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NP, PB1, and PB2 Viral Genes Contribute to Altered Replication of H5N1 Avian Influenza Viruses in Chickens▿ ‡

机译:NP,PB1和PB2病毒基因有助于改变H5N1禽流感病毒在鸡中的复制▿

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摘要

The virulence determinants for highly pathogenic avian influenza viruses (AIVs) are considered multigenic, although the best characterized virulence factor is the hemagglutinin (HA) cleavage site. The capability of influenza viruses to reassort gene segments is one potential way for new viruses to emerge with different virulence characteristics. To evaluate the role of other gene segments in virulence, we used reverse genetics to generate two H5N1 recombinant viruses with differing pathogenicity in chickens. Single-gene reassortants were used to determine which viral genes contribute to the altered virulence. Exchange of the PB1, PB2, and NP genes impacted replication of the reassortant viruses while also affecting the expression of specific host genes. Disruption of the parental virus' functional polymerase complexes by exchanging PB1 or PB2 genes decreased viral replication in tissues and consequently the pathogenicity of the viruses. In contrast, exchanging the NP gene greatly increased viral replication and expanded tissue tropism, thus resulting in decreased mean death times. Infection with the NP reassortant virus also resulted in the upregulation of gamma interferon and inducible nitric oxide synthase gene expression. In addition to the impact of PB1, PB2, and NP on viral replication, the HA, NS, and M genes also contributed to the pathogenesis of the reassortant viruses. While the pathogenesis of AIVs in chickens is clearly dependent on the interaction of multiple gene products, we have shown that single-gene reassortment events are sufficient to alter the virulence of AIVs in chickens.
机译:高致病性禽流感病毒(AIV)的毒力决定因素被认为是多基因的,尽管最具特征性的毒力因子是血凝素(HA)切割位点。流感病毒重新分配基因片段的能力是出现具有不同毒力特征的新病毒的一种潜在途径。为了评估其他基因片段在毒力中的作用,我们使用了反向遗传学来生成两种H5N1重组病毒,它们在鸡中具有不同的致病性。使用单基因重配子来确定哪些病毒基因有助于改变毒力。 PB1,PB2和NP基因的交换影响重配病毒的复制,同时也影响特定宿主基因的表达。通过交换PB1或PB2基因破坏亲代病毒的功能性聚合酶复合物会降低组织中的病毒复制,从而降低病毒的致病性。相反,交换NP基因大大增加了病毒复制并扩大了组织的向性,从而导致平均死亡时间减少。 NP重配病毒感染也导致γ干扰素的上调和诱导型一氧化氮合酶基因表达。除了PB1,PB2和NP对病毒复制的影响外,HA,NS和M基因也有助于重配病毒的发病。虽然鸡中AIV的发病机理明显取决于多种基因产物的相互作用,但我们已经表明,单基因重排事件足以改变鸡中AIV的毒力。

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