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首页> 外文期刊>Journal of Neuropathology and Experimental Neurology >Ovine PrP Genotype is Linked With Lesion Profile and Immunohistochemistry Patterns After Primary Transmission of Classical Scrapie to Wild-Type Mice
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Ovine PrP Genotype is Linked With Lesion Profile and Immunohistochemistry Patterns After Primary Transmission of Classical Scrapie to Wild-Type Mice

机译:绵羊PrP基因型与经典的scrapie初步传播到野生型小鼠后,与病灶和免疫组织化学模式相关。

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It is currently believed that primary transmission of classical scrapie to wild-type mice is inefficient and characterized by low attack rates and variable incubation periods and lesion profiles. Consequently, strain characterization of classical scrapie in these mice relies on subpassage. The aim of this study was to perform a retrospective analysis of lesion profiles and immunohistochemistry patterns after transmission of a large number of classical scrapie sources to wild-type mice and to investigate trends that might be used to characterize the agent without subpassaging. Scrapie field cases (n = 31) collected from individual farms between 1996 and 1999 were inoculated into RIII, C57BL, and VM mice and profiled using standard methodology and analyzed by immunohistochemistry. Using cluster analysis to resultant lesion profiles produced groups of similar lesion profiles in RIII and C57BL mice. We observed correlations between lesion profile clusters and the ovine prion protein (PrP) genotype. Immunohistochemistry indicated donor-mediated trends in the PrP pattern. These results indicate that ovine PrP genotype is a factor that is linked to both the lesion profile and the pattern of PrP deposition on primary transmission of classical scrapie to wild-type mice.
机译:目前认为,经典的瘙痒病向野生型小鼠的初次传播效率低下,其特征在于攻击率低,潜伏期和病变状况各不相同。因此,在这些小鼠中经典瘙痒病的菌株表征依赖于亚通道。这项研究的目的是在将大量经典的瘙痒病病源传播给野生型小鼠后,对病灶特征和免疫组化模式进行回顾性分析,并研究可能用于表征该药剂而未传代的趋势。将1996年至1999年间从各个农场收集的rap田病例(n = 31)接种到RIII,C57BL和VM小鼠中,并使用标准方法进行分析,并通过免疫组织化学进行分析。使用聚类分析得到的病变概况在RIII和C57BL小鼠中产生了相似的病变概况组。我们观察到病变轮廓簇与绵羊病毒蛋白(PrP)基因型之间的相关性。免疫组织化学表明PrP模式中供体介导的趋势。这些结果表明,绵羊PrP基因型是与损伤特征和经典瘙痒病向野生型小鼠初次传播时PrP沉积模式相关的因素。

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    Katy E. Beck, PhD, Rosemary E. Sallis, PhD, Richard Lockey, BSc, Marion M. Simmons, PhD, and John Spiropoulos, PhDFrom the Neuropathology Unit, Veterinary Laboratories Agency-Weybridge, New Haw, Addlestone, Surrey, United Kingdom.Send correspondence and reprint requests to: John Spiropoulos, PhD, Neuropathology Unit, Veterinary Laboratories Agency-Weybridge, New Haw, Addlestone, Surrey, KT15 3NB, United Kingdom, E-mail: j.spiropoulos@ vla.defra.gsi.gov.ukThis work was funded by the UK Department of the Environment, Food and Rural Affairs (Deffa), under projects SE1919 and SE1849.Supplemental digital content is available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal's Web site (www.jneuropath.com).,;

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