The S128N mutation combined with an additional potential N-linked glycosylation site at residue 133 in hemagglutinin affects the antigenicity of the human H7N9 virus

Wanli LiuThe Center for Disease Control and Prevention, Urumqi, Xinjiang Uygur Autonomous Region830001, China

Tian BaiNational Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention, Key Laboratory for Medical Virology, National Health and Family Planning Commission, Beijing102206, China

Jinlei GuoNational Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention, Key Laboratory for Medical Virology, National Health and Family Planning Commission, Beijing102206, China

Xinlan LiThe Center for Disease Control and Prevention, Urumqi, Xinjiang Uygur Autonomous Region830001, China

Lei YangNational Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention, Key Laboratory for Medical Virology, National Health and Family Planning Commission, Beijing102206, China

Xiaojun WangThe Center for Disease Control and Prevention, Urumqi, Xinjiang Uygur Autonomous Region830001, China

Junfeng GuoNational Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention, Key Laboratory for Medical Virology, National Health and Family Planning Commission, Beijing102206, China

Xin MaThe Center for Disease Control and Prevention, Urumqi, Xinjiang Uygur Autonomous Region830001, China

Xiyan LiNational Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention, Key Laboratory for Medical Virology, National Health and Family Planning Commission, Beijing102206, China

Hongbin LiuThe Center for Disease Control and Prevention, Urumqi, Xinjiang Uygur Autonomous Region830001, China

Jianfang ZhouNational Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention, Key Laboratory for Medical Virology, National Health and Family Planning Commission, Beijing102206, China

Dayan WangNational Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention, Key Laboratory for Medical Virology, National Health and Family Planning Commission, Beijing102206, China

Yue-Long ShuNational Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention, Key Laboratory for Medical Virology, National Health and Family Planning Commission, Beijing102206, ChinaCorrespondence[email protected]

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The S128N mutation combined with an additional potential N-linked glycosylation site at residue 133 in hemagglutinin affects the antigenicity of the human H7N9 virus

Table 1 Hemagglutination inhibition reactions of reassortant viruses containing single or multiple mutations

Supplementary Table S1

Supplementary Table S2

Supplementary Table S3

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The S128N mutation combined with an additional potential N-linked glycosylation site at residue 133 in hemagglutinin affects the antigenicity of the human H7N9 virus

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Table 1 Hemagglutination inhibition reactions of reassortant viruses containing single or multiple mutations

Supplementary Table S1

Supplementary Table S2

Supplementary Table S3

Related Research Data

Related research

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