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Preferential Inhibition of Herpes-Group Viruses by Phosphonoacetic Acid: Effect on Virus DNA Synthesis and Virus-Induced DNA Polymerase Activity
In tissue culture phosphonoacetic acid (PAA) specifically inhibited DNA synthesis of human cytomegalovirus (CMV), murine CMV, simian CMV, Epstein-Barr virus, and Herpesvirus saimiri. Fifty to one hundred micrograms per milliliter PAA completely inhibited viral DNA synthesis with no significant damag...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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1976
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2595326/ https://www.ncbi.nlm.nih.gov/pubmed/960726 |
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author | Huang, Eng-Shang Huang, Chien-Hui Huong, Shu-Mei Selgrade, Maryjane |
author_facet | Huang, Eng-Shang Huang, Chien-Hui Huong, Shu-Mei Selgrade, Maryjane |
author_sort | Huang, Eng-Shang |
collection | PubMed |
description | In tissue culture phosphonoacetic acid (PAA) specifically inhibited DNA synthesis of human cytomegalovirus (CMV), murine CMV, simian CMV, Epstein-Barr virus, and Herpesvirus saimiri. Fifty to one hundred micrograms per milliliter PAA completely inhibited viral DNA synthesis with no significant damage to host cell DNA synthesis. In vitro DNA polymerization assays showed that 10 μg/ml of PAA specifically inhibited partially purified human CMV-induced DNA polymerase, while little inhibition of host-cell DNA polymerase activity was found. The specific inhibition of herpes-group virus DNA synthesis with little toxicity to host cells suggests that PAA has great potential as an antiherpesvirus therapeutic agent. |
format | Text |
id | pubmed-2595326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1976 |
record_format | MEDLINE/PubMed |
spelling | pubmed-25953262008-12-05 Preferential Inhibition of Herpes-Group Viruses by Phosphonoacetic Acid: Effect on Virus DNA Synthesis and Virus-Induced DNA Polymerase Activity Huang, Eng-Shang Huang, Chien-Hui Huong, Shu-Mei Selgrade, Maryjane Yale J Biol Med Original Contributions In tissue culture phosphonoacetic acid (PAA) specifically inhibited DNA synthesis of human cytomegalovirus (CMV), murine CMV, simian CMV, Epstein-Barr virus, and Herpesvirus saimiri. Fifty to one hundred micrograms per milliliter PAA completely inhibited viral DNA synthesis with no significant damage to host cell DNA synthesis. In vitro DNA polymerization assays showed that 10 μg/ml of PAA specifically inhibited partially purified human CMV-induced DNA polymerase, while little inhibition of host-cell DNA polymerase activity was found. The specific inhibition of herpes-group virus DNA synthesis with little toxicity to host cells suggests that PAA has great potential as an antiherpesvirus therapeutic agent. 1976-03 /pmc/articles/PMC2595326/ /pubmed/960726 Text en |
spellingShingle | Original Contributions Huang, Eng-Shang Huang, Chien-Hui Huong, Shu-Mei Selgrade, Maryjane Preferential Inhibition of Herpes-Group Viruses by Phosphonoacetic Acid: Effect on Virus DNA Synthesis and Virus-Induced DNA Polymerase Activity |
title | Preferential Inhibition of Herpes-Group Viruses by Phosphonoacetic Acid: Effect on Virus DNA Synthesis and Virus-Induced DNA Polymerase Activity |
title_full | Preferential Inhibition of Herpes-Group Viruses by Phosphonoacetic Acid: Effect on Virus DNA Synthesis and Virus-Induced DNA Polymerase Activity |
title_fullStr | Preferential Inhibition of Herpes-Group Viruses by Phosphonoacetic Acid: Effect on Virus DNA Synthesis and Virus-Induced DNA Polymerase Activity |
title_full_unstemmed | Preferential Inhibition of Herpes-Group Viruses by Phosphonoacetic Acid: Effect on Virus DNA Synthesis and Virus-Induced DNA Polymerase Activity |
title_short | Preferential Inhibition of Herpes-Group Viruses by Phosphonoacetic Acid: Effect on Virus DNA Synthesis and Virus-Induced DNA Polymerase Activity |
title_sort | preferential inhibition of herpes-group viruses by phosphonoacetic acid: effect on virus dna synthesis and virus-induced dna polymerase activity |
topic | Original Contributions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2595326/ https://www.ncbi.nlm.nih.gov/pubmed/960726 |
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