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dc.creatorTerrab Benjelloun, Anasses
dc.creatorBenjamaa, Raniaes
dc.creatorMoujanni, Abdelkarimes
dc.creatorEddoha, Rabiaaes
dc.creatorBenbachir, Maryames
dc.creatorMoujahid, Abderrahmanes
dc.creatorNasser, Boubkeres
dc.creatorEssamadi, Abdel Khalides
dc.date.accessioned2022-05-18T16:24:59Z
dc.date.available2022-05-18T16:24:59Z
dc.date.issued2020
dc.identifier.citationTerrab Benjelloun, A., Benjamaa, R., Moujanni, A., Eddoha, R., Benbachir, M., Moujahid, A.,...,Nasser, B.Essamadi, A.K. (2020). Relationship among antibiotic residues and antibacterial activity of the endemic spurge honey (Euphorbia Resinifera o. Berg) from morocco. Emirates Journal of Food and Agriculture, 32 (11), 795-807.
dc.identifier.issn2079-052Xes
dc.identifier.issn2079-0538es
dc.identifier.urihttps://hdl.handle.net/11441/133455
dc.description.abstractAntibiotic-resistant bacteria continue to be of major health concern worldwide. In recent years, several reports and scientific articles claim the contamination of honey by antibiotics, detectable concentrations of antibiotic residues in honey are illegal. They, may cause hypersensitivity or resistance to drug therapy in humans, and are perceived by consumers as undesirable. In this sense, the purpose of this work was to examine the antibacterial activity of the Euphorbia resinifera (E. resinifera) honey against Escherichia coli and Staphylococcus aureus in vitro using the well-agar diffusion assay followed by dilution range to obtain more precise minimum inhibitory concentration values. The second aim is to evaluate the presence of antibiotics in honey using a screening test: Evidence Investigator™, an immuno-enzymatic method for detection of 27 antibiotic residues followed by a liquid chromatography-tandem mass spectrometry (LC-MS/MS) for confirmation of suspect samples; in order to assess the relationship between the presence of antibiotic residues and the antibacterial activity of honey. In this study, a total of 37 E. resinifera honey samples were analyzed. The results show that all samples of honey inhibited the growth of bacteria at the dilutions at 50% (v/v); the highest inhibition zone (25.98 ± 0.11 mm) was recorded from sample 5 for Staphylococcus aureus and (13.84 ± 1.10 mm) in sample 17 for Escherichia coli and that 50% (v/v) dilutions showed significant antibacterial effect compared to other dilutions (6.25, 12.5, 25% (v/v)). In all samples, there were no antibiotic residues detected except for one showing the detection of Trimethoprim at 6.48 µg kg-1. Our research is one of the first studies that relate the he relationship between the presence of antibiotic residues and the antibacterial activity of Euphorbia resinifera honey and showed that the antibacterial activity of honey might be due to the high osmotic nature, a low pH, its content of phenolic compounds and hydrogen peroxide and also to its content of methylglyoxal.es
dc.formatapplication/pdfes
dc.format.extent13 p.es
dc.language.isoenges
dc.publisherUnited Arab Emirates Universityes
dc.relation.ispartofEmirates Journal of Food and Agriculture, 32 (11), 795-807.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAntibacterial activityes
dc.subjectAntibiotic residueses
dc.subjectEuphorbia resinifera honeyes
dc.subjectLC-MS/MSes
dc.subjectMulti-arrayes
dc.subjectScreeninges
dc.titleRelationship among antibiotic residues and antibacterial activity of the endemic spurge honey (Euphorbia Resinifera o. Berg) from moroccoes
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Biología Vegetal y Ecologíaes
dc.relation.publisherversionhttps://doi.org/10.9755/ejfa.2020.v32.i11.2190es
dc.identifier.doi10.9755/ejfa.2020.v32.i11.2190es
dc.journaltitleEmirates Journal of Food and Agriculturees
dc.publication.volumen32es
dc.publication.issue11es
dc.publication.initialPage795es
dc.publication.endPage807es

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