Antimicrobial activity of nitrochalcone and pentyl caffeate against hospital pathogens results in decreased microbial adhesion and biofilm formation
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1080/08927014.2019.1574763 http://hdl.handle.net/11449/185622 |
Resumo: | The present study investigated the antimicrobial, anti-adhesion and anti-biofilm activity of the modified synthetic molecules nitrochalcone (NC-E05) and pentyl caffeate (C5) against microorganisms which have a high incidence in hospital-acquired infections. The compounds were further tested for their preliminary systemic toxicity in vivo. NC-E05 and C5 showed antimicrobial activity, with minimum inhibitory concentrations (MICs) ranging between 15.62 and 31.25g ml(-1). Treatment with NC-E05 and C5 at 1xMIC and/or 10xMIC significantly reduced mono or mixed-species biofilm formation and viability. At MIC/2, the compounds decreased microbial adhesion to HaCaT keratinocytes from 1 to 3h (p<0.0001). In addition, NC-E05 and C5 demonstrated low toxicity in vivo in the Galleria mellonella model at anti-biofilm concentrations. Thus, the chemical modification of these molecules proved to be effective in the proposed anti-biofilm activity, opening opportunities for the development of new antimicrobials. |
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Antimicrobial activity of nitrochalcone and pentyl caffeate against hospital pathogens results in decreased microbial adhesion and biofilm formationMixed biofilmnitrochalconepentyl caffeateStaphylococcus aureusCandida albicansThe present study investigated the antimicrobial, anti-adhesion and anti-biofilm activity of the modified synthetic molecules nitrochalcone (NC-E05) and pentyl caffeate (C5) against microorganisms which have a high incidence in hospital-acquired infections. The compounds were further tested for their preliminary systemic toxicity in vivo. NC-E05 and C5 showed antimicrobial activity, with minimum inhibitory concentrations (MICs) ranging between 15.62 and 31.25g ml(-1). Treatment with NC-E05 and C5 at 1xMIC and/or 10xMIC significantly reduced mono or mixed-species biofilm formation and viability. At MIC/2, the compounds decreased microbial adhesion to HaCaT keratinocytes from 1 to 3h (p<0.0001). In addition, NC-E05 and C5 demonstrated low toxicity in vivo in the Galleria mellonella model at anti-biofilm concentrations. Thus, the chemical modification of these molecules proved to be effective in the proposed anti-biofilm activity, opening opportunities for the development of new antimicrobials.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Univ Estadual Campinas, Dept Physiol Sci, Piracicaba Dent Sch, Piracicaba, SP, BrazilJulio de Mesquita Filho Univ, Dept Chem & Environm Sci, Sao Jose Do Rio Preto, BrazilUniv Sao Paulo, Dept Agri Food Ind Food & Nutr, Luiz de Queiroz Coll Agr, Piracicaba, BrazilJulio de Mesquita Filho Univ, Dept Chem & Environm Sci, Sao Jose Do Rio Preto, BrazilCNPq: 74335/2013-5CNPq: 132790/2018-1CAPES: 0.01Taylor & Francis LtdUniversidade Estadual de Campinas (UNICAMP)Universidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Almeida Sayao de Emeri, Fernanda Teresinha deRosalen, Pedro LuizPaganini, Eder Ramos [UNESP]Rocha Garcia, Mayara Aparecida [UNESP]Nazare, Ana Carolina [UNESP]Lazarini, Josy GoldoniAlencar, Severino Matias deRegasini, Luis Octavio [UNESP]Orlandi Sardi, Janaina de Cassia2019-10-04T12:36:57Z2019-10-04T12:36:57Z2019-04-03info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article129-142http://dx.doi.org/10.1080/08927014.2019.1574763Biofouling. Abingdon: Taylor & Francis Ltd, v. 35, n. 2, p. 129-142, 2019.0892-7014http://hdl.handle.net/11449/18562210.1080/08927014.2019.1574763WOS:000464691600001Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBiofoulinginfo:eu-repo/semantics/openAccess2021-10-23T12:39:48Zoai:repositorio.unesp.br:11449/185622Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-06T00:06:55.786888Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Antimicrobial activity of nitrochalcone and pentyl caffeate against hospital pathogens results in decreased microbial adhesion and biofilm formation |
title |
Antimicrobial activity of nitrochalcone and pentyl caffeate against hospital pathogens results in decreased microbial adhesion and biofilm formation |
spellingShingle |
Antimicrobial activity of nitrochalcone and pentyl caffeate against hospital pathogens results in decreased microbial adhesion and biofilm formation Almeida Sayao de Emeri, Fernanda Teresinha de Mixed biofilm nitrochalcone pentyl caffeate Staphylococcus aureus Candida albicans |
title_short |
Antimicrobial activity of nitrochalcone and pentyl caffeate against hospital pathogens results in decreased microbial adhesion and biofilm formation |
title_full |
Antimicrobial activity of nitrochalcone and pentyl caffeate against hospital pathogens results in decreased microbial adhesion and biofilm formation |
title_fullStr |
Antimicrobial activity of nitrochalcone and pentyl caffeate against hospital pathogens results in decreased microbial adhesion and biofilm formation |
title_full_unstemmed |
Antimicrobial activity of nitrochalcone and pentyl caffeate against hospital pathogens results in decreased microbial adhesion and biofilm formation |
title_sort |
Antimicrobial activity of nitrochalcone and pentyl caffeate against hospital pathogens results in decreased microbial adhesion and biofilm formation |
author |
Almeida Sayao de Emeri, Fernanda Teresinha de |
author_facet |
Almeida Sayao de Emeri, Fernanda Teresinha de Rosalen, Pedro Luiz Paganini, Eder Ramos [UNESP] Rocha Garcia, Mayara Aparecida [UNESP] Nazare, Ana Carolina [UNESP] Lazarini, Josy Goldoni Alencar, Severino Matias de Regasini, Luis Octavio [UNESP] Orlandi Sardi, Janaina de Cassia |
author_role |
author |
author2 |
Rosalen, Pedro Luiz Paganini, Eder Ramos [UNESP] Rocha Garcia, Mayara Aparecida [UNESP] Nazare, Ana Carolina [UNESP] Lazarini, Josy Goldoni Alencar, Severino Matias de Regasini, Luis Octavio [UNESP] Orlandi Sardi, Janaina de Cassia |
author2_role |
author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual de Campinas (UNICAMP) Universidade Estadual Paulista (Unesp) Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Almeida Sayao de Emeri, Fernanda Teresinha de Rosalen, Pedro Luiz Paganini, Eder Ramos [UNESP] Rocha Garcia, Mayara Aparecida [UNESP] Nazare, Ana Carolina [UNESP] Lazarini, Josy Goldoni Alencar, Severino Matias de Regasini, Luis Octavio [UNESP] Orlandi Sardi, Janaina de Cassia |
dc.subject.por.fl_str_mv |
Mixed biofilm nitrochalcone pentyl caffeate Staphylococcus aureus Candida albicans |
topic |
Mixed biofilm nitrochalcone pentyl caffeate Staphylococcus aureus Candida albicans |
description |
The present study investigated the antimicrobial, anti-adhesion and anti-biofilm activity of the modified synthetic molecules nitrochalcone (NC-E05) and pentyl caffeate (C5) against microorganisms which have a high incidence in hospital-acquired infections. The compounds were further tested for their preliminary systemic toxicity in vivo. NC-E05 and C5 showed antimicrobial activity, with minimum inhibitory concentrations (MICs) ranging between 15.62 and 31.25g ml(-1). Treatment with NC-E05 and C5 at 1xMIC and/or 10xMIC significantly reduced mono or mixed-species biofilm formation and viability. At MIC/2, the compounds decreased microbial adhesion to HaCaT keratinocytes from 1 to 3h (p<0.0001). In addition, NC-E05 and C5 demonstrated low toxicity in vivo in the Galleria mellonella model at anti-biofilm concentrations. Thus, the chemical modification of these molecules proved to be effective in the proposed anti-biofilm activity, opening opportunities for the development of new antimicrobials. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-10-04T12:36:57Z 2019-10-04T12:36:57Z 2019-04-03 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1080/08927014.2019.1574763 Biofouling. Abingdon: Taylor & Francis Ltd, v. 35, n. 2, p. 129-142, 2019. 0892-7014 http://hdl.handle.net/11449/185622 10.1080/08927014.2019.1574763 WOS:000464691600001 |
url |
http://dx.doi.org/10.1080/08927014.2019.1574763 http://hdl.handle.net/11449/185622 |
identifier_str_mv |
Biofouling. Abingdon: Taylor & Francis Ltd, v. 35, n. 2, p. 129-142, 2019. 0892-7014 10.1080/08927014.2019.1574763 WOS:000464691600001 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Biofouling |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
129-142 |
dc.publisher.none.fl_str_mv |
Taylor & Francis Ltd |
publisher.none.fl_str_mv |
Taylor & Francis Ltd |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808129585112416256 |