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Inactivation of non-enveloped virus by 1,5 iodonaphthyl azide
BACKGROUND: A photoactive hydrophobic agent 1,5-iodonaphthyl-azide (INA), has been previously shown to completely inactivate the enveloped viruses. INA sequesters into the lipid bilayer of the virus envelope and upon UV-irradiation bind to the hydrophobic domains of the envelope glycoproteins. In ou...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339248/ https://www.ncbi.nlm.nih.gov/pubmed/25879201 http://dx.doi.org/10.1186/s13104-015-1006-2 |
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author | Gupta, Paridhi Sharma, Anuj Mathias, Viard Raviv, Yossef Blumenthal, Robert Maheshwari, Radha K |
author_facet | Gupta, Paridhi Sharma, Anuj Mathias, Viard Raviv, Yossef Blumenthal, Robert Maheshwari, Radha K |
author_sort | Gupta, Paridhi |
collection | PubMed |
description | BACKGROUND: A photoactive hydrophobic agent 1,5-iodonaphthyl-azide (INA), has been previously shown to completely inactivate the enveloped viruses. INA sequesters into the lipid bilayer of the virus envelope and upon UV-irradiation bind to the hydrophobic domains of the envelope glycoproteins. In our earlier study, we have shown that the Venezuelan equine encephalitis virus (VEEV) genomic RNA was also inactivated during the inactivation of the virus with INA. FINDINGS: In the present study, we evaluated if the RNA inactivation property of INA can be used to inactivate non-enveloped RNA viruses. Encephalomyocarditis virus (EMCV) was used as a model non-enveloped virus. Treatment with INA followed by UV-irradiation resulted in complete inactivation of EMCV. RNA isolated from INA-inactivated EMCV was non-infectious and INA was found to be associated with the viral RNA genome. INA-inactivated EMCV induced robust total antibody response. However binding capacity of INA-inactivated EMCV to neutralizing antibody was inhibited. CONCLUSION: This is the first study to show that INA can completely inactivate non-enveloped virus. Our results suggest that the amino acid composition of the neutralizing epitope may interfere with the protective antibody response generated by the INA-inactivated non-enveloped virus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13104-015-1006-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4339248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43392482015-02-26 Inactivation of non-enveloped virus by 1,5 iodonaphthyl azide Gupta, Paridhi Sharma, Anuj Mathias, Viard Raviv, Yossef Blumenthal, Robert Maheshwari, Radha K BMC Res Notes Short Report BACKGROUND: A photoactive hydrophobic agent 1,5-iodonaphthyl-azide (INA), has been previously shown to completely inactivate the enveloped viruses. INA sequesters into the lipid bilayer of the virus envelope and upon UV-irradiation bind to the hydrophobic domains of the envelope glycoproteins. In our earlier study, we have shown that the Venezuelan equine encephalitis virus (VEEV) genomic RNA was also inactivated during the inactivation of the virus with INA. FINDINGS: In the present study, we evaluated if the RNA inactivation property of INA can be used to inactivate non-enveloped RNA viruses. Encephalomyocarditis virus (EMCV) was used as a model non-enveloped virus. Treatment with INA followed by UV-irradiation resulted in complete inactivation of EMCV. RNA isolated from INA-inactivated EMCV was non-infectious and INA was found to be associated with the viral RNA genome. INA-inactivated EMCV induced robust total antibody response. However binding capacity of INA-inactivated EMCV to neutralizing antibody was inhibited. CONCLUSION: This is the first study to show that INA can completely inactivate non-enveloped virus. Our results suggest that the amino acid composition of the neutralizing epitope may interfere with the protective antibody response generated by the INA-inactivated non-enveloped virus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13104-015-1006-2) contains supplementary material, which is available to authorized users. BioMed Central 2015-02-15 /pmc/articles/PMC4339248/ /pubmed/25879201 http://dx.doi.org/10.1186/s13104-015-1006-2 Text en © Gupta et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Short Report Gupta, Paridhi Sharma, Anuj Mathias, Viard Raviv, Yossef Blumenthal, Robert Maheshwari, Radha K Inactivation of non-enveloped virus by 1,5 iodonaphthyl azide |
title | Inactivation of non-enveloped virus by 1,5 iodonaphthyl azide |
title_full | Inactivation of non-enveloped virus by 1,5 iodonaphthyl azide |
title_fullStr | Inactivation of non-enveloped virus by 1,5 iodonaphthyl azide |
title_full_unstemmed | Inactivation of non-enveloped virus by 1,5 iodonaphthyl azide |
title_short | Inactivation of non-enveloped virus by 1,5 iodonaphthyl azide |
title_sort | inactivation of non-enveloped virus by 1,5 iodonaphthyl azide |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339248/ https://www.ncbi.nlm.nih.gov/pubmed/25879201 http://dx.doi.org/10.1186/s13104-015-1006-2 |
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