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一种用于检测和定量人鼻病毒的逆转录实时聚合酶链反应(RT real-time PCR)的开发。

Development of a RT real-time PCR for the detection and quantification of human rhinoviruses.

作者信息

Gambarino Stefano, Costa Cristina, Elia Mariateresa, Sidoti Francesca, Mantovani Samantha, Gruosso Valentina, Bergallo Massimiliano, Cavallo Rossana

机构信息

Department of Public Health and Microbiology, University of Turin, via Santena 9, 10126, Turin, Italy.

出版信息

Mol Biotechnol. 2009 Jul;42(3):350-7. doi: 10.1007/s12033-009-9164-x. Epub 2009 Mar 17.

Abstract

Human Rhinoviruses (HRV) are the most common viral agents, being responsible for upper as well as lower respiratory tract infections. Evidence demonstrating that HRV disease is not exclusively limited to the upper airways and may cause lower respiratory complications, together with the frequency of HRV infections and the increasing number of immunocompromised patients underline the need for including HRV in virological diagnostics of acute lower respiratory tract illness. This article describes the development and optimization of a reverse transcription (RT) real-time PCR assay for quantification of HRV RNA in clinical samples. Efficiency, sensitivity, specificity, inter- and intra-assay variability, and dynamic range have been determined. Subsequently, the assay has been validated on bronchoalveolar lavage (BAL) specimens obtained from immunocompetent and immunocompromised patients.

摘要

人鼻病毒(HRV)是最常见的病毒病原体,可引起上呼吸道和下呼吸道感染。有证据表明,HRV疾病不仅限于上呼吸道,还可能导致下呼吸道并发症,再加上HRV感染的频率以及免疫功能低下患者数量的增加,凸显了在急性下呼吸道疾病的病毒学诊断中纳入HRV检测的必要性。本文描述了一种用于定量临床样本中HRV RNA的逆转录(RT)实时PCR检测方法的开发和优化。已确定了该方法的效率、灵敏度、特异性、批间和批内变异性以及动态范围。随后,该检测方法在从免疫功能正常和免疫功能低下患者获取的支气管肺泡灌洗(BAL)标本上进行了验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33e3/7091102/c4688c2fbb47/12033_2009_9164_Fig1_HTML.jpg

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