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基于环介导等温扩增技术的碳青霉烯酶基因检测方法的评估。

Evaluation of LAMP-based assays for carbapenemase genes.

机构信息

Vitas Pharma Research Private Limited, TBI, University of Hyderabad, Hyderabad, India.

Department of Microbiology, Kasturba Medical College, Manipal, India.

出版信息

J Med Microbiol. 2019 Oct;68(10):1431-1437. doi: 10.1099/jmm.0.001050. Epub 2019 Aug 2.

Abstract

. Rapid and accurate detection of carbapenem resistance is a critical requirement for the selection of appropriate therapy and initiation of infection control measures. Although several tests are available, their use is limited by one or more factors. Phenotypic tests are lengthy, have variable sensitivity and specificity and do not generally identify the carbapenemase. Molecular assays overcome many of these issues but cost can be a barrier to adoption, particularly in low-resource settings. To address the need for affordable, molecular tools, we have assessed the performance characteristics of loop-mediated isothermal amplification (LAMP)-based assays for the major carbapenemase genes, bla, bla, bla, bla bla and bla.. The assays were validated using 1849 Gram-negative Indian clinical isolates obtained from seven hospitals and diagnostic centres.. The assays had diagnostic sensitivities of 98.14 %, 98.92 %, 100 %, 98.48 %, and diagnostic specificities of 98.94 %, 99.61 %, 97.42 %, 99.38 % for bla, bla, bla and bla, respectively. Due to a low number of isolates positive for bla and bla, the performance characteristics of assays for these two genes could not be suitably evaluated.. The performance characteristics suggest suitability for diagnostic and surveillance purposes.

摘要

. 快速准确地检测碳青霉烯类耐药性是选择适当治疗方法和启动感染控制措施的关键要求。虽然有几种检测方法可用,但由于一个或多个因素的限制,其使用受到限制。表型检测方法耗时较长,敏感性和特异性存在差异,并且通常无法识别碳青霉烯酶。分子检测方法克服了许多这些问题,但成本可能成为采用的障碍,尤其是在资源有限的环境中。为了解决对经济实惠的分子工具的需求,我们评估了基于环介导等温扩增(LAMP)的主要碳青霉烯酶基因,bla、bla、bla、bla bla 和 bla 的检测方法的性能特征。使用从七家医院和诊断中心获得的 1849 个革兰氏阴性印度临床分离株对检测方法进行了验证。检测方法对 bla、bla、bla 和 bla 的诊断敏感性分别为 98.14%、98.92%、100%、98.48%,诊断特异性分别为 98.94%、99.61%、97.42%、99.38%。由于 bla 和 bla 阳性分离株数量较少,无法对这两个基因的检测方法的性能特征进行适当评估。检测方法的性能特征表明其适合于诊断和监测目的。

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