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Inhibition by monensin of human cytomegalovirus DNA replication

Identifieur interne : 000184 ( Pmc/Corpus ); précédent : 000183; suivant : 000185

Inhibition by monensin of human cytomegalovirus DNA replication

Auteurs : C. J. Kaiser ; K. Radsak

Source :

RBID : PMC:7086728

Abstract

Summary

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.


Url:
DOI: 10.1007/BF01310716
PubMed: 3034210
PubMed Central: 7086728

Links to Exploration step

PMC:7086728

Le document en format XML

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<p>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.</p>
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<journal-id journal-id-type="nlm-ta">Arch Virol</journal-id>
<journal-id journal-id-type="iso-abbrev">Arch. Virol</journal-id>
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<journal-title>Archives of Virology</journal-title>
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<issn pub-type="ppub">0304-8608</issn>
<issn pub-type="epub">1432-8798</issn>
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<publisher-name>Springer-Verlag</publisher-name>
<publisher-loc>Vienna</publisher-loc>
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<article-id pub-id-type="pmc">7086728</article-id>
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<article-id pub-id-type="doi">10.1007/BF01310716</article-id>
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<subject>Original Papers</subject>
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<article-title>Inhibition by monensin of human cytomegalovirus DNA replication</article-title>
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<name>
<surname>Kaiser</surname>
<given-names>C. J.</given-names>
</name>
<xref ref-type="aff" rid="Aff1"></xref>
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<contrib contrib-type="author">
<name>
<surname>Radsak</surname>
<given-names>K.</given-names>
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<xref ref-type="aff" rid="Aff1"></xref>
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<aff id="Aff1">
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<institution-id institution-id-type="GRID">grid.10253.35</institution-id>
<institution-id institution-id-type="ISNI">0000000419369756</institution-id>
<institution>Zentrum für Hygiene und Medizinische Mikrobiologie,</institution>
<institution>Institut für Virologie der Philipps-Universität,</institution>
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Marburg, Germany</aff>
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<pub-date pub-type="ppub">
<year>1987</year>
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<volume>94</volume>
<issue>3</issue>
<fpage>229</fpage>
<lpage>245</lpage>
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<date date-type="accepted">
<day>18</day>
<month>11</month>
<year>1986</year>
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<copyright-statement>© Springer-Verlag 1987</copyright-statement>
<license>
<license-p>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.</license-p>
</license>
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<abstract id="Abs1">
<title>Summary</title>
<p>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.</p>
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<kwd-group xml:lang="en">
<title>Keywords</title>
<kwd>Infectious Disease</kwd>
<kwd>Polypeptide</kwd>
<kwd>Herpes Simplex</kwd>
<kwd>Viral Replication</kwd>
<kwd>Polymerase Activity</kwd>
</kwd-group>
<custom-meta-group>
<custom-meta>
<meta-name>issue-copyright-statement</meta-name>
<meta-value>© Springer-Verlag 1987</meta-value>
</custom-meta>
</custom-meta-group>
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<back>
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<fn>
<p>With 6 Figures</p>
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