Literature DB >> 27062579

1918 Influenza receptor binding domain variants bind and replicate in primary human airway cells regardless of receptor specificity.

A Sally Davis1, Daniel S Chertow2, Jason Kindrachuk3, Li Qi4, Louis M Schwartzman4, Jon Suzich2, Sara Alsaaty3, Carolea Logun3, James H Shelhamer3, Jeffery K Taubenberger5.   

Abstract

The 1918 influenza pandemic caused ~50 million deaths. Many questions remain regarding the origin, pathogenicity, and mechanisms of human adaptation of this virus. Avian-adapted influenza A viruses preferentially bind α2,3-linked sialic acids (Sia) while human-adapted viruses preferentially bind α2,6-linked Sia. A change in Sia preference from α2,3 to α2,6 is thought to be a requirement for human adaptation of avian influenza viruses. Autopsy data from 1918 cases, however, suggest that factors other than Sia preference played a role in viral binding and entry to human airway cells. Here, we evaluated binding and entry of five 1918 influenza receptor binding domain variants in a primary human airway cell model along with control avian and human influenza viruses. We observed that all five variants bound and entered cells efficiently and that Sia preference did not predict entry of influenza A virus to primary human airway cells evaluated in this model. Published by Elsevier Inc.

Entities:  

Keywords:  Hemagglutinin; Influenza A virus; Pandemic; Receptor binding

Mesh:

Substances:

Year:  2016        PMID: 27062579      PMCID: PMC4949484          DOI: 10.1016/j.virol.2016.03.025

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  34 in total

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Journal:  J Histochem Cytochem       Date:  2015-01-20       Impact factor: 2.479

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7.  Influenza virus receptor specificity and cell tropism in mouse and human airway epithelial cells.

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Authors:  John C Kash; Kathie-Anne Walters; A Sally Davis; Aline Sandouk; Louis M Schwartzman; Brett W Jagger; Daniel S Chertow; Qi Li; Rolf E Kuestner; Adrian Ozinsky; Jeffery K Taubenberger
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