Influenza A Virus Entry: Implications in Virulence and Future Therapeutics

Influenza A viruses have broad host tropism, being able to infect a range of hosts from wild fowl to swine to humans. This broad tropism makes highly pathogenic influenza A strains, such as H5N1, potentially dangerous to humans if they gain the ability to jump from an animal reservoir to humans. How...

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Main Authors: Emily Rumschlag-Booms, Lijun Rong
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Advances in Virology
Online Access:http://dx.doi.org/10.1155/2013/121924
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author Emily Rumschlag-Booms
Lijun Rong
author_facet Emily Rumschlag-Booms
Lijun Rong
author_sort Emily Rumschlag-Booms
collection DOAJ
description Influenza A viruses have broad host tropism, being able to infect a range of hosts from wild fowl to swine to humans. This broad tropism makes highly pathogenic influenza A strains, such as H5N1, potentially dangerous to humans if they gain the ability to jump from an animal reservoir to humans. How influenza A viruses are able to jump the species barrier is incompletely understood due to the complex genetic nature of the viral surface glycoprotein, hemagglutinin, which mediates entry, combined with the virus's ability to use various receptor linkages. Current therapeutics against influenza A include those that target the uncoating process after entry as well as those that prevent viral budding. While there are therapeutics in development that target entry, currently there are none clinically available. We review here the genetics of influenza A viruses that contribute to entry tropism, how these genetic alterations may contribute to receptor usage and species tropism, as well as how novel therapeutics can be developed that target the major surface glycoprotein, hemagglutinin.
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spelling doaj-art-a647585e4eb04028ad8966f969a437202025-02-03T05:49:27ZengWileyAdvances in Virology1687-86391687-86472013-01-01201310.1155/2013/121924121924Influenza A Virus Entry: Implications in Virulence and Future TherapeuticsEmily Rumschlag-Booms0Lijun Rong1Department of Biology, Northeastern Illinois University, Chicago, Chicago, IL 60625, USADepartment of Microbiology and Immunology, College of Medicine, University of Illinois at Chicago, IL 60612, USAInfluenza A viruses have broad host tropism, being able to infect a range of hosts from wild fowl to swine to humans. This broad tropism makes highly pathogenic influenza A strains, such as H5N1, potentially dangerous to humans if they gain the ability to jump from an animal reservoir to humans. How influenza A viruses are able to jump the species barrier is incompletely understood due to the complex genetic nature of the viral surface glycoprotein, hemagglutinin, which mediates entry, combined with the virus's ability to use various receptor linkages. Current therapeutics against influenza A include those that target the uncoating process after entry as well as those that prevent viral budding. While there are therapeutics in development that target entry, currently there are none clinically available. We review here the genetics of influenza A viruses that contribute to entry tropism, how these genetic alterations may contribute to receptor usage and species tropism, as well as how novel therapeutics can be developed that target the major surface glycoprotein, hemagglutinin.http://dx.doi.org/10.1155/2013/121924
spellingShingle Emily Rumschlag-Booms
Lijun Rong
Influenza A Virus Entry: Implications in Virulence and Future Therapeutics
Advances in Virology
title Influenza A Virus Entry: Implications in Virulence and Future Therapeutics
title_full Influenza A Virus Entry: Implications in Virulence and Future Therapeutics
title_fullStr Influenza A Virus Entry: Implications in Virulence and Future Therapeutics
title_full_unstemmed Influenza A Virus Entry: Implications in Virulence and Future Therapeutics
title_short Influenza A Virus Entry: Implications in Virulence and Future Therapeutics
title_sort influenza a virus entry implications in virulence and future therapeutics
url http://dx.doi.org/10.1155/2013/121924
work_keys_str_mv AT emilyrumschlagbooms influenzaavirusentryimplicationsinvirulenceandfuturetherapeutics
AT lijunrong influenzaavirusentryimplicationsinvirulenceandfuturetherapeutics