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Comprehensive Antigen Screening Identifies Moraxella catarrhalis Proteins That Induce Protection in a Mouse Pulmonary Clearance Model

Moraxella catarrhalis is one of the three most common causative bacterial pathogens of otitis media, however no effective vaccine against M. catarrhalis has been developed so far. To identify M. catarrhalis vaccine candidate antigens, we used carefully selected sera from children with otitis media a...

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Autores principales: Smidt, Margarita, Bättig, Patrick, Verhaegh, Suzanne J. C., Niebisch, Axel, Hanner, Markus, Selak, Sanja, Schüler, Wolfgang, Morfeldt, Eva, Hellberg, Christel, Nagy, Eszter, Lundberg, Urban, Hays, John P., Meinke, Andreas, Henriques-Normark, Birgitta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3650003/
https://www.ncbi.nlm.nih.gov/pubmed/23671716
http://dx.doi.org/10.1371/journal.pone.0064422
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author Smidt, Margarita
Bättig, Patrick
Verhaegh, Suzanne J. C.
Niebisch, Axel
Hanner, Markus
Selak, Sanja
Schüler, Wolfgang
Morfeldt, Eva
Hellberg, Christel
Nagy, Eszter
Lundberg, Urban
Hays, John P.
Meinke, Andreas
Henriques-Normark, Birgitta
author_facet Smidt, Margarita
Bättig, Patrick
Verhaegh, Suzanne J. C.
Niebisch, Axel
Hanner, Markus
Selak, Sanja
Schüler, Wolfgang
Morfeldt, Eva
Hellberg, Christel
Nagy, Eszter
Lundberg, Urban
Hays, John P.
Meinke, Andreas
Henriques-Normark, Birgitta
author_sort Smidt, Margarita
collection PubMed
description Moraxella catarrhalis is one of the three most common causative bacterial pathogens of otitis media, however no effective vaccine against M. catarrhalis has been developed so far. To identify M. catarrhalis vaccine candidate antigens, we used carefully selected sera from children with otitis media and healthy individuals to screen small-fragment genomic libraries that are expressed to display frame-selected peptides on a bacterial cell surface. This ANTIGENome technology led to the identification of 214 antigens, 23 of which were selected by in vitro or in vivo studies for additional characterization. Eight of the 23 candidates were tested in a Moraxella mouse pulmonary clearance model, and 3 of these antigens induced significantly faster bacterial clearance compared to adjuvant or to the previously characterized antigen OmpCD. The most significant protection data were obtained with the antigen MCR_1416 (Msp22), which was further investigated for its biological function by in vitro studies suggesting that Msp22 is a heme binding protein. This study comprises one of the most exhaustive studies to identify potential vaccine candidate antigens against the bacterial pathogen M. catarrhalis.
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spelling pubmed-36500032013-05-13 Comprehensive Antigen Screening Identifies Moraxella catarrhalis Proteins That Induce Protection in a Mouse Pulmonary Clearance Model Smidt, Margarita Bättig, Patrick Verhaegh, Suzanne J. C. Niebisch, Axel Hanner, Markus Selak, Sanja Schüler, Wolfgang Morfeldt, Eva Hellberg, Christel Nagy, Eszter Lundberg, Urban Hays, John P. Meinke, Andreas Henriques-Normark, Birgitta PLoS One Research Article Moraxella catarrhalis is one of the three most common causative bacterial pathogens of otitis media, however no effective vaccine against M. catarrhalis has been developed so far. To identify M. catarrhalis vaccine candidate antigens, we used carefully selected sera from children with otitis media and healthy individuals to screen small-fragment genomic libraries that are expressed to display frame-selected peptides on a bacterial cell surface. This ANTIGENome technology led to the identification of 214 antigens, 23 of which were selected by in vitro or in vivo studies for additional characterization. Eight of the 23 candidates were tested in a Moraxella mouse pulmonary clearance model, and 3 of these antigens induced significantly faster bacterial clearance compared to adjuvant or to the previously characterized antigen OmpCD. The most significant protection data were obtained with the antigen MCR_1416 (Msp22), which was further investigated for its biological function by in vitro studies suggesting that Msp22 is a heme binding protein. This study comprises one of the most exhaustive studies to identify potential vaccine candidate antigens against the bacterial pathogen M. catarrhalis. Public Library of Science 2013-05-09 /pmc/articles/PMC3650003/ /pubmed/23671716 http://dx.doi.org/10.1371/journal.pone.0064422 Text en © 2013 Smidt et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Smidt, Margarita
Bättig, Patrick
Verhaegh, Suzanne J. C.
Niebisch, Axel
Hanner, Markus
Selak, Sanja
Schüler, Wolfgang
Morfeldt, Eva
Hellberg, Christel
Nagy, Eszter
Lundberg, Urban
Hays, John P.
Meinke, Andreas
Henriques-Normark, Birgitta
Comprehensive Antigen Screening Identifies Moraxella catarrhalis Proteins That Induce Protection in a Mouse Pulmonary Clearance Model
title Comprehensive Antigen Screening Identifies Moraxella catarrhalis Proteins That Induce Protection in a Mouse Pulmonary Clearance Model
title_full Comprehensive Antigen Screening Identifies Moraxella catarrhalis Proteins That Induce Protection in a Mouse Pulmonary Clearance Model
title_fullStr Comprehensive Antigen Screening Identifies Moraxella catarrhalis Proteins That Induce Protection in a Mouse Pulmonary Clearance Model
title_full_unstemmed Comprehensive Antigen Screening Identifies Moraxella catarrhalis Proteins That Induce Protection in a Mouse Pulmonary Clearance Model
title_short Comprehensive Antigen Screening Identifies Moraxella catarrhalis Proteins That Induce Protection in a Mouse Pulmonary Clearance Model
title_sort comprehensive antigen screening identifies moraxella catarrhalis proteins that induce protection in a mouse pulmonary clearance model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3650003/
https://www.ncbi.nlm.nih.gov/pubmed/23671716
http://dx.doi.org/10.1371/journal.pone.0064422
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