Polyhexamethylene biguanide exposure leads to viral aggregation
This study reports the activity of two biguanides against MS2 bacteriophage used as a surrogate virus for nonenveloped mammalian viruses and provides an explanation as to their apparent limited efficacy. When tested in a standard suspension test, two polyhexamethylene biguanides (PHMB), VANTOCIL[tra...
Gespeichert in:
Veröffentlicht in: | Journal of applied microbiology 2010-06, Vol.108 (6), p.1880-1888 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1888 |
---|---|
container_issue | 6 |
container_start_page | 1880 |
container_title | Journal of applied microbiology |
container_volume | 108 |
creator | Pinto, F Maillard, J.-Y Denyer, S.P McGeechan, P |
description | This study reports the activity of two biguanides against MS2 bacteriophage used as a surrogate virus for nonenveloped mammalian viruses and provides an explanation as to their apparent limited efficacy. When tested in a standard suspension test, two polyhexamethylene biguanides (PHMB), VANTOCIL[trade mark sign] TG and COSMOCIL[trade mark sign] CQ, reduced the viability of MS2 by only 1-2 log₁₀ PFU ml⁻¹. Exposure time up to 30 min did not affect the activity of the biguanides, although both PHMB were shown to strongly interact with MS2 proteins. Inactivation kinetics and change in virus hydrophobicity suggested that PHMB induces the formation of viral aggregates. This hypothesis was supported using dynamic light scattering that showed an increase in viral aggregates sizes (up to 500 nm) in a concentration-dependent manner. It has been reported that viral aggregation is responsible for virus survival to the biocide exposure. Here, this might be the case, because the virucidal activity of the biguanides was modest and viral aggregation important. The formation of viral aggregates during virus exposure to PHMB was unlikely to overestimate the virucidal potential of the biguanides. |
doi_str_mv | 10.1111/j.1365-2672.2009.04596.x |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_749001040</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>744615164</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5046-2f6c94e2b33af14ca0fc2145ee18d042b505113218e8d8974e8c1dae6b55f82a3</originalsourceid><addsrcrecordid>eNqNkU1v1DAQhi1ERUvhL0AuiFOCx7Ed54BQVfGpVkWCnq2JM0mz8iaLvYHdf1-nuyrX-uKR_Lwz9mPGMuAFpPVhVUCpVS50JQrBeV1wqWpd7J6xs8eD5w-1zBWvxCl7GeOKcyi50i_YKdSmVlrBGfv0c_L7O9rhmrZ3e08jZc3QzzgOLWW020xxDpR5wjZm2yn7OwT0GfZ9oB63wzS-Yicd-kivj_s5u_3y-fflt_zq5uv3y4ur3CkudS467WpJoilL7EA65J0TIBURmJZL0SiuAEoBhkxr6kqScdAi6Uapzggsz9n7Q99NmP7MFLd2PURH3uNI0xxtJev0PC75E0ipQYGWiTQH0oUpxkCd3YRhjWFvgdvFs13ZRadddNrFs33wbHcp-uY4ZG7W1P4PHsUm4N0RwOjQdwFHN8RHTogqNZIqcR8P3L_B0_7JF7A_Lq6XKuXfHvIdThb7kGbc_hLLR4Mpq6quyntdJaFV</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>744615164</pqid></control><display><type>article</type><title>Polyhexamethylene biguanide exposure leads to viral aggregation</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Pinto, F ; Maillard, J.-Y ; Denyer, S.P ; McGeechan, P</creator><creatorcontrib>Pinto, F ; Maillard, J.-Y ; Denyer, S.P ; McGeechan, P</creatorcontrib><description>This study reports the activity of two biguanides against MS2 bacteriophage used as a surrogate virus for nonenveloped mammalian viruses and provides an explanation as to their apparent limited efficacy. When tested in a standard suspension test, two polyhexamethylene biguanides (PHMB), VANTOCIL[trade mark sign] TG and COSMOCIL[trade mark sign] CQ, reduced the viability of MS2 by only 1-2 log₁₀ PFU ml⁻¹. Exposure time up to 30 min did not affect the activity of the biguanides, although both PHMB were shown to strongly interact with MS2 proteins. Inactivation kinetics and change in virus hydrophobicity suggested that PHMB induces the formation of viral aggregates. This hypothesis was supported using dynamic light scattering that showed an increase in viral aggregates sizes (up to 500 nm) in a concentration-dependent manner. It has been reported that viral aggregation is responsible for virus survival to the biocide exposure. Here, this might be the case, because the virucidal activity of the biguanides was modest and viral aggregation important. The formation of viral aggregates during virus exposure to PHMB was unlikely to overestimate the virucidal potential of the biguanides.</description><identifier>ISSN: 1364-5072</identifier><identifier>EISSN: 1365-2672</identifier><identifier>DOI: 10.1111/j.1365-2672.2009.04596.x</identifier><identifier>PMID: 19895651</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Publishing Ltd</publisher><subject>activity ; Biguanides - pharmacology ; Biological and medical sciences ; Disinfectants - pharmacology ; Fundamental and applied biological sciences. Psychology ; Hydrophobic and Hydrophilic Interactions ; Levivirus - drug effects ; mechanisms of action ; Microbiology ; PHMB ; Viral Proteins - analysis ; virus ; viruses</subject><ispartof>Journal of applied microbiology, 2010-06, Vol.108 (6), p.1880-1888</ispartof><rights>2009 The Authors. Journal compilation © 2009 The Society for Applied Microbiology</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5046-2f6c94e2b33af14ca0fc2145ee18d042b505113218e8d8974e8c1dae6b55f82a3</citedby><cites>FETCH-LOGICAL-c5046-2f6c94e2b33af14ca0fc2145ee18d042b505113218e8d8974e8c1dae6b55f82a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2672.2009.04596.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2672.2009.04596.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22759645$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19895651$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pinto, F</creatorcontrib><creatorcontrib>Maillard, J.-Y</creatorcontrib><creatorcontrib>Denyer, S.P</creatorcontrib><creatorcontrib>McGeechan, P</creatorcontrib><title>Polyhexamethylene biguanide exposure leads to viral aggregation</title><title>Journal of applied microbiology</title><addtitle>J Appl Microbiol</addtitle><description>This study reports the activity of two biguanides against MS2 bacteriophage used as a surrogate virus for nonenveloped mammalian viruses and provides an explanation as to their apparent limited efficacy. When tested in a standard suspension test, two polyhexamethylene biguanides (PHMB), VANTOCIL[trade mark sign] TG and COSMOCIL[trade mark sign] CQ, reduced the viability of MS2 by only 1-2 log₁₀ PFU ml⁻¹. Exposure time up to 30 min did not affect the activity of the biguanides, although both PHMB were shown to strongly interact with MS2 proteins. Inactivation kinetics and change in virus hydrophobicity suggested that PHMB induces the formation of viral aggregates. This hypothesis was supported using dynamic light scattering that showed an increase in viral aggregates sizes (up to 500 nm) in a concentration-dependent manner. It has been reported that viral aggregation is responsible for virus survival to the biocide exposure. Here, this might be the case, because the virucidal activity of the biguanides was modest and viral aggregation important. The formation of viral aggregates during virus exposure to PHMB was unlikely to overestimate the virucidal potential of the biguanides.</description><subject>activity</subject><subject>Biguanides - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Disinfectants - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hydrophobic and Hydrophilic Interactions</subject><subject>Levivirus - drug effects</subject><subject>mechanisms of action</subject><subject>Microbiology</subject><subject>PHMB</subject><subject>Viral Proteins - analysis</subject><subject>virus</subject><subject>viruses</subject><issn>1364-5072</issn><issn>1365-2672</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1v1DAQhi1ERUvhL0AuiFOCx7Ed54BQVfGpVkWCnq2JM0mz8iaLvYHdf1-nuyrX-uKR_Lwz9mPGMuAFpPVhVUCpVS50JQrBeV1wqWpd7J6xs8eD5w-1zBWvxCl7GeOKcyi50i_YKdSmVlrBGfv0c_L7O9rhmrZ3e08jZc3QzzgOLWW020xxDpR5wjZm2yn7OwT0GfZ9oB63wzS-Yicd-kivj_s5u_3y-fflt_zq5uv3y4ur3CkudS467WpJoilL7EA65J0TIBURmJZL0SiuAEoBhkxr6kqScdAi6Uapzggsz9n7Q99NmP7MFLd2PURH3uNI0xxtJev0PC75E0ipQYGWiTQH0oUpxkCd3YRhjWFvgdvFs13ZRadddNrFs33wbHcp-uY4ZG7W1P4PHsUm4N0RwOjQdwFHN8RHTogqNZIqcR8P3L_B0_7JF7A_Lq6XKuXfHvIdThb7kGbc_hLLR4Mpq6quyntdJaFV</recordid><startdate>201006</startdate><enddate>201006</enddate><creator>Pinto, F</creator><creator>Maillard, J.-Y</creator><creator>Denyer, S.P</creator><creator>McGeechan, P</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201006</creationdate><title>Polyhexamethylene biguanide exposure leads to viral aggregation</title><author>Pinto, F ; Maillard, J.-Y ; Denyer, S.P ; McGeechan, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5046-2f6c94e2b33af14ca0fc2145ee18d042b505113218e8d8974e8c1dae6b55f82a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>activity</topic><topic>Biguanides - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Disinfectants - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hydrophobic and Hydrophilic Interactions</topic><topic>Levivirus - drug effects</topic><topic>mechanisms of action</topic><topic>Microbiology</topic><topic>PHMB</topic><topic>Viral Proteins - analysis</topic><topic>virus</topic><topic>viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pinto, F</creatorcontrib><creatorcontrib>Maillard, J.-Y</creatorcontrib><creatorcontrib>Denyer, S.P</creatorcontrib><creatorcontrib>McGeechan, P</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of applied microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pinto, F</au><au>Maillard, J.-Y</au><au>Denyer, S.P</au><au>McGeechan, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polyhexamethylene biguanide exposure leads to viral aggregation</atitle><jtitle>Journal of applied microbiology</jtitle><addtitle>J Appl Microbiol</addtitle><date>2010-06</date><risdate>2010</risdate><volume>108</volume><issue>6</issue><spage>1880</spage><epage>1888</epage><pages>1880-1888</pages><issn>1364-5072</issn><eissn>1365-2672</eissn><abstract>This study reports the activity of two biguanides against MS2 bacteriophage used as a surrogate virus for nonenveloped mammalian viruses and provides an explanation as to their apparent limited efficacy. When tested in a standard suspension test, two polyhexamethylene biguanides (PHMB), VANTOCIL[trade mark sign] TG and COSMOCIL[trade mark sign] CQ, reduced the viability of MS2 by only 1-2 log₁₀ PFU ml⁻¹. Exposure time up to 30 min did not affect the activity of the biguanides, although both PHMB were shown to strongly interact with MS2 proteins. Inactivation kinetics and change in virus hydrophobicity suggested that PHMB induces the formation of viral aggregates. This hypothesis was supported using dynamic light scattering that showed an increase in viral aggregates sizes (up to 500 nm) in a concentration-dependent manner. It has been reported that viral aggregation is responsible for virus survival to the biocide exposure. Here, this might be the case, because the virucidal activity of the biguanides was modest and viral aggregation important. The formation of viral aggregates during virus exposure to PHMB was unlikely to overestimate the virucidal potential of the biguanides.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Publishing Ltd</pub><pmid>19895651</pmid><doi>10.1111/j.1365-2672.2009.04596.x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1364-5072 |
ispartof | Journal of applied microbiology, 2010-06, Vol.108 (6), p.1880-1888 |
issn | 1364-5072 1365-2672 |
language | eng |
recordid | cdi_proquest_miscellaneous_749001040 |
source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | activity Biguanides - pharmacology Biological and medical sciences Disinfectants - pharmacology Fundamental and applied biological sciences. Psychology Hydrophobic and Hydrophilic Interactions Levivirus - drug effects mechanisms of action Microbiology PHMB Viral Proteins - analysis virus viruses |
title | Polyhexamethylene biguanide exposure leads to viral aggregation |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T16%3A48%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Polyhexamethylene%20biguanide%20exposure%20leads%20to%20viral%20aggregation&rft.jtitle=Journal%20of%20applied%20microbiology&rft.au=Pinto,%20F&rft.date=2010-06&rft.volume=108&rft.issue=6&rft.spage=1880&rft.epage=1888&rft.pages=1880-1888&rft.issn=1364-5072&rft.eissn=1365-2672&rft_id=info:doi/10.1111/j.1365-2672.2009.04596.x&rft_dat=%3Cproquest_cross%3E744615164%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=744615164&rft_id=info:pmid/19895651&rfr_iscdi=true |