Kim Jinsun, Shin Cha-Gyun
Department of Systems Biotechnology, Chung-Ang University, Ansung, Republic of Korea.
Anim Cells Syst (Seoul). 2020 Sep 15;24(5):282-288. doi: 10.1080/19768354.2020.1819413.
Interferon-induced transmembrane (IFITM) proteins as host restriction factors are known to inhibit the replication of several viruses. In this study, transient IFITM expression vectors were used to investigate whether IFITMs inhibit feline foamy viral (FFV) replication and which step of viral replication is inhibited. In our studies, viral production was significantly reduced when cells were infected with FFV at almost same times such as -3, 0, or 3 h post-transfection with IFITM vector. However viral production was not reduced even though cells were infected with FFV at 3 or 6 days post-transfection when production of IFITM proteins was maximized. Considering that IFITM expression was maximized at 3 days post-transfection, the stage of viral replication inhibited by IFITM appears to be the late step of viral replication. Moreover, the viral Gag proteins detected in the virus-infected cell lysates were proportionally correlated with viral titer of the culture supernatants. Therefore, it is likely that IFITMs can restrict production of FFV at the late step of viral replication.
干扰素诱导跨膜(IFITM)蛋白作为宿主限制因子,已知可抑制多种病毒的复制。在本研究中,使用瞬时IFITM表达载体来研究IFITM是否抑制猫泡沫病毒(FFV)复制以及抑制病毒复制的哪个步骤。在我们的研究中,当细胞在转染IFITM载体后几乎相同的时间(如转染后-3、0或3小时)感染FFV时,病毒产生显著减少。然而,当IFITM蛋白产生最大化时,即使细胞在转染后3或6天感染FFV,病毒产生也没有减少。考虑到IFITM表达在转染后3天最大化,IFITM抑制的病毒复制阶段似乎是病毒复制的后期步骤。此外,在病毒感染细胞裂解物中检测到的病毒Gag蛋白与培养上清液的病毒滴度呈比例相关。因此,IFITM很可能在病毒复制后期限制FFV的产生。