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本文引用的文献

1
Evolutionary patterns of eastern equine encephalitis virus in North versus South America suggest ecological differences and taxonomic revision.东马脑炎病毒在北美洲和南美洲的进化模式表明存在生态差异和分类修订。
J Virol. 2010 Jan;84(2):1014-25. doi: 10.1128/JVI.01586-09. Epub 2009 Nov 4.
2
Evaluation of chimeric Japanese encephalitis and dengue viruses for use in diagnostic plaque reduction neutralization tests.用于诊断蚀斑减少中和试验的嵌合日本脑炎病毒和登革病毒的评估。
Clin Vaccine Immunol. 2009 Jul;16(7):1052-9. doi: 10.1128/CVI.00095-09. Epub 2009 May 20.
3
Chimeric Sindbis/eastern equine encephalitis vaccine candidates are highly attenuated and immunogenic in mice.嵌合辛德毕斯病毒/东部马脑炎病毒候选疫苗在小鼠中高度减毒且具有免疫原性。
Vaccine. 2007 Oct 23;25(43):7573-81. doi: 10.1016/j.vaccine.2007.07.061. Epub 2007 Aug 15.
4
Recombinant alphaviruses are safe and useful serological diagnostic tools.重组甲病毒是安全且有用的血清学诊断工具。
Am J Trop Med Hyg. 2007 Apr;76(4):774-81.
5
Endemic eastern equine encephalitis in the Amazon region of Peru.秘鲁亚马逊地区的地方性东部马脑炎
Am J Trop Med Hyg. 2007 Feb;76(2):293-8.
6
Pseudotyped viruses permit rapid detection of neutralizing antibodies in human and equine serum against Venezuelan equine encephalitis virus.假型病毒可快速检测人和马血清中针对委内瑞拉马脑炎病毒的中和抗体。
Am J Trop Med Hyg. 2006 Oct;75(4):702-9.
7
High fidelity of yellow fever virus RNA polymerase.黄热病病毒RNA聚合酶的高保真度。
J Virol. 2004 Jan;78(2):1032-8. doi: 10.1128/jvi.78.2.1032-1038.2004.
8
Recombinant sindbis/Venezuelan equine encephalitis virus is highly attenuated and immunogenic.重组辛德毕斯/委内瑞拉马脑炎病毒高度减毒且具有免疫原性。
J Virol. 2003 Sep;77(17):9278-86. doi: 10.1128/jvi.77.17.9278-9286.2003.
9
Detection of North American eastern and western equine encephalitis viruses by nucleic acid amplification assays.通过核酸扩增检测北美东部和西部马脑炎病毒。
J Clin Microbiol. 2003 Jan;41(1):379-85. doi: 10.1128/JCM.41.1.379-385.2003.
10
Genetic and antigenic diversity among eastern equine encephalitis viruses from North, Central, and South America.来自北美洲、中美洲和南美洲的东部马脑炎病毒的遗传和抗原多样性。
Am J Trop Med Hyg. 1999 Oct;61(4):579-86. doi: 10.4269/ajtmh.1999.61.579.

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.

DOI:10.1128/CVI.05129-11
PMID:21752946
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3165225/
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。