Stefana Sabtcheva , Ivan Stoikov , Deyan Donchev , Sylvia Georgieva , Elina Dobreva , Ivan Nikolaev Ivanov
{"title":"Complete genome characterization of mcr-1-mediated colistin-resistant Escherichia coli from outpatients in Bulgaria","authors":"Stefana Sabtcheva , Ivan Stoikov , Deyan Donchev , Sylvia Georgieva , Elina Dobreva , Ivan Nikolaev Ivanov","doi":"10.1016/j.eimce.2024.10.006","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>This study reports the emergence of <em>mcr-1</em>-mediated colistin resistance in human <em>Escherichia coli</em> isolates from Bulgaria.</div></div><div><h3>Methods</h3><div>Three colistin-resistant <em>E. coli</em> isolates were obtained from outpatient urine specimens. They were subjected to PCR for detection of <em>mcr</em> genes and conjugation experiments. Whole-genome sequencing was employed to analyze the genomic characteristics of the isolates.</div></div><div><h3>Results</h3><div>PCR identified <em>mcr-1</em> in all isolates. In <em>E. coli</em> of sequence type (ST) 2067, <em>mcr-1.1</em> was found on a self-transmissible IncI2 plasmid, while <em>mcr-1.32</em> was chromosomal in the remaining two ST131 <em>E. coli</em> isolates. <em>E. coli</em> ST2067 co-harbored quinolones resistance mutations (<em>gyrA</em><sup>D87N</sup>, <em>gyrA</em><sup>S83L</sup>, <em>parC</em><sup>S80I</sup>), β-lactam (<em>bla</em><sub>TEM-30</sub>) and aminoglycoside (<em>aadA1</em>, <em>aac(3)-IId</em>) resistance genes.</div></div><div><h3>Conclusion</h3><div>This report further confirms the role of IncI2 conjugative plasmids in the dissemination of <em>mcr</em> genes. Our findings involving chromosomal <em>mcr-1</em> in high-risk ST131 <em>E. coli</em> strains from outpatients underscores the need for enhanced surveillance and systematic screening to combat colistin resistance.</div></div>","PeriodicalId":72916,"journal":{"name":"Enfermedades infecciosas y microbiologia clinica (English ed.)","volume":"43 2","pages":"Pages 97-101"},"PeriodicalIF":0.0000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Enfermedades infecciosas y microbiologia clinica (English ed.)","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2529993X25000140","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract
Introduction
This study reports the emergence of mcr-1-mediated colistin resistance in human Escherichia coli isolates from Bulgaria.
Methods
Three colistin-resistant E. coli isolates were obtained from outpatient urine specimens. They were subjected to PCR for detection of mcr genes and conjugation experiments. Whole-genome sequencing was employed to analyze the genomic characteristics of the isolates.
Results
PCR identified mcr-1 in all isolates. In E. coli of sequence type (ST) 2067, mcr-1.1 was found on a self-transmissible IncI2 plasmid, while mcr-1.32 was chromosomal in the remaining two ST131 E. coli isolates. E. coli ST2067 co-harbored quinolones resistance mutations (gyrAD87N, gyrAS83L, parCS80I), β-lactam (blaTEM-30) and aminoglycoside (aadA1, aac(3)-IId) resistance genes.
Conclusion
This report further confirms the role of IncI2 conjugative plasmids in the dissemination of mcr genes. Our findings involving chromosomal mcr-1 in high-risk ST131 E. coli strains from outpatients underscores the need for enhanced surveillance and systematic screening to combat colistin resistance.