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Plasminogen promotes influenza A virus replication through an annexin 2-dependent pathway in the absence of neuraminidase
41
Citations
37
References
2010
Year
Protease InhibitorsVirus StructureViral ReplicationMolecular VirologyProteolytic CleavageProtein FoldingAnnexin 2-Dependent PathwayPathogenesisViral PathogenesisImmunologyMolecular BiologyVirologyTrypsin-like ProteasesAlternative ProteaseMedicineViral Structural ProteinA Virus Replication
Proteolytic cleavage of haemagglutinin (HA) is essential for the infectivity of influenza A viruses (IAVs). This is usually mediated by trypsin-like proteases present in the respiratory tract. However, the ability to use plasminogen (PLG) as an alternative protease may contribute to pathogenesis of IAV infections and virus replication outside the respiratory tract. It was demonstrated previously that neuraminidase (NA) of the IAV strain A/WSN/33 can sequester PLG, allowing this virus to replicate in a PLG-dependent fashion. However, PLG also promotes replication of other IAVs, although its mode of action is poorly understood. Here, using NA-deficient viruses, we demonstrate that NA is not required for the binding of PLG and subsequent cleavage of HA. However, we demonstrate that the cellular protein annexin 2 (A2) can bind PLG and contributes to PLG-dependent cleavage of HA and subsequent IAV replication. Collectively, these results indicate that PLG promotes IAV replication in an A2-dependent fashion in the absence of NA.
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