Ralf Lopes, João Pedro Rueda Furlan, Micaela Santana Ramos, Lucas David Rodrigues Dos Santos, Rafael da Silva Rosa, Eliana Guedes Stehling
{"title":"<i>Klebsiella quasipneumoniae</i> subsp. <i>similipneumoniae</i> ST1859 O5:KL35 from Soil: First Report of <i>qnrE1</i> in the Environment.","authors":"Ralf Lopes, João Pedro Rueda Furlan, Micaela Santana Ramos, Lucas David Rodrigues Dos Santos, Rafael da Silva Rosa, Eliana Guedes Stehling","doi":"10.1089/mdr.2023.0075","DOIUrl":null,"url":null,"abstract":"<p><p>A <i>Klebsiella quasipneumoniae</i> subsp. <i>similipneumoniae</i> strain, named S915, belonging to the ST1859 O5:KL35, and harboring the plasmid-mediated quinolone resistance <i>qnrE1</i> gene, was isolated from a soil sample cultivated with lettuce in Brazil. The core genome multilocus sequence typing analysis revealed that S915 strain was most related to a clinical strain of Brazil. Comparative genomic analysis showed that ST1859 O5:KL35 strains have been circulating in clinical settings and are closely related to multidrug resistance and multimetal tolerance. Strain S915 presented a plasmid contig co-harboring the <i>qnrE1</i> gene and tellurite tolerance operon. The region harboring the <i>qnrE1</i> gene (IS<i>Ecp1</i>-<i>qnrE1</i>-<i>araJ</i>-<i>ahp</i>) shared high similarity with others from infected humans, ready-to-eat dish, and food-producing animals in Brazil. This is the first report of the plasmid-mediated <i>qnrE1</i> gene in the environment. Our findings evidence the initial dissemination of the <i>qnrE1</i> gene in the environment by the introduction of a clinical strain, which may be spread to different sectors, representing a One Health challenge.</p>","PeriodicalId":18701,"journal":{"name":"Microbial drug resistance","volume":" ","pages":"492-496"},"PeriodicalIF":2.3000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbial drug resistance","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1089/mdr.2023.0075","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/7/10 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0
Abstract
A Klebsiella quasipneumoniae subsp. similipneumoniae strain, named S915, belonging to the ST1859 O5:KL35, and harboring the plasmid-mediated quinolone resistance qnrE1 gene, was isolated from a soil sample cultivated with lettuce in Brazil. The core genome multilocus sequence typing analysis revealed that S915 strain was most related to a clinical strain of Brazil. Comparative genomic analysis showed that ST1859 O5:KL35 strains have been circulating in clinical settings and are closely related to multidrug resistance and multimetal tolerance. Strain S915 presented a plasmid contig co-harboring the qnrE1 gene and tellurite tolerance operon. The region harboring the qnrE1 gene (ISEcp1-qnrE1-araJ-ahp) shared high similarity with others from infected humans, ready-to-eat dish, and food-producing animals in Brazil. This is the first report of the plasmid-mediated qnrE1 gene in the environment. Our findings evidence the initial dissemination of the qnrE1 gene in the environment by the introduction of a clinical strain, which may be spread to different sectors, representing a One Health challenge.
期刊介绍:
Microbial Drug Resistance (MDR) is an international, peer-reviewed journal that covers the global spread and threat of multi-drug resistant clones of major pathogens that are widely documented in hospitals and the scientific community. The Journal addresses the serious challenges of trying to decipher the molecular mechanisms of drug resistance. MDR provides a multidisciplinary forum for peer-reviewed original publications as well as topical reviews and special reports.
MDR coverage includes:
Molecular biology of resistance mechanisms
Virulence genes and disease
Molecular epidemiology
Drug design
Infection control.