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利用唾液样本进行人狂犬病的生前诊断:实时荧光定量和传统逆转录聚合酶链反应技术的比较

Ante mortem diagnosis of human rabies using saliva samples: comparison of real time and conventional RT-PCR techniques.

作者信息

Nagaraj T, Vasanth Joel P, Desai Anita, Kamat Anupa, Madhusudana S N, Ravi V

机构信息

Department of Neurovirology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India.

出版信息

J Clin Virol. 2006 May;36(1):17-23. doi: 10.1016/j.jcv.2006.01.009. Epub 2006 Feb 28.

Abstract

BACKGROUND

Rabies is an enzootic and fatal disease and is still a major problem in developing countries. Ante mortem diagnosis in human cases is necessary for medical management of the patient and to ensure appropriate post-exposure treatment of contacts. Both conventional RT-PCR and Real time PCR (TaqMan) have been described for the detection of rabies virus RNA from saliva and tissue respectively, however to date, there have been no studies comparing conventional and real time PCR assays for detection of rabies virus nucleic acid using saliva samples for ante mortem diagnosis.

OBJECTIVES

In this study, we evaluated the utility of conventional RT-PCR and SYBR Green I Real time PCR in the ante mortem diagnosis of rabies using saliva samples.

STUDY DESIGN

Saliva samples collected from twenty-four patients presenting with typical clinical manifestations of rabies were tested in the two assays.

RESULTS

Amongst the 24 samples tested, 21 samples (87.5%) were positive by either of the two molecular methods. Of these 21, rabies virus RNA was detected in 6/21 in the conventional RT-PCR assay while SYBR Green I Real time PCR could detect RNA in 18/21 samples.

CONCLUSION

Real time PCR assay was more sensitive than conventional RT-PCR assay (sensitivity 75% versus 37%, p=0.0189). This study highlights the utility of molecular diagnostic tests in establishing ante mortem diagnosis of rabies using saliva samples within a few hours.

摘要

背景

狂犬病是一种地方性动物传染病且具有致命性,在发展中国家仍然是一个主要问题。对人类病例进行生前诊断对于患者的医疗管理以及确保对接触者进行适当的暴露后治疗至关重要。传统逆转录聚合酶链反应(RT-PCR)和实时荧光定量聚合酶链反应(TaqMan)已分别用于从唾液和组织中检测狂犬病病毒RNA,然而迄今为止,尚无研究比较使用唾液样本进行生前诊断时传统PCR和实时荧光定量PCR检测狂犬病病毒核酸的效果。

目的

在本研究中,我们评估了传统RT-PCR和SYBR Green I实时荧光定量PCR在使用唾液样本进行狂犬病生前诊断中的效用。

研究设计

对从24例出现狂犬病典型临床表现的患者采集的唾液样本进行这两种检测。

结果

在检测的24个样本中,两种分子方法中的任何一种检测出21个样本(87.5%)呈阳性。在这21个样本中,传统RT-PCR检测出6/21的样本中存在狂犬病病毒RNA,而SYBR Green I实时荧光定量PCR能检测出18/21样本中的RNA。

结论

实时荧光定量PCR检测比传统RT-PCR检测更敏感(敏感性分别为75%和37%,p = 0.0189)。本研究突出了分子诊断检测在数小时内利用唾液样本进行狂犬病生前诊断的效用。

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