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Species specific differences in use of ANP32 proteins by influenza A virus

Long, JS; Idoko-Akoh, A; Mistry, B; Goldhill, D; Staller, E; Schreyer, J; Ross, C; Goodbourn, S; Shelton, H; Skinner, MA; et al. Long, JS; Idoko-Akoh, A; Mistry, B; Goldhill, D; Staller, E; Schreyer, J; Ross, C; Goodbourn, S; Shelton, H; Skinner, MA; Sang, H; McGrew, MJ; Barclay, W (2019) Species specific differences in use of ANP32 proteins by influenza A virus. Elife, 8. e45066. ISSN 2050-084X https://doi.org/10.7554/eLife.45066
SGUL Authors: Goodbourn, Stephen Edward Ross, Craig Stephen

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Abstract

Influenza A viruses (IAV) are subject to species barriers that prevent frequent zoonotic transmission and pandemics. One of these barriers is the poor activity of avian IAV polymerases in human cells. Differences between avian and mammalian ANP32 proteins underlie this host range barrier. Human ANP32A and ANP32B homologues both support function of human-adapted influenza polymerase but do not support efficient activity of avian IAV polymerase which requires avian ANP32A. We show here that the gene currently designated as avian ANP32B is evolutionarily distinct from mammalian ANP32B, and that chicken ANP32B does not support IAV polymerase activity even of human-adapted viruses. Consequently, IAV relies solely on chicken ANP32A to support its replication in chicken cells. Amino acids 129I and 130N, accounted for the inactivity of chicken ANP32B. Transfer of these residues to chicken ANP32A abolished support of IAV polymerase. Understanding ANP32 function will help develop antiviral strategies and aid the design of influenza virus resilient genome edited chickens.

Item Type: Article
Additional Information: © 2019, Long et al. This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use and redistribution provided that the original author and source are credited.
Keywords: ANP32A, ANP32B, Influenza, chicken, gene editing, human, infectious disease, microbiology, polymerase, virus
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Elife
ISSN: 2050-084X
Language: eng
Dates:
DateEvent
4 June 2019Published
29 April 2019Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
BB/K002465/1Biotechnology and Biological Sciences Research Councilhttp://dx.doi.org/10.13039/501100000268
205100Wellcome Trusthttp://dx.doi.org/10.13039/100004440
Imperial College President's ScholarshipImperial College Londonhttp://dx.doi.org/10.13039/501100000761
Principal's Career DevelopmentUniversity Of Edinburghhttp://dx.doi.org/10.13039/501100000848
105396/Z/14/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
BB/R007292/1Biotechnology and Biological Sciences Research Councilhttp://dx.doi.org/10.13039/501100000268
BBS/E/I/00007034Biotechnology and Biological Sciences Research Councilhttp://dx.doi.org/10.13039/501100000268
BB/P013732/1Biotechnology and Biological Sciences Research Councilhttp://dx.doi.org/10.13039/501100000268
BB/P013759/1Biotechnology and Biological Sciences Research Councilhttp://dx.doi.org/10.13039/501100000268
PubMed ID: 31159925
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/110840
Publisher's version: https://doi.org/10.7554/eLife.45066

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