Immunoreactive cell wall proteins of Clostridium difficile identified by human sera

1 Centre for Molecular Microbiology and Infection, Division of Cell and Molecular Biology, Imperial College, London SW7 2AZ, UK 2 Centre for Food Safety, School of Agriculture, Food Science and Veterinary Medicine, University College Dublin, Belfield, Dublin 4, Ireland 3 Department of Medicine for t...

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Veröffentlicht in:Journal of medical microbiology 2008-06, Vol.57 (6), p.750-756
Hauptverfasser: Wright, Anne, Drudy, Denise, Kyne, Lorraine, Brown, Katherine, Fairweather, Neil F
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container_end_page 756
container_issue 6
container_start_page 750
container_title Journal of medical microbiology
container_volume 57
creator Wright, Anne
Drudy, Denise
Kyne, Lorraine
Brown, Katherine
Fairweather, Neil F
description 1 Centre for Molecular Microbiology and Infection, Division of Cell and Molecular Biology, Imperial College, London SW7 2AZ, UK 2 Centre for Food Safety, School of Agriculture, Food Science and Veterinary Medicine, University College Dublin, Belfield, Dublin 4, Ireland 3 Department of Medicine for the Older Person, Mater Misericordiae University Hospital, Dublin 7, Ireland Correspondence Neil F. Fairweather n.fairweather{at}imperial.ac.uk Received 24 July 2007 Accepted 19 October 2007 Clostridium difficile is a leading cause of nosocomial infection in the developed world, causing antibiotic-associated disease in susceptible populations. The identity of immunogenic proteins is important in understanding the pathogenesis of disease and in the design of vaccines. This study analysed the sera of six patients infected during a hospital outbreak of a C. difficile ribotype 017 strain. Using a proteomics-based approach, cell wall proteins were separated by two-dimensional PAGE, and immunoreactive proteins were revealed by reaction with patient sera. The identity of immunoreactive proteins was established by MS. Forty-two different proteins were identified in total. All patient sera reacted with at least one component of the surface-layer protein (SLP), four reacted with both components (high- and low-molecular-mass SLPs), and five reacted with one other cell wall protein, suggesting that these are immunodominant antigens. The role of these proteins as potential vaccine candidates and their roles in pathogenesis deserve further study. Abbreviations: 2DE, two-dimensional PAGE; CDAD, Clostridium difficile -associated disease; ECL, enhanced chemiluminescence; HRP, horseradish peroxidase; IPG, immobilized pH gradient; MALDI, matrix-associated laser desorption/ionization; MS/MS, tandem mass spectrometry; SLP, surface-layer protein. The complete dataset of immunoreactive proteins identified in this study is available as supplementary data with the online version of this paper.
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Fairweather n.fairweather{at}imperial.ac.uk Received 24 July 2007 Accepted 19 October 2007 Clostridium difficile is a leading cause of nosocomial infection in the developed world, causing antibiotic-associated disease in susceptible populations. The identity of immunogenic proteins is important in understanding the pathogenesis of disease and in the design of vaccines. This study analysed the sera of six patients infected during a hospital outbreak of a C. difficile ribotype 017 strain. Using a proteomics-based approach, cell wall proteins were separated by two-dimensional PAGE, and immunoreactive proteins were revealed by reaction with patient sera. The identity of immunoreactive proteins was established by MS. Forty-two different proteins were identified in total. All patient sera reacted with at least one component of the surface-layer protein (SLP), four reacted with both components (high- and low-molecular-mass SLPs), and five reacted with one other cell wall protein, suggesting that these are immunodominant antigens. The role of these proteins as potential vaccine candidates and their roles in pathogenesis deserve further study. Abbreviations: 2DE, two-dimensional PAGE; CDAD, Clostridium difficile -associated disease; ECL, enhanced chemiluminescence; HRP, horseradish peroxidase; IPG, immobilized pH gradient; MALDI, matrix-associated laser desorption/ionization; MS/MS, tandem mass spectrometry; SLP, surface-layer protein. 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Fairweather n.fairweather{at}imperial.ac.uk Received 24 July 2007 Accepted 19 October 2007 Clostridium difficile is a leading cause of nosocomial infection in the developed world, causing antibiotic-associated disease in susceptible populations. The identity of immunogenic proteins is important in understanding the pathogenesis of disease and in the design of vaccines. This study analysed the sera of six patients infected during a hospital outbreak of a C. difficile ribotype 017 strain. Using a proteomics-based approach, cell wall proteins were separated by two-dimensional PAGE, and immunoreactive proteins were revealed by reaction with patient sera. The identity of immunoreactive proteins was established by MS. Forty-two different proteins were identified in total. 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Fairweather n.fairweather{at}imperial.ac.uk Received 24 July 2007 Accepted 19 October 2007 Clostridium difficile is a leading cause of nosocomial infection in the developed world, causing antibiotic-associated disease in susceptible populations. The identity of immunogenic proteins is important in understanding the pathogenesis of disease and in the design of vaccines. This study analysed the sera of six patients infected during a hospital outbreak of a C. difficile ribotype 017 strain. Using a proteomics-based approach, cell wall proteins were separated by two-dimensional PAGE, and immunoreactive proteins were revealed by reaction with patient sera. The identity of immunoreactive proteins was established by MS. Forty-two different proteins were identified in total. 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subjects Antibodies, Bacterial - blood
Antibodies, Bacterial - immunology
Bacterial Proteins - immunology
Bacterial Proteins - metabolism
Cell Wall - immunology
Cell Wall - metabolism
Clostridium difficile
Clostridium difficile - immunology
Clostridium difficile - metabolism
Clostridium Infections - blood
Clostridium Infections - immunology
Humans
Immune Sera - immunology
Proteomics
title Immunoreactive cell wall proteins of Clostridium difficile identified by human sera
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