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Interferon-induced Sus scrofa Mx1 blocks endocytic traffic of incoming influenza A virus particles

机译:干扰素诱导的Sus scrofa Mx1阻断传入的甲型流感病毒颗粒的内吞运输

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摘要

The interferon-induced Mx proteins of vertebrates are dynamin-like GTPases, some isoforms of which can additionally inhibit the life cycle of certain RNA viruses. Here we show that the porcine Mx1 protein (poMx1) inhibits replication of influenza A virus and we attempt to identify the step at which the viral life cycle is blocked. In infected cells expressing poMx1, the level of transcripts encoding the viral nucleoprotein is significantly lower than normal, even when secondary transcription is prevented by exposure to cycloheximide. This reveals that a pretranscriptional block participates to the anti-influenza activity. Binding and internalization of incoming virus particles are normal in the presence of poMx1 but centripetal traffic to the late endosomes is interrupted. Surprisingly but decisively, poMx1 significantly alters binding of early endosome autoantigen 1 to early endosomes and/or early endosome size and spatial distribution. This is compatible with impairment of traffic of the endocytic vesicles to the late endosomes.
机译:干扰素诱导的脊椎动物Mx蛋白是类似动力蛋白的GTPases,其某些同工型还可以抑制某些RNA病毒的生命周期。在这里,我们表明猪Mx1蛋白(poMx1)抑制了甲型流感病毒的复制,我们试图确定阻断病毒生命周期的步骤。在表达poMx1的受感染细胞中,编码病毒核蛋白的转录物水平显着低于正常水平,即使通过暴露于环己酰亚胺可防止二次转录。这表明转录前阻断参与抗流感活性。在poMx1存在下,传入病毒颗粒的结合和内在化是正常的,但向晚期内体的向心运输被中断。出人意料但决定性的是,poMx1显着改变了早期内体自身抗原1与早期内体和/或早期内体大小和空间分布的结合。这与内吞小泡向晚期内体的运输的损害是相容的。

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