Host Cell Restriction Factors that Limit Influenza A Infection

Viral infection of different cell types induces a unique spectrum of host defence genes, including interferon-stimulated genes (ISGs) and genes encoding other proteins with antiviral potential. Although hundreds of ISGs have been described, the vast majority have not been functionally characterised....

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Published inViruses Vol. 9; no. 12; p. 376
Main Authors Villalón-Letelier, Fernando, Brooks, Andrew G, Saunders, Philippa M, Londrigan, Sarah L, Reading, Patrick C
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 07.12.2017
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Abstract Viral infection of different cell types induces a unique spectrum of host defence genes, including interferon-stimulated genes (ISGs) and genes encoding other proteins with antiviral potential. Although hundreds of ISGs have been described, the vast majority have not been functionally characterised. Cellular proteins with putative antiviral activity (hereafter referred to as "restriction factors") can target various steps in the virus life-cycle. In the context of influenza virus infection, restriction factors have been described that target virus entry, genomic replication, translation and virus release. Genome wide analyses, in combination with ectopic overexpression and/or gene silencing studies, have accelerated the identification of restriction factors that are active against influenza and other viruses, as well as providing important insights regarding mechanisms of antiviral activity. Herein, we review current knowledge regarding restriction factors that mediate anti-influenza virus activity and consider the viral countermeasures that are known to limit their impact. Moreover, we consider the strengths and limitations of experimental approaches to study restriction factors, discrepancies between in vitro and in vivo studies, and the potential to exploit restriction factors to limit disease caused by influenza and other respiratory viruses.
AbstractList Viral infection of different cell types induces a unique spectrum of host defence genes, including interferon-stimulated genes (ISGs) and genes encoding other proteins with antiviral potential. Although hundreds of ISGs have been described, the vast majority have not been functionally characterised. Cellular proteins with putative antiviral activity (hereafter referred to as "restriction factors") can target various steps in the virus life-cycle. In the context of influenza virus infection, restriction factors have been described that target virus entry, genomic replication, translation and virus release. Genome wide analyses, in combination with ectopic overexpression and/or gene silencing studies, have accelerated the identification of restriction factors that are active against influenza and other viruses, as well as providing important insights regarding mechanisms of antiviral activity. Herein, we review current knowledge regarding restriction factors that mediate anti-influenza virus activity and consider the viral countermeasures that are known to limit their impact. Moreover, we consider the strengths and limitations of experimental approaches to study restriction factors, discrepancies between in vitro and in vivo studies, and the potential to exploit restriction factors to limit disease caused by influenza and other respiratory viruses.
Author Villalón-Letelier, Fernando
Brooks, Andrew G
Londrigan, Sarah L
Saunders, Philippa M
Reading, Patrick C
AuthorAffiliation 2 WHO Collaborating Centre for Reference and Research on Influenza, Victorian Infectious Diseases Reference Laboratory at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC 3000, Australia
1 Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC 3000, Australia; fvillalon@student.unimelb.edu.au (F.V.-L.); agbrooks@unimelb.edu.au (A.G.B.); philippa.saunders@unimelb.edu.au (P.M.S.); sarahll@unimelb.edu.au (S.L.L.)
AuthorAffiliation_xml – name: 1 Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC 3000, Australia; fvillalon@student.unimelb.edu.au (F.V.-L.); agbrooks@unimelb.edu.au (A.G.B.); philippa.saunders@unimelb.edu.au (P.M.S.); sarahll@unimelb.edu.au (S.L.L.)
– name: 2 WHO Collaborating Centre for Reference and Research on Influenza, Victorian Infectious Diseases Reference Laboratory at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC 3000, Australia
Author_xml – sequence: 1
  givenname: Fernando
  surname: Villalón-Letelier
  fullname: Villalón-Letelier, Fernando
  email: fvillalon@student.unimelb.edu.au
  organization: Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC 3000, Australia. fvillalon@student.unimelb.edu.au
– sequence: 2
  givenname: Andrew G
  surname: Brooks
  fullname: Brooks, Andrew G
  email: agbrooks@unimelb.edu.au
  organization: Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC 3000, Australia. agbrooks@unimelb.edu.au
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  givenname: Philippa M
  surname: Saunders
  fullname: Saunders, Philippa M
  email: philippa.saunders@unimelb.edu.au
  organization: Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC 3000, Australia. philippa.saunders@unimelb.edu.au
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  givenname: Sarah L
  surname: Londrigan
  fullname: Londrigan, Sarah L
  email: sarahll@unimelb.edu.au
  organization: Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC 3000, Australia. sarahll@unimelb.edu.au
– sequence: 5
  givenname: Patrick C
  surname: Reading
  fullname: Reading, Patrick C
  email: preading@unimelb.edu.au, preading@unimelb.edu.au
  organization: WHO Collaborating Centre for Reference and Research on Influenza, Victorian Infectious Diseases Reference Laboratory at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC 3000, Australia. preading@unimelb.edu.au
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29215570$$D View this record in MEDLINE/PubMed
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Issue 12
Keywords influenza
replication
restriction factor
interferon-stimulated gene
innate
Language English
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Snippet Viral infection of different cell types induces a unique spectrum of host defence genes, including interferon-stimulated genes (ISGs) and genes encoding other...
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SubjectTerms Animals
Antiviral activity
Gene silencing
Genomes
Host-Pathogen Interactions
Humans
Immunologic Factors - metabolism
Infections
Influenza
Influenza A
Influenza A virus - immunology
innate
Interferon
interferon-stimulated gene
replication
restriction factor
Review
Viral infections
Viruses
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Title Host Cell Restriction Factors that Limit Influenza A Infection
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