当前位置: X-MOL 学术Eur. J. Clin. Microbiol. Infect. Dis. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Rapid detection of NDM and VIM carbapenemase encoding genes by recombinase polymerase amplification and lateral flow–based detection
European Journal of Clinical Microbiology & Infectious Diseases ( IF 3.7 ) Pub Date : 2021-05-11 , DOI: 10.1007/s10096-021-04267-6
Abdulrahman K S Ayfan 1, 2 , Joanne Macdonald 3 , Patrick N A Harris 1, 4 , Claire Heney 4 , David L Paterson 1 , Ella Trembizki 1 , Claire Y T Wang 5 , David M Whiley 1, 4 , Hosam M Zowawi 1, 6, 7 , Adam D Irwin 1, 5
Affiliation  

Carbapenemase-producing organisms (CPOs) pose a serious clinical threat and rapid detection tools are essential to aid in patient management. We developed rapid and simple molecular tests to detect blaNDM-type and blaVIM-type carbapenemase genes using recombinase polymerase amplification (RPA) combined with a lateral flow detection. The tests could provide results in approximately 15 min when using DNA extracts, with limits of detection of 9.2 copies/μl for the blaNDM-type assay and 7.5 copies/μl for blaVIM-type assay, and successfully detected all isolates harbouring the carbapenemase encoding genes in a panel of 57 isolates. These RPA tests may be suitable for use in low-resource settings to tailor rapid implementation of infection control precautions and antibiotic stewardship.



中文翻译:

通过重组酶聚合酶扩增和基于侧向流动的检测快速检测 NDM 和 VIM 碳青霉烯酶编码基因

产碳青霉烯酶的生物体 (CPO) 构成严重的临床威胁,快速检测工具对于帮助患者管理至关重要。我们开发了快速而简单的分子测试,使用重组酶聚合酶扩增 (RPA) 结合侧向流动检测来检测bla NDM 型bla VIM 型碳青霉烯酶基因。使用 DNA 提取物时,测试可在大约 15 分钟内提供结果,bla NDM 型检测的检测限为 9.2拷贝/μl,bla VIM 型检测的检测限为7.5 拷贝/μl化,并成功检测到在 57 个分离株中含有碳青霉烯酶编码基因的所有分离株。这些 RPA 测试可能适用于资源匮乏的环境,以便快速实施感染控制预防措施和抗生素管理。

更新日期:2021-05-11
down
wechat
bug