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Isolation and characterization of cidofovir resistant vaccinia viruses
BACKGROUND: The emergence of drug resistant viruses, together with the possibility of increased virulence, is an important concern in the development of new antiviral compounds. Cidofovir (CDV) is a phosphonate nucleotide that is approved for use against cytomegalovirus retinitis and for the emergen...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2397383/ https://www.ncbi.nlm.nih.gov/pubmed/18479513 http://dx.doi.org/10.1186/1743-422X-5-58 |
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author | Becker, Marie N Obraztsova, Maria Kern, Earl R Quenelle, Debra C Keith, Kathy A Prichard, Mark N Luo, Ming Moyer, Richard W |
author_facet | Becker, Marie N Obraztsova, Maria Kern, Earl R Quenelle, Debra C Keith, Kathy A Prichard, Mark N Luo, Ming Moyer, Richard W |
author_sort | Becker, Marie N |
collection | PubMed |
description | BACKGROUND: The emergence of drug resistant viruses, together with the possibility of increased virulence, is an important concern in the development of new antiviral compounds. Cidofovir (CDV) is a phosphonate nucleotide that is approved for use against cytomegalovirus retinitis and for the emergency treatment of smallpox or complications following vaccination. One mode of action for CDV has been demonstrated to be the inhibition of the viral DNA polymerase. RESULTS: We have isolated several CDV resistant (CDV(R)) vaccinia viruses through a one step process, two of which have unique single mutations within the DNA polymerase. An additional resistant virus isolate provides evidence of a second site mutation within the genome involved in CDV resistance. The CDV(R )viruses were 3–7 fold more resistant to the drug than the parental viruses. The virulence of the CDV(R )viruses was tested in mice inoculated intranasally and all were found to be attenuated. CONCLUSION: Resistance to CDV in vaccinia virus can be conferred individually by at least two different mutations within the DNA polymerase gene. Additional genes may be involved. This one step approach for isolating resistant viruses without serial passage and in the presence of low doses of drug minimizes unintended secondary mutations and is applicable to other potential antiviral agents. |
format | Text |
id | pubmed-2397383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-23973832008-05-29 Isolation and characterization of cidofovir resistant vaccinia viruses Becker, Marie N Obraztsova, Maria Kern, Earl R Quenelle, Debra C Keith, Kathy A Prichard, Mark N Luo, Ming Moyer, Richard W Virol J Research BACKGROUND: The emergence of drug resistant viruses, together with the possibility of increased virulence, is an important concern in the development of new antiviral compounds. Cidofovir (CDV) is a phosphonate nucleotide that is approved for use against cytomegalovirus retinitis and for the emergency treatment of smallpox or complications following vaccination. One mode of action for CDV has been demonstrated to be the inhibition of the viral DNA polymerase. RESULTS: We have isolated several CDV resistant (CDV(R)) vaccinia viruses through a one step process, two of which have unique single mutations within the DNA polymerase. An additional resistant virus isolate provides evidence of a second site mutation within the genome involved in CDV resistance. The CDV(R )viruses were 3–7 fold more resistant to the drug than the parental viruses. The virulence of the CDV(R )viruses was tested in mice inoculated intranasally and all were found to be attenuated. CONCLUSION: Resistance to CDV in vaccinia virus can be conferred individually by at least two different mutations within the DNA polymerase gene. Additional genes may be involved. This one step approach for isolating resistant viruses without serial passage and in the presence of low doses of drug minimizes unintended secondary mutations and is applicable to other potential antiviral agents. BioMed Central 2008-05-14 /pmc/articles/PMC2397383/ /pubmed/18479513 http://dx.doi.org/10.1186/1743-422X-5-58 Text en Copyright © 2008 Becker 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 Becker, Marie N Obraztsova, Maria Kern, Earl R Quenelle, Debra C Keith, Kathy A Prichard, Mark N Luo, Ming Moyer, Richard W Isolation and characterization of cidofovir resistant vaccinia viruses |
title | Isolation and characterization of cidofovir resistant vaccinia viruses |
title_full | Isolation and characterization of cidofovir resistant vaccinia viruses |
title_fullStr | Isolation and characterization of cidofovir resistant vaccinia viruses |
title_full_unstemmed | Isolation and characterization of cidofovir resistant vaccinia viruses |
title_short | Isolation and characterization of cidofovir resistant vaccinia viruses |
title_sort | isolation and characterization of cidofovir resistant vaccinia viruses |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2397383/ https://www.ncbi.nlm.nih.gov/pubmed/18479513 http://dx.doi.org/10.1186/1743-422X-5-58 |
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