Epitopes described in "Identification of T-cell epitopes in Francisella tularensis using an ordered protein array of serological targets."

Article Authors:Michael D Valentino; Zachary J Maben; Lucinda L Hensley; Matthew D Woolard; Thomas H Kawula; Jeffrey A Frelinger; John G Frelinger
Article Title:Identification of T-cell epitopes in Francisella tularensis using an ordered protein array of serological targets.
Reference Detail
Reference ID:1021609
Abstract:Francisella tularensis is a Gram-negative intracellular bacterium that is the causative agent of tularaemia. Concerns regarding its use as a bioterrorism agent have led to a renewed interest in the biology of infection, host response and pathogenesis. A robust T-cell response is critical to confer protection against F. tularensis. However, characterization of the cellular immune response has been hindered by the paucity of tools to examine the anti-Francisella immune response at the molecular level. We set out to combine recent advances of genomics with solid-phase antigen delivery coupled with a T-cell functional assay to identify T-cell epitopes. A subset of clones, encoding serological targets, was selected from an F. tularensis SchuS4 ordered genomic library and subcloned into a bacterial expression vector to test the feasibility of this approach. Proteins were expressed and purified individually employing the BioRobot 3000 in a semi-automated purification method. The purified proteins were coupled to beads, delivered to antigen-presenting cells for processing, and screened with Francisella-specific T-cell hybridomas of unknown specificity. We identified cellular reactivity against the pathogenicity protein IglB, and the chaperone proteins GroEL and DnaK. Further analyses using genetic deletions and synthetic peptides were performed to identify the minimal peptide epitopes. Priming with the peptide epitopes before infection with F. tularensis LVS increased the frequency of antigen-specific CD4 T cells as assessed by intracellular interferon- staining. These results illustrate the feasibility of screening an arrayed protein library that should be applicable to a variety of pathogens.
Affiliations:Department of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA. jfrelinger@gmail.com.
Reference Type:Literature
PubMed ID:21214540
Journal Volume:132
Article Pages:348-60
Journal ISSN:0019-2805
Article Chemical List:Bacterial Proteins;Epitopes, T-Lymphocyte
Article MeSH List:Animals; Bacterial Proteins(immunology); CD4-Positive T-Lymphocytes(immunology); Epitopes, T-Lymphocyte(immunology); Francisella tularensis(immunology); Hybridomas; Immunoblotting; Mice; Mice, Inbred C57BL; Protein Array Analysis(methods); Tularemia(immunology)
Curation Last Updated:2015-07-30 20:39:07