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Identification and characterization of viral defective RNA genomes in influenza B virus

机译:乙型流感病毒中病毒缺陷RNA基因组的鉴定和表征

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摘要

Influenza B virus (FLUBV) is an important pathogen that infects humans and causes seasonal influenza epidemics. To date, little is known about defective genomes of FLUBV and their roles in viral replication. In this study, by using a next-generation sequencing approach, we analyzed total mRNAs extracted from A549 cells infected with B/Brisbane/60/2008 virus (Victoria lineage), and identified four defective FLUBV genomes with two (PB1∆A and PB1∆B) from the polymerase basic subunit 1 (PB1) segment and the other two (M∆A and M∆B) from the matrix (M) protein-encoding segment. These defective genomes contained significant deletions in the central regions with each having the potential for encoding a novel polypeptide. Significantly, each of the discovered defective RNAs can potently inhibit the replication of B/Yamanashi/166/98 (Yamagata lineage). Furthermore, PB1∆A was able to interfere modestly with influenza A virus (FLUAV) replication. In summary, our study provides important initial insights into FLUBV defective-interfering genomes, which can be further explored to achieve better understanding of the replication, pathogenesis and evolution of FLUBV.
机译:乙型流感病毒(FLUBV)是一种重要的病原体,可感染人类并引起季节性流感流行。迄今为止,关于FLUBV的缺陷基因组及其在病毒复制中的作用还知之甚少。在这项研究中,我们使用下一代测序方法,分析了从感染B / Brisbane / 60/2008病毒(维多利亚世系)的A549细胞中提取的总mRNA,并鉴定了四个缺陷的FLUBV基因组,其中两个(PB1∆A和PB1)聚合酶基础亚基1(PB1)片段中的∆B),矩阵(M)蛋白质编码片段中的另外两个(M∆A和M∆B)。这些有缺陷的基因组在中央区域包含显着的缺失,每个具有编码新多肽的潜力。重要的是,每个发现的有缺陷的RNA都可以有效抑制B / Yamanashi / 166/98(Yamagata谱系)的复制。此外,PB1ΔA能够适度地干扰甲型流感病毒(FLUAV)的复制。总而言之,我们的研究为FLUBV缺陷干扰基因组提供了重要的初步见识,可以进一步探索以更好地理解FLUBV的复制,发病机理和进化。

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