A single amino acid substitution in 1918 influenza virus hemagglutinin changes receptor binding specificity

L Glaser, J Stevens, D Zamarin, IA Wilson… - Journal of …, 2005 - Am Soc Microbiol
L Glaser, J Stevens, D Zamarin, IA Wilson, A García-Sastre, TM Tumpey, CF Basler
Journal of virology, 2005Am Soc Microbiol
The receptor binding specificity of influenza viruses may be important for host restriction of
human and avian viruses. Here, we show that the hemagglutinin (HA) of the virus that
caused the 1918 influenza pandemic has strain-specific differences in its receptor binding
specificity. The A/South Carolina/1/18 HA preferentially binds the α2, 6 sialic acid (human)
cellular receptor, whereas the A/New York/1/18 HA, which differs by only one amino acid,
binds both the α2, 6 and the α2, 3 sialic acid (avian) cellular receptors. Compared to the …
Abstract
The receptor binding specificity of influenza viruses may be important for host restriction of human and avian viruses. Here, we show that the hemagglutinin (HA) of the virus that caused the 1918 influenza pandemic has strain-specific differences in its receptor binding specificity. The A/South Carolina/1/18 HA preferentially binds the α2,6 sialic acid (human) cellular receptor, whereas the A/New York/1/18 HA, which differs by only one amino acid, binds both the α2,6 and the α2,3 sialic acid (avian) cellular receptors. Compared to the conserved consensus sequence in the receptor binding site of avian HAs, only a single amino acid at position 190 was changed in the A/New York/1/18 HA. Mutation of this single amino acid back to the avian consensus resulted in a preference for the avian receptor.
American Society for Microbiology