在体外对美罗培南敏感的肠杆菌中检测碳青霉烯酶。

Luana Silva Dornelles, Mariana Preussler Mott, Gabriela da Silva Collar, Luciana Giordani, Rodrigo Minuto Paiva, Larissa Lutz
{"title":"在体外对美罗培南敏感的肠杆菌中检测碳青霉烯酶。","authors":"Luana Silva Dornelles, Mariana Preussler Mott, Gabriela da Silva Collar, Luciana Giordani, Rodrigo Minuto Paiva, Larissa Lutz","doi":"10.1016/j.eimce.2024.07.008","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Carbapenemase-producing Enterobacterales (CPE) is a global threat. We evaluate the prevalence of CPE among isolates categorized as meropenem-susceptible, but that meet the European Committee on Antimicrobial Susceptibility Testing (EUCAST) screening cut-off values for carbapenemase detection, and analyze the susceptibility of these isolates to new available drugs.</p><p><strong>Methods: </strong>We analyzed 257 isolates from patients hospitalized in a tertiary hospital in Brazil, from July 2022 to April 2023. Only isolates that met the screening cut-off values established by EUCAST for detection of carbapenemases were analyzed (i.e. meropenem inhibition zones of 25-27mm by disk diffusion). The detection of carbapenemases was performed by immnunochromatographic testing and confirmed by high-resolution melting-PCR (HRM-qPCR).</p><p><strong>Results: </strong>We identified 12 (4.7%) CPE including 7 KPC, 4 NDM, and 1 OXA-48-like. The isolates were susceptible to ceftazidime-avibactam (72.7%), meropenem-vaborbactam (100%), imipenem-relebactam (63.6%) and ceftolozane-tazobactam (36.4%).</p><p><strong>Conclusion: </strong>We highlight the importance of tracking carbapenemases for epidemiological control and therapeutic guidance.</p>","PeriodicalId":72916,"journal":{"name":"Enfermedades infecciosas y microbiologia clinica (English ed.)","volume":"43 1","pages":"32-35"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Detection of carbapenemases in Enterobacterales susceptible in vitro to meropenem.\",\"authors\":\"Luana Silva Dornelles, Mariana Preussler Mott, Gabriela da Silva Collar, Luciana Giordani, Rodrigo Minuto Paiva, Larissa Lutz\",\"doi\":\"10.1016/j.eimce.2024.07.008\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Carbapenemase-producing Enterobacterales (CPE) is a global threat. We evaluate the prevalence of CPE among isolates categorized as meropenem-susceptible, but that meet the European Committee on Antimicrobial Susceptibility Testing (EUCAST) screening cut-off values for carbapenemase detection, and analyze the susceptibility of these isolates to new available drugs.</p><p><strong>Methods: </strong>We analyzed 257 isolates from patients hospitalized in a tertiary hospital in Brazil, from July 2022 to April 2023. Only isolates that met the screening cut-off values established by EUCAST for detection of carbapenemases were analyzed (i.e. meropenem inhibition zones of 25-27mm by disk diffusion). The detection of carbapenemases was performed by immnunochromatographic testing and confirmed by high-resolution melting-PCR (HRM-qPCR).</p><p><strong>Results: </strong>We identified 12 (4.7%) CPE including 7 KPC, 4 NDM, and 1 OXA-48-like. The isolates were susceptible to ceftazidime-avibactam (72.7%), meropenem-vaborbactam (100%), imipenem-relebactam (63.6%) and ceftolozane-tazobactam (36.4%).</p><p><strong>Conclusion: </strong>We highlight the importance of tracking carbapenemases for epidemiological control and therapeutic guidance.</p>\",\"PeriodicalId\":72916,\"journal\":{\"name\":\"Enfermedades infecciosas y microbiologia clinica (English ed.)\",\"volume\":\"43 1\",\"pages\":\"32-35\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-01-01\",\"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://doi.org/10.1016/j.eimce.2024.07.008\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Enfermedades infecciosas y microbiologia clinica (English ed.)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.eimce.2024.07.008","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

产碳青霉烯酶肠杆菌(CPE)是一种全球性威胁。我们评估了被归类为美罗培尼敏感但符合欧洲抗微生物药物敏感性试验委员会(EUCAST)筛选碳青霉烯酶检测临界值的分离株中CPE的患病率,并分析了这些分离株对现有新药的敏感性。方法:对2022年7月至2023年4月在巴西某三级医院住院的257株分离株进行分析。仅分析符合EUCAST建立的碳青霉烯酶检测筛选临界值的分离株(即圆盘扩散法美罗培南抑制区为25-27mm)。碳青霉烯酶采用免疫层析检测,高分辨率熔融pcr (HRM-qPCR)检测。结果:我们鉴定了12例(4.7%)CPE,包括7例KPC, 4例NDM和1例oxa -48样。对头孢他啶-阿维巴坦(72.7%)、美罗培恩-瓦波巴坦(100%)、亚胺培南-瑞巴坦(63.6%)和头孢洛赞-他唑巴坦(36.4%)敏感。结论:我们强调追踪碳青霉烯酶对流行病学控制和治疗指导的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of carbapenemases in Enterobacterales susceptible in vitro to meropenem.

Introduction: Carbapenemase-producing Enterobacterales (CPE) is a global threat. We evaluate the prevalence of CPE among isolates categorized as meropenem-susceptible, but that meet the European Committee on Antimicrobial Susceptibility Testing (EUCAST) screening cut-off values for carbapenemase detection, and analyze the susceptibility of these isolates to new available drugs.

Methods: We analyzed 257 isolates from patients hospitalized in a tertiary hospital in Brazil, from July 2022 to April 2023. Only isolates that met the screening cut-off values established by EUCAST for detection of carbapenemases were analyzed (i.e. meropenem inhibition zones of 25-27mm by disk diffusion). The detection of carbapenemases was performed by immnunochromatographic testing and confirmed by high-resolution melting-PCR (HRM-qPCR).

Results: We identified 12 (4.7%) CPE including 7 KPC, 4 NDM, and 1 OXA-48-like. The isolates were susceptible to ceftazidime-avibactam (72.7%), meropenem-vaborbactam (100%), imipenem-relebactam (63.6%) and ceftolozane-tazobactam (36.4%).

Conclusion: We highlight the importance of tracking carbapenemases for epidemiological control and therapeutic guidance.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
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