Wu Wei, Zhang Shuo, Qu Jing, Zhang Quanfu, Li Chuan, Li Jiandong, Jin Cong, Liang Mifang, Li Dexin
Key laboratory of Medical Virology, Ministry of Health, Department of Viral Hemorrhagic Fever, National Institute for Viral Disease Control and Prevention, China CDC, Beijing 102206, China.
Key laboratory of Medical Virology, Ministry of Health, Department of Viral Hemorrhagic Fever, National Institute for Viral Disease Control and Prevention, China CDC, Beijing 102206, China.
Virus Res. 2014 Jul 17;187:84-90. doi: 10.1016/j.virusres.2013.12.037. Epub 2014 Mar 12.
Viral hemorrhagic fevers (VHFs) are worldwide diseases caused by several kinds of viruses. With the emergence of new viruses, advanced diagnostic methods are urgently needed for identification of VHFs. Based on Luminex xMAP technology, a rapid, sensitive, multi-pathogen and high-throughput method which could simultaneously detect hemorrhagic fever viruses (HFVs) specific IgG antibodies was developed. Recombinant antigens of nine HFVs including Hantaan virus (HTNV), Seoul virus (SEOV), Puumala virus (PUUV), Andes virus (ANDV), Sin Nombre virus (SNV), Crimean-Congo hemorrhagic fever virus (CCHFV), Rift Valley fever virus (RVFV), Severe fever with thrombocytopenia syndrome bunyavirus (SFTSV) and dengue virus (DENV) were produced and purified from a prokaryotic expression system and the influence of the coupling amount was investigated. Cross-reactions among antigens and their rabbit immune sera were evaluated. Serum samples collected from 51 laboratory confirmed hemorrhagic fever with renal syndrome (HFRS) patients, 43 confirmed SFTS patients and 88 healthy donors were analyzed. Results showed that recombinant nucleocapsid protein of the five viruses belonging to the genus Hantavirus, had serological cross-reactivity with their corresponding rabbit immune sera, but not apparent with immune sera of other four viruses. Evaluation of this new method with clinical serum samples showed 98.04% diagnostic sensitivity for HFRS, 90.70% for SFTS detection and the specificity was ranging from 66.67% to 100.00%. The multiplexed Luminex-based immunoassay has firstly been established in our study, which provides a potentially reliable diagnostic tool for IgG antibody detection of VHFs.
病毒性出血热(VHFs)是由多种病毒引起的全球性疾病。随着新病毒的出现,迫切需要先进的诊断方法来识别VHFs。基于Luminex xMAP技术,开发了一种快速、灵敏、多病原体且高通量的方法,该方法能够同时检测出血热病毒(HFVs)特异性IgG抗体。从原核表达系统中制备并纯化了包括汉坦病毒(HTNV)、汉城病毒(SEOV)、普马拉病毒(PUUV)、安第斯病毒(ANDV)、辛诺柏病毒(SNV)、克里米亚-刚果出血热病毒(CCHFV)、裂谷热病毒(RVFV)、严重发热伴血小板减少综合征布尼亚病毒(SFTSV)和登革病毒(DENV)在内的9种HFVs的重组抗原,并研究了偶联量的影响。评估了抗原与其兔免疫血清之间的交叉反应。分析了从51例实验室确诊的肾综合征出血热(HFRS)患者、43例确诊的SFTS患者和88名健康供体采集的血清样本。结果表明,属于汉坦病毒属的5种病毒的重组核衣壳蛋白与其相应的兔免疫血清具有血清学交叉反应,但与其他4种病毒的免疫血清无明显交叉反应。用临床血清样本对该新方法进行评估,结果显示对HFRS的诊断敏感性为98.04%,对SFTS的检测敏感性为90.70%,特异性在66.67%至100.00%之间。本研究首次建立了基于Luminex的多重免疫分析方法,为VHFs的IgG抗体检测提供了一种潜在可靠的诊断工具。