Identification of Immunogenic and Virulence-Associated Campylobacter jejuni Proteins Lene N. Nielsen a , b , Thomas A. Luijkx c , e , Christina S. Vegge b , Christina Kofoed Johnsen a , f , Piet Nuijten c , Brendan W. Wren d , Hanne Ingmer b and Karen A. Krogfelt a a Department of Microbiological Surveillance and Research f Unit for Electron Microscopy, Statens Serum Institut, Copenhagen, Denmark b University of Copenhagen, Department of Veterinary Disease Biology, Copenhagen, Denmark c Merck, Nobilon International B.V., Boxmeer, The Netherlands d London School of Hygiene and Tropical Medicine, London, United Kingdom e Antimmune BV, Nijmegen, The Netherlands ABSTRACT With the aim of identifying proteins important for host interaction and virulence, we have screened an expression library of NCTC 11168 Campylobacter jejuni genes for highly immunogenic proteins. A commercial C. jejuni open reading frame (ORF) library consisting of more than 1,600 genes was transformed into the Escherichia coli expression strain BL21(DE3), resulting in 2,304 clones. This library was subsequently screened for immunogenic proteins using antibodies raised in rabbit against a clinical isolate of C. jejuni ; this resulted in 52 highly reactive clones representing 25 different genes after sequencing. Selected candidate genes were inactivated in C. jejuni NCTC 11168, and the virulence was examined using INT 407 epithelial cell line and motility, biofilm, autoagglutination, and serum resistance assays. These investigations revealed C. jejuni antigen 0034c (Cj0034c) to be a novel virulence factor and support the usefulness of the method. Further, several antigens were tested as vaccine candidates in two mouse models, in which Cj0034c, Cj0404, and Cj0525c resulted in a reduction of invasion in spleen and liver after challenge.
Identification of Immunogenic and Virulence-Associated Campylobacter jejuni Proteins
Abstract
Identification of Immunogenic and Virulence-Associated Campylobacter jejuni Proteins Lene N. Nielsen a , b , Thomas A. Luijkx c , e , Christina S. Vegge b , Christina Kofoed Johnsen a , f , Piet Nuijten c , Brendan W. Wren d , Hanne Ingmer b and Karen A. Krogfelt a a Department of Microbiological Surveillance and Research f Unit for Electron Microscopy, Statens Serum Institut, Copenhagen, Denmark b University of Copenhagen, Department of Veterinary Disease Biology, Copenhagen, Denmark c Merck, Nobilon International B.V., Boxmeer, The Netherlands d London School of Hygiene and Tropical Medicine, London, United Kingdom e Antimmune BV, Nijmegen, The Netherlands ABSTRACT With the aim of identifying proteins important for host interaction and virulence, we have screened an expression library of NCTC 11168 Campylobacter jejuni genes for highly immunogenic proteins. A commercial C. jejuni open reading frame (ORF) library consisting of more than 1,600 genes was transformed into the Escherichia coli expression strain BL21(DE3), resulting in 2,304 clones. This library was subsequently screened for immunogenic proteins using antibodies raised in rabbit against a clinical isolate of C. jejuni ; this resulted in 52 highly reactive clones representing 25 different genes after sequencing. Selected candidate genes were inactivated in C. jejuni NCTC 11168, and the virulence was examined using INT 407 epithelial cell line and motility, biofilm, autoagglutination, and serum resistance assays. These investigations revealed C. jejuni antigen 0034c (Cj0034c) to be a novel virulence factor and support the usefulness of the method. Further, several antigens were tested as vaccine candidates in two mouse models, in which Cj0034c, Cj0404, and Cj0525c resulted in a reduction of invasion in spleen and liver after challenge.Preview Only. This article cannot be rented because we do not currently have permission from the publisher.
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Identification of Immunogenic and Virulence-Associated Campylobacter jejuni Proteins
Nielsen, Lene N.; Luijkx, Thomas A.; Vegge, Christina S.; Johnsen, Christina Kofoed; Nuijten, Piet; Wren, Brendan W.; Ingmer, Hanne; Krogfelt, Karen A.
Follow Clinical and Vaccine Immunology
, Volume 19 (2): 113
American Society For Microbiology – Feb 1, 2012
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