Elena Addis, Ilaria Unali, Anna Bertoncelli, Anna Ventura, Riccardo Cecchetto, Annarita Mazzariol
{"title":"意大利北部一家医院在耐多药筛选过程中分离出的基因不相关的肺炎克雷伯菌株中存在不同的 OXA 碳青霉烯酶。","authors":"Elena Addis, Ilaria Unali, Anna Bertoncelli, Anna Ventura, Riccardo Cecchetto, Annarita Mazzariol","doi":"10.1089/mdr.2023.0134","DOIUrl":null,"url":null,"abstract":"<p><p><i>Klebsiella pneumoniae</i> is one of the main opportunistic pathogens that cause a broad spectrum of diseases with increasingly frequent acquisition of resistance to antibiotics, namely carbapenems. This study focused on the characterization of 23 OXA-48-like carbapenemase-producing <i>K. pneumoniae</i> isolates using phenotypic and molecular tests. Phenotypic determination of the presence of β-lactamases was performed using the extended-spectrum beta-lactamase (ESBL) NP test, and phenotypic determination of the presence of carbapenemase was based on the Carba NP test. Antimicrobial susceptibility tests were performed to assess the resistance against carbapenems. Molecular characterization of ESBL genes and carbapenemase genes (<i>bla<sub>OXA-48</sub></i>, <i>bla<sub>KPC</sub></i>, <i>bla<sub>VIM</sub></i>, and <i>bla<sub>NDM</sub></i>) was performed using polymerase chain reaction (PCR) techniques. In addition, <i>K. pneumoniae</i> strains were analyzed for their relatedness using multilocus sequence typing PCR analysis based on the Institut Pasteur protocol, which produces allelic profiles that contain their evolutionary and geographic pattern. Following further Sanger sequencing of the <i>bla<sub>OXA-48</sub></i> genes, no genetic mutations were found. Some OXA-48-producing <i>K. pneumoniae</i> isolates coharbored <i>bla<sub>KPC</sub></i>, <i>bla<sub>NDM</sub></i>, and <i>bla<sub>VIM</sub></i> genes, which encode other carbapenemases that can hydrolyze carbapenem antibiotics. The final part of the study focused on the characterization of the plasmid profiles of all isolates to better understand the spreading of the IncL/M <i>bla<sub>OXA-48</sub></i> plasmid gene. The plasmid profile also revealed other incompatibility groups, suggesting that other plasmid genes are spreading in <i>K. pneumoniae</i> isolates, which can coharbor and spread different carbapenemases simultaneously.</p>","PeriodicalId":18701,"journal":{"name":"Microbial drug resistance","volume":" ","pages":"127-133"},"PeriodicalIF":2.3000,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Different OXA-Carbapenemases in Genetically Unrelated <i>Klebsiella pneumoniae</i> Strains Isolated in a North Italian Hospital During Multidrug Resistance Screening.\",\"authors\":\"Elena Addis, Ilaria Unali, Anna Bertoncelli, Anna Ventura, Riccardo Cecchetto, Annarita Mazzariol\",\"doi\":\"10.1089/mdr.2023.0134\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Klebsiella pneumoniae</i> is one of the main opportunistic pathogens that cause a broad spectrum of diseases with increasingly frequent acquisition of resistance to antibiotics, namely carbapenems. This study focused on the characterization of 23 OXA-48-like carbapenemase-producing <i>K. pneumoniae</i> isolates using phenotypic and molecular tests. Phenotypic determination of the presence of β-lactamases was performed using the extended-spectrum beta-lactamase (ESBL) NP test, and phenotypic determination of the presence of carbapenemase was based on the Carba NP test. Antimicrobial susceptibility tests were performed to assess the resistance against carbapenems. Molecular characterization of ESBL genes and carbapenemase genes (<i>bla<sub>OXA-48</sub></i>, <i>bla<sub>KPC</sub></i>, <i>bla<sub>VIM</sub></i>, and <i>bla<sub>NDM</sub></i>) was performed using polymerase chain reaction (PCR) techniques. In addition, <i>K. pneumoniae</i> strains were analyzed for their relatedness using multilocus sequence typing PCR analysis based on the Institut Pasteur protocol, which produces allelic profiles that contain their evolutionary and geographic pattern. Following further Sanger sequencing of the <i>bla<sub>OXA-48</sub></i> genes, no genetic mutations were found. Some OXA-48-producing <i>K. pneumoniae</i> isolates coharbored <i>bla<sub>KPC</sub></i>, <i>bla<sub>NDM</sub></i>, and <i>bla<sub>VIM</sub></i> genes, which encode other carbapenemases that can hydrolyze carbapenem antibiotics. The final part of the study focused on the characterization of the plasmid profiles of all isolates to better understand the spreading of the IncL/M <i>bla<sub>OXA-48</sub></i> plasmid gene. The plasmid profile also revealed other incompatibility groups, suggesting that other plasmid genes are spreading in <i>K. pneumoniae</i> isolates, which can coharbor and spread different carbapenemases simultaneously.</p>\",\"PeriodicalId\":18701,\"journal\":{\"name\":\"Microbial drug resistance\",\"volume\":\" \",\"pages\":\"127-133\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2024-03-01\",\"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.2023.0134\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/2 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"INFECTIOUS DISEASES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbial drug resistance","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1089/mdr.2023.0134","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/2 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
Different OXA-Carbapenemases in Genetically Unrelated Klebsiella pneumoniae Strains Isolated in a North Italian Hospital During Multidrug Resistance Screening.
Klebsiella pneumoniae is one of the main opportunistic pathogens that cause a broad spectrum of diseases with increasingly frequent acquisition of resistance to antibiotics, namely carbapenems. This study focused on the characterization of 23 OXA-48-like carbapenemase-producing K. pneumoniae isolates using phenotypic and molecular tests. Phenotypic determination of the presence of β-lactamases was performed using the extended-spectrum beta-lactamase (ESBL) NP test, and phenotypic determination of the presence of carbapenemase was based on the Carba NP test. Antimicrobial susceptibility tests were performed to assess the resistance against carbapenems. Molecular characterization of ESBL genes and carbapenemase genes (blaOXA-48, blaKPC, blaVIM, and blaNDM) was performed using polymerase chain reaction (PCR) techniques. In addition, K. pneumoniae strains were analyzed for their relatedness using multilocus sequence typing PCR analysis based on the Institut Pasteur protocol, which produces allelic profiles that contain their evolutionary and geographic pattern. Following further Sanger sequencing of the blaOXA-48 genes, no genetic mutations were found. Some OXA-48-producing K. pneumoniae isolates coharbored blaKPC, blaNDM, and blaVIM genes, which encode other carbapenemases that can hydrolyze carbapenem antibiotics. The final part of the study focused on the characterization of the plasmid profiles of all isolates to better understand the spreading of the IncL/M blaOXA-48 plasmid gene. The plasmid profile also revealed other incompatibility groups, suggesting that other plasmid genes are spreading in K. pneumoniae isolates, which can coharbor and spread different carbapenemases simultaneously.
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.