Changes in the NS1 gene of avian influenza viruses isolated in Thailand affect expression of type I interferon in primary chicken embryonic fibroblast cells.

Indian Journal of Virology Pub Date : 2013-12-01 Epub Date: 2013-08-28 DOI:10.1007/s13337-013-0158-8
Chutamas Thepmalee, Phanchana Sanguansermsri, Naratchala Suwanankhon, Chanpen Chamnanpood, Pornchai Chamnanpood, Sutatip Pongcharoen, Pannika R Niumsap, Damratsamon Surangkul, Donruedee Sanguansermsri
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引用次数: 5

Abstract

The non-structural protein 1 (NS1) of avian influenza virus was defined as one of the virulent factors. To understand the effect of NS1 protein of influenza virus H5N1 isolated in Thailand on type I (α/β) interferon (IFN) synthesis, five reverse genetic viruses were constructed and used as models. The viruses were generated using NS genomic segment from A/Peurto Rico/8/1934 (H1N1) and four avian influenza viruses isolated from the first outbreak in Thailand. All the viruses have the rest of the genome from A/Peurto Rico/8/1934 (H1N1). The constructed viruses were named (1) NS1 PR8/34, (2) NS1 wild type, (3) NS1 L15FD53G, (4) NS1 N171I and (5) NS1 E71K, respectively. The type I (α/β) IFN gene expression in control and infected primary chicken embryonic fibroblast cells were analyzed by quantitative polymerase chain reaction. The results show that the inhibition of IFN-β gene expression by NS1 wild type infected cells is stronger than NS1 N171I, NS1 E71K, NS1 PR8/34 and NS1 L15FD53G, respectively. The data suggest that the difference of amino acid sequence of NS1 protein contributes to the IFN-β antagonist. In contrast, the difference of the NS1 protein does not influence in the IFN-α antagonistic activity.

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泰国分离的禽流感病毒NS1基因的改变影响了鸡胚成纤维细胞中I型干扰素的表达。
禽流感病毒的非结构蛋白1 (NS1)被确定为致毒因子之一。为了解泰国H5N1型流感病毒NS1蛋白对ⅰ型(α/β)干扰素(IFN)合成的影响,构建了5种反向遗传病毒作为模型。这些病毒是利用A/波多黎各/8/1934 (H1N1)禽流感病毒的NS基因组片段和从泰国首次暴发中分离的4种禽流感病毒产生的。所有的病毒都有A/波多黎各/8/1934 (H1N1)病毒基因组的其余部分。构建的病毒分别命名为(1)NS1 PR8/34、(2)NS1野生型、(3)NS1 L15FD53G、(4)NS1 N171I和(5)NS1 E71K。采用定量聚合酶链反应分析了ⅰ型(α/β) IFN基因在对照和感染原代鸡胚成纤维细胞中的表达。结果表明,NS1野生型感染细胞对IFN-β基因表达的抑制作用分别强于NS1 N171I、NS1 E71K、NS1 PR8/34和NS1 L15FD53G。提示NS1蛋白氨基酸序列的差异对IFN-β拮抗剂的作用有一定的影响。相反,NS1蛋白的差异不影响IFN-α的拮抗活性。
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来源期刊
Indian Journal of Virology
Indian Journal of Virology 医学-病毒学
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6-12 weeks
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