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甲型流感病毒基因组片段非特异性包装的证据。

Evidence for segment-nonspecific packaging of the influenza a virus genome.

作者信息

Bancroft Christa T, Parslow Tristram G

机构信息

Department of Pathology, University of California, San Francisco, California 94143-0511, USA.

出版信息

J Virol. 2002 Jul;76(14):7133-9. doi: 10.1128/jvi.76.14.7133-7139.2002.

Abstract

The influenza A virus genome is composed of eight negative-sense RNA segments (called vRNAs), all of which must be packaged to produce an infectious virion. It is not clear whether individual vRNAs are packaged specifically or at random, however, and the total vRNA capacity of the virion is unknown. We have created modified forms of the viral nucleoprotein (NP), neuraminidase (NA), and nonstructural (NS) vRNAs that encode green or yellow fluorescent proteins and studied the efficiency with which these are packaged by using a plasmid-based influenza A virus assembly system. Packaging was assessed precisely and quantitatively by scoring transduction of the fluorescent markers in a single-round infectivity assay with a flow cytometer. We found that, under conditions in which virions are limiting, pairs of alternatively tagged vRNAs compete for packaging but do so in a nonspecific manner. Reporters representing different vRNAs were not packaged additively, as would be expected under specific packaging, but instead appeared to compete for a common niche in the virion. Moreover, 3 to 5% of transduction-competent viruses were found to incorporate two alternative reporters, regardless of whether those reporters represented the same or different vRNAs - a finding compatible with random, but not with specific, packaging. Probabilistic estimates suggest that in order to achieve this level of dual transduction by chance alone, each influenza A virus virion must package an average of 9 to 11 vRNAs.

摘要

甲型流感病毒基因组由八个负链RNA片段(称为vRNAs)组成,所有这些片段都必须被包装才能产生具有感染性的病毒粒子。然而,目前尚不清楚单个vRNAs是被特异性包装还是随机包装,并且病毒粒子的总vRNA容量也未知。我们创建了编码绿色或黄色荧光蛋白的病毒核蛋白(NP)、神经氨酸酶(NA)和非结构(NS)vRNAs的修饰形式,并使用基于质粒的甲型流感病毒组装系统研究了它们被包装的效率。通过在单轮感染性试验中使用流式细胞仪对荧光标记的转导进行评分,精确且定量地评估包装情况。我们发现,在病毒粒子有限的条件下,成对的交替标记vRNAs会竞争包装,但这种竞争是非特异性的。代表不同vRNAs的报告基因并不是像特异性包装情况下预期的那样进行累加包装,而是似乎在病毒粒子中竞争一个共同的空间。此外,发现3%至5%具有转导能力的病毒会掺入两个交替的报告基因,无论这些报告基因代表相同还是不同的vRNAs——这一发现与随机包装相符,但与特异性包装不符。概率估计表明,仅靠偶然要达到这种双重转导水平,每个甲型流感病毒粒子平均必须包装9至11个vRNAs。

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