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使用实时逆转录聚合酶链反应杂交探针法直接从临床标本中特异性检测肠道病毒71型。

Specific detection of enterovirus 71 directly from clinical specimens using real-time RT-PCR hybridization probe assay.

作者信息

Tan Eng Lee, Chow Vincent Tak Kwong, Kumarasinghe Gamini, Lin Raymond Tze Pin, Mackay Ian M, Sloots Theo P, Poh Chit Laa

机构信息

Department of Microbiology, Faculty of Medicine, National University of Singapore, Singapore.

出版信息

Mol Cell Probes. 2006 Apr;20(2):135-40. doi: 10.1016/j.mcp.2005.11.003. Epub 2006 Feb 7.

Abstract

Enterovirus 71 (EV71) is one of the main causative agents of hand, foot and mouth disease (HFMD) in young children. Infections caused by EV71 could lead to many complications, ranging from brainstem encephalitis to pulmonary oedema, resulting in high mortality. Thus, rapid detection of the virus is required to enable measures to be implemented in preventing widespread transmission. Based on primers and probes targeting at the VP1 region, a real-time reverse-transcriptase polymerase chain reaction (RT-PCR) hybridization probe assay was developed for specific detection of EV71 from clinical specimens. Quantitative analysis showed that the assay was able to detect as low as 5 EV71 viral copies and EV71 was detected from 46 of the 55 clinical specimens obtained from pediatric patients suffering from HFMD during the period from 2000 to 2003 in Singapore. This study showed that the single tube real-time RT-PCR assay developed in this study can be applied as a rapid and sensitive method for specific detection of EV71 directly from clinical specimens.

摘要

肠道病毒71型(EV71)是幼儿手足口病(HFMD)的主要病原体之一。EV71引起的感染可导致许多并发症,从脑干脑炎到肺水肿,导致高死亡率。因此,需要快速检测该病毒,以便采取措施防止其广泛传播。基于针对VP1区域的引物和探针,开发了一种实时逆转录聚合酶链反应(RT-PCR)杂交探针检测法,用于从临床标本中特异性检测EV71。定量分析表明,该检测法能够检测低至5个EV71病毒拷贝,并且在2000年至2003年期间从新加坡患有手足口病的儿科患者获得的55份临床标本中的46份中检测到了EV71。这项研究表明,本研究中开发的单管实时RT-PCR检测法可作为一种快速、灵敏的方法,直接从临床标本中特异性检测EV71。

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