代谢干扰通过抑制vRNA合成损害甲型流感病毒的复制。

Jens Kleinehr, Chiara Robin Bojarzyn, Michael Schöfbänker, Katharina Daniel, Stephan Ludwig, Eike R Hrincius
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引用次数: 0

摘要

为了复制,病毒利用宿主细胞的代谢来合成病毒成分。最近,我们可以证明糖酵解的抑制通过损害病毒聚合酶作为转录酶或复制酶的调节来干扰IAV复制。在这里,我们研究了与糖酵解直接或间接相关的其他代谢途径是如何影响IAV复制和聚合酶调控的。因此,我们抑制了谷氨酰胺水解、脂肪酸合成(FAS)、氧化磷酸化(OXPHOS)和戊糖磷酸途径(PPP)。抑制这些代谢途径导致病毒滴度显著降低。此外,对谷氨酰胺解酶、FAS和OXPHOS的抑制使细胞糖酵解和呼吸网络不平衡,导致病毒转录期延长,而复制明显减少。我们的数据表明,影响细胞糖酵解和呼吸平衡会损害病毒聚合酶的动态调节,导致病毒基因组RNA和病毒颗粒的合成减少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolic interference impairs influenza A virus replication by dampening vRNA synthesis.

For replication, viruses exploit the host cell metabolism for biosynthesis of viral components. Recently, we could show that inhibition of glycolysis interfered with IAV replication by impairing the regulation of the viral polymerase as a transcriptase or replicase. Here, we investigated how IAV replication and polymerase regulation is influenced by other metabolic pathways which are directly or indirectly linked to glycolysis. Therefore, we inhibited glutaminolysis, fatty acid synthesis (FAS), oxidative phosphorylation (OXPHOS), and the pentose phosphate pathway (PPP). Inhibition of these metabolic pathways led to a significant reduction of viral titers. Furthermore, the inhibition of glutaminolysis, FAS and OXPHOS unbalanced the cellular glycolysis and respiration network leading to a prolonged phase of viral transcription while replication was strongly decreased. Our data indicate that affecting the cellular glycolysis and respiration balance impairs the dynamic regulation of the viral polymerase, resulting in reduced synthesis of viral genomic RNA and viral particles.

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