David Badenas-Alzugaray, Laura Valour, Alexander Tristancho-Baró, Rossi Núñez-Medina, Ana María Milagro-Beamonte, Carmen Torres-Manrique, Beatriz Gilaberte-Angós, Ana Isabel López-Calleja, Antonio Rezusta-López
{"title":"Characterization of <i>Pseudomonas kurunegalensis</i> by Whole-Genome Sequencing from a Clinical Sample: New Challenges in Identification.","authors":"David Badenas-Alzugaray, Laura Valour, Alexander Tristancho-Baró, Rossi Núñez-Medina, Ana María Milagro-Beamonte, Carmen Torres-Manrique, Beatriz Gilaberte-Angós, Ana Isabel López-Calleja, Antonio Rezusta-López","doi":"10.3390/reports8030104","DOIUrl":null,"url":null,"abstract":"<p><p><b>Backgoround:</b> The genus <i>Pseudomonas</i> encompasses metabolically versatile bacteria widely distributed in diverse environments, including clinical settings. Among these, <i>Pseudomonas kurunegalensis</i> is a recently described environmental species with limited clinical characterization. <b>Objective and Methods:</b> In this study, we report the genomic and phenotypic characterization of a <i>P. kurunegalensis</i> isolate, Pam1317368, recovered from a catheterized urine sample of a post-renal transplant patient without symptoms of urinary tract infection. Initial identification by MALDI-TOF MS misclassified the isolate as <i>Pseudomonas monteilii</i>. Whole-genome sequencing and average nucleotide identity (ANI) analysis (≥95%) confirmed its identity as <i>P. kurunegalensis</i>. The methodology included genomic DNA extraction, Illumina sequencing, genome assembly, ANI calculation, antimicrobial susceptibility testing, resistance gene identification and phylogenetic analysis. <b>Results:</b> Antimicrobial susceptibility testing revealed multidrug resistance, including carbapenem resistance mediated by the metallo-β-lactamase gene <i>VIM-2</i>. Additional resistance determinants included genes conferring resistance to fluoroquinolones and aminoglycosides. Phylogenetic analysis placed the isolate within the <i>P. kurunegalensis</i> clade, closely related to environmental strains. <b>Conclusions:</b> Although the clinical significance of this finding remains unclear, the presence of clinically relevant resistance genes in an environmental <i>Pseudomonas</i> species isolated from a human sample highlights the value of genomic surveillance and accurate species-level identification in clinical microbiology.</p>","PeriodicalId":74664,"journal":{"name":"Reports (MDPI)","volume":"8 3","pages":""},"PeriodicalIF":0.8000,"publicationDate":"2025-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12266002/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reports (MDPI)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/reports8030104","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Backgoround: The genus Pseudomonas encompasses metabolically versatile bacteria widely distributed in diverse environments, including clinical settings. Among these, Pseudomonas kurunegalensis is a recently described environmental species with limited clinical characterization. Objective and Methods: In this study, we report the genomic and phenotypic characterization of a P. kurunegalensis isolate, Pam1317368, recovered from a catheterized urine sample of a post-renal transplant patient without symptoms of urinary tract infection. Initial identification by MALDI-TOF MS misclassified the isolate as Pseudomonas monteilii. Whole-genome sequencing and average nucleotide identity (ANI) analysis (≥95%) confirmed its identity as P. kurunegalensis. The methodology included genomic DNA extraction, Illumina sequencing, genome assembly, ANI calculation, antimicrobial susceptibility testing, resistance gene identification and phylogenetic analysis. Results: Antimicrobial susceptibility testing revealed multidrug resistance, including carbapenem resistance mediated by the metallo-β-lactamase gene VIM-2. Additional resistance determinants included genes conferring resistance to fluoroquinolones and aminoglycosides. Phylogenetic analysis placed the isolate within the P. kurunegalensis clade, closely related to environmental strains. Conclusions: Although the clinical significance of this finding remains unclear, the presence of clinically relevant resistance genes in an environmental Pseudomonas species isolated from a human sample highlights the value of genomic surveillance and accurate species-level identification in clinical microbiology.