Molecular Epidemiology of Vancomycin-Resistant Enterococci during 2021 in a tertiary care hospital in Greece.

IF 1.5 4区 医学 Q4 MICROBIOLOGY
New Microbiologica Pub Date : 2024-12-01
Eleni Panidou-Tsoulou, Georgios Meletis, Charalampos Kotzamanidis, Esmeralda Dushku, Virginia Giantzi, Areti Tychala, Angeliki Kassomenaki, Paraskevi Mantzana, Lemonia Skoura, Efthymia Protonotariou
{"title":"Molecular Epidemiology of Vancomycin-Resistant Enterococci during 2021 in a tertiary care hospital in Greece.","authors":"Eleni Panidou-Tsoulou, Georgios Meletis, Charalampos Kotzamanidis, Esmeralda Dushku, Virginia Giantzi, Areti Tychala, Angeliki Kassomenaki, Paraskevi Mantzana, Lemonia Skoura, Efthymia Protonotariou","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The present study aimed to determine the resistance mechanisms and clonal relationships among vancomycin-resistant Enterococci (VRE) isolated in AHEPA University Hospital during the pandemic year 2021. Overall, 140 clinical VRE were isolated during the study period and 44 were randomly selected for molecular analysis. A multiplex PCR was employed to detect vancomycin resistance genes (vanA, vanB, vanC, vanD, vanE, vanG) using specific primers. Additionally, pulsed-field gel electrophoresis (PFGE) was performed to assess the clonal relatedness of the selected isolates. The multiplex PCR showed that 36 of the 44 studied strains (81.9%) harbored the vanA gene whereas, 7 of 44 (15.9%) co-harbored the vanA and vanB resistance genes; one isolate had a negative PCR result. PFGE analysis unveiled 37 distinct electrophoretic patterns among the 44 VRE isolates with a similarity threshold of 75%. These patterns were clustered into 4 distinct branches. Our findings indicate a polyclonal distribution of vanA genes among the studied isolates and the notable concomitant presence of vanA/vanB genotypes. Furthermore, these results highlight the worsening that took place during the COVID-19 pandemic period regarding antibiotic resistance rates, underscoring the imperative need for stringent infection control measures and active surveillance.</p>","PeriodicalId":54723,"journal":{"name":"New Microbiologica","volume":"47 4","pages":"350-354"},"PeriodicalIF":1.5000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Microbiologica","FirstCategoryId":"3","ListUrlMain":"","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The present study aimed to determine the resistance mechanisms and clonal relationships among vancomycin-resistant Enterococci (VRE) isolated in AHEPA University Hospital during the pandemic year 2021. Overall, 140 clinical VRE were isolated during the study period and 44 were randomly selected for molecular analysis. A multiplex PCR was employed to detect vancomycin resistance genes (vanA, vanB, vanC, vanD, vanE, vanG) using specific primers. Additionally, pulsed-field gel electrophoresis (PFGE) was performed to assess the clonal relatedness of the selected isolates. The multiplex PCR showed that 36 of the 44 studied strains (81.9%) harbored the vanA gene whereas, 7 of 44 (15.9%) co-harbored the vanA and vanB resistance genes; one isolate had a negative PCR result. PFGE analysis unveiled 37 distinct electrophoretic patterns among the 44 VRE isolates with a similarity threshold of 75%. These patterns were clustered into 4 distinct branches. Our findings indicate a polyclonal distribution of vanA genes among the studied isolates and the notable concomitant presence of vanA/vanB genotypes. Furthermore, these results highlight the worsening that took place during the COVID-19 pandemic period regarding antibiotic resistance rates, underscoring the imperative need for stringent infection control measures and active surveillance.

2021年期间希腊一家三级医院耐万古霉素肠球菌的分子流行病学研究
本研究旨在确定2021年大流行年在AHEPA大学医院分离的万古霉素耐药肠球菌(VRE)的耐药机制和克隆关系。总体而言,在研究期间分离出140例临床VRE,随机选择44例进行分子分析。利用特异引物,采用多重PCR检测万古霉素耐药基因(vanA、vanB、vanC、vanD、vanE、vanG)。此外,采用脉冲场凝胶电泳(PFGE)来评估所选分离株的克隆亲缘性。多重PCR结果显示,44株菌株中有36株(81.9%)携带vanA基因,7株(15.9%)同时携带vanA和vanB抗性基因;1株PCR结果为阴性。PFGE分析显示44株VRE分离株有37种不同的电泳模式,相似阈值为75%。这些图案聚集成4个不同的分支。我们的研究结果表明,在所研究的分离株中,vanA基因存在多克隆分布,并且明显存在vanA/vanB基因型。此外,这些结果强调了在2019冠状病毒病大流行期间抗生素耐药率的恶化,强调了采取严格的感染控制措施和积极监测的迫切需要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
New Microbiologica
New Microbiologica 生物-微生物学
CiteScore
2.20
自引率
5.60%
发文量
40
审稿时长
6-12 weeks
期刊介绍: The publication, diffusion and furtherance of research and study on all aspects of basic and clinical Microbiology and related fields are the chief aims of the journal.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信