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利用重组截短型NcSAG1通过酶联免疫吸附测定法对牛新孢子虫感染进行血清学诊断

Serodiagnosis of Neospora caninum infection in cattle by enzyme-linked immunosorbent assay with recombinant truncated NcSAG1.

作者信息

Chahan Bayin, Gaturaga Irungu, Huang Xiaohong, Liao Min, Fukumoto Shinya, Hirata Haruyuki, Nishikawa Yoshihumi, Suzuki Hiroshi, Sugimoto Chihiro, Nagasawa Hideyuki, Fujisaki Kozo, Igarashi Ikuo, Mikami Takeshi, Xuan Xuenan

机构信息

National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Inada-cho, Obihiro, Hokkaido 080-8555, Japan.

出版信息

Vet Parasitol. 2003 Dec 30;118(3-4):177-85. doi: 10.1016/j.vetpar.2003.10.010.

Abstract

Neospora caninum is a veterinary medically important pathogen capable of causing abortion in cattle and neuromuscular paralysis in dogs. The surface antigen 1 of N. caninum (NcSAG1) is an important candidate for the development of a diagnostic reagent for neosporosis. In order to establish an effective diagnostic method, the gene encoding truncated NcSAG1 (NcSAG1t) lacking a signal peptide and C-terminal hydrophobic regions was cloned and expressed in Escherichia coli as a fusion protein with glutathione S-transferase (GST). The purified GST-NcSAG1t was tested in an enzyme-linked immunosorbent assay (ELISA) for the detection of N. caninum antibodies in cattle. The ELISA with GST-NcSAG1t clearly differentiated between immunofluorescent antibody test (IFAT)-positive and -negative sera from cattle. In addition, the ELISA detected no cross-reactivity with sera from mice experimentally infected with the closely related parasite Toxoplasma gondii. Field serum samples collected from cattle in Brazil were examined for the diagnosis of neosporosis by using the ELISA. Of the 197 samples analyzed, 66 (33.5%) samples were positive for antibodies to N. caninum. Of the 66 ELISA-positive samples, 60 (90%) samples were confirmed as positive by Western blot analysis with whole parasite antigens. These results suggest that the recombinant NcSAG1t could be a reliable reagent for use as an antigen in ELISA for the serodiagnosis of N. caninum infection in cattle.

摘要

犬新孢子虫是一种在兽医学上具有重要意义的病原体,能够导致牛流产和犬神经肌肉麻痹。犬新孢子虫的表面抗原1(NcSAG1)是开发新孢子虫病诊断试剂的重要候选物。为了建立一种有效的诊断方法,编码缺失信号肽和C端疏水区域的截短型NcSAG1(NcSAG1t)的基因被克隆,并在大肠杆菌中作为与谷胱甘肽S-转移酶(GST)的融合蛋白进行表达。纯化后的GST-NcSAG1t在酶联免疫吸附测定(ELISA)中用于检测牛体内的犬新孢子虫抗体。使用GST-NcSAG1t的ELISA能够清晰地区分牛的免疫荧光抗体试验(IFAT)阳性和阴性血清。此外,该ELISA检测到与实验感染密切相关寄生虫刚地弓形虫的小鼠血清无交叉反应。利用ELISA对从巴西牛采集的现场血清样本进行新孢子虫病诊断检测。在分析的197个样本中,66个(33.5%)样本的犬新孢子虫抗体呈阳性。在66个ELISA阳性样本中,60个(90%)样本通过全寄生虫抗原的蛋白质印迹分析被确认为阳性。这些结果表明,重组NcSAG1t可作为一种可靠的试剂,用作ELISA中的抗原,用于牛犬新孢子虫感染的血清学诊断。

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