Characterization and cloning of T24, a Taenia solium antigen diagnostic for cysticercosis

被引:85
作者
Hancock, K [1 ]
Pattabhi, S
Whitfield, FW
Yushak, ML
Lane, WS
Garciac, HH
Gonzalez, AE
Gilman, RH
Tsang, VCW
机构
[1] Ctr Dis Control & Prevent, Div Parasit Dis, Atlanta, GA 30333 USA
[2] Harvard Univ, Microchem & Proteom Anal Facil, Cambridge, MA 02138 USA
[3] Inst Ciencias Neurol, Dept Transmissible Dis, Lima, Peru
[4] Univ Peruana Cayetano Heredia, Dept Microbiol, Lima, Peru
[5] Univ Nacl Mayor San Marcos, Sch Vet Med, Lima 14, Peru
[6] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Int Hlth, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
Taenia solium; cysticercosis; neurocysticercosis; diagnostic antigen; recombinant protein; Western blot;
D O I
10.1016/j.molbiopara.2006.02.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The third and final diagnostic antigen of the lentil lectin purified glycoproteins (LLGP) extracted from the larval stage of Taenia solium has been characterized, cloned, and expressed. T24 is an integral membrane protein that belongs to the tetraspanin superfamily. It migrates at a position corresponding to 24-kDa and as it homodimer at 42-kDa. Antibodies from cysticercosis patients recognize secondary structure epitopes that are dependent upon correctly formed disulfide bonds. A portion of T24, the large, extracellular loop domain, was expressed in an immunologically reactive form in insect cells. When tested in a Western blot assay with a large battery of serum samples, this protein, T24H, has a sensitivity of 94% (101/107), for detecting cases of cysticercosis with two or more viable cysts, and a specificity of 98% (284/290). The identification and expression of T24H sets the stage for the development of an ELISA suitable for testing single samples and for large-scale serosurveys that is not dependent upon the isolation and purification of antigens from parasite materials. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:109 / 117
页数:9
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