Publication: Enterocin AS-48 as Evidence for the Use of Bacteriocins as New Leishmanicidal Agents
| dc.contributor.author | Abengózar, María Ángeles | |
| dc.contributor.author | Cebrián, Rubén | |
| dc.contributor.author | Saugar, Jose Maria | |
| dc.contributor.author | Garate, Teresa | |
| dc.contributor.author | Valdivia, Eva | |
| dc.contributor.author | Martínez-Bueno, Manuel | |
| dc.contributor.author | Maqueda, Mercedes | |
| dc.contributor.author | Rivas, Luis | |
| dc.contributor.funder | Instituto de Salud Carlos III | |
| dc.contributor.funder | Unión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF) | |
| dc.date.accessioned | 2019-06-06T11:17:24Z | |
| dc.date.available | 2019-06-06T11:17:24Z | |
| dc.date.issued | 2017 | |
| dc.description.abstract | We report the feasibility of enterocin AS-48, a circular cationic peptide produced by Enterococcus faecalis, as a new leishmanicidal agent. AS-48 is lethal to Leishmania promastigotes as well as to axenic and intracellular amastigotes at low micromolar concentrations, with scarce cytotoxicity to macrophages. AS-48 induced a fast bioenergetic collapse of L. donovani promastigotes but only a partial permeation of their plasma membrane with limited entrance of vital dyes, even at concentrations beyond its full lethality. Fluoresceinated AS-48 was visualized inside parasites by confocal microscopy and seen to cause mitochondrial depolarization and reactive oxygen species production. Altogether, AS-48 appeared to have a mixed leishmanicidal mechanism that includes both plasma membrane permeabilization and additional intracellular targets, with mitochondrial dysfunctionality being of special relevance. This complex leishmanicidal mechanism of AS-48 persisted even for the killing of intracellular amastigotes, as evidenced by transmission electron microscopy. We demonstrated the potentiality of AS-48 as a new and safe leishmanicidal agent, expanding the growing repertoire of eukaryotic targets for bacteriocins, and our results provide a proof of mechanism for the search of new leishmanicidal bacteriocins, whose diversity constitutes an almost endless source for new structures at moderate production cost and whose safe use on food preservation is well established. | es_ES |
| dc.description.peerreviewed | Sí | es_ES |
| dc.description.sponsorship | L.R. was supported by grants from the Fondo de Investigaciones Sanitarias-ISCIII-FEDER (PI12-02706), Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016 (SAF2015-65740-R and SAF2013-48971-C2-1-R), Subdirección General de Redes y Centros de Investigación Cooperativa-FEDER (RICET RD12/0018/0007, RD12/0018/0011, RD16CIII/003/004, and RD16/0027/0010) and CSIC (PIE 201620E038), the European Regional Development Funds (ERDF), and the Research Group General (BIO160, UGR). | es_ES |
| dc.format.number | 4 | es_ES |
| dc.format.volume | 61 | es_ES |
| dc.identifier.citation | Antimicrob Agents Chemother. 2017 Mar 24;61(4). pii: e02288-16. | es_ES |
| dc.identifier.doi | 10.1128/AAC.02288-16 | es_ES |
| dc.identifier.e-issn | 1098-6596 | es_ES |
| dc.identifier.issn | 0066-4804 | es_ES |
| dc.identifier.journal | Antimicrobial agents and chemotherapy | es_ES |
| dc.identifier.pubmedID | 28167557 | es_ES |
| dc.identifier.uri | http://hdl.handle.net/20.500.12105/7750 | |
| dc.language.iso | eng | es_ES |
| dc.publisher | American Society for Microbiology (ASM) | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/PI12-02706 | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/SAF2015-65740-R | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/SAF2013-48971-C2-1-R | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/RD12/0018/0007 | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/RD12/0018/0011 | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/RD16CIII/003/004 | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/RD16/0027/0010 | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/PIE201620E038 | es_ES |
| dc.relation.publisherversion | https://doi.org/10.1128/AAC.02288-16 | es_ES |
| dc.repisalud.centro | ISCIII::Centro Nacional de Microbiología | es_ES |
| dc.repisalud.institucion | ISCIII | es_ES |
| dc.rights.accessRights | open access | es_ES |
| dc.rights.license | Atribución-NoComercial-CompartirIgual 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | * |
| dc.subject | Antimicrobial peptide | es_ES |
| dc.subject | Bioenergetics | es_ES |
| dc.subject | Enterocin AS-48 | es_ES |
| dc.subject | Intracellular parasite | es_ES |
| dc.subject.mesh | Adenosine Triphosphate | es_ES |
| dc.subject.mesh | Antiprotozoal Agents | es_ES |
| dc.subject.mesh | Bacteriocins | es_ES |
| dc.subject.mesh | Cell Membrane | es_ES |
| dc.subject.mesh | Cell Membrane Permeability | es_ES |
| dc.subject.mesh | Cell Survival | es_ES |
| dc.subject.mesh | Enterococcus faecalis | es_ES |
| dc.subject.mesh | Fluorescent Dyes | es_ES |
| dc.subject.mesh | Inhibitory Concentration 50 | es_ES |
| dc.subject.mesh | Leishmania | es_ES |
| dc.subject.mesh | Life Cycle Stages | es_ES |
| dc.subject.mesh | Macrophages | es_ES |
| dc.subject.mesh | Microscopy, Electron | es_ES |
| dc.subject.mesh | Mitochondria | es_ES |
| dc.subject.mesh | Species Specificity | es_ES |
| dc.title | Enterocin AS-48 as Evidence for the Use of Bacteriocins as New Leishmanicidal Agents | es_ES |
| dc.type | journal article | es_ES |
| dc.type.hasVersion | AM | es_ES |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | 2036bb40-097f-406a-b634-f77164674c2b | |
| relation.isAuthorOfPublication | 3d704a19-fdd1-4b31-97da-1c2cd59180d1 | |
| relation.isAuthorOfPublication.latestForDiscovery | 2036bb40-097f-406a-b634-f77164674c2b |
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