Quantitative Proteomic Analysis of Host—Pathogen Interactions: A Study of Acinetobacter baumannii Responses to Host Airways

UDC.coleccionInvestigaciónes_ES
UDC.departamentoBioloxíaes_ES
UDC.departamentoFisioterapia, Medicina e Ciencias Biomédicases_ES
UDC.institutoCentroCICA - Centro Interdisciplinar de Química e Bioloxíaes_ES
UDC.institutoCentroINIBIC - Instituto de Investigacións Biomédicas de A Coruñaes_ES
UDC.journalTitleBMC Genomicses_ES
UDC.startPageArticle number: 422es_ES
UDC.volume16 (2015)es_ES
dc.contributor.authorMéndez Arredondo, José Antonio
dc.contributor.authorMateos, Jesús
dc.contributor.authorBeceiro Casas, Alejandro
dc.contributor.authorLópez Díaz, María
dc.contributor.authorTomás, María
dc.contributor.authorPoza, Margarita
dc.contributor.authorBou, Germán
dc.date.accessioned2025-04-15T11:13:13Z
dc.date.available2025-04-15T11:13:13Z
dc.date.issued2015-05-30
dc.descriptionAdditional files: 1. Workflow of the proteomic experiment -- 2. Histopathology shows signs of consolidated pneumonia in infected animals -- 3. Prediction of exoproteins -- 4. RT-PCR analysis of different genes. Primers and Univesal ProbeLibrary (UPL, Roche) probes used in this study -- 5. Protein identification data.es_ES
dc.description.abstract[Abstract] Background: Acinetobacter baumannii is a major health problem. The most common infection caused by A. baumannii is hospital acquired pneumonia, and the associated mortality rate is approximately 50 %. Neither in vivo nor ex vivo expression profiling has been performed at the proteomic or transcriptomic level for pneumonia caused by A. baumannii. In this study, we characterized the proteome of A. baumannii under conditions that simulate those found in the airways, to gain some insight into how A. baumannii adapts to the host and to improve knowledge about the pathogenesis and virulence of this bacterium. A clinical strain of A. baumannii was grown under different conditions: in the presence of bronchoalveolar lavage fluid from infected rats, of RAW 264.7 cells to simulate conditions in the respiratory tract and in control conditions. We used iTRAQ labelling and LC-MALDI-TOF/TOF to investigate how A. baumannii responds on exposure to macrophages/BALF. Results: 179 proteins showed differential expression. In both models, proteins involved in the following processes were over-expressed: (i) pathogenesis and virulence (OmpA, YjjK); (ii) cell wall/membrane/envelope biogenesis (MurC); (iii) energy production and conversion (acetyl-CoA hydrolase); and (iv) translation (50S ribosomal protein L9). Proteins involved in the following were under-expressed: (i) lipid metabolism (short-chain dehydrogenase); (ii) amino acid metabolism and transport (aspartate aminotransferase); (iii) unknown function (DNA-binding protein); and (iv) inorganic ion transport and metabolism (hydroperoxidase). Conclusions: We observed alterations in cell wall synthesis and identified 2 upregulated virulence-associated proteins with >15 peptides/protein in both ex vivo models (OmpA and YjjK), suggesting that these proteins are fundamental for pathogenesis and virulence in the airways. This study is the first comprehensive overview of the ex vivo proteome of A. baumannii and is an important step towards identification of diagnostic biomarkers, novel drug targets and potential vaccine candidates in the fight against pneumonia caused by A. baumannii.es_ES
dc.description.sponsorshipThis study was funded by grants from the European Community, FP7, ID: 278232 (MagicBullet), and by the Plan Nacional de I+D+I 2008-2011 and Instituto de Salud Carlos III, Subdirección General de Redes y Centros de Investigación Cooperativa, Ministerio de Economía y Competitividad, Spanish Network for Research in Infectious Diseases (REIPI RD12/0015/0014), cofinanced by the European Development Regional Fund (EDRF) “A Way to Achieve Europe.” M. T. and A.B. were financially supported by the Miguel Servet Programme ISCIII-FEDER (CP09/00033 and CP13/00226, respectively). This work was supported by the National Plans for Scientific Research, Development and Technological Innovation 2008-2011 and 2013-2016 and funded by the ISCIII- General Subdirection of Assesment and Promotion of the Research – European Regional Development Fund (ERDF) “A way of making Europe”: PI10/00056 and PI13/02390 to M. T., PI11/01034 to M.P., PI12/00552 to G.B. and PI14/00059 to M.P. and A.B.es_ES
dc.identifier.citationMéndez, J.A., Mateos, J., Beceiro, A. et al. Quantitative proteomic analysis of host—pathogen interactions: a study of Acinetobacter baumannii responses to host airways. BMC Genomics 16, 422 (2015). https://doi.org/10.1186/s12864-015-1608-zes_ES
dc.identifier.doi10.1186/s12864-015-1608-z
dc.identifier.issn1471-2164
dc.identifier.urihttp://hdl.handle.net/2183/41763
dc.language.isoenges_ES
dc.publisherSpringer Naturees_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/278232es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO/Plan Nacional de I+D+i 2008-2011/RD12%2F0015%2F0014/ES/Enfermedades infecciosases_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICINN/Plan Nacional de I+D+i 2008-2011/CP09%2F00033/ES/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CP13%2F00226/ES/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICINN/Plan Nacional de I+D+i 2008-2011/PI10%2F00056/ES/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/PI13%2F02390/ES/Relación entre Quorum Sensing y mecanismos de resistencia en patógenos nosocomiales. Nuevas Terapias Antivirulentas/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICINN/Plan nacional de I+D+i 2008-2011/PI11%2F01034/ES/Genómica y transcriptómica de biofilms de Acinetobacter baumannii/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO/Plan Nacional de I+D+i 2008-2011/PI12%2F00552/ES/Estudios preclínicos con D-aminoácidos para atenuar la virulencia de Acinetobacter baumannii y otros patógenos multirresistentes: Una nueva estrategia para erradicar una infección/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/PI14%2F00059/ES/Nuevas estrategias frente al patógeno multirresistente Acinetobacter baumannii: silenciamiento (siRNA) bacteriano y nuevos inhibidores químicos. Evaluación en estudios preclínicos/es_ES
dc.relation.urihttps://doi.org/10.1186/s12864-015-1608-zes_ES
dc.rightsAtribución 4.0 Internacionales_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectProteomees_ES
dc.subjectAcinetobacter baumanniies_ES
dc.subjectHost-pathogen interactiones_ES
dc.subjectEx vivoes_ES
dc.subjectVirulencees_ES
dc.titleQuantitative Proteomic Analysis of Host—Pathogen Interactions: A Study of Acinetobacter baumannii Responses to Host Airwayses_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublicationa68d08dc-09ba-453e-8928-7c08e5b14a4b
relation.isAuthorOfPublication909e08d1-6ed1-4b99-9e9e-c64eb72e7dea
relation.isAuthorOfPublication.latestForDiscoverya68d08dc-09ba-453e-8928-7c08e5b14a4b

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