Inhibition of feline (FIPV) and human (SARS) coronavirus by semisynthetic derivatives of glycopeptide antibiotics
Identifieur interne : 001105 ( Pmc/Checkpoint ); précédent : 001104; suivant : 001106Inhibition of feline (FIPV) and human (SARS) coronavirus by semisynthetic derivatives of glycopeptide antibiotics
Auteurs : Jan Balzarini [Belgique] ; Els Keyaerts [Belgique] ; Leen Vijgen [Belgique] ; Herman Egberink [Pays-Bas] ; Erik De Clercq [Belgique] ; Marc Van Ranst [Belgique] ; Svetlana S. Printsevskaya [Russie] ; Eugenia N. Olsufyeva [Russie] ; Svetlana E. Solovieva [Russie] ; Maria N. Preobrazhenskaya [Russie]Source :
- Antiviral Research [ 0166-3542 ] ; 2006.
Abstract
Various semisynthetic derivatives of glycopeptide antibiotics including vancomycin, eremomycin, teicoplanin, ristocetin A and DA-40926 have been evaluated for their inhibitory activity against feline infectious peritonitis virus (FIPV) and human (SARS-CoV, Frankfurt-1 strain) coronavirus in cell culture in comparison with their activity against human immunodeficiency virus (HIV). Several glycopeptide derivatives modified with hydrophobic substituents showed selective antiviral activity. For the most active compounds, the 50% effective concentrations (EC50) were in the lower micromolar range. In general, removal of the carbohydrate parts of the molecules did not affect the antiviral activity of the compounds. Some compounds showed inhibitory activity against both, whereas other compounds proved inhibitory to either, FIPV or SARS-CoV. There was no close correlation between the EC50 values of the glycopeptide derivatives for FIPV or SARS-CoV.
Url:
DOI: 10.1016/j.antiviral.2006.03.005
PubMed: 16675038
PubMed Central: 7114212
Affiliations:
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<author><name sortKey="Printsevskaya, Svetlana S" sort="Printsevskaya, Svetlana S" uniqKey="Printsevskaya S" first="Svetlana S." last="Printsevskaya">Svetlana S. Printsevskaya</name>
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<author><name sortKey="Olsufyeva, Eugenia N" sort="Olsufyeva, Eugenia N" uniqKey="Olsufyeva E" first="Eugenia N." last="Olsufyeva">Eugenia N. Olsufyeva</name>
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<author><name sortKey="Preobrazhenskaya, Maria N" sort="Preobrazhenskaya, Maria N" uniqKey="Preobrazhenskaya M" first="Maria N." last="Preobrazhenskaya">Maria N. Preobrazhenskaya</name>
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<series><title level="j">Antiviral Research</title>
<idno type="ISSN">0166-3542</idno>
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<front><div type="abstract" xml:lang="en"><p>Various semisynthetic derivatives of glycopeptide antibiotics including vancomycin, eremomycin, teicoplanin, ristocetin A and DA-40926 have been evaluated for their inhibitory activity against feline infectious peritonitis virus (FIPV) and human (SARS-CoV, Frankfurt-1 strain) coronavirus in cell culture in comparison with their activity against human immunodeficiency virus (HIV). Several glycopeptide derivatives modified with hydrophobic substituents showed selective antiviral activity. For the most active compounds, the 50% effective concentrations (EC<sub>50</sub>
) were in the lower micromolar range. In general, removal of the carbohydrate parts of the molecules did not affect the antiviral activity of the compounds. Some compounds showed inhibitory activity against both, whereas other compounds proved inhibitory to either, FIPV or SARS-CoV. There was no close correlation between the EC<sub>50</sub>
values of the glycopeptide derivatives for FIPV or SARS-CoV.</p>
</div>
</front>
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<biblStruct><analytic><author><name sortKey="Trani, A" uniqKey="Trani A">A. Trani</name>
</author>
<author><name sortKey="Ferrari, P" uniqKey="Ferrari P">P. Ferrari</name>
</author>
<author><name sortKey="Pallanza, R" uniqKey="Pallanza R">R. Pallanza</name>
</author>
<author><name sortKey="Ciabatti, R" uniqKey="Ciabatti R">R. Ciabatti</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Tresnan, D B" uniqKey="Tresnan D">D.B. Tresnan</name>
</author>
<author><name sortKey="Levis, R" uniqKey="Levis R">R. Levis</name>
</author>
<author><name sortKey="Holmes, K V" uniqKey="Holmes K">K.V. Holmes</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Walsh, C T" uniqKey="Walsh C">C.T. Walsh</name>
</author>
</analytic>
</biblStruct>
</listBibl>
</div1>
</back>
</TEI>
<pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Antiviral Res</journal-id>
<journal-id journal-id-type="iso-abbrev">Antiviral Res</journal-id>
<journal-title-group><journal-title>Antiviral Research</journal-title>
</journal-title-group>
<issn pub-type="ppub">0166-3542</issn>
<issn pub-type="epub">1872-9096</issn>
<publisher><publisher-name>Elsevier B.V.</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">16675038</article-id>
<article-id pub-id-type="pmc">7114212</article-id>
<article-id pub-id-type="publisher-id">S0166-3542(06)00072-6</article-id>
<article-id pub-id-type="doi">10.1016/j.antiviral.2006.03.005</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Inhibition of feline (FIPV) and human (SARS) coronavirus by semisynthetic derivatives of glycopeptide antibiotics</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Balzarini</surname>
<given-names>Jan</given-names>
</name>
<email>jan.balzarini@rega.kuleuven.be</email>
<xref rid="aff1" ref-type="aff">a</xref>
<xref rid="cor1" ref-type="corresp">⁎</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Keyaerts</surname>
<given-names>Els</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Vijgen</surname>
<given-names>Leen</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Egberink</surname>
<given-names>Herman</given-names>
</name>
<xref rid="aff2" ref-type="aff">b</xref>
</contrib>
<contrib contrib-type="author"><name><surname>De Clercq</surname>
<given-names>Erik</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Van Ranst</surname>
<given-names>Marc</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Printsevskaya</surname>
<given-names>Svetlana S.</given-names>
</name>
<xref rid="aff3" ref-type="aff">c</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Olsufyeva</surname>
<given-names>Eugenia N.</given-names>
</name>
<xref rid="aff3" ref-type="aff">c</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Solovieva</surname>
<given-names>Svetlana E.</given-names>
</name>
<xref rid="aff3" ref-type="aff">c</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Preobrazhenskaya</surname>
<given-names>Maria N.</given-names>
</name>
<xref rid="aff3" ref-type="aff">c</xref>
</contrib>
</contrib-group>
<aff id="aff1"><label>a</label>
Rega Institute for Medical Research, K.U. Leuven, Minderbroedersstraat 10, B-3000 Leuven, Belgium</aff>
<aff id="aff2"><label>b</label>
Institute of Virology, Faculty of Veterinary Medicine, University of Utrecht, Utrecht, The Netherlands</aff>
<aff id="aff3"><label>c</label>
Gause Institute of New Antibiotics, Russian Academy of Medical Sciences, Moscow, Russia</aff>
<author-notes><corresp id="cor1"><label>⁎</label>
Corresponding author. Tel.: +32 16 337352; fax: + 32 16 337340. <email>jan.balzarini@rega.kuleuven.be</email>
</corresp>
</author-notes>
<pub-date pub-type="pmc-release"><day>6</day>
<month>4</month>
<year>2006</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub"><month>10</month>
<year>2006</year>
</pub-date>
<pub-date pub-type="epub"><day>6</day>
<month>4</month>
<year>2006</year>
</pub-date>
<volume>72</volume>
<issue>1</issue>
<fpage>20</fpage>
<lpage>33</lpage>
<history><date date-type="received"><day>25</day>
<month>1</month>
<year>2006</year>
</date>
<date date-type="accepted"><day>14</day>
<month>3</month>
<year>2006</year>
</date>
</history>
<permissions><copyright-statement>Copyright © 2006 Elsevier B.V. All rights reserved.</copyright-statement>
<copyright-year>2006</copyright-year>
<copyright-holder>Elsevier B.V.</copyright-holder>
<license><license-p>Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.</license-p>
</license>
</permissions>
<abstract><p>Various semisynthetic derivatives of glycopeptide antibiotics including vancomycin, eremomycin, teicoplanin, ristocetin A and DA-40926 have been evaluated for their inhibitory activity against feline infectious peritonitis virus (FIPV) and human (SARS-CoV, Frankfurt-1 strain) coronavirus in cell culture in comparison with their activity against human immunodeficiency virus (HIV). Several glycopeptide derivatives modified with hydrophobic substituents showed selective antiviral activity. For the most active compounds, the 50% effective concentrations (EC<sub>50</sub>
) were in the lower micromolar range. In general, removal of the carbohydrate parts of the molecules did not affect the antiviral activity of the compounds. Some compounds showed inhibitory activity against both, whereas other compounds proved inhibitory to either, FIPV or SARS-CoV. There was no close correlation between the EC<sub>50</sub>
values of the glycopeptide derivatives for FIPV or SARS-CoV.</p>
</abstract>
<kwd-group><title>Keywords</title>
<kwd>Coronaviruses</kwd>
<kwd>FIPV</kwd>
<kwd>SARS</kwd>
<kwd>Glycopeptide antibiotics</kwd>
<kwd>Vancomycin</kwd>
<kwd>Teicoplanin</kwd>
<kwd>Eremomycin</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
<affiliations><list><country><li>Belgique</li>
<li>Pays-Bas</li>
<li>Russie</li>
</country>
<region><li>District fédéral central</li>
<li>Utrecht (province)</li>
</region>
<settlement><li>Moscou</li>
<li>Utrecht</li>
</settlement>
</list>
<tree><country name="Belgique"><noRegion><name sortKey="Balzarini, Jan" sort="Balzarini, Jan" uniqKey="Balzarini J" first="Jan" last="Balzarini">Jan Balzarini</name>
</noRegion>
<name sortKey="De Clercq, Erik" sort="De Clercq, Erik" uniqKey="De Clercq E" first="Erik" last="De Clercq">Erik De Clercq</name>
<name sortKey="Keyaerts, Els" sort="Keyaerts, Els" uniqKey="Keyaerts E" first="Els" last="Keyaerts">Els Keyaerts</name>
<name sortKey="Van Ranst, Marc" sort="Van Ranst, Marc" uniqKey="Van Ranst M" first="Marc" last="Van Ranst">Marc Van Ranst</name>
<name sortKey="Vijgen, Leen" sort="Vijgen, Leen" uniqKey="Vijgen L" first="Leen" last="Vijgen">Leen Vijgen</name>
</country>
<country name="Pays-Bas"><region name="Utrecht (province)"><name sortKey="Egberink, Herman" sort="Egberink, Herman" uniqKey="Egberink H" first="Herman" last="Egberink">Herman Egberink</name>
</region>
</country>
<country name="Russie"><region name="District fédéral central"><name sortKey="Printsevskaya, Svetlana S" sort="Printsevskaya, Svetlana S" uniqKey="Printsevskaya S" first="Svetlana S." last="Printsevskaya">Svetlana S. Printsevskaya</name>
</region>
<name sortKey="Olsufyeva, Eugenia N" sort="Olsufyeva, Eugenia N" uniqKey="Olsufyeva E" first="Eugenia N." last="Olsufyeva">Eugenia N. Olsufyeva</name>
<name sortKey="Preobrazhenskaya, Maria N" sort="Preobrazhenskaya, Maria N" uniqKey="Preobrazhenskaya M" first="Maria N." last="Preobrazhenskaya">Maria N. Preobrazhenskaya</name>
<name sortKey="Solovieva, Svetlana E" sort="Solovieva, Svetlana E" uniqKey="Solovieva S" first="Svetlana E." last="Solovieva">Svetlana E. Solovieva</name>
</country>
</tree>
</affiliations>
</record>
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