Department of Virology and Parasitology, Fujita Health University School of Medicine, Aichi, Japan.
EMBO J. 2012 Feb 1;31(3):754-66. doi: 10.1038/emboj.2011.429. Epub 2011 Nov 29.
Phosphatidylinositol 4-kinase IIIβ (PI4KB) is a host factor required for genome RNA replication of enteroviruses, small non-enveloped viruses belonging to the family Picornaviridae. Here, we demonstrated that PI4KB is also essential for genome replication of another picornavirus, Aichi virus (AiV), but is recruited to the genome replication sites by a different strategy from that utilized by enteroviruses. AiV non-structural proteins, 2B, 2BC, 2C, 3A, and 3AB, interacted with a Golgi protein, acyl-coenzyme A binding domain containing 3 (ACBD3). Furthermore, we identified previously unknown interaction between ACBD3 and PI4KB, which provides a novel manner of Golgi recruitment of PI4KB. Knockdown of ACBD3 or PI4KB suppressed AiV RNA replication. The viral proteins, ACBD3, PI4KB, and phophatidylinositol-4-phosphate (PI4P) localized to the viral RNA replication sites. AiV replication and recruitment of PI4KB to the RNA replication sites were not affected by brefeldin A, in contrast to those in enterovirus infection. These results indicate that a viral protein/ACBD3/PI4KB complex is formed to synthesize PI4P at the AiV RNA replication sites and plays an essential role in viral RNA replication.
磷脂酰肌醇 4-激酶 IIIβ(PI4KB)是肠道病毒(属于小 RNA 病毒科的无包膜病毒)基因组 RNA 复制所必需的宿主因子。在这里,我们证明 PI4KB 对于另一种小 RNA 病毒——Aichi 病毒(AiV)的基因组复制也是必需的,但它被招募到基因组复制位点的策略与肠道病毒不同。AiV 的非结构蛋白 2B、2BC、2C、3A 和 3AB 与一种高尔基蛋白酰基辅酶 A 结合域包含 3(ACBD3)相互作用。此外,我们鉴定了之前未知的 ACBD3 和 PI4KB 之间的相互作用,这为 PI4KB 的高尔基招募提供了一种新方式。ACBD3 或 PI4KB 的敲低抑制了 AiV RNA 复制。病毒蛋白、ACBD3、PI4KB 和磷酸肌醇-4-磷酸(PI4P)定位于病毒 RNA 复制位点。与肠道病毒感染不同,Brefeldin A 对 AiV 复制和 PI4KB 向 RNA 复制位点的招募没有影响。这些结果表明,病毒蛋白/ACBD3/PI4KB 复合物的形成是为了在 AiV RNA 复制位点合成 PI4P,并在病毒 RNA 复制中发挥重要作用。