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Determination of Spontaneous Mutation Frequencies in Measles Virus under Nonselective Conditions

机译:非选择性条件下麻疹病毒自发突变频率的测定

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摘要

There is a paradox between the remarkable genetic stability of measles virus (MV) in the field and the high mutation rates implied by the frequency of the appearance of monoclonal antibody escape mutants generated when the virus is pressured to revert in vitro (S. J. Schrag, P. A. Rota, and W. J. Bellini, J. Virol. 73:51–54, 1999). We established a highly sensitive assay to determine frequencies of various categories of mutations in large populations of wild-type and laboratory-adapted MVs using recombinant viruses containing an additional transcription unit (ATU) encoding enhanced green fluorescent protein (EGFP). Single and double mutations were made in the fluorophore of EGFP to ablate fluorescence. The frequencies of reversion mutants in the population were determined by measuring the appearance of fluorescence indicating a revertant virus. This allows mutation rates to be measured under nonselective conditions, as phenotypic reversion to fluorescence requires only either a single- or a double-nucleotide change and amino acid substitution, which does not affect the length of the nonessential reporter protein expressed from the ATU. Mutation rates in MV are the same for wild-type and laboratory-adapted viruses, and they are an order of magnitude lower than the previous measurement assessed under selective conditions. The actual mutation rate for MV is approximately 1.8 × 10−6 per base per replication event.
机译:麻疹病毒在野外的显着遗传稳定性与高压力产生率之间存在矛盾,这种高突变率是由压力迫使其在体外恢复产生的单克隆抗体逃逸突变体出现频率暗示的(SJ Schrag,PA Rota和WJ Bellini,J。Virol。73:51–54,1999)。我们建立了一种高度敏感的测定方法,以使用包含编码增强型绿色荧光蛋白(EGFP)的附加转录单位(ATU)的重组病毒,确定野生型和实验室适应性MV大种群中各种类别突变的频率。在EGFP的荧光团中进行单突变和双突变以消除荧光。群体中回复突变体的频率通过测量指示回复病毒的荧光外观来确定。这允许在非选择性条件下测量突变率,因为表型回复荧光仅需要单核苷酸或双核苷酸变化和氨基酸取代,而这不会影响从ATU表达的非必需报道蛋白的长度。 MV中的突变率与野生型和实验室适应病毒相同,并且比选择性条件下评估的先前测量值低一个数量级。每个复制事件中,MV的实际突变率约为每碱基1.8×10 -6

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