Evaluation of Babesia bigemina 200 kDa recombinant antigen in enzyme-linked immunosorbent assay

被引:6
|
作者
Altangerel, Khukhuu [1 ]
Alhassan, Andy [1 ]
Iseki, Hiroshi [1 ]
Sivakumar, Thillaiampalam [1 ]
Boldbaatar, Damdinsuren [2 ]
Yokoyama, Naoaki [1 ]
Igarashi, Ikuo [1 ]
机构
[1] Obihiro Univ Agr & Vet Med, Natl Res Ctr Protozoan Dis, Obihiro, Hokkaido 0808555, Japan
[2] Kagoshima Univ, Fac Agr, Dept Frontier Vet Med, Lab Emerging Infect Dis, Kagoshima 8900065, Japan
基金
日本学术振兴会;
关键词
RHOPTRY-ASSOCIATED PROTEIN-1; BOVIS; ANTIBODIES; INFECTION; CATTLE; EXPRESSION; DIAGNOSIS; RESISTANCE; STATE; CELLS;
D O I
10.1007/s00436-009-1392-2
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
A truncated fragment of the gene encoding the 200-kDa protein (P200) of Babesia bigemina was cloned into a plasmid vector, pGEX-4 T-1 and expressed in Escherichia coli as a glutathione-S-transferase fused protein. An indirect enzyme-linked immunosorbent assay (ELISA) using the rp200/CT detected specific antibodies in cattle experimentally infected with B. bigemina. Furthermore, the antigen did not cross-react with antibodies to Babesia bovis, a closely related Babesia parasite indicating that rp200/CT is a specific antigen for the diagnosis of B. bigemina infection. Additionally, ELISA using p200/CT and polymerase chain reaction were conducted on serum and corresponding DNA samples obtained from field cattle to evaluate the diagnostic utility of the p200/CT antigen. Results from the current study suggest that p200/CT ELISA is a sensitive and specific method for improved serodiagnosis of B. bigemina infection.
引用
收藏
页码:249 / 254
页数:6
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