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Inhibition by monensin of human cytomegalovirus DNA replication
Monensin, at concentrations which depended on the multiplicity of infection, was found to prevent DNA replication of human cytomegalovirus (HCMV) as well as production of viral progeny in human foreskin fibroblasts. The drug did not affect DNA replication of herpes simplex virus. Inhibition of conse...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
1987
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086728/ https://www.ncbi.nlm.nih.gov/pubmed/3034210 http://dx.doi.org/10.1007/BF01310716 |
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author | Kaiser, C. J. Radsak, K. |
author_facet | Kaiser, C. J. Radsak, K. |
author_sort | Kaiser, C. J. |
collection | PubMed |
description | Monensin, at concentrations which depended on the multiplicity of infection, was found to prevent DNA replication of human cytomegalovirus (HCMV) as well as production of viral progeny in human foreskin fibroblasts. The drug did not affect DNA replication of herpes simplex virus. Inhibition of consecutive HCMV DNA synthesis was also observed following delayed addition of the drug within 12–24 hours postinfection, but was fully reversible upon its removal. Viral replication proceeded, however, without impairment in cultures treated with monensin prior to infection. Induction of viral DNA polymerase activity was not impeded by the inhibitor. Analysis of protein- and glycoprotein synthesis revealed that monensin interfered with the production of a number of HCMV-specific polypeptides. Furthermore, evidence was obtained that the drug may hinder intracellular transport of a 135 kd glycopolypeptide. |
format | Online Article Text |
id | pubmed-7086728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1987 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-70867282020-03-23 Inhibition by monensin of human cytomegalovirus DNA replication Kaiser, C. J. Radsak, K. Arch Virol Original Papers Monensin, at concentrations which depended on the multiplicity of infection, was found to prevent DNA replication of human cytomegalovirus (HCMV) as well as production of viral progeny in human foreskin fibroblasts. The drug did not affect DNA replication of herpes simplex virus. Inhibition of consecutive HCMV DNA synthesis was also observed following delayed addition of the drug within 12–24 hours postinfection, but was fully reversible upon its removal. Viral replication proceeded, however, without impairment in cultures treated with monensin prior to infection. Induction of viral DNA polymerase activity was not impeded by the inhibitor. Analysis of protein- and glycoprotein synthesis revealed that monensin interfered with the production of a number of HCMV-specific polypeptides. Furthermore, evidence was obtained that the drug may hinder intracellular transport of a 135 kd glycopolypeptide. Springer-Verlag 1987 /pmc/articles/PMC7086728/ /pubmed/3034210 http://dx.doi.org/10.1007/BF01310716 Text en © Springer-Verlag 1987 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Papers Kaiser, C. J. Radsak, K. Inhibition by monensin of human cytomegalovirus DNA replication |
title | Inhibition by monensin of human cytomegalovirus DNA replication |
title_full | Inhibition by monensin of human cytomegalovirus DNA replication |
title_fullStr | Inhibition by monensin of human cytomegalovirus DNA replication |
title_full_unstemmed | Inhibition by monensin of human cytomegalovirus DNA replication |
title_short | Inhibition by monensin of human cytomegalovirus DNA replication |
title_sort | inhibition by monensin of human cytomegalovirus dna replication |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086728/ https://www.ncbi.nlm.nih.gov/pubmed/3034210 http://dx.doi.org/10.1007/BF01310716 |
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