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In Vitro Antibacterial Activity of Propyl-Propane-Thiosulfinate and Propyl-Propane-Thiosulfonate Derived from Allium spp. against Gram-Negative and Gram-Positive Multidrug-Resistant Bacteria Isolated from Human Samples.

dc.contributor.authorSorlozano-Puerto, Antonio
dc.contributor.authorAlbertuz-Crespo, Maria
dc.contributor.authorLopez-Machado, Isaac
dc.contributor.authorAriza-Romero, Juan Jose
dc.contributor.authorBaños-Arjona, Alberto
dc.contributor.authorExposito-Ruiz, Manuela
dc.contributor.authorGutierrez-Fernandez, Jose
dc.date.accessioned2023-01-25T10:23:11Z
dc.date.available2023-01-25T10:23:11Z
dc.date.issued2018-09-17
dc.description.abstractThe aim of this study was to compare the in vitro antibacterial activity of two compounds derived from Alliaceae, PTS (propyl-propane-thiosulfinate), and PTSO (propyl-propane-thiosulfonate), with that of other antibiotics commonly used against bacteria isolated from humans. A total of 212 gram-negative bacilli and 267 gram-positive cocci isolated from human clinical samples and resistant to at least one group of antibiotics were selected. In order to determine the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) to various antibiotics as well as PTS and PTSO, all isolates underwent broth microdilution assay. PTS showed moderate activity against Enterobacteriaceae with MIC50 (and MBC50) and MIC90 (and MBC90) values of 256-512 mg/L, while PTSO showed greater activity with MIC50 and MIC90 values of 64-128 mg/L and MBC50 and MBC90 values of 128-512 mg/L. These data show the bactericidal activity of both compounds and indicate that PTSO was more active than PTS against this group of bacteria. Both compounds showed lower activity against P. aeruginosa (MIC50 = 1024 mg/L, MIC90 = 2048 mg/L, MBC50 = 2048 mg/L, and MBC90 = 2048 mg/L, for PTS; MIC50 = 512 mg/L, MIC90 = 1024 mg/L, MBC50 = 512 mg/L, and MBC90 = 2048 mg/L, for PTSO) compared to those obtained in others nonfermenting gram-negative bacilli (MIC50 = 128 mg/L, MIC90 = 512 mg/L, MBC50 = 128 mg/L, and MBC90 = 512 mg/L, for PTS; MIC50 = 64 mg/L, MIC90 = 256 mg/L, MBC50 = 64 mg/L, and MBC90 = 256 mg/L, for PTSO) and also indicate the bactericidal activity of both compounds against these groups of bacteria. Finally, the activity against S. aureus, E. faecalis, and S. agalactiae was higher than that observed against enterobacteria, especially in the case of PTSO (MIC50 = 8 mg/L, MIC90 = 8 mg/L, MBC50 = 32 mg/L, and MBC90 = 64 mg/L, in S. aureus; MIC50 = 4 mg/L, MIC90 = 8 mg/L, MBC50 = 8 mg/L, and MBC90 = 16 mg/L, in E. faecalis and S. agalactiae). PTS and PTSO have a significant broad spectrum antibacterial activity against multiresistant bacteria isolated from human clinical samples. Preliminary results in present work provide basic and useful information for development and potential use of these compounds in the treatment of human infections.
dc.identifier.doi10.1155/2018/7861207
dc.identifier.essn2314-6141
dc.identifier.pmcPMC6166382
dc.identifier.pmid30310819
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6166382/pdf
dc.identifier.unpaywallURLhttp://downloads.hindawi.com/journals/bmri/2018/7861207.pdf
dc.identifier.urihttp://hdl.handle.net/10668/13068
dc.journal.titleBioMed research international
dc.journal.titleabbreviationBiomed Res Int
dc.language.isoen
dc.organizationHospital Universitario Virgen de las Nieves
dc.page.number7861207
dc.pubmedtypeJournal Article
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshAllium
dc.subject.meshAnti-Bacterial Agents
dc.subject.meshBacteria
dc.subject.meshBacterial Infections
dc.subject.meshDrug Resistance, Multiple, Bacterial
dc.subject.meshHumans
dc.subject.meshMicrobial Sensitivity Tests
dc.subject.meshPlant Extracts
dc.subject.meshPropane
dc.subject.meshThiosulfonic Acids
dc.titleIn Vitro Antibacterial Activity of Propyl-Propane-Thiosulfinate and Propyl-Propane-Thiosulfonate Derived from Allium spp. against Gram-Negative and Gram-Positive Multidrug-Resistant Bacteria Isolated from Human Samples.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number2018
dspace.entity.typePublication

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