4.8 Article

The 150-Loop Restricts the Host Specificity of Human H10N8 Influenza Virus

期刊

CELL REPORTS
卷 19, 期 2, 页码 235-245

出版社

CELL PRESS
DOI: 10.1016/j.celrep.2017.03.054

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资金

  1. NIH [R56 AI117675, AI114730, U54 GM094586]
  2. VENI grant from the Netherlands Organization for Scientific Research (NWO)
  3. Rubicon grant from the Netherlands Organization for Scientific Research (NWO)
  4. MEERVOUD grant from the NWO
  5. federal funds from the NIH NCI [Y1-CO-1020]
  6. NIGMS [Y1-GM-1104]
  7. US Department of Energy (DOE), Basic Energy Sciences, Office of Science [DE-AC02-06CH11357]
  8. DOE Office of Biological and Environmental Research
  9. NIH NIGMS [P41GM103393]
  10. National Center for Research Resources [P41RR001209]

向作者/读者索取更多资源

Adaptation of influenza A viruses to new hosts are rare events but are the basis for emergence of new influenza pandemics in the human population. Thus, understanding the processes involved in such events is critical for anticipating potential pandemic threats. In 2013, the first case of human infection by an avian H10N8 virus was reported, yet the H10 hemagglutinin (HA) maintains avian receptor specificity. However, the 150-loop of H10 HA, as well as related H7 and H15 subtypes, contains a two-residue insert that can potentially block human receptor binding. Mutation of the 150-loop on the background of Q226L and G228S mutations, which arose in the receptor-binding site of human pandemic H2 and H3 viruses, resulted in acquisition of human-type receptor specificity. Crystal structures of H10 HA mutants with human and avian receptor analogs, receptor-binding studies, and tissue staining experiments illustrate the important role of the 150-loop in H10 receptor specificity.

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