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首页> 外文期刊>Molecular and Cellular Probes: The Location, Diagnosis and Monitoring of Disease by Specific Molecules and Cell Lines >Specific detection of enterovirus 71 directly from clinical specimens using real-time RT-PCR hybridization probe assay.
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Specific detection of enterovirus 71 directly from clinical specimens using real-time RT-PCR hybridization probe assay.

机译:使用实时RT-PCR杂交探针测定法直接从临床样本中特异性检测肠病毒71。

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摘要

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 detectionof EV71 directly from clinical specimens.
机译:肠病毒71(EV71)是幼儿手足口病(HFMD)的主要病原体之一。 EV71引起的感染可能导致许多并发症,从脑干脑炎到肺水肿,导致高死亡率。因此,需要快速检测病毒以使得能够采取措施来防止广泛传播。基于针对VP1区域的引物和探针,开发了实时逆转录聚合酶链反应(RT-PCR)杂交探针测定法,用于从临床标本中特异性检测EV71。定量分析表明,该方法能够检测低至5份EV71病毒拷贝,并且在2000年至2003年新加坡的55例患手足口病的儿科患者的临床样本中,有46份检测到EV71。这项研究表明,这项研究中开发的单管实时RT-PCR测定法可作为一种快速灵敏的方法直接从临床样本中特异性检测EV71。

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