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酶联免疫吸附测定法检测牛血清中抗犬新孢子虫重组主要表面抗原(Nc-p43)片段的IgG抗体。

ELISA detection of IgG antibody against a recombinant major surface antigen (Nc-p43) fragment of Neospora caninum in bovine sera.

作者信息

Ahn Hye-Jin, Kim Sera, Kim Dae-Yong, Nam Ho-Woo

机构信息

Department of Parasitology and Catholic Institute of Parasitic Diseases, Catholic University of Korea, College of Medicine, Seoul 137-701, Korea.

出版信息

Korean J Parasitol. 2003 Sep;41(3):175-7. doi: 10.3347/kjp.2003.41.3.175.

Abstract

An ELISA was established to measure bovine IgG directed against the recombinant antigenic determinant of Nc-p43, a major surface antigen of Neospora caninum. In a previous study, two thirds of the C-terminal of the molecule was expressed as a 6 x His tagged protein (Ncp43P) for ELISA using 2/3 of the N-terminal of SAG1 from Toxoplasma gondii as a control (TgSAG1A). Among 852 cattle sera collected from stock farms scattered nation-wide, 103 sera (12.1%) were found to react with Ncp43P positively, but no positive reaction was observed with TgSAG1A. This study shows that Ncp43P could be available as an efficient antigen for the diagnosis of neosporosis in cattle. Furthermore, it together with TgSAG1A, could be useful for the differential diagnosis of N. caninum and T. gondii infections in other mammals.

摘要

建立了一种酶联免疫吸附测定法(ELISA),用于检测针对犬新孢子虫主要表面抗原Nc-p43重组抗原决定簇的牛IgG。在先前的一项研究中,该分子C端的三分之二被表达为6×组氨酸标签蛋白(Ncp43P)用于ELISA,使用来自刚地弓形虫SAG1 N端的三分之二作为对照(TgSAG1A)。在从全国范围内分散的养殖场收集的852份牛血清中,发现103份血清(12.1%)与Ncp43P呈阳性反应,但与TgSAG1A未观察到阳性反应。本研究表明,Ncp43P可作为诊断牛新孢子虫病的有效抗原。此外,它与TgSAG1A一起,可用于其他哺乳动物中犬新孢子虫和刚地弓形虫感染的鉴别诊断。

相似文献

本文引用的文献

1
Review of Neospora caninum and neosporosis in animals.动物新孢子虫及新孢子虫病综述。
Korean J Parasitol. 2003 Mar;41(1):1-16. doi: 10.3347/kjp.2003.41.1.1.
4
In vitro isolation and characterization of bovine Neospora caninum in Korea.
Vet Parasitol. 2000 Jun 10;90(1-2):147-54. doi: 10.1016/s0304-4017(00)00224-7.
7
An enzyme-linked immunosorbent assay (ELISA) for serological diagnosis of Neospora sp. infection in cattle.
J Vet Diagn Invest. 1995 Jul;7(3):352-9. doi: 10.1177/104063879500700310.

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