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首页> 外文期刊>Biologicals: Journal of the International Association of Biological Standardization >Application of a real time Polymerase Chain Reaction (PCR) assay for the early diagnosis of human leptospirosis in Sri Lanka
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Application of a real time Polymerase Chain Reaction (PCR) assay for the early diagnosis of human leptospirosis in Sri Lanka

机译:实时聚合酶链反应(PCR)分析在斯里兰卡人类钩端螺旋体病的早期诊断中的应用

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摘要

Leptospirosis has a major impact on health in Sri Lanka but is probably grossly under-recognized due to difficulties in clinical diagnosis and lack of diagnostic laboratory services. The objective of this study was to establish and evaluate a SYBR Green-based real-time Polymerase Chain Reaction (rt-PCR) assay for early, rapid and definitive laboratory diagnosis of leptospirosis in Sri Lanka. The rt-PCR assay was established and analytical specificity and sensitivity were determined using reference DNA samples. Evaluation of the assay for diagnosis of clinical samples was performed using two panels of serum samples obtained from 111 clinically suspected adult patients. Patients were confirmed as leptospirosis (n = 65) and non-leptospirosis (n = 30) by the Patoc MAT. Other 16 samples gave ambiguous results. The analytical sensitivity of the rt-PCR was approximately 60 genome copies and no cross-reactivity was observed with saprophytic Leptospira spp. and other pathogenic microorganisms. Based on confirmation with Patoc-MAT on paired samples this corresponds to a diagnostic sensitivity and specificity of 67.7% (44/65) and 90.0% (27/30), respectively. This study showed that rt-PCR has the potential to facilitate rapid and definitive diagnosis of leptospirosis during early phase of infection in Sri Lanka. (C) 2016 International Alliance for Biological Standardization. Published by Elsevier Ltd. All rights reserved.
机译:钩端螺旋体病对斯里兰卡的健康有重大影响,但由于临床诊断困难和缺乏诊断实验室服务,因此可能被严重忽视。这项研究的目的是建立和评估基于SYBR Green的实时聚合酶链反应(rt-PCR)分析方法,用于斯里兰卡钩端螺旋体病的早期,快速和确定性实验室诊断。建立了rt-PCR分析,并使用参考DNA样品确定了分析特异性和灵敏度。使用从111名临床可疑成年患者中获得的两份血清样品,对用于诊断临床样品的分析方法进行评估。 Patoc MAT将患者确认为钩端螺旋体病(n = 65)和非钩端螺旋体病(n = 30)。其他16个样本给出的结果不明确。 rt-PCR的分析灵敏度约为60个基因组拷贝,并且与腐生钩端螺旋体属的物种没有观察到交叉反应。和其他病原微生物。根据Patoc-MAT对配对样品的确认,这分别相当于诊断灵敏度和特异性分别为67.7%(44/65)和90.0%(27/30)。这项研究表明,rt-PCR可能有助于在斯里兰卡感染早期对钩端螺旋体病进行快速,明确的诊断。 (C)2016国际生物标准化联盟。由Elsevier Ltd.出版。保留所有权利。

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