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Identification of antigenic epitopes in the haemagglutinin protein of H7 avian influenza virus
Authors:Lu Yao  Yuqing Chen  Xingbo Wang  Zhenwei Bi  Qian Xiao  Jing Lei
Institution:1. MOE Joint International Research Laboratory of Animal Health and Food Safety, Institute of Immunology, Nanjing Agricultural University, Nanjing, People’s Republic of China;2. Jiangsu Engineering Laboratory of Animal Immunology, Institute of Immunology, Nanjing Agricultural University, Nanjing, People’s Republic of China;3. Jiangsu Detection Center of Terrestrial Wildlife Disease, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, People’s Republic of China;4. Key Laboratory of Animal Virology, Ministry of Agriculture, Zhejiang University, Hangzhou, People’s Republic of China;5. Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University, Hangzhou, People’s Republic of China
Abstract:ABSTRACT

The H7 subtype avian influenza virus (AIV) has been reported to infect not only poultry but also humans. The haemagglutinin (HA) protein is the major surface antigen of AIV and plays an important role in viral infection. In this study, five monoclonal antibodies (mAbs, 2F8, 3F6, 5C11, 5E2 and 5C12) against the HA protein of H7 virus were produced and characterized. Epitope mapping indicated that 103RESGSS107 was the minimal linear epitope recognized by the mAbs 2F8/3F6/5C11, and mAbs 5E2/5C12 recognized the epitope 103-145aa. The protein sequence alignment of HA indicated that the two epitopes were not found in other subtypes of AIV, and none of the five mAbs cross-reacted with other subtypes, suggesting these mAbs are specific to H7 virus. The epitope 103RESGSS107 was highly conserved among Eurasian lineage strains of H7 AIV, whereas three amino acid substitutions (E104R, E104K and E104G) in the epitope occurred in 98.44% of North-American lineage strains. Any of these single mutations prevented the mutated epitope from being recognized by mAbs 2F8/3F6/5C11; thus, these mAbs can distinguish between Eurasian and North-American lineages of H7 strains. Furthermore, the mAbs 2F8, 3F6 and 5C11 could be highly blocked with H7-positive serum in blocking assays, revealing that 103RESGSS107 may be a dominant epitope stimulating the production of antibodies during viral infection. These results may facilitate future investigations into the structure and function of HA protein, as well as surveillance and detection of H7 virus.

RESEARCH HIGHLIGHTS
  • Five mAbs against HA protein of H7 AIV were generated and characterized.

  • Two novel epitopes 103RESGSS107 and 103-145aa were identified.

  • The epitope 103RESGSS107 differs between Eurasian and North-American lineages.

  • The mAbs 2F8, 3F6 and 5C11 could distinguish two lineages of H7 strains.

Keywords:Avian influenza virus  monoclonal antibody  H7  epitope  haemagglutinin  identification
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