Clinic for Gastroenterology, Hepatology and Infectiology, Medical Faculty, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany.
Institute for Pharmaceutical and Medicinal Chemistry, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany.
Viruses. 2021 Mar 18;13(3):504. doi: 10.3390/v13030504.
Non-human primates (NHP) are an important source of viruses that can spillover to humans and, after adaptation, spread through the host population. Whereas HIV-1 and HTLV-1 emerged as retroviral pathogens in humans, a unique class of retroviruses called foamy viruses (FV) with zoonotic potential are occasionally detected in bushmeat hunters or zookeepers. Various FVs are endemic in numerous mammalian natural hosts, such as primates, felines, bovines, and equines, and other animals, but not in humans. They are apathogenic, and significant differences exist between the viral life cycles of FV and other retroviruses. Importantly, FVs replicate in the presence of many well-defined retroviral restriction factors such as TRIM5α, BST2 (Tetherin), MX2, and APOBEC3 (A3). While the interaction of A3s with HIV-1 is well studied, the escape mechanisms of FVs from restriction by A3 is much less explored. Here we review the current knowledge of FV biology, host restriction factors, and FV-host interactions with an emphasis on the consequences of FV regulatory protein Bet binding to A3s and outline crucial open questions for future studies.
非人类灵长类动物(NHP)是一种重要的病毒来源,可以溢出到人类,并在适应后在宿主群体中传播。虽然 HIV-1 和 HTLV-1 作为人类中的逆转录病毒病原体出现,但一类具有动物源性的称为泡沫病毒(FV)的独特逆转录病毒偶尔会在狩猎者或动物园管理员的野味中被检测到。各种 FV 在许多哺乳动物的自然宿主中流行,如灵长类动物、猫科动物、牛科动物和马科动物以及其他动物,但在人类中不存在。它们是无致病性的,FV 与其他逆转录病毒的病毒生命周期存在显著差异。重要的是,FV 在许多明确定义的逆转录病毒限制因子(如 TRIM5α、BST2(Tetherin)、MX2 和 APOBEC3(A3))的存在下复制。虽然 A3 与 HIV-1 的相互作用研究得很好,但 FV 逃避 A3 限制的机制研究得较少。本文综述了 FV 生物学、宿主限制因子以及 FV-宿主相互作用的最新知识,重点介绍了 FV 调节蛋白 Bet 与 A3 结合的后果,并概述了未来研究的关键问题。