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Published in: Archives of Virology 6/2010

01-06-2010 | Original Article

Three amino acid changes in PB1-F2 of highly pathogenic H5N1 avian influenza virus affect pathogenicity in mallard ducks

Authors: Henju Marjuki, Christoph Scholtissek, John Franks, Nicholas J. Negovetich, Jerry R. Aldridge, Rachelle Salomon, David Finkelstein, Robert G. Webster

Published in: Archives of Virology | Issue 6/2010

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Abstract

Despite reports that the PB1-F2 protein contributes to influenza virus pathogenicity in the mouse model, little is known about its significance in avian hosts. In our previous study, the A/Vietnam/1203/04 (H5N1) wild-type virus (wtVN1203) was more lethal to mallard ducks than a reverse genetics (rg)-derived VN1203. In search of potential viral factors responsible for this discrepancy, we found that synonymous mutations (SMs) had been inadvertently introduced into three genes of the rgVN1203 (rgVN1203/SM-3). Of 11 SMs in the PB1 gene, three resided in the PB1-F2 open reading frame, caused amino acid (aa) substitutions in the PB1-F2 protein, and reduced virus lethality in mallard ducks. The wtVN1203 and recombinant viruses with repairs to these three aa’s (rgVN1203/R-PB1-F2) or with repairs to all 11 SMs (rgVN1203/R-PB1) were significantly more pathogenic than rgVN1203/SM-3. In cultured cells, repairing three mutations in PB1-F2 increased viral polymerase activity and expression levels of viral RNA.
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Metadata
Title
Three amino acid changes in PB1-F2 of highly pathogenic H5N1 avian influenza virus affect pathogenicity in mallard ducks
Authors
Henju Marjuki
Christoph Scholtissek
John Franks
Nicholas J. Negovetich
Jerry R. Aldridge
Rachelle Salomon
David Finkelstein
Robert G. Webster
Publication date
01-06-2010
Publisher
Springer Vienna
Published in
Archives of Virology / Issue 6/2010
Print ISSN: 0304-8608
Electronic ISSN: 1432-8798
DOI
https://doi.org/10.1007/s00705-010-0666-4

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