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Idiopathic Brainstem Neuronal Chromatolysis (IBNC): a novel prion protein related disorder of cattle?

机译:特发性脑干神经元染色体溶解症(IBNC):一种与牛的pr蛋白相关的新型疾病?

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Background The epidemic form of Bovine Spongiform Encephalopathy (BSE) is generally considered to have been caused by a single prion strain but at least two strain variants of cattle prion disorders have recently been recognized. An additional neurodegenerative condition, idiopathic brainstem neuronal chromatolysis and hippocampal sclerosis (IBNC), a rare neurological disease of adult cattle, was also recognised in a sub-set of cattle submitted under the BSE Orders in which lesions of BSE were absent. Between the years of 1988 and 1991 IBNC occurred in Scotland with an incidence of 7 cases per 100,000 beef suckler cows over the age of 6 years. Results When the brains of 15 IBNC cases were each tested by immunohistochemistry, all showed abnormal labelling for prion protein (PrP). Immunohistological labelling for PrP was also present in the retina of a single case available for examination. The pattern of PrP labelling in brain is distinct from that seen in other ruminant prion diseases and is absent from brains with other inflammatory conditions and from normal control brains. Brains of IBNC cattle do not reveal abnormal PrP isoforms when tested by the commercial BioRad or Idexx test kits and do not reveal PrPres when tested by Western blotting using stringent proteinase digestion methods. However, some weakly protease resistant isoforms of PrP may be detected when tissues are examined using mild proteinase digestion techniques. Conclusion The study shows that a distinctive neurological disorder of cattle, which has some clinical similarities to BSE, is associated with abnormal PrP labelling in brain but the pathology and biochemistry of IBNC are distinct from BSE. The study is important either because it raises the possibility of a significant increase in the scope of prion disease or because it demonstrates that widespread and consistent PrP alterations may not be confined to prion diseases. Further studies, including transmission experiments, are needed to establish whether IBNC is a condition in which prion protein is abnormally regulated or it is yet a further example of an infectious cattle prion disease.
机译:背景技术牛海绵状脑病(BSE)的流行形式通常被认为是由单一病毒株引起的,但是最近已认识到牛cattle病毒病的至少两种株变体。在没有BSE病变的BSE指令下提交的一组亚型牛中,也认识到了另一种神经退行性疾病,即特发性脑干神经元色解和海马硬化(IBNC),这是成年牛的一种罕见的神经系统疾病。在1988年至1991年之间,IBNC在苏格兰发生,每6岁以上的100,000头奶牛出现7例。结果分别对15例IBNC病例的大脑进行免疫组织化学检测时,均显示abnormal蛋白(PrP)标记异常。 PrP的免疫组织学标记还存在于可检查的单个病例的视网膜中。大脑中PrP标记的模式与其他反刍病毒疾病中所见的模式不同,患有其他炎症性疾病的大脑和正常对照大脑中均没有。通过商业化的BioRad或Idexx测试试剂盒进行测试时,IBNC牛的大脑不会显示出异常的PrP亚型,而使用严格的蛋白酶消化方法进行的蛋白质印迹测试时,则不会显示出PrP res 。但是,使用温和的蛋白酶消化技术检查组织时,可能会检测到PrP的一些弱蛋白酶抗性亚型。结论研究表明,牛的一种特殊的神经系统疾病与BSE有一定的临床相似性,与脑中PrP标记异常有关,但IBNC的病理和生化与BSE有所不同。该研究很重要,因为它增加了病毒疾病范围显着增加的可能性,或者因为它表明广泛且一致的PrP改变可能不限于not病毒疾病。需要进一步的研究,包括传播实验,以确定IBNC是is病毒蛋白异常调节的病状还是传染性牛病毒病的又一例子。

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