作者: Zhi-Yong Yang , Yue Huang , Lakshmanan Ganesh , Kwanyee Leung , Wing-Pui Kong
DOI: 10.1128/JVI.78.11.5642-5650.2004
关键词:
摘要: The severe acute respiratory syndrome coronavirus (SARS-CoV) synthesizes several putative viral envelope proteins, including the spike (S), membrane (M), and small (E) glycoproteins. Although these proteins likely are essential for replication, their specific roles in SARS-CoV entry have not been defined. In this report, we show that S glycoprotein mediates through pH-dependent endocytosis. Further, define its cellular tropism demonstrate virus transmission occurs cell-mediated transfer by dendritic cells. was used successfully to pseudotype replication-defective retroviral lentiviral vectors readily infected Vero cells as well primary pulmonary renal epithelial from human, nonhuman primate, and, a lesser extent, feline species. of reporter similar wild-type, replication-competent SARS-CoV, binding purified susceptible target demonstrated flow cytometry. myeloid were able interact with bind virus, could be SARS-CoV. However, synapse-like structure. Both infection direct inhibited anti-S antisera, indicating strategies directed toward gene product confer therapeutic benefit antiviral drugs or development SARS vaccine.