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Proteomic Profiling of the Outer Membrane Fraction of the Obligate Intracellular Bacterial Pathogen Ehrlichia ruminantium

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  • معلومة اضافية
    • Contributors:
      Contrôle des maladies animales exotiques et émergentes (UMR CMAEE); Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Institut National de la Recherche Agronomique (INRA); Instituto de Biologia Experimental e Tecnológica (IBET); Instituto de Tecnologia Química e Biológica António Xavier (ITQB); Universidade Nova de Lisboa = NOVA University Lisbon (NOVA); Université des Antilles et de la Guyane (UAG); FEDER grant, "Risque en sante animale et vegetale" FED 1/1.4-30305 PAUILF Identification des proteines de la membrane externe de la Rickettsiales Ehrlichia ruminantium par une approche de proteomique Fundacao para a Ciencia e Tecnologia (FCT) PTDC/CVT/114118/2009 PEst-OE/EQB/LA0004/2011 SFRH/BPD/45978/2008
    • بيانات النشر:
      HAL CCSD
      Public Library of Science
    • الموضوع:
      2015
    • Collection:
      CIRAD: HAL (Recherche agronomique pour le développement / Agricultural Research for Development)
    • نبذة مختصرة :
      International audience ; The outer membrane proteins (OMPs) of Gram-negative bacteria play a crucial role in virulence and pathogenesis. Identification of these proteins represents an important goal for bacterial proteomics, because it aids in vaccine development. Here, we have developed such an approach for Ehrlichia ruminantium, the obligate intracellular bacterium that causes heartwater. A preliminary whole proteome analysis of elementary bodies, the extracellular infectious form of the bacterium, had been performed previously, but information is limited about OMPs in this organism and about their role in the protective immune response. Identification of OMPs is also essential for understanding Ehrlichia’s OM architecture, and how the bacterium interacts with the host cell environment. First, we developed an OMP extraction method using the ionic detergent sarkosyl, which enriched the OM fraction. Second, proteins were separated via one-dimensional electrophoresis, and digested peptides were analyzed via nano-liquid chromatographic separation coupled with mass spectrometry (LCMALDI-TOF/TOF). Of 46 unique proteins identified in the OM fraction, 18 (39%) were OMPs, including 8 proteins involved in cell structure and biogenesis, 4 in transport/virulence, 1 porin, and 5 proteins of unknown function. These experimental data were compared to the predicted subcellular localization of the entire E. ruminantium proteome, using three different algorithms. This work represents the most complete proteome characterization of the OM fraction in Ehrlichia spp. The study indicates that suitable subcellular fractionation experiments combined with straightforward computational analysis approaches are powerful for determining the predominant subcellular localization of the experimentally observed proteins.We identified proteins potentially involved in E. ruminantium athogenesis, which are good novel targets for candidate vaccines. Thus, combining bioinformatics and proteomics, we discovered new OMPs for E. ruminantium that are ...
    • Relation:
      hal-01203402; https://hal.univ-antilles.fr/hal-01203402; https://hal.univ-antilles.fr/hal-01203402/document; https://hal.univ-antilles.fr/hal-01203402/file/2015_Moumene_PLOSONE-1.pdf; PRODINRA: 320053; WOS: 000350683900014
    • الرقم المعرف:
      10.1371/journal.pone.0116758
    • Rights:
      http://creativecommons.org/licenses/by/ ; info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.FB9A9C67