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一种用于检测痰液样本中肺炎链球菌、b型流感嗜血杆菌和结核分枝杆菌复合群的多重降落PCR。

A multiplex touchdown PCR for detection of Streptococcus pneumoniae, Haemophilus influenzae type b and Mycobacterium tuberculosis complex in sputum samples.

作者信息

Luo Y C, Du P, Zhao J Z, Duan X J, Hou Y J, Pan H, Shao S H

机构信息

School of Medical Science and Laboratory Medicine, Jiangsu University, Zhenjiang 212013, China.

出版信息

Trop Biomed. 2012 Sep;29(3):422-8.

Abstract

Rapid and accurate detection of Streptococcus pneumoniae (Sp), Haemophilus influenzae type b (Hib) and Mycobacterium tuberculosis complex (MTBC) in sputum by conventional methods remains problematic. Primers based on capsular polysaccharide biosynthesis gene (cpsA), the region II of the capsulation locus (cap), the insertion sequence IS6110 were designed for Sp, Hib, MTBC respectively. These primers were incorporated in a multiplex touchdown PCR assay for simultaneous detection of Sp, Hib and MTBC. The multiplex touchdown PCR assay was evaluated using standard strains and clinical sputum samples. The multiplex touchdown PCR assay showed 100% specificity in identifying Sp, Hib, MTBC from pure culture of standard strains. The sensitivities of the multiplex touchdown PCR assay were 94%, 98%, 98% for detection of Sp, Hib and MTBC respectively based on culture results while evaluated using 492 consecutive qualified clinical sputum samples; the specificities were all 100%. This highly sensitive and specific multiplex touchdown PCR assay offers a rapid and simple method for detection of Sp, Hib and MTBC in clinical sputum samples.

摘要

采用传统方法在痰液中快速准确地检测肺炎链球菌(Sp)、b型流感嗜血杆菌(Hib)和结核分枝杆菌复合群(MTBC)仍然存在问题。分别基于荚膜多糖生物合成基因(cpsA)、荚膜形成位点区域II(cap)、插入序列IS6110设计了用于Sp、Hib、MTBC的引物。将这些引物用于多重降落式聚合酶链反应(PCR)检测,以同时检测Sp、Hib和MTBC。使用标准菌株和临床痰液样本对多重降落式PCR检测进行评估。多重降落式PCR检测在从标准菌株的纯培养物中鉴定Sp、Hib、MTBC时显示出100%的特异性。在使用492份连续合格的临床痰液样本进行评估时,基于培养结果,多重降落式PCR检测对Sp、Hib和MTBC检测的灵敏度分别为94%、98%、98%;特异性均为100%。这种高灵敏度和特异性的多重降落式PCR检测为临床痰液样本中Sp、Hib和MTBC的检测提供了一种快速简便的方法。

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