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Antiviral activity of gliotoxin, gentian violet and brilliant green against Nipah and Hendra virus in vitro

BACKGROUND: Using a recently described monolayer assay amenable to high throughput screening format for the identification of potential Nipah virus and Hendra virus antivirals, we have partially screened a low molecular weight compound library (>8,000 compounds) directly against live virus infect...

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Autores principales: Aljofan, Mohamad, Sganga, Michael L, Lo, Michael K, Rootes, Christina L, Porotto, Matteo, Meyer, Adam G, Saubern, Simon, Moscona, Anne, Mungall, Bruce A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2781006/
https://www.ncbi.nlm.nih.gov/pubmed/19889218
http://dx.doi.org/10.1186/1743-422X-6-187
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author Aljofan, Mohamad
Sganga, Michael L
Lo, Michael K
Rootes, Christina L
Porotto, Matteo
Meyer, Adam G
Saubern, Simon
Moscona, Anne
Mungall, Bruce A
author_facet Aljofan, Mohamad
Sganga, Michael L
Lo, Michael K
Rootes, Christina L
Porotto, Matteo
Meyer, Adam G
Saubern, Simon
Moscona, Anne
Mungall, Bruce A
author_sort Aljofan, Mohamad
collection PubMed
description BACKGROUND: Using a recently described monolayer assay amenable to high throughput screening format for the identification of potential Nipah virus and Hendra virus antivirals, we have partially screened a low molecular weight compound library (>8,000 compounds) directly against live virus infection and identified twenty eight promising lead molecules. Initial single blind screens were conducted with 10 μM compound in triplicate with a minimum efficacy of 90% required for lead selection. Lead compounds were then further characterised to determine the median efficacy (IC(50)), cytotoxicity (CC(50)) and the in vitro therapeutic index in live virus and pseudotype assay formats. RESULTS: While a number of leads were identified, the current work describes three commercially available compounds: brilliant green, gentian violet and gliotoxin, identified as having potent antiviral activity against Nipah and Hendra virus. Similar efficacy was observed against pseudotyped Nipah and Hendra virus, vesicular stomatitis virus and human parainfluenza virus type 3 while only gliotoxin inhibited an influenza A virus suggesting a non-specific, broad spectrum activity for this compound. CONCLUSION: All three of these compounds have been used previously for various aspects of anti-bacterial and anti-fungal therapy and the current results suggest that while unsuitable for internal administration, they may be amenable to topical antiviral applications, or as disinfectants and provide excellent positive controls for future studies.
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spelling pubmed-27810062009-11-24 Antiviral activity of gliotoxin, gentian violet and brilliant green against Nipah and Hendra virus in vitro Aljofan, Mohamad Sganga, Michael L Lo, Michael K Rootes, Christina L Porotto, Matteo Meyer, Adam G Saubern, Simon Moscona, Anne Mungall, Bruce A Virol J Research BACKGROUND: Using a recently described monolayer assay amenable to high throughput screening format for the identification of potential Nipah virus and Hendra virus antivirals, we have partially screened a low molecular weight compound library (>8,000 compounds) directly against live virus infection and identified twenty eight promising lead molecules. Initial single blind screens were conducted with 10 μM compound in triplicate with a minimum efficacy of 90% required for lead selection. Lead compounds were then further characterised to determine the median efficacy (IC(50)), cytotoxicity (CC(50)) and the in vitro therapeutic index in live virus and pseudotype assay formats. RESULTS: While a number of leads were identified, the current work describes three commercially available compounds: brilliant green, gentian violet and gliotoxin, identified as having potent antiviral activity against Nipah and Hendra virus. Similar efficacy was observed against pseudotyped Nipah and Hendra virus, vesicular stomatitis virus and human parainfluenza virus type 3 while only gliotoxin inhibited an influenza A virus suggesting a non-specific, broad spectrum activity for this compound. CONCLUSION: All three of these compounds have been used previously for various aspects of anti-bacterial and anti-fungal therapy and the current results suggest that while unsuitable for internal administration, they may be amenable to topical antiviral applications, or as disinfectants and provide excellent positive controls for future studies. BioMed Central 2009-11-04 /pmc/articles/PMC2781006/ /pubmed/19889218 http://dx.doi.org/10.1186/1743-422X-6-187 Text en Copyright ©2009 Aljofan et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Aljofan, Mohamad
Sganga, Michael L
Lo, Michael K
Rootes, Christina L
Porotto, Matteo
Meyer, Adam G
Saubern, Simon
Moscona, Anne
Mungall, Bruce A
Antiviral activity of gliotoxin, gentian violet and brilliant green against Nipah and Hendra virus in vitro
title Antiviral activity of gliotoxin, gentian violet and brilliant green against Nipah and Hendra virus in vitro
title_full Antiviral activity of gliotoxin, gentian violet and brilliant green against Nipah and Hendra virus in vitro
title_fullStr Antiviral activity of gliotoxin, gentian violet and brilliant green against Nipah and Hendra virus in vitro
title_full_unstemmed Antiviral activity of gliotoxin, gentian violet and brilliant green against Nipah and Hendra virus in vitro
title_short Antiviral activity of gliotoxin, gentian violet and brilliant green against Nipah and Hendra virus in vitro
title_sort antiviral activity of gliotoxin, gentian violet and brilliant green against nipah and hendra virus in vitro
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2781006/
https://www.ncbi.nlm.nih.gov/pubmed/19889218
http://dx.doi.org/10.1186/1743-422X-6-187
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