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Effect of ginger essential oil and 6-gingerol on a multispecies biofilm of Listeria monocytogenes, Salmonella Typhimurium, and Pseudomonas aeruginosa

dc.contributor.authordos Santos, Emanoelli Aparecida Rodrigues [UNESP]
dc.contributor.authorTadielo, Leonardo Ereno [UNESP]
dc.contributor.authorSchmiedt, Jhennifer Arruda
dc.contributor.authorPossebon, Fábio Sossai [UNESP]
dc.contributor.authorPereira, Maria Olivia
dc.contributor.authorPereira, Juliano Gonçalves [UNESP]
dc.contributor.authordos Santos Bersot, Luciano
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionFederal University of Paraná
dc.contributor.institutionUniversity of Minho
dc.date.accessioned2025-04-29T18:06:34Z
dc.date.issued2023-12-01
dc.description.abstractThe objective of this study was to evaluate the potential antimicrobial and antibiofilm effect of ginger essential oil (GEO) and 6-gingerol on a multispecies biofilm formed by Listeria monocytogenes, Salmonella Typhimurium, and Pseudomonas aeruginosa on a polypropylene surface. The minimum inhibitory concentration concentrations obtained for GEO were 100 and 50 mg/mL and for 6-gingerol 1.25 mg/mL. Sessile cell counts ranged within 5.35–7.35 log CFU/cm2 in the control biofilm, with the highest sessile growth at 72 h. GEO treatments acted on the total population regardless of concentration at 1 and 48 h. L. monocytogenes behaved similarly to the total population, showing GEO action at 1 h and keeping the same pattern at 48, 72, and 96 h. Better action on S. Typhimurium was obtained at times of 1, 72, and 96 h. P. aeruginosa showed logarithmic reduction only when treated with GEO 50 mg at 24 h. As for 6-gingerol, in general, there was no significant action (p > 0.05) on the evaluated sessile cells. GEO showed antimicrobial activity against L. monocytogenes, S. Typhimurium, and P. aeruginosa, acting as an inhibitor of biofilm formation. As for 6-gingerol, it was considered a possible antimicrobial agent but without efficacy during biofilm formation.en
dc.description.affiliationSchool of Veterinary Medicine and Animal Science São Paulo State University (UNESP), Distrito de Rubião Jr, SN
dc.description.affiliationDepartment of Veterinary Sciences Federal University of Paraná, Palotina Campus, Rua Pioneiro, Jardim Dallas, PR
dc.description.affiliationBiological Engineering Center University of Minho, Gualtar Campus
dc.description.affiliationUnespSchool of Veterinary Medicine and Animal Science São Paulo State University (UNESP), Distrito de Rubião Jr, SN
dc.format.extent3041-3049
dc.identifierhttp://dx.doi.org/10.1007/s42770-023-01075-2
dc.identifier.citationBrazilian Journal of Microbiology, v. 54, n. 4, p. 3041-3049, 2023.
dc.identifier.doi10.1007/s42770-023-01075-2
dc.identifier.issn1678-4405
dc.identifier.issn1517-8382
dc.identifier.scopus2-s2.0-85169820533
dc.identifier.urihttps://hdl.handle.net/11449/297431
dc.language.isoeng
dc.relation.ispartofBrazilian Journal of Microbiology
dc.sourceScopus
dc.subjectAntibacterial
dc.subjectAntibiofilm
dc.subjectControl methods
dc.subjectEssential oils
dc.titleEffect of ginger essential oil and 6-gingerol on a multispecies biofilm of Listeria monocytogenes, Salmonella Typhimurium, and Pseudomonas aeruginosaen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication9ca5a87b-0c83-43fa-b290-6f8a4202bf99
relation.isOrgUnitOfPublication.latestForDiscovery9ca5a87b-0c83-43fa-b290-6f8a4202bf99
unesp.author.orcid0000-0001-6011-3232[1]
unesp.author.orcid0000-0003-4731-849X[2]
unesp.author.orcid0000-0002-7539-840X[3]
unesp.author.orcid0000-0002-0118-6164[4]
unesp.author.orcid0000-0002-4307-3985[5]
unesp.author.orcid0000-0002-8713-7506[6]
unesp.author.orcid0000-0001-7013-5574[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina Veterinária e Zootecnia, Botucatupt

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