Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Pathogen-Associated Malignancies Integrated Research Center (PAM IRC), Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
PLoS Pathog. 2024 Jul 29;20(7):e1012170. doi: 10.1371/journal.ppat.1012170. eCollection 2024 Jul.
While Merkel cell polyomavirus (MCPyV or MCV) is an abundant virus frequently shed from healthy skin, it is one of the most lethal tumor viruses in immunocompromised individuals, highlighting the crucial role of host immunity in controlling MCPyV oncogenic potential. Despite its prevalence, very little is known about how MCPyV interfaces with the host immune response to maintain asymptomatic persistent infection and how inadequate control of MCPyV infection triggers MCC tumorigenesis. In this study, we discovered that the MCPyV protein, known as the Alternative Large Tumor Open Reading Frame (ALTO), also referred to as middle T, effectively primes and activates the STING signaling pathway. It recruits Src kinase into the complex of STING downstream kinase TBK1 to trigger its autophosphorylation, which ultimately activates the subsequent antiviral immune response. Combining single-cell analysis with both loss- and gain-of-function studies of MCPyV infection, we demonstrated that the activity of ALTO leads to a decrease in MCPyV replication. Thus, we have identified ALTO as a crucial viral factor that modulates the STING-TBK1 pathway, creating a negative feedback loop that limits viral infection and maintains a delicate balance with the host immune system. Our study reveals a novel mechanism by which a tumorigenic virus-encoded protein can link Src function in cell proliferation to the activation of innate immune signaling, thereby controlling viral spread, and sustaining persistent infection. Our previous findings suggest that STING also functions as a tumor suppressor in MCPyV-driven oncogenesis. This research provides a foundation for investigating how disruptions in the finely tuned virus-host balance, maintained by STING, could alter the fate of MCPyV infection, potentially encouraging malignancy.
Merkel 细胞多瘤病毒(MCPyV 或 MCV)是一种在健康皮肤中经常脱落的丰富病毒,但它是免疫功能低下个体中最致命的肿瘤病毒之一,这突显了宿主免疫在控制 MCPyV 致癌潜力方面的关键作用。尽管 MCPyV 很普遍,但人们对其如何与宿主免疫反应相互作用以维持无症状持续性感染以及宿主免疫反应控制不足如何引发 MCC 肿瘤发生知之甚少。在这项研究中,我们发现 MCPyV 蛋白,称为替代大肿瘤开放阅读框(ALTO),也称为中 T,有效地启动和激活 STING 信号通路。它将Src 激酶募集到 STING 下游激酶 TBK1 的复合物中,触发其自身磷酸化,从而最终激活随后的抗病毒免疫反应。我们结合单细胞分析以及 MCPyV 感染的功能丧失和获得功能研究,证明了 ALTO 的活性导致 MCPyV 复制减少。因此,我们确定 ALTO 是一种关键的病毒因子,可调节 STING-TBK1 途径,形成负反馈回路,限制病毒感染并与宿主免疫系统保持微妙平衡。我们的研究揭示了一种新的机制,即致癌病毒编码蛋白可以将细胞增殖中的 Src 功能与先天免疫信号的激活联系起来,从而控制病毒的传播并维持持续性感染。我们之前的研究结果表明,STING 也在 MCPyV 驱动的肿瘤发生中作为肿瘤抑制因子发挥作用。这项研究为研究 STING 维持的精细病毒-宿主平衡的破坏如何改变 MCPyV 感染的命运,从而可能促进恶性肿瘤提供了基础。