Cargando…
The Antiviral Effect of the Chemical Compounds Targeting DED/EDh Motifs of the Viral Proteins on Lymphocytic Choriomeningitis Virus and SARS-CoV-2
Arenaviruses and coronaviruses include several human pathogenic viruses, such as Lassa virus, Lymphocytic choriomeningitis virus (LCMV), SARS-CoV, MERS-CoV, and SARS-CoV-2. Although these viruses belong to different virus families, they possess a common motif, the DED/EDh motif, known as an exonucle...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310078/ https://www.ncbi.nlm.nih.gov/pubmed/34202565 http://dx.doi.org/10.3390/v13071220 |
_version_ | 1783728673890762752 |
---|---|
author | Ngwe Tun, Mya Myat Morita, Kouichi Ishikawa, Takeshi Urata, Shuzo |
author_facet | Ngwe Tun, Mya Myat Morita, Kouichi Ishikawa, Takeshi Urata, Shuzo |
author_sort | Ngwe Tun, Mya Myat |
collection | PubMed |
description | Arenaviruses and coronaviruses include several human pathogenic viruses, such as Lassa virus, Lymphocytic choriomeningitis virus (LCMV), SARS-CoV, MERS-CoV, and SARS-CoV-2. Although these viruses belong to different virus families, they possess a common motif, the DED/EDh motif, known as an exonuclease (ExoN) motif. In this study, proof-of-concept studies, in which the DED/EDh motif in these viral proteins, NP for arenaviruses, and nsp14 for coronaviruses, could be a drug target, were performed. Docking simulation studies between two structurally different chemical compounds, ATA and PV6R, and the DED/EDh motifs in these viral proteins indicated that these compounds target DED/EDh motifs. The concentration which exhibited modest cell toxicity was used with these compounds to treat LCMV and SARS-CoV-2 infections in two different cell lines, A549 and Vero 76 cells. Both ATA and PV6R inhibited the post-entry step of LCMV and SARS-CoV-2 infection. These studies strongly suggest that DED/EDh motifs in these viral proteins could be a drug target to combat two distinct viral families, arenaviruses and coronaviruses. |
format | Online Article Text |
id | pubmed-8310078 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83100782021-07-25 The Antiviral Effect of the Chemical Compounds Targeting DED/EDh Motifs of the Viral Proteins on Lymphocytic Choriomeningitis Virus and SARS-CoV-2 Ngwe Tun, Mya Myat Morita, Kouichi Ishikawa, Takeshi Urata, Shuzo Viruses Article Arenaviruses and coronaviruses include several human pathogenic viruses, such as Lassa virus, Lymphocytic choriomeningitis virus (LCMV), SARS-CoV, MERS-CoV, and SARS-CoV-2. Although these viruses belong to different virus families, they possess a common motif, the DED/EDh motif, known as an exonuclease (ExoN) motif. In this study, proof-of-concept studies, in which the DED/EDh motif in these viral proteins, NP for arenaviruses, and nsp14 for coronaviruses, could be a drug target, were performed. Docking simulation studies between two structurally different chemical compounds, ATA and PV6R, and the DED/EDh motifs in these viral proteins indicated that these compounds target DED/EDh motifs. The concentration which exhibited modest cell toxicity was used with these compounds to treat LCMV and SARS-CoV-2 infections in two different cell lines, A549 and Vero 76 cells. Both ATA and PV6R inhibited the post-entry step of LCMV and SARS-CoV-2 infection. These studies strongly suggest that DED/EDh motifs in these viral proteins could be a drug target to combat two distinct viral families, arenaviruses and coronaviruses. MDPI 2021-06-24 /pmc/articles/PMC8310078/ /pubmed/34202565 http://dx.doi.org/10.3390/v13071220 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ngwe Tun, Mya Myat Morita, Kouichi Ishikawa, Takeshi Urata, Shuzo The Antiviral Effect of the Chemical Compounds Targeting DED/EDh Motifs of the Viral Proteins on Lymphocytic Choriomeningitis Virus and SARS-CoV-2 |
title | The Antiviral Effect of the Chemical Compounds Targeting DED/EDh Motifs of the Viral Proteins on Lymphocytic Choriomeningitis Virus and SARS-CoV-2 |
title_full | The Antiviral Effect of the Chemical Compounds Targeting DED/EDh Motifs of the Viral Proteins on Lymphocytic Choriomeningitis Virus and SARS-CoV-2 |
title_fullStr | The Antiviral Effect of the Chemical Compounds Targeting DED/EDh Motifs of the Viral Proteins on Lymphocytic Choriomeningitis Virus and SARS-CoV-2 |
title_full_unstemmed | The Antiviral Effect of the Chemical Compounds Targeting DED/EDh Motifs of the Viral Proteins on Lymphocytic Choriomeningitis Virus and SARS-CoV-2 |
title_short | The Antiviral Effect of the Chemical Compounds Targeting DED/EDh Motifs of the Viral Proteins on Lymphocytic Choriomeningitis Virus and SARS-CoV-2 |
title_sort | antiviral effect of the chemical compounds targeting ded/edh motifs of the viral proteins on lymphocytic choriomeningitis virus and sars-cov-2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310078/ https://www.ncbi.nlm.nih.gov/pubmed/34202565 http://dx.doi.org/10.3390/v13071220 |
work_keys_str_mv | AT ngwetunmyamyat theantiviraleffectofthechemicalcompoundstargetingdededhmotifsoftheviralproteinsonlymphocyticchoriomeningitisvirusandsarscov2 AT moritakouichi theantiviraleffectofthechemicalcompoundstargetingdededhmotifsoftheviralproteinsonlymphocyticchoriomeningitisvirusandsarscov2 AT ishikawatakeshi theantiviraleffectofthechemicalcompoundstargetingdededhmotifsoftheviralproteinsonlymphocyticchoriomeningitisvirusandsarscov2 AT uratashuzo theantiviraleffectofthechemicalcompoundstargetingdededhmotifsoftheviralproteinsonlymphocyticchoriomeningitisvirusandsarscov2 AT ngwetunmyamyat antiviraleffectofthechemicalcompoundstargetingdededhmotifsoftheviralproteinsonlymphocyticchoriomeningitisvirusandsarscov2 AT moritakouichi antiviraleffectofthechemicalcompoundstargetingdededhmotifsoftheviralproteinsonlymphocyticchoriomeningitisvirusandsarscov2 AT ishikawatakeshi antiviraleffectofthechemicalcompoundstargetingdededhmotifsoftheviralproteinsonlymphocyticchoriomeningitisvirusandsarscov2 AT uratashuzo antiviraleffectofthechemicalcompoundstargetingdededhmotifsoftheviralproteinsonlymphocyticchoriomeningitisvirusandsarscov2 |