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dc.contributor.authorMónaco, Amy-
dc.contributor.authorCanales-Huerta, Nicole-
dc.contributor.authorJara-Wilde, Jorge-
dc.contributor.authorHärtel, Steffen-
dc.contributor.authorChabalgoity, José Alejandro-
dc.contributor.authorMoreno, María-
dc.contributor.authorScavone, Paola-
dc.date.accessioned2024-01-03T13:32:01Z-
dc.date.available2024-01-03T13:32:01Z-
dc.date.issued2021-
dc.identifier.citationMÓNACO, A., CANALES-HUERTA, N., JARA-WILDE, J. y otros. Salmonella Typhimurium Triggers Extracellular Traps Release in Murine Macrophages. Frontiers in cellular and infection microbiology [en línea] 2021,11. DOI: 10.3389/fcimb.2021.639768es
dc.identifier.urihttps://hdl.handle.net/20.500.12008/42099-
dc.description.abstractSalmonella comprises two species and more than 2500 serovars with marked differences in host specificity, and is responsible for a wide spectrum of diseases, ranging from localized gastroenteritis to severe life-threatening invasive disease. The initiation of the host inflammatory response, triggered by many Pathogen-Associated Molecular Patterns (PAMPs) that Salmonella possesses, recruits innate immune cells in order to restrain the infection at the local site. Neutrophils are known for killing bacteria through oxidative burst, amid other mechanisms. Amongst those mechanisms for controlling bacteria, the release of Extracellular Traps (ETs) represents a newly described pathway of programmed cell death known as ETosis. Particularly, Neutrophil Extracellular Traps (NETs) were first described in 2004 and since then, a number of reports have demonstrated their role as a novel defense mechanism against different pathogens. This released net-like material is composed of cellular DNA decorated with histones and cellular proteins. These structures have shown ability to trap, neutralize and kill different kinds of microorganisms, ranging from viruses and bacteria to fungi and parasites. Salmonella was one of the first microorganisms that were reported to be killed by NETs and several studies have confirmed the observation and deepened into its variants. Nevertheless, much less is known about their counterparts in other immune cells, e.g. Macrophage Extracellular Traps (METs) and Salmonella-induced MET release has never been reported so far. In this work, we observed the production of METs induced by Salmonella enterica serovar Typhimurium and recorded their effect on bacteria, showing for the first time that macrophages can also release extracellular DNA traps upon encounter with Salmonella Typhimurium. Additionally we show that METs effectively immobilize and reduce Salmonella survival in a few minutes, suggesting METs as a novel immune-mediated defense mechanism against Salmonella infection. Of note, this phenomenon was confirmed in primary macrophages, since MET release was also observed in bone marrow-derived macrophages infected with Salmonella. The evidence of this peculiar mechanism provides new incipient insights into macrophages´ role against Salmonella infection and can help to design new strategies for the clinical control of this transcendental pathogen.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenes
dc.relation.ispartofFrontiers in cellular and infection microbiology. 2021, 11es
dc.rightsLas obras depositadas en el Repositorio se rigen por la Ordenanza de los Derechos de la Propiedad Intelectual de la Universidad de la República.(Res. Nº 91 de C.D.C. de 8/III/1994 – D.O. 7/IV/1994) y por la Ordenanza del Repositorio Abierto de la Universidad de la República (Res. Nº 16 de C.D.C. de 07/10/2014)es
dc.subjectSalmonellaes
dc.subjectMacrophageses
dc.subjectExtracellular trapses
dc.subjectMETes
dc.subjectDefense mechanismes
dc.titleSalmonella Typhimurium Triggers Extracellular Traps Release in Murine Macrophageses
dc.typeArtículoes
dc.contributor.filiacionMónaco Amy, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Desarrollo Biotecnológico-
dc.contributor.filiacionCanales-Huerta Nicole, University of Chile, Faculty of Medicine. Institute of Biomedical Sciences ICBM, Integrative Biology Program, Laboratorio de Análisis de Imágenes Científicas SCIAN-Lab-
dc.contributor.filiacionJara-Wilde Jorge, University of Chile, Faculty of Medicine. Institute of Biomedical Sciences ICBM, Integrative Biology Program, Laboratorio de Análisis de Imágenes Científicas SCIAN-Lab-
dc.contributor.filiacionHärtel Steffen, University of Chile, Faculty of Medicine. Institute of Biomedical Sciences ICBM, Integrative Biology Program, Laboratorio de Análisis de Imágenes Científicas SCIAN-Lab-
dc.contributor.filiacionChabalgoity José Alejandro, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Desarrollo Biotecnológico-
dc.contributor.filiacionMoreno María, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Desarrollo Biotecnológico-
dc.contributor.filiacionScavone Paola, Ministerio de Educación y Cultura, Instituto de Investigaciones Biológicas Clemente Estable, Departamento de Microbiología-
dc.rights.licenceLicencia Creative Commons Atribución (CC - By 4.0)es
dc.identifier.doi10.3389/fcimb.2021.639768-
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