Carrera Monica, Sagripanti Jose-Luis
Laboratory of the Association of Biochemists and Pharmacists (COFYB, Argentina), Buenos Aires CP 1184, Argentina.
J Virol Methods. 2009 Jul;159(1):29-33. doi: 10.1016/j.jviromet.2009.02.021. Epub 2009 Mar 3.
The aim of this study was to design and construct a non-virulent simulant to replace several pathogenic viruses in the development of detection and identification methods in biodefense. A non-infectious simulant was designed and engineered to include the nucleic acid signature of VEEV (Venezuelan Equine Encephalitis virus), Influenza virus, Rift Valley Fever virus, Machupo virus, Lassa virus, Yellow Fever virus, Ebola virus, Eastern Equine Encephalitis virus, Junin virus, Marburg virus, Dengue virus, and Crimean-Congo virus, all in a single construct. The nucleic acid sequences of all isolates available for each virus species were aligned using ClustalW software in order to obtain conserved regions of the viral genomes. Specific primers were designed to permit the identification and differentiation between viral threat agents. A chimera of 3143 base pairs was engineered to produce 13 PCR amplicons of different sizes. PCR amplification of the simulant with virus-specific primers revealed products of the predicted length, in bands of similar intensity, and without detectable unspecific products by electrophoresis analysis. The simulant described could reduce the need to use infectious viruses in the development of detection and diagnostic methods, and could also be useful as a non-virulent positive control in nucleic acid-based tests against biological threat agents.
本研究的目的是设计并构建一种无毒模拟物,以在生物防御检测和鉴定方法的开发中替代多种致病病毒。设计并构建了一种非感染性模拟物,使其包含委内瑞拉马脑炎病毒(VEEV)、流感病毒、裂谷热病毒、马丘波病毒、拉沙病毒、黄热病病毒、埃博拉病毒、东部马脑炎病毒、胡宁病毒、马尔堡病毒、登革病毒和克里米亚-刚果病毒的核酸特征,所有这些都包含在一个单一构建体中。使用ClustalW软件对每种病毒物种的所有可用分离株的核酸序列进行比对,以获得病毒基因组的保守区域。设计了特异性引物,以实现对病毒威胁因子的鉴定和区分。构建了一个3143个碱基对的嵌合体,以产生13个不同大小的PCR扩增产物。用病毒特异性引物对模拟物进行PCR扩增,结果显示产物长度符合预期,条带强度相似,且电泳分析未检测到非特异性产物。所述模拟物可减少在检测和诊断方法开发中使用感染性病毒的需求,也可作为针对生物威胁因子的基于核酸检测的无毒阳性对照。