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Identification of a novel splice variant form of the influenza A virus M2 ion channel with an antigenically distinct ectodomain.

Abstract:
Segment 7 of influenza A virus produces up to four mRNAs. Unspliced transcripts encode M1, spliced mRNA2 encodes the M2 ion channel, while protein products from spliced mRNAs 3 and 4 have not previously been identified. The M2 protein plays important roles in virus entry and assembly, and is a target for antiviral drugs and vaccination. Surprisingly, M2 is not essential for virus replication in a laboratory setting, although its loss attenuates the virus. To better understand how IAV might replicate without M2, we studied the reversion mechanism of an M2-null virus. Serial passage of a virus lacking the mRNA2 splice donor site identified a single nucleotide pseudoreverting mutation, which restored growth in cell culture and virulence in mice by upregulating mRNA4 synthesis rather than by reinstating mRNA2 production. We show that mRNA4 encodes a novel M2-related protein (designated M42) with an antigenically distinct ectodomain that can functionally replace M2 despite showing clear differences in intracellular localisation, being largely retained in the Golgi compartment. We also show that the expression of two distinct ion channel proteins is not unique to laboratory-adapted viruses but, most notably, was also a feature of the 1983 North American outbreak of H5N2 highly pathogenic avian influenza virus. In identifying a 14th influenza A polypeptide, our data reinforce the unexpectedly high coding capacity of the viral genome and have implications for virus evolution, as well as for understanding the role of M2 in the virus life cycle.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1371/journal.ppat.1002998

Authors


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Institution:
University of Oxford
Division:
MSD
Department:
Pathology Dunn School
Role:
Author


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Funding agency for:
Fodor, E
Grant:
G0700848


Publisher:
Public Library of Science
Journal:
PLoS pathogens More from this journal
Volume:
8
Issue:
11
Pages:
e1002998
Publication date:
2012-01-01
DOI:
EISSN:
1553-7374
ISSN:
1553-7366


Language:
English
Keywords:
Pubs id:
pubs:358315
UUID:
uuid:a531e265-7622-4556-8c37-1e800e5ddd56
Local pid:
pubs:358315
Source identifiers:
358315
Deposit date:
2013-11-16

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