Diversity of Functionally Permissive Sequences in the Receptor-Binding Site of Influenza Hemagglutinin

Cell Host Microbe. 2017 Jun 14;21(6):742-753.e8. doi: 10.1016/j.chom.2017.05.011.

Abstract

Influenza A virus hemagglutinin (HA) initiates viral entry by engaging host receptor sialylated glycans via its receptor-binding site (RBS). The amino acid sequence of the RBS naturally varies across avian and human influenza virus subtypes and is also evolvable. However, functional sequence diversity in the RBS has not been fully explored. Here, we performed a large-scale mutational analysis of the RBS of A/WSN/33 (H1N1) and A/Hong Kong/1/1968 (H3N2) HAs. Many replication-competent mutants not yet observed in nature were identified, including some that could escape from an RBS-targeted broadly neutralizing antibody. This functional sequence diversity is made possible by pervasive epistasis in the RBS 220-loop and can be buffered by avidity in viral receptor binding. Overall, our study reveals that the HA RBS can accommodate a much greater range of sequence diversity than previously thought, which has significant implications for the complex evolutionary interrelationships between receptor specificity and immune escape.

Keywords: X-ray crystallography; deep mutational scanning; epistasis; evolution; hemagglutinin; immune escape; influenza A virus; receptor-binding site; sequence diversity.

MeSH terms

  • Amino Acid Sequence
  • Antibodies, Viral / immunology
  • Antigenic Variation / genetics
  • Antigenic Variation / immunology
  • Antigens, Viral / genetics
  • Base Sequence
  • Binding Sites / genetics*
  • Binding Sites / immunology
  • Crystallography, X-Ray / instrumentation
  • Evolution, Molecular
  • HEK293 Cells
  • Hemagglutinin Glycoproteins, Influenza Virus / chemistry
  • Hemagglutinin Glycoproteins, Influenza Virus / genetics*
  • Hemagglutinin Glycoproteins, Influenza Virus / immunology
  • Humans
  • Immune Evasion*
  • Influenza A Virus, H1N1 Subtype / genetics*
  • Influenza A Virus, H1N1 Subtype / immunology
  • Influenza A Virus, H3N2 Subtype / genetics*
  • Influenza A Virus, H3N2 Subtype / immunology
  • Influenza, Human / virology
  • Mutation
  • Protein Conformation
  • Receptors, Virus / genetics*
  • Receptors, Virus / immunology
  • Sequence Analysis
  • Virus Internalization

Substances

  • Antibodies, Viral
  • Antigens, Viral
  • Hemagglutinin Glycoproteins, Influenza Virus
  • Receptors, Virus