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使用蛋白质印迹技术对源自巴西的边缘无形体纯分离株的抗原谱进行分析。

Antigenic profile of a pure isolate of Anaplasma marginale of Brazilian origin, using a western blot technique.

作者信息

Patarroyo J H, Henckel D J, Prates A A, Mafra C L

机构信息

Departamento de Medicina Veterinária, Universidade Federal de Viçosa, Minas Gerais, Brazil.

出版信息

Vet Parasitol. 1994 Mar;52(1-2):129-37. doi: 10.1016/0304-4017(94)90042-6.

Abstract

Anaplasma marginale initial bodies of the Brazilian isolate AUFV1 were purified from infected erythrocytes using a combination of lysis, ultrasonic disruption and differential centrifugation. Initial bodies were solubilised with a buffer containing protease inhibitors and non-ionic detergents. Immunochemical analysis by the Western blot technique revealed at least five proteins with apparent molecular weights (MW) of 105, 100, 97, 87 and 38 kDa when homologous sera were used as primary antibodies. Sera from cattle from Mato Grosso do Sul State in Brazil revealed five proteins of 105, 100, 87, 38 and 25 kDa; other heterologous sera obtained from Illinois, USA, bound to four antigens with MW of 105, 100, 87 and 38 kDa, the latter being stronger and broader than the others. No bands were observed in the non-infected erythrocyte control when the different A. marginale sera or antibodies against Babesia bovis and Babesia bigemina were used. Antibodies from cattle infected with the A. marginale isolates bound to proteins of 105, 100, 87 and 38 kDa, indicating that there are at least four peptides common to the isolates. The major surface proteins, designated MSP-1, MSP-2 and MSP-3, are also present in the Brazilian isolate AUFV1 and the sample from the National Research Centre of Beef Cattle in Mato Grosso do Sul State. One practical consideration of this study is the possibility of cross-protection between different Anaplasma isolates including some from Brazil.

摘要

使用裂解、超声破碎和差速离心相结合的方法,从感染的红细胞中纯化巴西分离株AUFV1的边缘无形体原生小体。原生小体用含有蛋白酶抑制剂和非离子去污剂的缓冲液溶解。当使用同源血清作为一抗时,通过蛋白质印迹技术进行的免疫化学分析显示至少有5种蛋白质,其表观分子量(MW)分别为105、100、97、87和38 kDa。来自巴西南马托格罗索州牛的血清显示出分子量为105、100、87、38和25 kDa的5种蛋白质;从美国伊利诺伊州获得的其他异源血清与分子量为105、100、87和38 kDa的4种抗原结合,其中分子量为38 kDa的抗原条带比其他条带更强更宽。当使用不同的边缘无形体血清或抗牛巴贝斯虫和双芽巴贝斯虫的抗体时,在未感染红细胞的对照中未观察到条带。感染边缘无形体分离株的牛的抗体与分子量为105、100、87和38 kDa的蛋白质结合,表明这些分离株至少有4种共同的肽段。主要表面蛋白,即MSP-1、MSP-2和MSP-3,也存在于巴西分离株AUFV1和南马托格罗索州肉牛国家研究中心的样本中。本研究的一个实际考虑因素是不同无形体分离株之间,包括一些来自巴西的分离株之间交叉保护的可能性。

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