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dc.creatorFernandez-Garcia, Lauraes
dc.creatorAmbroa, A.es
dc.creatorBlasco, L.es
dc.creatorBleriot, Inéses
dc.creatorLópez, Maríaes
dc.creatorÁlvarez-Marín, Rocíoes
dc.creatorRodríguez-Baño, Jesúses
dc.creatorPachón Díaz, Jerónimoes
dc.creatorTomás, Maríaes
dc.date.accessioned2020-10-06T18:27:26Z
dc.date.available2020-10-06T18:27:26Z
dc.date.issued2018-12-17
dc.identifier.citationFernandez-Garcia, L., Ambroa, A., Blasco, L., Bleriot, I., López, M., Alvarez-Marin, R.,...,Tomás, M. (2018). Relationship Between the Quorum Network (Sensing/Quenching) and Clinical Features of Pneumonia and Bacteraemia Caused by A. baumannii. Frontiers in microbiology, 9
dc.identifier.issn1664-302Xes
dc.identifier.urihttps://hdl.handle.net/11441/101754
dc.description.abstractAcinetobacter baumannii (Ab) is one of the most important pathogens associated with nosocomial infections, especially pneumonia. Interest in the Quorum network, i.e., Quorum Sensing (QS)/Quorum Quenching (QQ), in this pathogen has grown in recent years. The Quorum network plays an important role in regulating diverse virulence factors such as surface motility and bacterial competition through the type VI secretion system (T6SS), which is associated with bacterial invasiveness. In the present study, we investigated 30 clinical strains of A. baumannii isolated in the “II Spanish Study of A. baumannii GEIH-REIPI 2000-2010” (Genbank Umbrella Bioproject PRJNA422585), a multicentre study describing the relationship between the Quorum network in A. baumannii and the development of pneumonia and associated bacteraemia. Expression of the aidA gene (encoding the AidA protein, QQ enzyme) was lower (P < 0.001) in strains of A. baumannii isolated from patients with bacteraemic pneumonia than in strains isolated from patients with non-bacteraemic pneumonia. Moreover, aidA expression in the first type of strain was not regulated in the presence of environmental stress factors such as the 3-oxo-C12-HSL molecule (substrate of AidA protein, QQ activation) or H2O2 (inhibitor of AidA protein, QS activation). However, in the A. baumannii strains isolated from patients with non-bacteraemic pneumonia, aidA gene expression was regulated by stressors such as 3-oxo-C12-HSL and H2O2. In an in vivo Galleria mellonella model of A. baumannii infection, the A. baumannii ATCC 17978 strain was associated with higher mortality (100% at 24 h) than the mutant, abaI-deficient, strain (carrying a synthetase enzyme of Acyl homoserine lactone molecules) (70% at 24 h). These data suggest that the QS (abaR and abaI genes)/QQ (aidA gene) network affects the development of secondary bacteraemia in pneumonia patients and also the virulence of A. baumannii.es
dc.description.sponsorshipNational Plan for Scientific Researches
dc.description.sponsorshipTechnological Development and Innovation PI16/01163es
dc.description.sponsorshipISCIII-Deputy General Directorate for Evaluation and Promotion of Research-European Regional Development Fund A way of Making Europees
dc.description.sponsorshipInstituto de Salud Carlos IIIes
dc.description.sponsorshipMiguel Servet Research Programme SERGAS and ISCIIIes
dc.description.sponsorshipXunta de Galicia (GAIN, Axencia de Innovación)es
dc.formatapplication/pdfes
dc.format.extent11es
dc.language.isoenges
dc.publisherFrontiers Research Foundationes
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectQuorumes
dc.subjectPneumoniaes
dc.subjectSensinges
dc.subjectQuenchinges
dc.subjectBacteraemiaes
dc.subjectAcinetobacteres
dc.titleRelationship Between the Quorum Network (Sensing/Quenching) and Clinical Features of Pneumonia and Bacteraemia Caused by A. baumanniies
dc.typeinfo:eu-repo/semantics/articlees
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Medicinaes
dc.relation.projectIDPI16/01163es
dc.relation.projectIDRD16/0016/0001es
dc.relation.projectIDRD16/0016/0006es
dc.relation.projectIDRD16/0016/0008es
dc.relation.projectIDRD16/0016/0009es
dc.relation.projectIDRD16/0016/0010es
dc.identifier.doi10.3389/fmicb.2018.03105es
dc.journaltitleFrontiers in microbiologyes
dc.publication.volumen9es

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