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Susceptibility to scrapie and disease phenotype in sheep: cross-PRNP genotype experimental transmissions with natural sources

机译:绵羊对瘙痒病和疾病表型的易感性:天然来源的交叉PRNP基因型实验传播

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摘要

It has long been established that the sheep Prnp genotype influences the susceptibility to scrapie, and some studies suggest that it can also determine several aspects of the disease phenotype. Other studies, however, indicate that the source of infection may also play a role in such phenotype. To address this question an experiment was set up in which either of two different natural scrapie sources, AAS from AA136 Suffolk and VVC from VV136 Cheviot sheep, were inoculated into AA136, VA136 and VV136 sheep recipients (n = 52). The immunohistochemical (IHC) profile of disease-associated PrP (PrPd) accumulation in the brain of recipient sheep was highly consistent upon codon 136 homologous and semi-homologous transmission, but could be either similar to or different from those of the inoculum donors. In contrast, the IHC profiles were highly variable upon heterologous transmission (VVC to AA136 and AAS to VV136). Furthermore, sheep of the same Prnp genotype could exhibit different survival times and PrPd profiles depending on the source of infection, and a correlation was observed between IHC and Western blot profiles. It was found that additional polymorphisms at codons 112 or 141 of AA136 recipients resulted in a delayed appearance of clinical disease or even in protection from infection. The results of this study strongly suggest that the scrapie phenotype in sheep results from a complex interaction between source, donor and recipient factors, and that the Prnp genotype of the recipient sheep does not explain the variability observed upon codon 136 heterologous transmissions, arguing for other genetic factors to be involved.
机译:长期以来,已经确定绵羊Prnp基因型会影响瘙痒病的易感性,一些研究表明它也可以确定该疾病表型的几个方面。然而,其他研究表明,感染源也可能在这种表型中起作用。为了解决这个问题,建立了一个实验,将两种不同的天然瘙痒病源,分别来自AA136 Suffolk的AAS和来自VV136 Cheviot绵羊的VVC接种到AA136,VA136和VV136绵羊接受者中(n = 52)。 136号密码子同源和半同源传播后,受体绵羊大脑中与疾病相关的PrP(PrP d )积累的免疫组织化学(IHC)谱高度一致,但可以相似或不同从接种者的那些。相反,在异源传播时(从VVC到AA136,从AAS到VV136),IHC配置文件变化很大。此外,根据感染源的不同,具有相同Prnp基因型的绵羊可能表现出不同的存活时间和PrP d 特征,并且观察到IHC和Western印迹特征之间存在相关性。发现在AA136受体的第112或141位密码子处的额外多态性导致临床疾病的出现延迟,甚至导致免受感染。这项研究的结果有力地表明,绵羊的瘙痒病表型是由来源,供体和受体因素之间复杂的相互作用引起的,并且受体绵羊的Prnp基因型不能解释在密码子136异源传播中观察到的变异性,这是其他原因的结果。涉及的遗传因素。

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