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

被引:0
|
作者
Khukhuu Altangerel
Andy Alhassan
Hiroshi Iseki
Thillaiampalam Sivakumar
Damdinsuren Boldbaatar
Naoaki Yokoyama
Ikuo Igarashi
机构
[1] Obihiro University of Agriculture and Veterinary Medicine,National Research Center for Protozoan Diseases
[2] Kagoshima University,Laboratory of Emerging Infectious Diseases, Department of Frontier Veterinary Medicine, Faculty of Agriculture
来源
Parasitology Research | 2009年 / 105卷
关键词
Polymerase Chain Reaction; Babesia; Babesiosis; Infected Cattle; Ampicillin Sodium;
D O I
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中图分类号
学科分类号
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.
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页码:249 / 254
页数:5
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