Pig paramyxovirus of the blue eye disease binding to a 116 kDa glycoprotein expressed in pig neuronal membranes.

M. L. Mendoza-Magaña, M. Ramírez-Herrera, J. M. Dueñas-Jiménez, S. Dueñas-Jiménez
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引用次数: 7

Abstract

UNLABELLED Pig paramyxovirus of the blue eye disease (PPBED) is a novel member of the paramyxoviridac family which infects pigs. In neonatal pigs it causes neurological damage, whereas in adult pigs it affects the reproductive function. As PPBED damages the new-born pig central nervous system (CNS), it is important to study whether PPBED binds to the membrane proteins of all brain tissue, or selectively binds to neuronal tissue of the brain stem, olfactory bulb, hippocampus, cerebellum, frontal, temporal and parietal brain cortex. It is also important to establish whether it also infects neurones obtained from new-born, 60-day-old and adult pigs, and the role of carbohydrate residues in virus binding. The effect on virus binding of polyclonal antibodies against viral envelope proteins was also studied. Binding studies were performed using dot blot and virus overlay protein binding assays. PPBED was able to bind to membrane proteins from all brain regions, particularly to a protein band of approximately 116 kDa. Neuraminidase treatment of neuronal membrane proteins decreased virus binding; subsequent treatments with beta-galactosidase and manosidase did not increase virus binding inhibition. N-glycosidase F and trypsin also decreased virus binding, but not the O-glycanase. Antibodies against viral haemagglutinin-neuraminidase blocked virus binding more efficiently than antibodies against viral fusion protein. IN CONCLUSION (1) PPBFD is able to bind to pig neurones of all brain regions studied and at all ages analysed; (2) a 116 kDa membrane protein containing sialic acid residues with an N-linked oligosaccharide chain was specifically recognized; (3) PPBED haemagglutinin-neuraminidase protein seems to play a central role in neural receptor recognition.
猪蓝眼病副粘病毒与猪神经元膜表达的116 kDa糖蛋白结合。
猪蓝眼病副粘病毒(PPBED)是一种感染猪的副粘病毒家族的新成员。在新生猪中,它会引起神经损伤,而在成年猪中,它会影响生殖功能。由于PPBED对新生猪中枢神经系统(CNS)有损伤,因此研究PPBED是与所有脑组织的膜蛋白结合,还是选择性地与脑干、嗅球、海马、小脑、大脑额叶、颞叶和顶叶皮层的神经元组织结合具有重要意义。同样重要的是确定它是否也感染从新生、60日龄和成年猪获得的神经元,以及碳水化合物残基在病毒结合中的作用。研究了病毒包膜蛋白多克隆抗体对病毒结合的影响。结合研究采用点印迹法和病毒覆盖蛋白结合法。PPBED能够与大脑所有区域的膜蛋白结合,特别是与大约116 kDa的蛋白带结合。神经氨酸酶处理神经元膜蛋白降低病毒结合;随后用-半乳糖苷酶和马诺苷酶处理没有增加病毒结合抑制。n -糖苷酶F和胰蛋白酶也降低病毒结合,但o -糖苷酶没有。抗病毒血凝素-神经氨酸酶抗体比抗病毒融合蛋白抗体更有效地阻断病毒结合。结论(1)PPBFD能够结合所研究的所有脑区和所有年龄的猪神经元;(2)特异性识别了含有n -寡糖链唾液酸残基的116 kDa膜蛋白;(3) PPBED血凝素-神经氨酸酶蛋白似乎在神经受体识别中起核心作用。
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