Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, 393 Middle Huaxia Road, Shanghai 201210, China.
School of Life Science and Technology, ShanghaiTech University, 393 Middle Huaxia Road, Shanghai 201210, China.
Viruses. 2024 Feb 9;16(2):272. doi: 10.3390/v16020272.
Cross-species spillover to humans of coronaviruses (CoVs) from wildlife animal reservoirs poses marked and global threats to human and animal health. Recently, sporadic infection of canine coronavirus-human pneumonia-2018 (CCoV-HuPn-2018) in hospitalized patients with pneumonia genetically related to canine and feline coronavirus were identified. In addition, swine acute diarrhea syndrome coronavirus (SADS-CoV) had the capability of broad tropism to cultured cells including from humans. Together, the transmission of Alphacoronaviruses that originated in wildlife to humans via intermediate hosts was responsible for the high-impact emerging zoonosis. Entry of CoV is mainly mediated by Spike and formation of a typical six helix bundle (6-HB) structure in the postfusion state of Spike is pivotal. Here, we present the complete fusion core structures of CCoV-HuPn-2018 and SADS-CoV from Alphacoronavirus at 2.10 and 2.59 Å, respectively. The overall structure of the CCoV-HuPn-2018 fusion core is similar to Alphacoronavirus like HCoV-229E, while SADS-CoV is analogous to Betacoronavirus like SARS-CoV-2. Collectively, we provide a structural basis for the development of pan-CoV small molecules and polypeptides based on the HR1-HR2 complex, concerning CCoV-HuPn-2018 and SADS-CoV.
跨物种从野生动物动物库溢出到人类的冠状病毒 (CoVs) 对人类和动物健康构成显著的全球威胁。最近,在与犬冠状病毒-人类肺炎-2018(CCoV-HuPn-2018)相关的住院肺炎患者中鉴定出了与犬和猫冠状病毒有关的散发性感染。此外,猪急性腹泻综合征冠状病毒(SADS-CoV)具有广泛的嗜性,可以感染包括人类在内的培养细胞。总之,源自野生动物的 Alphacoronaviruses 通过中间宿主传播到人类,导致了高影响的新兴人畜共患病。CoV 的进入主要是由 Spike 介导的, Spike 在融合后状态下形成典型的六螺旋束(6-HB)结构至关重要。在这里,我们以 2.10 和 2.59 Å 的分辨率呈现了来自 Alphacoronavirus 的 CCoV-HuPn-2018 和 SADS-CoV 的完整融合核心结构。CCoV-HuPn-2018 融合核心的整体结构类似于 Alphacoronavirus 样 HCoV-229E,而 SADS-CoV 则类似于 Betacoronavirus 样 SARS-CoV-2。总的来说,我们为基于 HR1-HR2 复合物的泛 CoV 小分子和多肽的开发提供了结构基础,涉及 CCoV-HuPn-2018 和 SADS-CoV。