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Activity of the antimicrobial peptide P34 against bovine alphaherpesvirus type 1
Previous studies have demonstrated the antimicrobial activity of the peptide P34. In this study, the antiviral potential of P34 and the in vitro mechanism of action were investigated against bovine alphaherpesvirus type 1 (BoHV1). P34 exhibited low toxicity, a high selectivity index (22.9) and a per...
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Published in: | Ciência rural 2017, Vol.47 (6) |
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creator | Castro, Clarissa Caetano de Silva, Débora Scopel e Costa, Géssica Aracéli Fischer, Geferson Vargas, Gilberto D’Avila Brandelli, Adriano Lima, Marcelo de Motta, Amanda de Souza da Hübner, Silvia de Oliveira |
description | Previous studies have demonstrated the antimicrobial activity of the peptide P34. In this study, the antiviral potential of P34 and the in vitro mechanism of action were investigated against bovine alphaherpesvirus type 1 (BoHV1). P34 exhibited low toxicity, a high selectivity index (22.9) and a percentage of inhibition of up to 100% in MDBK cells. Results from antiviral assays indicated that P34 did not interact with cell receptors, but it was able to inhibit the viral penetration immediately after pre-adsorption. In addition, BoHV1 growth curve in MDBK cells in the presence of P34 revealed a significant reduction in virus titer only 8h post-infection, also suggesting an important role at late stages of the replicative cycle. Virucidal effect was observed only in cytotoxic concentrations of the peptide. These findings showed that the antimicrobial peptide P34 may be considered as a potential novel inhibitor of in vitro herpesviruses and must encourage further investigation of its antiherpetic activity in animal models as well as against a wide spectrum of viruses.
RESUMO: A atividade antimicrobiana do peptídeo P34 já foi previamente demonstrada. Neste estudo, o potencial antiviral do P34 e o mecanismo de ação in vitro contra o alfaherpesvírus bovino tipo 1 (BoHV1) foram investigados. O P34 exibiu baixa toxicidade, alto índice de seletividade (22.9) e percentagem de inibição viral de até 100% em células MDBK. Os resultados dos ensaios antivirais indicaram que não interage com receptores celulares, mas é capaz de inibir a penetração viral, imediatamente após a pré-adsorção. Além disso, a curva de crescimento do BoHV1 em células MDBK na presença do P34 revelou uma significativa redução no título somente após 8h de infecção, sugerindo também uma importante atividade do peptídeo nas fases finais do ciclo replicativo. Efeito virucida frente / BoHV1 foi observado apenas em concentrações citotóxicas do peptídeo. Os dados obtidos indicam que o peptídeo antimicrobiano P34 pode ser considerado um potencial composto inibidor de herpesvírus, in vitro, e estimulam posteriores investigações sobre sua atividade anti-herpética em modelos animais, bem como contra outros vírus. |
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RESUMO: A atividade antimicrobiana do peptídeo P34 já foi previamente demonstrada. Neste estudo, o potencial antiviral do P34 e o mecanismo de ação in vitro contra o alfaherpesvírus bovino tipo 1 (BoHV1) foram investigados. O P34 exibiu baixa toxicidade, alto índice de seletividade (22.9) e percentagem de inibição viral de até 100% em células MDBK. Os resultados dos ensaios antivirais indicaram que não interage com receptores celulares, mas é capaz de inibir a penetração viral, imediatamente após a pré-adsorção. Além disso, a curva de crescimento do BoHV1 em células MDBK na presença do P34 revelou uma significativa redução no título somente após 8h de infecção, sugerindo também uma importante atividade do peptídeo nas fases finais do ciclo replicativo. Efeito virucida frente / BoHV1 foi observado apenas em concentrações citotóxicas do peptídeo. Os dados obtidos indicam que o peptídeo antimicrobiano P34 pode ser considerado um potencial composto inibidor de herpesvírus, in vitro, e estimulam posteriores investigações sobre sua atividade anti-herpética em modelos animais, bem como contra outros vírus.</description><identifier>ISSN: 0103-8478</identifier><identifier>ISSN: 1678-4596</identifier><identifier>EISSN: 0103-8478</identifier><identifier>EISSN: 1678-4596</identifier><identifier>DOI: 10.1590/0103-8478cr20160668</identifier><language>eng ; por</language><publisher>Santa Maria: Universidade Federal de Santa Maria Centro de Ciencias Rurais</publisher><subject>AGRONOMY ; Animal models ; Antiinfectives and antibacterials ; Antimicrobial activity ; Antimicrobial agents ; Antimicrobial peptides ; antiviral ; Cattle industry ; Cytotoxicity ; Gram-positive bacteria ; herpesvírus ; Infections ; Peptides ; peptídeo ; Selectivity ; Spectrum analysis ; Statistical analysis ; Toxicity ; Viruses</subject><ispartof>Ciência rural, 2017, Vol.47 (6)</ispartof><rights>2017. This work is published under http://creativecommons.org/licenses/by/4.0/deed.en (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>This work is licensed under a Creative Commons Attribution 4.0 International License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-5b43952852803f298257ddcad1d6b66470374bea89c1fffd686efb2fe3a70aea3</citedby><cites>FETCH-LOGICAL-c357t-5b43952852803f298257ddcad1d6b66470374bea89c1fffd686efb2fe3a70aea3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2492279621/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2492279621?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,4024,24150,25753,27923,27924,27925,37012,44590,74998</link.rule.ids></links><search><creatorcontrib>Castro, Clarissa Caetano de</creatorcontrib><creatorcontrib>Silva, Débora Scopel e</creatorcontrib><creatorcontrib>Costa, Géssica Aracéli</creatorcontrib><creatorcontrib>Fischer, Geferson</creatorcontrib><creatorcontrib>Vargas, Gilberto D’Avila</creatorcontrib><creatorcontrib>Brandelli, Adriano</creatorcontrib><creatorcontrib>Lima, Marcelo de</creatorcontrib><creatorcontrib>Motta, Amanda de Souza da</creatorcontrib><creatorcontrib>Hübner, Silvia de Oliveira</creatorcontrib><title>Activity of the antimicrobial peptide P34 against bovine alphaherpesvirus type 1</title><title>Ciência rural</title><addtitle>Cienc. Rural</addtitle><description>Previous studies have demonstrated the antimicrobial activity of the peptide P34. In this study, the antiviral potential of P34 and the in vitro mechanism of action were investigated against bovine alphaherpesvirus type 1 (BoHV1). P34 exhibited low toxicity, a high selectivity index (22.9) and a percentage of inhibition of up to 100% in MDBK cells. Results from antiviral assays indicated that P34 did not interact with cell receptors, but it was able to inhibit the viral penetration immediately after pre-adsorption. In addition, BoHV1 growth curve in MDBK cells in the presence of P34 revealed a significant reduction in virus titer only 8h post-infection, also suggesting an important role at late stages of the replicative cycle. Virucidal effect was observed only in cytotoxic concentrations of the peptide. These findings showed that the antimicrobial peptide P34 may be considered as a potential novel inhibitor of in vitro herpesviruses and must encourage further investigation of its antiherpetic activity in animal models as well as against a wide spectrum of viruses.
RESUMO: A atividade antimicrobiana do peptídeo P34 já foi previamente demonstrada. Neste estudo, o potencial antiviral do P34 e o mecanismo de ação in vitro contra o alfaherpesvírus bovino tipo 1 (BoHV1) foram investigados. O P34 exibiu baixa toxicidade, alto índice de seletividade (22.9) e percentagem de inibição viral de até 100% em células MDBK. Os resultados dos ensaios antivirais indicaram que não interage com receptores celulares, mas é capaz de inibir a penetração viral, imediatamente após a pré-adsorção. Além disso, a curva de crescimento do BoHV1 em células MDBK na presença do P34 revelou uma significativa redução no título somente após 8h de infecção, sugerindo também uma importante atividade do peptídeo nas fases finais do ciclo replicativo. Efeito virucida frente / BoHV1 foi observado apenas em concentrações citotóxicas do peptídeo. Os dados obtidos indicam que o peptídeo antimicrobiano P34 pode ser considerado um potencial composto inibidor de herpesvírus, in vitro, e estimulam posteriores investigações sobre sua atividade anti-herpética em modelos animais, bem como contra outros vírus.</description><subject>AGRONOMY</subject><subject>Animal models</subject><subject>Antiinfectives and antibacterials</subject><subject>Antimicrobial activity</subject><subject>Antimicrobial agents</subject><subject>Antimicrobial peptides</subject><subject>antiviral</subject><subject>Cattle industry</subject><subject>Cytotoxicity</subject><subject>Gram-positive bacteria</subject><subject>herpesvírus</subject><subject>Infections</subject><subject>Peptides</subject><subject>peptídeo</subject><subject>Selectivity</subject><subject>Spectrum analysis</subject><subject>Statistical analysis</subject><subject>Toxicity</subject><subject>Viruses</subject><issn>0103-8478</issn><issn>1678-4596</issn><issn>0103-8478</issn><issn>1678-4596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpNUV1rGzEQPEIDcZ38grwI8ux09XGS7jGYtgkEYkj7LPb0EctcrIskG_zve66LU1jYZZgZhtmmuaVwT9sOvgEFvtBCaZsZUAlS6otmdka__HdfNV9L2QAwxYWYNasHW-M-1gNJgdS1J7it8T3anPqIAxn9WKPzZMUFwTeM21JJn_ZxOxGHcY1rn0df9jHvCqmH0RN63VwGHIq_-bfnze8f338tHxfPLz-flg_PC8tbVRdtL3jXMj0N8MA6zVrlnEVHneylFAq4Er1H3VkaQnBSSx96FjxHBeiRz5unk69LuDFjju-YDyZhNH-BlN8M5hrt4A0qRa3VrmeMCsug0z6AaJFCaKnjcvK6P3kVG_2QzCbt8nYKb16PtZljbVOtCgAkTEI6Ce5OgjGnj50v9VPCRMeY6iQ7sviJNbVZSvbhHJOCOf7NnO0__8b_ANGih-g</recordid><startdate>2017</startdate><enddate>2017</enddate><creator>Castro, Clarissa Caetano de</creator><creator>Silva, Débora Scopel e</creator><creator>Costa, Géssica Aracéli</creator><creator>Fischer, Geferson</creator><creator>Vargas, Gilberto D’Avila</creator><creator>Brandelli, Adriano</creator><creator>Lima, Marcelo de</creator><creator>Motta, Amanda de Souza da</creator><creator>Hübner, Silvia de Oliveira</creator><general>Universidade Federal de Santa Maria Centro de Ciencias Rurais</general><general>Universidade Federal de Santa Maria</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X2</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>M0K</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>GPN</scope><scope>DOA</scope></search><sort><creationdate>2017</creationdate><title>Activity of the antimicrobial peptide P34 against bovine alphaherpesvirus type 1</title><author>Castro, Clarissa Caetano de ; Silva, Débora Scopel e ; Costa, Géssica Aracéli ; Fischer, Geferson ; Vargas, Gilberto D’Avila ; Brandelli, Adriano ; Lima, Marcelo de ; Motta, Amanda de Souza da ; Hübner, Silvia de Oliveira</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-5b43952852803f298257ddcad1d6b66470374bea89c1fffd686efb2fe3a70aea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng ; por</language><creationdate>2017</creationdate><topic>AGRONOMY</topic><topic>Animal models</topic><topic>Antiinfectives and antibacterials</topic><topic>Antimicrobial activity</topic><topic>Antimicrobial agents</topic><topic>Antimicrobial peptides</topic><topic>antiviral</topic><topic>Cattle industry</topic><topic>Cytotoxicity</topic><topic>Gram-positive bacteria</topic><topic>herpesvírus</topic><topic>Infections</topic><topic>Peptides</topic><topic>peptídeo</topic><topic>Selectivity</topic><topic>Spectrum analysis</topic><topic>Statistical analysis</topic><topic>Toxicity</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Castro, Clarissa Caetano de</creatorcontrib><creatorcontrib>Silva, Débora Scopel e</creatorcontrib><creatorcontrib>Costa, Géssica Aracéli</creatorcontrib><creatorcontrib>Fischer, Geferson</creatorcontrib><creatorcontrib>Vargas, Gilberto D’Avila</creatorcontrib><creatorcontrib>Brandelli, Adriano</creatorcontrib><creatorcontrib>Lima, Marcelo de</creatorcontrib><creatorcontrib>Motta, Amanda de Souza da</creatorcontrib><creatorcontrib>Hübner, Silvia de Oliveira</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Agricultural Science Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>SciTech Premium Collection</collection><collection>Agricultural Science Database</collection><collection>ProQuest - Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>SciELO</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Ciência rural</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Castro, Clarissa Caetano de</au><au>Silva, Débora Scopel e</au><au>Costa, Géssica Aracéli</au><au>Fischer, Geferson</au><au>Vargas, Gilberto D’Avila</au><au>Brandelli, Adriano</au><au>Lima, Marcelo de</au><au>Motta, Amanda de Souza da</au><au>Hübner, Silvia de Oliveira</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Activity of the antimicrobial peptide P34 against bovine alphaherpesvirus type 1</atitle><jtitle>Ciência rural</jtitle><addtitle>Cienc. Rural</addtitle><date>2017</date><risdate>2017</risdate><volume>47</volume><issue>6</issue><issn>0103-8478</issn><issn>1678-4596</issn><eissn>0103-8478</eissn><eissn>1678-4596</eissn><abstract>Previous studies have demonstrated the antimicrobial activity of the peptide P34. In this study, the antiviral potential of P34 and the in vitro mechanism of action were investigated against bovine alphaherpesvirus type 1 (BoHV1). P34 exhibited low toxicity, a high selectivity index (22.9) and a percentage of inhibition of up to 100% in MDBK cells. Results from antiviral assays indicated that P34 did not interact with cell receptors, but it was able to inhibit the viral penetration immediately after pre-adsorption. In addition, BoHV1 growth curve in MDBK cells in the presence of P34 revealed a significant reduction in virus titer only 8h post-infection, also suggesting an important role at late stages of the replicative cycle. Virucidal effect was observed only in cytotoxic concentrations of the peptide. These findings showed that the antimicrobial peptide P34 may be considered as a potential novel inhibitor of in vitro herpesviruses and must encourage further investigation of its antiherpetic activity in animal models as well as against a wide spectrum of viruses.
RESUMO: A atividade antimicrobiana do peptídeo P34 já foi previamente demonstrada. Neste estudo, o potencial antiviral do P34 e o mecanismo de ação in vitro contra o alfaherpesvírus bovino tipo 1 (BoHV1) foram investigados. O P34 exibiu baixa toxicidade, alto índice de seletividade (22.9) e percentagem de inibição viral de até 100% em células MDBK. Os resultados dos ensaios antivirais indicaram que não interage com receptores celulares, mas é capaz de inibir a penetração viral, imediatamente após a pré-adsorção. Além disso, a curva de crescimento do BoHV1 em células MDBK na presença do P34 revelou uma significativa redução no título somente após 8h de infecção, sugerindo também uma importante atividade do peptídeo nas fases finais do ciclo replicativo. Efeito virucida frente / BoHV1 foi observado apenas em concentrações citotóxicas do peptídeo. Os dados obtidos indicam que o peptídeo antimicrobiano P34 pode ser considerado um potencial composto inibidor de herpesvírus, in vitro, e estimulam posteriores investigações sobre sua atividade anti-herpética em modelos animais, bem como contra outros vírus.</abstract><cop>Santa Maria</cop><pub>Universidade Federal de Santa Maria Centro de Ciencias Rurais</pub><doi>10.1590/0103-8478cr20160668</doi><oa>free_for_read</oa></addata></record> |
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subjects | AGRONOMY Animal models Antiinfectives and antibacterials Antimicrobial activity Antimicrobial agents Antimicrobial peptides antiviral Cattle industry Cytotoxicity Gram-positive bacteria herpesvírus Infections Peptides peptídeo Selectivity Spectrum analysis Statistical analysis Toxicity Viruses |
title | Activity of the antimicrobial peptide P34 against bovine alphaherpesvirus type 1 |
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