Takano Tomomi, Wakayama Yumeho, Doki Tomoyoshi
Laboratory of Veterinary Infectious Disease, School of Veterinary Medicine, Kitasato University, Towada, Aomori 034-8628, Japan.
Pathogens. 2019 Dec 16;8(4):300. doi: 10.3390/pathogens8040300.
Feline coronavirus (FCoV) is a pathogen causing a lethal infectious disease in cats, feline infectious peritonitis. It has two serotypes (type I FCoV and type II FCoV). According to our previous study, type I FCoV infection is inhibited by compounds inducing intracellular cholesterol accumulation, whereas type II FCoV infection is not inhibited. Intracellular cholesterol accumulation was reported to disrupt late endosome function. Based on these findings, types I and II FCoV are considered to enter the cytosol through late and early endosomes, respectively. We investigated whether the antiviral activities of a late endosome trafficking inhibitor and cholesterol-accumulating agents are different between the FCoV serotypes. The late endosome trafficking inhibitor did not inhibit type II FCoV infection, but it inhibited type I FCoV infection. Type I FCoV infection was inhibited by cholesterol-accumulating triazoles, but not by non-cholesterol-accumulating triazoles. These phenomena were observed in both feline cell lines and feline primary macrophages. This study provides additional information on the differences in intracellular reproductive cycle between type I and type II FCoV.
猫冠状病毒(FCoV)是一种可导致猫致命性传染病——猫传染性腹膜炎的病原体。它有两种血清型(I型FCoV和II型FCoV)。根据我们之前的研究,诱导细胞内胆固醇积累的化合物可抑制I型FCoV感染,而II型FCoV感染则不受抑制。据报道,细胞内胆固醇积累会破坏晚期内体功能。基于这些发现,I型和II型FCoV被认为分别通过晚期和早期内体进入细胞质。我们研究了晚期内体运输抑制剂和胆固醇积累剂对不同FCoV血清型的抗病毒活性是否存在差异。晚期内体运输抑制剂不抑制II型FCoV感染,但可抑制I型FCoV感染。积累胆固醇的三唑类化合物可抑制I型FCoV感染,但不积累胆固醇的三唑类化合物则无此作用。在猫细胞系和猫原代巨噬细胞中均观察到了这些现象。本研究为I型和II型FCoV细胞内复制周期的差异提供了更多信息。