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Development and Characterization of Double-Antibody Sandwich ELISA for Detection of Zika Virus Infection

机译:用于检测寨卡病毒感染的双抗体夹心ELISA的开发与表征

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Zika virus (ZIKV) is an emerging mosquito-transmitted flavivirus that can cause severe disease, including congenital birth defect and Guillain?Barré syndrome during pregnancy. Although, several molecular diagnostic methods have been developed to detect the ZIKV, these methods pose challenges as they cannot detect early viral infection. Furthermore, these methods require the extraction of RNA, which is easy to contaminate. Nonstructural protein 1 (NS1) is an important biomarker for early diagnosis of the virus, and the detection methods associated with the NS1 protein have recently been reported. The aim of this study was to develop a rapid and sensitive detection method for the detection of the ZIKV based on the NS1 protein. The sensitivity of this method is 120 ng mL ?1 and it detected the ZIKV in the supernatant and lysates of Vero and BHK cells, as well as the sera of tree shrews infected with the ZIKV. Without the isolation of the virus and the extraction of the RNA, our method can be used as a primary screening test as opposed to other diagnosis methods that detect the ZIKV.
机译:寨卡病毒(ZIKV)是一种新兴的由蚊子传播的黄病毒,可引起严重疾病,包括先天性先天缺陷和妊娠期的Guillain?Barré综合征。尽管已经开发了几种分子诊断方法来检测ZIKV,但是由于这些方法无法检测到早期病毒感染,因此带来了挑战。此外,这些方法需要提取容易被污染的RNA。非结构蛋白1(NS1)是病毒早期诊断的重要生物标志物,最近已报道了与NS1蛋白相关的检测方法。这项研究的目的是开发一种快速灵敏的检测方法,用于检测基于NS1蛋白的ZIKV。该方法的灵敏度为120 ng mL?1,可检测Vero和BHK细胞的上清液和裂解物中的ZIKV,以及感染ZIKV的树the的血清。无需分离病毒和提取RNA,与检测ZIKV的其他诊断方法相比,我们的方法可以用作主要的筛选测试。

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