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。

IF 2.3 4区 医学 Q3 INFECTIOUS DISEASES
Microbial drug resistance Pub Date : 2024-03-01 Epub Date: 2024-01-02 DOI:10.1089/mdr.2023.0134
Elena Addis, Ilaria Unali, Anna Bertoncelli, Anna Ventura, Riccardo Cecchetto, Annarita Mazzariol
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引用次数: 0

摘要

肺炎克雷伯氏菌是主要的机会性病原体之一,可引起多种疾病,并对抗生素(即碳青霉烯类)产生越来越频繁的耐药性。本研究采用表型和分子检测方法,重点研究了 23 株产 OXA-48 类碳青霉烯酶肺炎克雷伯菌分离株的特征。使用广谱β-内酰胺酶(ESBL)NP测试对β-内酰胺酶的存在进行表型测定,使用Carba NP测试对碳青霉烯酶的存在进行表型测定。抗菌药物药敏试验用于评估对碳青霉烯类的耐药性。利用聚合酶链反应(PCR)技术对 ESBL 基因和碳青霉烯酶基因(blaOXA-48、blaKPC、blaVIM 和 blaNDM)进行了分子鉴定。此外,还根据巴斯德研究所(Institut Pasteur)的方案,使用多焦点序列分型 PCR 分析法分析了肺炎克氏菌菌株的亲缘关系,该方法可产生包含其进化和地理模式的等位基因图谱。进一步对 blaOXA-48 基因进行桑格测序后,没有发现基因突变。一些产生 OXA-48 的肺炎克雷伯菌分离株共轭 blaKPC、blaNDM 和 blaVIM 基因,这些基因编码可水解碳青霉烯类抗生素的其他碳青霉烯酶。研究的最后一部分侧重于分析所有分离株的质粒特征,以更好地了解 IncL/M blaOXA-48 质粒基因的传播情况。质粒图谱还揭示了其他不相容群,表明其他质粒基因正在肺炎克雷伯菌分离株中传播,这些质粒基因可以同时共生和传播不同的碳青霉烯酶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

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来源期刊
Microbial drug resistance
Microbial drug resistance 医学-传染病学
CiteScore
6.00
自引率
3.80%
发文量
118
审稿时长
6-12 weeks
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.
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