Recognition of N -Glycolylneuraminic Acid Linked to Galactose by the α2,3 Linkage Is Associated with Intestinal Replication of Influenza A Virus in Ducks

Author:

Ito Toshihiro1,Suzuki Yasuo2,Suzuki Takashi2,Takada Ayato3,Horimoto Taisuke4,Wells Krisna5,Kida Hiroshi3,Otsuki Koichi1,Kiso Makoto6,Ishida Hideharu6,Kawaoka Yoshihiro75

Affiliation:

1. Department of Veterinary Public Health, Faculty of Agriculture, Tottori University, Tottori 680-8553,1

2. Department of Biochemistry, University of Shizuoka, School of Pharmaceutical Science, Shizuoka 422-8002,2

3. Laboratory of Microbiology, Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo 060-0818,3

4. Department of Veterinary Microbiology, College of Agriculture, Osaka Prefecture University, Sakai 599-6231,4

5. Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin—Madison, Madison, Wisconsin 537065

6. Department of Applied Bioorganic Chemistry, Gifu University, Gifu 501-1193,6 and

7. Institute of Medical Science, University of Tokyo, Minato-ku, Tokyo 108-8639,7 and

Abstract

ABSTRACT The hemagglutinin (HA) of H3 human influenza viruses does not support viral replication in duck intestine despite its avian origin. A Leu-to-Gln mutation at position 226 and a Ser-to-Gly mutation at position 228 in the HA of human A/Udorn/307/72 (H3N2) permit a reassortant virus [human Udorn HA, with all other genes from A/mallard/New York/6750/78 (H2N2)] to replicate in ducks. To understand the molecular basis of this change in host range restriction, we investigated the receptor specificity of duck influenza viruses as well as of human-duck virus reassortants. The results indicate that the recognition of a glycoconjugate moiety possessing N -glycolneuramic acid (NeuGc) linked to galactose by the α2,3 linkage (NeuGcα2,3Gal) is associated with viral replication in duck intestine. Immunofluorescence assays with NeuGcα2,3Gal-specific antiserum detected this moiety primarily on the crypt epithelial cells of duck colon. Such recognition, together with biochemical evidence of NeuGc in crypt cells, correlated exactly with the ability of the virus to replicate in duck colon. These results suggest that recognition of the NeuGcα2,3-Gal moiety plays an important role in the enterotropism of avian influenza viruses.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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