Actividad antibacteriana del péptido LfcinB (20-25)4 contra aislados clínicos multirresistentes de E. coli Y S. aureus

dc.contributor.advisorRivera Monroy, Zuly Jenny
dc.contributor.advisorParra Giraldo, Claudia Marcela
dc.contributor.authorBonilla Velásquez, Laura Daniela
dc.contributor.researchgroupSíntesis y aplicación de moléculas peptídicasspa
dc.date.accessioned2021-08-20T15:36:37Z
dc.date.available2021-08-20T15:36:37Z
dc.date.issued2021-05-30
dc.descriptionTexto
dc.descriptionilustraciones, gráficas, tablasspa
dc.description.abstractLos péptidos antimicrobianos (PAMs) constituyen una alternativa terapéutica para el desarrollo de tratamientos de enfermedades infecciosas, que podrían contrarrestar el ascendente número de microorganismos resistentes a antibióticos que han incrementado el problema de salud pública a nivel mundial. La OMS en el año 2018, reportó la aparición de cepas resistentes y multirresistentes, bacterias como Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii y Staphylococcus aureus, han desarrollado mecanismos de resistencia frente a los antibióticos de primera línea, evidenciando la ineficacia de los fármacos utilizados comúnmente. Como una estrategia para ampliar las alternativas terapéuticas los péptidos derivados de la Lactoferricina Bovina (LfcinB), que contienen el motivo mínimo de actividad antimicrobiana RRWQWR, han sido evaluados contra cepas de referencia Gram positivas y Gram negativas, esta investigación ha permitido enfocar el péptido tetramérico LfcinB (20-25)4 con actividad antibacteriana promisoria. Dando continuidad a esta investigación, en el presente trabajo se evaluó la actividad antibacteriana de LfcinB (20-25)4 contra aislados clínicos de S. aureus y E. coli los cuales presentan diferentes perfiles de resistencia. Se determinó que el péptido tetramérico presenta actividad contra los aislados clínicos evaluados, con Concentraciones Mínimas Inhibitorias (CMI) en el rango de 11 μM a 22 μM para bacterias Gram positivas y 5 μM a 22 μM para Gram negativas; estos resultados muestran que este péptido LfcinB (20-25)4 con actividad antibacteriana, tanto en cepas de referencia como en aislados clínicos, es una alternativa viable para el desarrollo de nuevos agentes terapéuticos. (Texto tomado de la fuente)spa
dc.description.abstractAntimicrobial peptides (PAMs) are an alternative to the development of new antibacterial therapies, which could counteract the ascending number of antibiotic- resistant microorganisms that have increased the global public health problem. In the latest WHO reports in 2018, it indicates that bacteria such as Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii and Staphylococcus aureus, exhibit resistance against first-line antibiotics and are classified as resistant and multidrug-resistant strains, demonstrating the inefficiency of drugs worldwide. Within this context, peptides derived from Lactoferricin Bovina (LfcinB) containing the minimum motif, have been evaluated against Gram-positive and Gram-negative reference strains. In this work, the tetrameric peptide LfcinB (20- 25)4 was evaluated against clinical isolates of S. aureus and E. coli that have been classified as multidrug-resistant by the Institute of Cancerology of Bogota, with a new identification through MALDI TOF. The activity of this peptide was demonstrated against the clinical isolates evaluated, having a minimal inhibitory concentration (MIC) within the range of 11 – 22μM for Gram-positive bacteria and 5 – 22μM for Gram negatives. In addition, the activity in combination with ciprofloxacin was evaluated for one of the isolates with higher percentages of antibiotic resistance, resulting in an additive effect that maintained the concentration of the peptide. All these results show that the tetrameric peptide LfcinB (20-25)4 with antibacterial activity, is a viable alternative for the development of new therapeutic agents. (Text taken from source)eng
dc.description.degreelevelMaestríaspa
dc.description.degreenameMagíster en Ciencias - Microbiologíaspa
dc.description.researchareaMicrobiologíaspa
dc.format.extent93 páginasspa
dc.format.mimetypeapplication/pdfspa
dc.identifier.instnameUniversidad Nacional de Colombiaspa
dc.identifier.reponameRepositorio Institucional Universidad Nacional de Colombiaspa
dc.identifier.repourlhttps://repositorio.unal.edu.co/spa
dc.identifier.urihttps://repositorio.unal.edu.co/handle/unal/79982
dc.language.isospaspa
dc.publisherUniversidad Nacional de Colombiaspa
dc.publisher.branchUniversidad Nacional de Colombia - Sede Bogotáspa
dc.publisher.departmentInstituto de Biotecnología (IBUN)spa
dc.publisher.facultyFacultad de Cienciasspa
dc.publisher.placeBogotá, Colombiaspa
dc.publisher.programBogotá - Ciencias - Maestría en Ciencias - Microbiologíaspa
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dc.rightsDerechos reservados al autor, 2021spa
dc.rights.accessrightsinfo:eu-repo/semantics/openAccessspa
dc.rights.licenseReconocimiento 4.0 Internacionalspa
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/spa
dc.subject.ddc610 - Medicina y salud::615 - Farmacología y terapéuticaspa
dc.subject.decsAntibacterianos
dc.subject.decsAnti-Bacterial Agents
dc.subject.decsEnfermedades transmisibles
dc.subject.decsCommunicable Diseases
dc.subject.proposalLactoferricina Bovinaspa
dc.subject.proposalActividad antibacterianaspa
dc.subject.proposalAislados clínicosspa
dc.subject.proposalMultirresistentesspa
dc.subject.proposalPéptidos antimicrobianosspa
dc.subject.proposalBovine lactoferricineng
dc.subject.proposalAntibacterial activityeng
dc.subject.proposalClinical isolateseng
dc.subject.proposalAntimicrobial peptideseng
dc.titleActividad antibacteriana del péptido LfcinB (20-25)4 contra aislados clínicos multirresistentes de E. coli Y S. aureusspa
dc.title.translatedAntibacterial activity of the LfcinB (20-25) 4 peptide against multi-resistant clinical isolates of E. coli and S. aureuseng
dc.typeTrabajo de grado - Maestríaspa
dc.type.coarhttp://purl.org/coar/resource_type/c_bdccspa
dc.type.coarversionhttp://purl.org/coar/version/c_ab4af688f83e57aaspa
dc.type.contentTextspa
dc.type.driverinfo:eu-repo/semantics/masterThesisspa
dc.type.redcolhttp://purl.org/redcol/resource_type/TMspa
dc.type.versioninfo:eu-repo/semantics/acceptedVersionspa
dcterms.audienceEspecializadaspa
oaire.accessrightshttp://purl.org/coar/access_right/c_abf2spa
oaire.awardtitleDiseño y obtención de nuevos agentes antibacterianos basados en dendrímero péptido – resorcinareno: Una alternativa para combatir la resistencia bacteriana.spa
oaire.fundernameMINCIENCIAS (COLCIENCIAS)spa

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