Immunodominant Francisella tularensis antigens identified using proteome microarray. Crown Copyright 2007 Dstl

被引:88
作者
Eyles, Jim E.
Unal, Berkay
Hartley, Margaret Gill
Newstead, Sarah L.
Flick-Smith, Helen
Prior, Joann L.
Oyston, Petra C. F.
Randall, Arlo
Mu, Yunxiang
Hirst, Siddiqua
Molina, Douglas M.
Davies, D. Huw
Milne, Tim
Griffin, Kate F.
Baldi, Pierre
Titball, Rick W.
Felgner, Philip L.
机构
[1] DSTL, Salisbury SP4 0JQ, Wilts, England
[2] Univ Calif Irvine, Dept Med, Irvine, CA 92717 USA
[3] Univ Calif Irvine, Sch Informat & Comp Sci, Irvine, CA 92717 USA
[4] Univ Calif Irvine, Inst Genom & Bioinformat, Irvine, CA 92717 USA
[5] ImmPORT Therapeut, Irvine, CA USA
[6] London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1, England
关键词
adjuvant; microarray; tularemia; vaccine;
D O I
10.1002/pmic.200600985
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Stimulation of protective immune responses against intracellular pathogens is difficult to achieve using non-replicating vaccines. BALB/c mice immunized by intramuscular injection with killed Francisella tularensis (live vaccine strain) adjuvanted with preformed immune stimulating complexes admixed with CpG, were protected when systemically challenged with a highly virulent strain of F. tularensis (Schu S4). Serum from immunized mice was used to probe a whole proteome microarray in order to identify immunodominant antigens. Eleven out of the top 12 immunodominant antigens have been previously described as immunoreactive in F. tularensis. However, 31 previously unreported immunoreactive antigens were revealed using this approach. Twenty four (50%) of the ORFs on the immunodominant hit list belonged to the category of surface or membrane associated proteins compared to only 22% of the entire proteome. There were eight hypothetical protein hits and eight hits from proteins associated with different aspects of metabolism. The chip also allowed us to readily determine the IgG subclass bias, towards individual or multiple antigens, in protected and unprotected animals. These data give insight into the protective immune response and have potentially important implications for the rational design of non-living vaccines for tularemia and other intracellular pathogens.
引用
收藏
页码:2172 / 2183
页数:12
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