <i>Pseudomonas aeruginosa</i>, originating from Portugal and Taiwan, which are associated with various pathologies. The results revealed significant genetic diversity among the isolates, with each exhibiting a distinct genetic profile. A prevalence of sequence type ST235 was observed, characterizing it as a high-risk clone, and serotyping indicated a predominance of type O11, associated with chronic respiratory infections in cystic fibrosis (CF) patients. The phylogenetic analysis demonstrated genetic diversity among the isolates, with distinct clades and complex evolutionary relationships. Additionally, transposable elements such as Tn3 and IS6 were identified in all isolates, highlighting their importance in the mobility of antibiotic resistance genes. An analysis of antimicrobial resistance profiles revealed pan-drug resistance in all isolates, with a high prevalence of genes conferring resistance to β-lactams and aminoglycosides. Furthermore, additional analyses revealed mutations in regulatory networks and specific loci previously implicated in colistin resistance, such as <i>pmrA</i>, <i>cprS</i>, <i>phoO</i>, and others, suggesting a possible contribution to the observed resistant phenotype. This study has a strong impact because it not only reveals the genetic diversity and resistance mechanisms in <i>P. aeruginosa</i> but also identifies mutations in regulatory genes associated with colistin resistance.
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spelling doaj-art-bccd7835c4ed45cf8ef695601c9fbf962025-08-20T02:28:18ZengMDPI AGPathogens2076-08172025-04-0114438710.3390/pathogens14040387Mutational Analysis of Colistin-Resistant <i>Pseudomonas aeruginosa</i> Isolates: From Genomic Background to Antibiotic ResistanceTelma De Sousa0Hsin-Yao Wang1Ting-Wei Lin2Manuela Caniça3Miguel J. N. Ramos4Daniela Santos5Catarina Silva6Sónia Saraiva7Racha Beyrouthy8Richard Bonnet9Michel Hébraud10Gilberto Igrejas11Patrícia Poeta12MicroART—Antibiotic Resistance Team, Department of Veterinary Sciences, University of Trás-os-Montes and Alto Douro, 5000-801 Vila Real, PortugalDepartment of Laboratory Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan 333, TaiwanDepartment of Laboratory Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan 333, TaiwanNational Reference Laboratory of Antibiotic Resistance and Healthcare Associated Infections, Department of Infectious Diseases, National Institute of Health Dr. Ricardo Jorge, 1649-016 Lisbon, PortugalNational Reference Laboratory of Antibiotic Resistance and Healthcare Associated Infections, Department of Infectious Diseases, National Institute of Health Dr. Ricardo Jorge, 1649-016 Lisbon, PortugalNational Reference Laboratory of Antibiotic Resistance and Healthcare Associated Infections, Department of Infectious Diseases, National Institute of Health Dr. Ricardo Jorge, 1649-016 Lisbon, PortugalMicroART—Antibiotic Resistance Team, Department of Veterinary Sciences, University of Trás-os-Montes and Alto Douro, 5000-801 Vila Real, PortugalMicroART—Antibiotic Resistance Team, Department of Veterinary Sciences, University of Trás-os-Montes and Alto Douro, 5000-801 Vila Real, PortugalInstitut National de la Santé et de la Recherche Médicale, (UMR1071), Institute National de la Recherche Agronomique (USC-2018), Université Clermont Auvergne, 63000 Clermont-Ferrand, FranceInstitut National de la Santé et de la Recherche Médicale, (UMR1071), Institute National de la Recherche Agronomique (USC-2018), Université Clermont Auvergne, 63000 Clermont-Ferrand, FranceINRAE, Université Clermont Auvergne, UMR Microbiologie Environnement Digestif Santé (MEDiS), 63122 Saint-Genès-Champanelle, FranceDepartment of Genetics and Biotechnology, University of Trás-os-Montes and Alto Douro, 5000-801 Vila Real, PortugalMicroART—Antibiotic Resistance Team, Department of Veterinary Sciences, University of Trás-os-Montes and Alto Douro, 5000-801 Vila Real, PortugalThis study analyzed eleven isolates of colistin-resistant <i>Pseudomonas aeruginosa</i>, originating from Portugal and Taiwan, which are associated with various pathologies. The results revealed significant genetic diversity among the isolates, with each exhibiting a distinct genetic profile. A prevalence of sequence type ST235 was observed, characterizing it as a high-risk clone, and serotyping indicated a predominance of type O11, associated with chronic respiratory infections in cystic fibrosis (CF) patients. The phylogenetic analysis demonstrated genetic diversity among the isolates, with distinct clades and complex evolutionary relationships. Additionally, transposable elements such as Tn3 and IS6 were identified in all isolates, highlighting their importance in the mobility of antibiotic resistance genes. An analysis of antimicrobial resistance profiles revealed pan-drug resistance in all isolates, with a high prevalence of genes conferring resistance to β-lactams and aminoglycosides. Furthermore, additional analyses revealed mutations in regulatory networks and specific loci previously implicated in colistin resistance, such as <i>pmrA</i>, <i>cprS</i>, <i>phoO</i>, and others, suggesting a possible contribution to the observed resistant phenotype. This study has a strong impact because it not only reveals the genetic diversity and resistance mechanisms in <i>P. aeruginosa</i> but also identifies mutations in regulatory genes associated with colistin resistance.https://www.mdpi.com/2076-0817/14/4/387<i>Pseudomonas aeruginosa</i>colistin resistanceWGSmutationsantibiotic resistance
spellingShingle Telma De Sousa
Hsin-Yao Wang
Ting-Wei Lin
Manuela Caniça
Miguel J. N. Ramos
Daniela Santos
Catarina Silva
Sónia Saraiva
Racha Beyrouthy
Richard Bonnet
Michel Hébraud
Gilberto Igrejas
Patrícia Poeta
Mutational Analysis of Colistin-Resistant <i>Pseudomonas aeruginosa</i> Isolates: From Genomic Background to Antibiotic Resistance
Pathogens
<i>Pseudomonas aeruginosa</i>
colistin resistance
WGS
mutations
antibiotic resistance
title Mutational Analysis of Colistin-Resistant <i>Pseudomonas aeruginosa</i> Isolates: From Genomic Background to Antibiotic Resistance
title_full Mutational Analysis of Colistin-Resistant <i>Pseudomonas aeruginosa</i> Isolates: From Genomic Background to Antibiotic Resistance
title_fullStr Mutational Analysis of Colistin-Resistant <i>Pseudomonas aeruginosa</i> Isolates: From Genomic Background to Antibiotic Resistance
title_full_unstemmed Mutational Analysis of Colistin-Resistant <i>Pseudomonas aeruginosa</i> Isolates: From Genomic Background to Antibiotic Resistance
title_short Mutational Analysis of Colistin-Resistant <i>Pseudomonas aeruginosa</i> Isolates: From Genomic Background to Antibiotic Resistance
title_sort mutational analysis of colistin resistant i pseudomonas aeruginosa i isolates from genomic background to antibiotic resistance
topic <i>Pseudomonas aeruginosa</i>
colistin resistance
WGS
mutations
antibiotic resistance
url https://www.mdpi.com/2076-0817/14/4/387
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