Unravelling the Immunomodulatory Effects of Viral Ion Channels, towards the Treatment of Disease

The current COVID-19 pandemic has highlighted the need for the research community to develop a better understanding of viruses, in particular their modes of infection and replicative lifecycles, to aid in the development of novel vaccines and much needed anti-viral therapeutics. Several viruses expr...

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Autores principales: Siobhan Gargan, Nigel J. Stevenson
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/77e3e8461d934d59bc46ac5dc465039f
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spelling oai:doaj.org-article:77e3e8461d934d59bc46ac5dc465039f2021-11-25T19:12:58ZUnravelling the Immunomodulatory Effects of Viral Ion Channels, towards the Treatment of Disease10.3390/v131121651999-4915https://doaj.org/article/77e3e8461d934d59bc46ac5dc465039f2021-10-01T00:00:00Zhttps://www.mdpi.com/1999-4915/13/11/2165https://doaj.org/toc/1999-4915The current COVID-19 pandemic has highlighted the need for the research community to develop a better understanding of viruses, in particular their modes of infection and replicative lifecycles, to aid in the development of novel vaccines and much needed anti-viral therapeutics. Several viruses express proteins capable of forming pores in host cellular membranes, termed “Viroporins”. They are a family of small hydrophobic proteins, with at least one amphipathic domain, which characteristically form oligomeric structures with central hydrophilic domains. Consequently, they can facilitate the transport of ions through the hydrophilic core. Viroporins localise to host membranes such as the endoplasmic reticulum and regulate ion homeostasis creating a favourable environment for viral infection. Viroporins also contribute to viral immune evasion via several mechanisms. Given that viroporins are often essential for virion assembly and egress, and as their structural features tend to be evolutionarily conserved, they are attractive targets for anti-viral therapeutics. This review discusses the current knowledge of several viroporins, namely Influenza A virus (IAV) M2, Human Immunodeficiency Virus (HIV)-1 Viral protein U (Vpu), Hepatitis C Virus (HCV) p7, Human Papillomavirus (HPV)-16 E5, Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV) Open Reading Frame (ORF)3a and Polyomavirus agnoprotein. We highlight the intricate but broad immunomodulatory effects of these viroporins and discuss the current antiviral therapies that target them; continually highlighting the need for future investigations to focus on novel therapeutics in the treatment of existing and future emergent viruses.Siobhan GarganNigel J. StevensonMDPI AGarticlevirusesion channelsviroporinsimmune evasionimmune modulationinfluenzaMicrobiologyQR1-502ENViruses, Vol 13, Iss 2165, p 2165 (2021)
institution DOAJ
collection DOAJ
language EN
topic viruses
ion channels
viroporins
immune evasion
immune modulation
influenza
Microbiology
QR1-502
spellingShingle viruses
ion channels
viroporins
immune evasion
immune modulation
influenza
Microbiology
QR1-502
Siobhan Gargan
Nigel J. Stevenson
Unravelling the Immunomodulatory Effects of Viral Ion Channels, towards the Treatment of Disease
description The current COVID-19 pandemic has highlighted the need for the research community to develop a better understanding of viruses, in particular their modes of infection and replicative lifecycles, to aid in the development of novel vaccines and much needed anti-viral therapeutics. Several viruses express proteins capable of forming pores in host cellular membranes, termed “Viroporins”. They are a family of small hydrophobic proteins, with at least one amphipathic domain, which characteristically form oligomeric structures with central hydrophilic domains. Consequently, they can facilitate the transport of ions through the hydrophilic core. Viroporins localise to host membranes such as the endoplasmic reticulum and regulate ion homeostasis creating a favourable environment for viral infection. Viroporins also contribute to viral immune evasion via several mechanisms. Given that viroporins are often essential for virion assembly and egress, and as their structural features tend to be evolutionarily conserved, they are attractive targets for anti-viral therapeutics. This review discusses the current knowledge of several viroporins, namely Influenza A virus (IAV) M2, Human Immunodeficiency Virus (HIV)-1 Viral protein U (Vpu), Hepatitis C Virus (HCV) p7, Human Papillomavirus (HPV)-16 E5, Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV) Open Reading Frame (ORF)3a and Polyomavirus agnoprotein. We highlight the intricate but broad immunomodulatory effects of these viroporins and discuss the current antiviral therapies that target them; continually highlighting the need for future investigations to focus on novel therapeutics in the treatment of existing and future emergent viruses.
format article
author Siobhan Gargan
Nigel J. Stevenson
author_facet Siobhan Gargan
Nigel J. Stevenson
author_sort Siobhan Gargan
title Unravelling the Immunomodulatory Effects of Viral Ion Channels, towards the Treatment of Disease
title_short Unravelling the Immunomodulatory Effects of Viral Ion Channels, towards the Treatment of Disease
title_full Unravelling the Immunomodulatory Effects of Viral Ion Channels, towards the Treatment of Disease
title_fullStr Unravelling the Immunomodulatory Effects of Viral Ion Channels, towards the Treatment of Disease
title_full_unstemmed Unravelling the Immunomodulatory Effects of Viral Ion Channels, towards the Treatment of Disease
title_sort unravelling the immunomodulatory effects of viral ion channels, towards the treatment of disease
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/77e3e8461d934d59bc46ac5dc465039f
work_keys_str_mv AT siobhangargan unravellingtheimmunomodulatoryeffectsofviralionchannelstowardsthetreatmentofdisease
AT nigeljstevenson unravellingtheimmunomodulatoryeffectsofviralionchannelstowardsthetreatmentofdisease
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