Animal Infectious Disease Laboratory, School of Veterinary Medicine, Yangzhou University, 48 East Wenhui Road, Yangzhou, 225009, Jiangsu Province, China.
Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonosis, Yangzhou University, Yangzhou, Jiangsu, China.
Med Microbiol Immunol. 2018 Nov;207(5-6):255-269. doi: 10.1007/s00430-018-0548-z. Epub 2018 Jul 4.
PA-X, a fusion protein belonging to influenza A viruses (IAVs), integrating the N-terminal 191 amino acids of PA gene and the ribosomal frame-shifting product that lengthens out to 41 or 61 amino acids. Since its discovery in 2012, multiple functions have been attributed to this small protein, including a process, where wide-spread protein synthesis in infected host cells is shut down (called host shutoff), and viral replication, polymerase activity, viral-induced cell apoptosis, PA nuclear localization, and virulence are modulated. However, many of its proposed functions may be specific to strain, subtype, host, or cell line. In this review, we start by describing the well-defined global host-shutoff ability of PA-X and the potential mechanisms underlying it. We move on to the role played by PA-X in modulating innate and acquired immune responses in the host. We then systematically discuss the role played by PA-X in modulating the virulence of influenza viruses of different subtypes and host origins, and finish with a general overview of the research advances made in identifying the host cell partners that interact with PA-X. To uncover possible clues about the differential effects of PA-X in modulating viral virulence, we focus on systemically evaluating polymorphisms in PA-X from various viral subtypes and hosts, including avian and human H5N1, H5N6, H9N2, and H7N9 viruses. Finally, we conclude with a proposition regarding the possible future research directions for this important protein.
PA-X 是一种融合蛋白,属于甲型流感病毒(IAVs),它整合了 PA 基因的 N 端 191 个氨基酸和核糖体移码产物,延长至 41 或 61 个氨基酸。自 2012 年发现以来,这种小蛋白被赋予了多种功能,包括广泛抑制感染宿主细胞中蛋白质合成的过程(称为宿主关闭)以及病毒复制、聚合酶活性、病毒诱导的细胞凋亡、PA 核定位和毒力等功能。然而,它的许多提议的功能可能是特定于菌株、亚型、宿主或细胞系的。在这篇综述中,我们首先描述了 PA-X 明确的全球宿主关闭能力及其潜在的机制。接着,我们讨论了 PA-X 在调节宿主固有和获得性免疫反应中的作用。然后,我们系统地讨论了 PA-X 在调节不同亚型和宿主来源的流感病毒毒力中的作用,并概述了鉴定与 PA-X 相互作用的宿主细胞伙伴的研究进展。为了揭示 PA-X 在调节病毒毒力方面的差异作用的可能线索,我们重点系统评估了来自各种病毒亚型和宿主的 PA-X 中的多态性,包括禽源和人源 H5N1、H5N6、H9N2 和 H7N9 病毒。最后,我们提出了关于这个重要蛋白未来研究方向的建议。