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ERDRP-0519 inhibits feline coronavirus in vitro
BACKGROUND: Coronaviruses (CoVs) are major human and animal pathogens and antiviral drugs are pursued as a complementary strategy, chiefly if vaccines are not available. Feline infectious peritonitis (FIP) is a fatal systemic disease of felids caused by FIP virus (FIPV), a virulent pathotype of feli...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8787031/ https://www.ncbi.nlm.nih.gov/pubmed/35078478 http://dx.doi.org/10.1186/s12917-022-03153-3 |
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author | Camero, Michele Lanave, Gianvito Catella, Cristiana Lucente, Maria Stella Sposato, Alessio Mari, Viviana Tempesta, Maria Martella, Vito Buonavoglia, Alessio |
author_facet | Camero, Michele Lanave, Gianvito Catella, Cristiana Lucente, Maria Stella Sposato, Alessio Mari, Viviana Tempesta, Maria Martella, Vito Buonavoglia, Alessio |
author_sort | Camero, Michele |
collection | PubMed |
description | BACKGROUND: Coronaviruses (CoVs) are major human and animal pathogens and antiviral drugs are pursued as a complementary strategy, chiefly if vaccines are not available. Feline infectious peritonitis (FIP) is a fatal systemic disease of felids caused by FIP virus (FIPV), a virulent pathotype of feline enteric coronavirus (FeCoV). Some antiviral drugs active on FIPV have been identified, but they are not available in veterinary medicine. ERDRP-0519 (ERDRP) is a non-nucleoside inhibitor, targeting viral RNA polymerase, effective against morbilliviruses in vitro and in vivo. RESULTS: The antiviral efficacy of ERDRP against a type II FIPV was evaluated in vitro in Crandell Reese Feline Kidney (CRFK) cells. ERDRP significantly inhibited replication of FIPV in a dose-dependent manner. Viral infectivity was decreased by up to 3.00 logarithms in cell cultures whilst viral load, estimated by quantification of nucleic acids, was reduced by nearly 3.11 logaritms. CONCLUSIONS: These findings confirm that ERDRP is highly effective against a CoV. Experiments will be necessary to assess whether ERDRP is suitable for treatment of FIPV in vivo. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12917-022-03153-3. |
format | Online Article Text |
id | pubmed-8787031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87870312022-01-25 ERDRP-0519 inhibits feline coronavirus in vitro Camero, Michele Lanave, Gianvito Catella, Cristiana Lucente, Maria Stella Sposato, Alessio Mari, Viviana Tempesta, Maria Martella, Vito Buonavoglia, Alessio BMC Vet Res Research BACKGROUND: Coronaviruses (CoVs) are major human and animal pathogens and antiviral drugs are pursued as a complementary strategy, chiefly if vaccines are not available. Feline infectious peritonitis (FIP) is a fatal systemic disease of felids caused by FIP virus (FIPV), a virulent pathotype of feline enteric coronavirus (FeCoV). Some antiviral drugs active on FIPV have been identified, but they are not available in veterinary medicine. ERDRP-0519 (ERDRP) is a non-nucleoside inhibitor, targeting viral RNA polymerase, effective against morbilliviruses in vitro and in vivo. RESULTS: The antiviral efficacy of ERDRP against a type II FIPV was evaluated in vitro in Crandell Reese Feline Kidney (CRFK) cells. ERDRP significantly inhibited replication of FIPV in a dose-dependent manner. Viral infectivity was decreased by up to 3.00 logarithms in cell cultures whilst viral load, estimated by quantification of nucleic acids, was reduced by nearly 3.11 logaritms. CONCLUSIONS: These findings confirm that ERDRP is highly effective against a CoV. Experiments will be necessary to assess whether ERDRP is suitable for treatment of FIPV in vivo. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12917-022-03153-3. BioMed Central 2022-01-25 /pmc/articles/PMC8787031/ /pubmed/35078478 http://dx.doi.org/10.1186/s12917-022-03153-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Camero, Michele Lanave, Gianvito Catella, Cristiana Lucente, Maria Stella Sposato, Alessio Mari, Viviana Tempesta, Maria Martella, Vito Buonavoglia, Alessio ERDRP-0519 inhibits feline coronavirus in vitro |
title | ERDRP-0519 inhibits feline coronavirus in vitro |
title_full | ERDRP-0519 inhibits feline coronavirus in vitro |
title_fullStr | ERDRP-0519 inhibits feline coronavirus in vitro |
title_full_unstemmed | ERDRP-0519 inhibits feline coronavirus in vitro |
title_short | ERDRP-0519 inhibits feline coronavirus in vitro |
title_sort | erdrp-0519 inhibits feline coronavirus in vitro |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8787031/ https://www.ncbi.nlm.nih.gov/pubmed/35078478 http://dx.doi.org/10.1186/s12917-022-03153-3 |
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