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Insights into the antiviral activity of phospholipases A(2) (PLA(2)s) from snake venoms

Viruses are associated with several human diseases that infect a large number of individuals, hence directly affecting global health and economy. Owing to the lack of efficient vaccines, antiviral therapy and emerging resistance strains, many viruses are considered as a potential threat to public he...

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Autores principales: Teixeira, S.C., Borges, B.C., Oliveira, V.Q., Carregosa, L.S., Bastos, L.A., Santos, I.A., Jardim, A.C.G., Melo, F.F., Freitas, L.M., Rodrigues, V.M., Lopes, D.S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368918/
https://www.ncbi.nlm.nih.gov/pubmed/32698062
http://dx.doi.org/10.1016/j.ijbiomac.2020.07.178
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author Teixeira, S.C.
Borges, B.C.
Oliveira, V.Q.
Carregosa, L.S.
Bastos, L.A.
Santos, I.A.
Jardim, A.C.G.
Melo, F.F.
Freitas, L.M.
Rodrigues, V.M.
Lopes, D.S.
author_facet Teixeira, S.C.
Borges, B.C.
Oliveira, V.Q.
Carregosa, L.S.
Bastos, L.A.
Santos, I.A.
Jardim, A.C.G.
Melo, F.F.
Freitas, L.M.
Rodrigues, V.M.
Lopes, D.S.
author_sort Teixeira, S.C.
collection PubMed
description Viruses are associated with several human diseases that infect a large number of individuals, hence directly affecting global health and economy. Owing to the lack of efficient vaccines, antiviral therapy and emerging resistance strains, many viruses are considered as a potential threat to public health. Therefore, researches have been developed to identify new drug candidates for future treatments. Among them, antiviral research based on natural molecules is a promising approach. Phospholipases A(2) (PLA(2)s) isolated from snake venom have shown significant antiviral activity against some viruses such as Dengue virus, Human Immunodeficiency virus, Hepatitis C virus and Yellow fever virus, and have emerged as an attractive alternative strategy for the development of novel antiviral therapy. Thus, this review provides an overview of remarkable findings involving PLA(2)s from snake venom that possess antiviral activity, and discusses the mechanisms of action mediated by PLA(2)s against different stages of virus replication cycle. Additionally, molecular docking simulations were performed by interacting between phospholipids from Dengue virus envelope and PLA(2)s from Bothrops asper snake venom. Studies on snake venom PLA(2)s highlight the potential use of these proteins for the development of broad-spectrum antiviral drugs.
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spelling pubmed-73689182020-07-20 Insights into the antiviral activity of phospholipases A(2) (PLA(2)s) from snake venoms Teixeira, S.C. Borges, B.C. Oliveira, V.Q. Carregosa, L.S. Bastos, L.A. Santos, I.A. Jardim, A.C.G. Melo, F.F. Freitas, L.M. Rodrigues, V.M. Lopes, D.S. Int J Biol Macromol Review Viruses are associated with several human diseases that infect a large number of individuals, hence directly affecting global health and economy. Owing to the lack of efficient vaccines, antiviral therapy and emerging resistance strains, many viruses are considered as a potential threat to public health. Therefore, researches have been developed to identify new drug candidates for future treatments. Among them, antiviral research based on natural molecules is a promising approach. Phospholipases A(2) (PLA(2)s) isolated from snake venom have shown significant antiviral activity against some viruses such as Dengue virus, Human Immunodeficiency virus, Hepatitis C virus and Yellow fever virus, and have emerged as an attractive alternative strategy for the development of novel antiviral therapy. Thus, this review provides an overview of remarkable findings involving PLA(2)s from snake venom that possess antiviral activity, and discusses the mechanisms of action mediated by PLA(2)s against different stages of virus replication cycle. Additionally, molecular docking simulations were performed by interacting between phospholipids from Dengue virus envelope and PLA(2)s from Bothrops asper snake venom. Studies on snake venom PLA(2)s highlight the potential use of these proteins for the development of broad-spectrum antiviral drugs. Published by Elsevier B.V. 2020-12-01 2020-07-19 /pmc/articles/PMC7368918/ /pubmed/32698062 http://dx.doi.org/10.1016/j.ijbiomac.2020.07.178 Text en © 2020 Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Review
Teixeira, S.C.
Borges, B.C.
Oliveira, V.Q.
Carregosa, L.S.
Bastos, L.A.
Santos, I.A.
Jardim, A.C.G.
Melo, F.F.
Freitas, L.M.
Rodrigues, V.M.
Lopes, D.S.
Insights into the antiviral activity of phospholipases A(2) (PLA(2)s) from snake venoms
title Insights into the antiviral activity of phospholipases A(2) (PLA(2)s) from snake venoms
title_full Insights into the antiviral activity of phospholipases A(2) (PLA(2)s) from snake venoms
title_fullStr Insights into the antiviral activity of phospholipases A(2) (PLA(2)s) from snake venoms
title_full_unstemmed Insights into the antiviral activity of phospholipases A(2) (PLA(2)s) from snake venoms
title_short Insights into the antiviral activity of phospholipases A(2) (PLA(2)s) from snake venoms
title_sort insights into the antiviral activity of phospholipases a(2) (pla(2)s) from snake venoms
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368918/
https://www.ncbi.nlm.nih.gov/pubmed/32698062
http://dx.doi.org/10.1016/j.ijbiomac.2020.07.178
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