Department of Microbiology, University of Pennsylvania, Philadelphia, PA 19104, USA.
J Virol Methods. 2010 Feb;163(2):416-23. doi: 10.1016/j.jviromet.2009.11.004. Epub 2009 Nov 10.
Andes virus (ANDV), a member of the Hantavirus genus in the family Bunyaviridae, causes an acute disease characteristic of New-World hantaviruses called hantavirus pulmonary syndrome (HPS). HPS is a highly pathogenic disease with a case-fatality rate of 40%. ANDV is the only hantavirus reported to spread directly from human-to-human. The aim of the present study was to develop a quantitative and high-throughput pseudovirion assay to study ANDV infection and neutralization in biosafety level 2 facilities (BSL-2). This pseudovirion assay is based on incorporation of ANDV glycoproteins onto replication-defective vesicular stomatitis virus (VSV) cores in which the gene for the surface G protein has been replaced by that encoding Renilla luciferase. Infection by the pseudovirions can be quantified by luciferase activity of infected cell lysates. ANDV pseudovirions were neutralized by ANDV-specific antisera, and there was good concordance between specificity and neutralization titers of ANDV hamster sera as determined by our pseudovirion assay and a commonly used plaque reduction neutralization titer (PRNT) assay. In addition, the pseudovirions were used to evaluate the requirements for ANDV entry, like pH dependency and the role of beta3 integrin, the reported receptor for other pathogenic hantaviruses, on entry.
安第斯病毒(ANDV)是布尼亚病毒科汉坦病毒属的一种病毒,可引起一种称为汉坦病毒肺综合征(HPS)的急性疾病,这种疾病是新出现的世界汉坦病毒的特征。HPS 是一种高致病性疾病,病死率为 40%。ANDV 是唯一报道可直接在人与人之间传播的汉坦病毒。本研究的目的是开发一种定量和高通量的假病毒测定法,以在生物安全 2 级设施(BSL-2)中研究 ANDV 感染和中和作用。这种假病毒测定法基于将 ANDV 糖蛋白掺入复制缺陷型水疱性口炎病毒(VSV)核心中,其中表面 G 蛋白的基因已被编码 Renilla 荧光素的基因所取代。通过感染细胞裂解物的荧光素酶活性来定量感染假病毒。ANDV 假病毒被 ANDV 特异性抗血清中和,并且我们的假病毒测定法和常用的蚀斑减少中和滴度(PRNT)测定法确定的 ANDV 仓鼠血清的特异性和中和效价之间具有良好的一致性。此外,还使用假病毒来评估 ANDV 进入的要求,例如 pH 依赖性和β3 整合素的作用,β3 整合素是其他致病性汉坦病毒的报告受体,在进入过程中起作用。