School of Molecular Bioscience, University of Sydney, Sydney, NSW 2006, Australia.
Anal Chem. 2013 Jan 15;85(2):1097-105. doi: 10.1021/ac302962u. Epub 2013 Jan 2.
Parainfluenza viruses (PIVs) are one of the most common causes of respiratory tract infections in children and can be life-threatening when the airway becomes obstructed. Infection results in a spectrum of respiratory disease symptoms that makes diagnosis difficult. A new proteotyping approach employing high-resolution mass spectrometry is shown to be able to distinguish common human serotypes of the PIV from the perspective of all surface and internal viral proteins. The detection of signature peptides, conserved in sequence and unique in mass, within the spectra of these protein or whole virus digests enables the parainfluenza virus to be identified and typed and for it to be distinguished from the influenza virus. Given that the approach is more rapid and direct than conventional reverse transcriptase polymerase chain reaction (RT-PCR), and that it can be implemented with high sample throughout at a comparable sensitivity, it affords an effective new means with which to characterize the virus at the molecular level.
副黏病毒(PIV)是儿童呼吸道感染的最常见原因之一,当气道阻塞时可危及生命。感染会导致一系列呼吸道疾病症状,使诊断变得困难。一种新的蛋白质组学方法采用高分辨率质谱,能够从所有表面和内部病毒蛋白的角度来区分常见的人类 PIV 血清型。在这些蛋白质或整个病毒消化物的光谱中检测到保守的特征肽,在质量上是独特的,这使得副黏病毒能够被识别和分型,并与流感病毒区分开来。鉴于该方法比传统的逆转录聚合酶链反应(RT-PCR)更快、更直接,并且可以以更高的样本通量实现,具有可比的灵敏度,因此它为在分子水平上对病毒进行特征分析提供了一种有效的新方法。