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Inhibition of influenza A virus replication by influenza B virus nucleoprotein: An insight into interference between influenza A and B viruses
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Metadata
Document Title
Inhibition of influenza A virus replication by influenza B virus nucleoprotein: An insight into interference between influenza A and B viruses
Author
Wanitchang A, Narkpuk J, Jaru-Ampornpan P, Jengarn J, Jongkaewwattana A
Name from Authors Collection
Scopus Author ID
25824516500
Scopus Author ID
55279790400
Affiliations
National Science & Technology Development Agency - Thailand; National Center Genetic Engineering & Biotechnology (BIOTEC)
Type
Article
Source Title
VIROLOGY
ISSN
0042-6822
Year
2012
Volume
432
Issue
1
Open Access
Bronze
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI
10.1016/j.virol.2012.06.016
Format
Abstract
Given that co-infection of cells with equivalent titers of influenza A and B viruses (FluA and FluB) has been shown to result in suppression of FluA growth, it is possible that FluB-specific proteins might hinder FluA polymerase activity and replication. We addressed this possibility by individually determining the effect of each gene of FluB on the FluA polymerase assay and found that the nucleoprotein of FluB (NPFluB) inhibits polymerase activity of FluA in a dose-dependent manner. Mutational analyses of NPFluB suggest that functional NPFluB is necessary for this inhibition. Slower growth of FluA was also observed in MOCK cells stably expressing NPFluB. Further analysis of NPFluB indicated that it does not affect nuclear import of NPFluA. Taken together, these findings suggest a novel role of NPFluB in inhibiting replication of FluA, providing more insights into the mechanism of interference between FluA and FluB and the lack of reassortants between them. (C) 2012 Elsevier Inc. All rights reserved.
Industrial Classification
Knowledge Taxonomy Level 1
Knowledge Taxonomy Level 2
Knowledge Taxonomy Level 3
Funding Sponsor
National Science Development Agency (NSTDA) [CPMO-P-00-20386]
License
Copyright
Rights
Elsevier Inc.
Publication Source
WOS