Middle East respiratory syndrome coronavirus and bat coronavirus HKU9 both can utilize GRP78 for attachment onto host cells
Hin ChuDepartments of Microbiology andChe-Man ChanDepartments of Microbiology andXi ZhangDepartments of Microbiology andYixin WangDepartments of Microbiology andShuofeng YuanDepartments of Microbiology andJie ZhouDepartments of Microbiology andRex Au-YeungPathologyKong‐Hung SzeDepartments of Microbiology andDong YangDepartments of Microbiology andHuiping ShuaiDepartments of Microbiology andYuxin HouDepartments of Microbiology andCun LiDepartments of Microbiology andXiaoyu ZhaoDepartments of Microbiology andVincent Kwok‐Man PoonDepartments of Microbiology andSze LeungDepartments of Microbiology andMan Lung YeungCarol Yu Centre for InfectionJinghua Yanthe CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101Guangwen Luthe West China Hospital Emergency Department, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, and Collaborative Innovation Center of Biotherapy, Chengdu, Sichuan 610041, andDong‐Yan JinSchool of Biomedical Sciences, andGeorge F. Gaothe CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101Jasper Fuk‐Woo ChanCarol Yu Centre for InfectionKwok‐Yung YuenCarol Yu Centre for Infection
2018en
ABI
Аннотация
, the lineage C MERS-CoV and the lineage D bCoV-HKU9. The capacity of GRP78 to facilitate surface attachment of both a human coronavirus and a phylogenetically related bat coronavirus exemplifies the need for continuous surveillance of the evolution of animal coronaviruses to monitor their potential for human adaptations.
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