Laboratory of Veterinary Public Health, College of Veterinary Medicine, Chungnam National University, Daejeon, Republic of Korea.
Research Institute of Veterinary Medicine, Chungnam National University, Daejeon, Republic of Korea.
Emerg Microbes Infect. 2022 Dec;11(1):2176-2183. doi: 10.1080/22221751.2022.2114850.
Swine acute diarrhea syndrome coronavirus (SADS-CoV) was reported in China in 2017 and is a causative agent of porcine enteric disease. Recent studies indicate that cells from various hosts are susceptible to SADS-CoV, suggesting the zoonotic potential of this virus. However, little is known about the mechanisms through which this virus enters cells. In this study, we investigated the role of furin in SADS-CoV spike (S)-mediated cell - cell fusion and entry. We found that the SADS-CoV S protein induced the fusion of various cells. Cell - cell fusion was inhibited by the proprotein convertase inhibitor dec-RVKR-cmk, and between cells transfected with mutant S proteins resistant to furin cleavage. These findings revealed that furin-induced cleavage of the SADS-CoV S protein is required for cell - cell fusion. Using mutagenesis analysis, we demonstrated that furin cleaves the SADS-CoV S protein near the S1/S2 cleavage site, RYVR and AVRR. We used pseudotyped viruses to determine whether furin-induced S cleavage is also required for viral entry. Pseudotyped viruses expressing S proteins with a mutated furin cleavage site could be transduced into target cells, indicating that furin-induced cleavage is not required for pseudotyped virus entry. Our data indicate that S cleavage is critical for SADS-CoV S-mediated cell - cell fusion and suggest that furin might be a host target for SADS-CoV antivirals.
猪急性腹泻综合征冠状病毒(SADS-CoV)于 2017 年在中国被报道,是一种引起猪肠道疾病的病原体。最近的研究表明,来自各种宿主的细胞容易感染 SADS-CoV,表明该病毒具有人畜共患病的潜力。然而,对于该病毒进入细胞的机制知之甚少。在本研究中,我们研究了弗林蛋白酶在 SADS-CoV 刺突(S)介导的细胞-细胞融合和进入中的作用。我们发现 SADS-CoV S 蛋白诱导了各种细胞的融合。细胞-细胞融合被蛋白水解酶抑制剂 dec-RVKR-cmk 抑制,并且在对弗林蛋白酶切割具有抗性的突变 S 蛋白转染的细胞之间被抑制。这些发现表明,SADS-CoV S 蛋白的弗林蛋白酶诱导切割对于细胞-细胞融合是必需的。通过突变分析,我们证明弗林蛋白酶在 S1/S2 切割位点附近切割 SADS-CoV S 蛋白,RYVR 和 AVRR。我们使用假型病毒来确定弗林蛋白酶诱导的 S 切割是否也需要病毒进入。能够转导靶细胞的假型病毒表达具有突变弗林蛋白酶切割位点的 S 蛋白,表明弗林蛋白酶诱导的切割对于假型病毒进入不是必需的。我们的数据表明 S 切割对于 SADS-CoV S 介导的细胞-细胞融合至关重要,并表明弗林蛋白酶可能是 SADS-CoV 抗病毒药物的宿主靶标。