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作 者:Dandi Li Mengxuan Wang Tongyao Mao Mingwen Wang Qing Zhang Hong Wang Lili Pang Xiaoman Sun Zhaojun Duan
机构地区:[1]National Health Commission Key Laboratory for Medical Virology and Viral Diseases,Beijing 102206,China [2]National Institute for Viral Disease Control and Prevention,China CDC,Beijing 102206,China
出 处:《Virologica Sinica》2021年第5期1187-1196,共10页中国病毒学(英文版)
基 金:the participation of the ProteinGlycan Interaction Resource of the CFG(supporting grant R24 GM098791);the National Center for Functional Glycomics(NCFG)at Beth Israel Deaconess Medical Center,Harvard Medical School(supporting grant P41 GM103694);supported by grants from the National Natural Science Foundation of China(NSFC)(No.21934005);National Key Research and Development Program of China(2018YFC1200602)。
摘 要:P[3]rotavirus(RV)has been identified in many species,including human,simian,dog,and bat.Several glycans,including sialic acid,histo-blood group antigens(HBGAs)are reported as RV attachment factors.The glycan binding specificity of different P[3]RV VP8*s were investigated in this study.Human HCR3 A and dog P[3]RV VP8*s recognized glycans with terminal sialic acid and hemagglutinated the red blood cells,while bat P[3]VP8*showed neither binding to glycans nor hemagglutination.However,the bat P[3]VP8*mutant of C189 Y obtained the ability to hemagglutinate the red blood cells,while human P[3]HCR3 A/M2-102 mutants of Y189 C lost the ability.Sequence alignment and structural analysis indicated that residue 189 played an important role in the ligand recognition and may contribute to the cross-species transmission.Structural superimposition exhibited that bat P[3]VP8*model was quite different from the simian P[3]Rhesus rotavirus(RRV)P[3]VP8*,indicating that bat P[3]RV was relatively distinct and partially contributed to the no binding to tested glycans.These results promote our understanding of P[3]VP8*/glycans interactions and the potential transmission of bat/human P[3]RVs,offering more insight into the RV infection and prevalence.
关 键 词:Bat rotavirus VP8* Glycan binding specificity HEMAGGLUTINATION Sialic acid
分 类 号:R373[医药卫生—病原生物学]
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