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Flaviviral NS4b, chameleon and jack-in-the-box roles in viral replication and pathogenesis, and a molecular target for antiviral intervention

机译:黄病毒NS4b,变色龙和即兴发挥作用在病毒复制和发病机理中的作用,以及抗病毒干预的分子靶标

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Dengue virus and other flaviviruses such as the yellow fever, West Nile, and Japanese encephalitis viruses are emerging vector-borne human pathogens that affect annually more than 100 million individuals and that may cause debilitating and potentially fatal hemorrhagic and encephalitic diseases. Currently, there are no specific antiviral drugs for the treatment of flavivirus-associated disease. A better understanding of the flavivirus-host interactions during the different events of the flaviviral life cycle may be essential when developing novel antiviral strategies. The flaviviral non-structural protein 4b (NS4b) appears to play an important role in flaviviral replication by facilitating the formation of the viral replication complexes and in counteracting innate immune responses such as the following: (i) type I IFN signaling; (ii) RNA interference; (iii) formation of stress granules; and (iv) the unfolded protein response. Intriguingly, NS4b has recently been shown to constitute an excellent target for the selective inhibition of flavivirus replication. We here review the current knowledge on NS4b. (c) 2015 The Authors. Reviews in Medical Virology published by John Wiley & Sons Ltd.
机译:登革热病毒和其他黄病毒,例如黄热病,西尼罗河病毒和日本脑炎病毒,是新兴的媒介传播人类病原体,每年影响一亿多人,并可能导致虚弱的和潜在的致命性出血性和脑病。当前,尚无用于治疗黄病毒相关疾病的特异性抗病毒药物。在开发新的抗病毒策略时,更好地了解黄病毒生命周期不同事件期间的黄病毒-宿主相互作用可能至关重要。黄病毒非结构蛋白4b(NS4b)通过促进病毒复制复合物的形成和抵抗先天性免疫应答(例如以下情况),在黄病毒复制中起着重要作用:(i)I型IFN信号传导; (ii)RNA干扰; (iii)形成应力颗粒; (iv)展开的蛋白质反应。有趣的是,最近已证明NS4b构成了选择性抑制黄病毒复制的极佳靶标。我们在这里回顾有关NS4b的最新知识。 (c)2015作者。 John Wiley&Sons Ltd.发表的《医学病毒学评论》。

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