Functional Analysis of Sulfatide in Influenza A Virus Infection and Replication

Methods Mol Biol. 2022:2556:97-122. doi: 10.1007/978-1-0716-2635-1_9.

Abstract

3-O-sulfation synthesizes sulfatide in the galactose moiety of galactosylceramide. Sulfatide is expressed in many organs such as the gastrointestinal tract, trachea, kidney, and central nervous system. Influenza A virus binds not only to glycoconjugates terminally containing sialic acid as a viral binding receptor but also to sulfatide not containing sialic acid. On the surface of infected cells, the envelope glycoprotein hemagglutinin of influenza A virus interacts with sulfatide. This interaction enhances the nuclear export of viral ribonucleoprotein complexes, resulting in efficient progeny viruses. Inhibiting this interaction would be a new potent anti-influenza drug that suppresses the progeny virus production in the infected cells.

Keywords: Baculovirus protein expression system; Hemagglutinin; Influenza virus; Sulfatide; Virus replication.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Galactose
  • Galactosylceramides
  • Glycoproteins
  • Hemagglutinins
  • Humans
  • Influenza A virus*
  • Influenza, Human*
  • N-Acetylneuraminic Acid
  • Receptors, Virus
  • Ribonucleoproteins
  • Sulfoglycosphingolipids

Substances

  • Galactosylceramides
  • Glycoproteins
  • Hemagglutinins
  • Receptors, Virus
  • Ribonucleoproteins
  • Sulfoglycosphingolipids
  • N-Acetylneuraminic Acid
  • Galactose