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吉氏巴贝斯虫:采用重组BgTRAP酶联免疫吸附试验对犬感染进行血清学诊断。

Babesia gibsoni: Serodiagnosis of infection in dogs by an enzyme-linked immunosorbent assay with recombinant BgTRAP.

作者信息

Goo Youn-Kyoung, Jia Honglin, Aboge G Oluga, Terkawi M Alaa, Kuriki Ken, Nakamura Chinatsu, Kumagai Akiko, Zhou Jinlin, Lee Eung-goo, Nishikawa Yoshifumi, Igarashi Ikuo, Fujisaki Kozo, 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

Exp Parasitol. 2008 Apr;118(4):555-60. doi: 10.1016/j.exppara.2007.11.010. Epub 2007 Nov 22.

Abstract

The thrombospondin-related adhesive protein of Babesia gibsoni (BgTRAP) is known as an immunodominant antigen and is, therefore, considered as a candidate for the development of a diagnostic reagent for canine babesiosis. The recombinant BgTRAP (rBgTRAP) expressed in Escherichia coli was tested in an enzyme-linked immunosorbent assay (ELISA) for detecting antibodies to B. gibsoni in dogs. The ELISA with rBgTRAP clearly differentiated between B. gibsoni-infected dog sera and specific pathogen-free (SPF) dog sera. The sera collected from dogs experimentally infected with closely related parasites, B. canis canis, B. canis vogeli, B. canis rossi, and Neospora caninum, showed no cross-reactivity by the ELISA with rBgTRAP. A total of 107 blood samples collected from dogs that had been diagnosed as having babesiosis at veterinary hospitals in Japan were examined for the diagnosis of B. gibsoni infection by the ELISA and PCR. Ninety-six (89.7%) and 89 (83.2%) of the tested samples were positive by the ELISA and PCR, respectively, while 11 (10.3%) and 4 (3.7%) were ELISA+/PCR- and ELISA-/PCR+, respectively. In addition, the sensitivity of the ELISA with rBgTRAP was much higher than that of previously established ELISAs with rBgP50, rBgSA1, and rBgP32. These results indicate that the rBgTRAP is the most promising diagnostic antigen for the detection of an antibody to B. gibsoni in dogs and that the combined ELISA/PCR approach could provide the most reliable diagnosis for clinical sites.

摘要

犬吉氏巴贝斯虫的血小板反应蛋白相关黏附蛋白(BgTRAP)是一种免疫显性抗原,因此被认为是开发犬巴贝斯虫病诊断试剂的候选抗原。在酶联免疫吸附测定(ELISA)中对大肠杆菌表达的重组BgTRAP(rBgTRAP)进行检测,以检测犬体内针对吉氏巴贝斯虫的抗体。含有rBgTRAP的ELISA能够清晰地区分感染吉氏巴贝斯虫的犬血清和无特定病原体(SPF)犬血清。用ELISA检测感染密切相关寄生虫——犬巴贝斯虫、韦氏巴贝斯虫、罗氏巴贝斯虫和犬新孢子虫的犬血清,结果显示无交叉反应。从日本兽医医院诊断为患有巴贝斯虫病的犬只采集了107份血样,通过ELISA和PCR检测吉氏巴贝斯虫感染情况。ELISA检测的96份(89.7%)和PCR检测的89份(83.2%)样本呈阳性,而ELISA+/PCR-和ELISA-/PCR+的样本分别为11份(10.3%)和4份(3.7%)。此外,含有rBgTRAP的ELISA的灵敏度远高于先前建立的含有rBgP50、rBgSA1和rBgP32的ELISA。这些结果表明,rBgTRAP是检测犬体内吉氏巴贝斯虫抗体最有前景的诊断抗原,并且ELISA/PCR联合检测方法可为临床提供最可靠的诊断。

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