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辛德毕斯病毒/东部马脑炎嵌合病毒在用于虫媒病毒病诊断的蚀斑减少中和试验中的应用。

Use of sindbis/eastern equine encephalitis chimeric viruses in plaque reduction neutralization tests for arboviral disease diagnostics.

作者信息

Johnson B W, Kosoy O, Wang E, Delorey M, Russell B, Bowen R A, Weaver S C

机构信息

Diagnostic and Reference Laboratory, Centers for Disease Control and Prevention, 3150 Rampart Road, Fort Collins, CO 80521, USA.

出版信息

Clin Vaccine Immunol. 2011 Sep;18(9):1486-91. doi: 10.1128/CVI.05129-11. Epub 2011 Jul 13.

Abstract

Eastern equine encephalitis virus (EEEV) is a highly virulent, mosquito-borne alphavirus that causes severe and often fatal neurological disease in humans and horses in eastern North American, the Caribbean, and Mexico and throughout Central and South America. EEEV infection is diagnosed serologically by anti-EEEV-specific IgM detection, with confirmation by the plaque reduction neutralization test (PRNT), which is highly specific for alphaviruses. Live virus is used in the PRNT procedure, which currently requires biosafety level 3 containment facilities and select agent security in the case of EEEV. These requirements restrict the ability of public health laboratories to conduct PRNTs. Sindbis virus (SINV)/EEEV recombinant constructs have been engineered to express the immunogenic structural proteins from 2 wild-type EEEV strains in an attenuated form. These SINV/EEEVs, which are not classified as select agents, were evaluated as alternative diagnostic reagents in a PRNT using human, equine, and murine sera. The results indicate that the chimeric viruses exhibit specificity comparable to that of wild-type EEEV, with only a slight reduction in sensitivity. Considering their benefits in increased safety and reduced regulatory requirements, these chimeric viruses should be highly useful in diagnostic laboratories throughout the Americas.

摘要

东部马脑炎病毒(EEEV)是一种高致病性、由蚊子传播的甲病毒,在北美东部、加勒比地区、墨西哥以及中美洲和南美洲各地,可导致人类和马匹患上严重且往往致命的神经系统疾病。EEEV感染通过检测抗EEEV特异性IgM进行血清学诊断,并通过蚀斑减少中和试验(PRNT)加以确认,该试验对甲病毒具有高度特异性。PRNT程序中使用活病毒,就EEEV而言,目前需要生物安全3级防护设施和特定病原体安全措施。这些要求限制了公共卫生实验室进行PRNT的能力。辛德毕斯病毒(SINV)/EEEV重组构建体已被设计成以减毒形式表达来自2种野生型EEEV毒株的免疫原性结构蛋白。这些未被归类为特定病原体的SINV/EEEV在使用人、马和鼠血清的PRNT中作为替代诊断试剂进行了评估。结果表明,嵌合病毒表现出与野生型EEEV相当的特异性,敏感性仅略有降低。鉴于其在提高安全性和降低监管要求方面的优势,这些嵌合病毒在美洲各地的诊断实验室中应会非常有用。

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