Neu5Gc binding loss of subtype H7 influenza A virus facilitates adaptation to gallinaceous poultry following transmission from waterbirds

Author:

Guan Minhui123ORCID,DeLiberto Thomas J.4ORCID,Feng Aijing123,Zhang Jieze5,Li Tao6,Wang Shuaishuai7,Li Lei7,Killian Mary Lea8,Praena Beatriz123,Giri Emily123,Deliberto Shelagh T.4,Hang Jun6,Olivier Alicia9,Torchetti Mia Kim8,Tao Yizhi Jane10ORCID,Parrish Colin11ORCID,Wan Xiu-Feng12312ORCID

Affiliation:

1. Center for Influenza and Emerging Infectious Diseases (CIEID), University of Missouri, Columbia, Missouri, USA

2. Department of Molecular Microbiology and Immunology, School of Medicine, University of Missouri, Columbia, Missouri, USA

3. Bond Life Sciences Center, University of Missouri, Columbia, Missouri, USA

4. US Department of Agriculture Animal and Plant Health Inspection Service, Fort Collins, Colorado, USA

5. Department of Bioengineering, Rice University, Houston, Texas, USA

6. Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA

7. Department of Chemistry and Center for Diagnostics and Therapeutics, Georgia State University, Atlanta, Georgia, USA

8. National Veterinary Services Laboratories, Veterinary Services, U.S. Department of Agriculture, Ames, Iowa, USA

9. Department of Pathobiology and Population Medicine, College of Veterinary Medicine, Mississippi State University, Mississippi State, Mississippi, USA

10. Department of BioSciences, Rice University, Houston, Texas, USA

11. Department of Microbiology and Immunology, College of Veterinary Medicine, Baker Institute for Animal Health, Cornell University, Ithaca, New York, USA

12. Department of Electrical Engineering and Computer Science, College of Engineering, University of Missouri, Columbia, Missouri, USA

Abstract

ABSTRACT Between 2013 and 2018, the novel A/Anhui/1/2013 (AH/13)-lineage H7N9 virus caused at least five waves of outbreaks in humans, totaling 1,567 confirmed human cases in China. Surveillance data indicated a disproportionate distribution of poultry infected with this AH/13-lineage virus, and laboratory experiments demonstrated that this virus can efficiently spread among chickens but not among Pekin ducks. The underlying mechanism of this selective transmission remains unclear. In this study, we demonstrated the absence of Neu5Gc expression in chickens across all respiratory and gastrointestinal tissues. However, Neu5Gc expression varied among different duck species and even within the tissues of the same species. The AH/13-lineage viruses exclusively bind to acetylneuraminic acid (Neu5Ac), in contrast to wild waterbird H7 viruses that bind both Neu5Ac and N-glycolylneuraminic acid (Neu5Gc). The level of Neu5Gc expression influences H7 virus replication and facilitates adaptive mutations in these viruses. In summary, our findings highlight the critical role of Neu5Gc in affecting the host range and interspecies transmission dynamics of H7 viruses among avian species. IMPORTANCE Migratory waterfowl, gulls, and shorebirds are natural reservoirs for influenza A viruses (IAVs) that can occasionally spill over to domestic poultry, and ultimately humans. This study showed wild-type H7 IAVs from waterbirds initially bind to glycan receptors terminated with N-acetylneuraminic acid (Neu5Ac) or N-glycolylneuraminic acid (Neu5Gc). However, after enzootic transmission in chickens, the viruses exclusively bind to Neu5Ac. The absence of Neu5Gc expression in gallinaceous poultry, particularly chickens, exerts selective pressure, shaping IAV populations, and promoting the acquisition of adaptive amino acid substitutions in the hemagglutinin protein. This results in the loss of Neu5Gc binding and an increase in virus transmissibility in gallinaceous poultry, particularly chickens. Consequently, the transmission capability of these poultry-adapted H7 IAVs in wild water birds decreases. Timely intervention, such as stamping out, may help reduce virus adaptation to domestic chicken populations and lower the risk of enzootic outbreaks, including those caused by IAVs exhibiting high pathogenicity.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

Welch Foundation

National Science Foundation

Publisher

American Society for Microbiology

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