Suppr超能文献

英国非典型瘙痒病病例的朊蛋白基因型

PrP genotypes of atypical scrapie cases in Great Britain.

作者信息

Saunders G C, Cawthraw S, Mountjoy S J, Hope J, Windl O

机构信息

Department of TSE Molecular Biology, Veterinary Laboratories Agency, New Haw, Addlestone, Surrey KT15 3NB, UK.

出版信息

J Gen Virol. 2006 Nov;87(Pt 11):3141-3149. doi: 10.1099/vir.0.81779-0.

Abstract

Great Britain and elsewhere have detected atypical scrapie infection in sheep with PrP genotypes thought to be genetically resistant to the classical form of scrapie. DNA sequencing of the PrP gene of British atypical scrapie cases (n=69), classical scrapie cases (n=59) and scrapie-free controls (n=138) was undertaken to identify whether PrP variants, other than the three well-characterized polymorphic codons, influenced susceptibility to atypical scrapie infection. Four non-synonymous changes, M112T, M137T, L141F and P241S, were detected that are most probably associated with the A(136)R(154)Q(171) haplotype. Only the PrP variant containing a phenylalanine residue at amino acid position 141 was found to be associated more commonly with the atypical scrapie cases. In addition to the single nucleotide polymorphisms associated with the ARQ allele, two out of nine atypical scrapie cases with the ARR/ARR genotype were found to contain a 24 bp insertion, leading to an additional octapeptide repeat. In terms of PrP genetics, one classification of the GB scrapie cases examined in this study would place animals carrying any homozygous or heterozygous combination of ARR, AHQ or AF(141)RQ alleles, or any one of these alleles when paired with ARQ, as being susceptible to atypical scrapie infection, and animals heterozygous or homozygous for VRQ or homozygous for ARQ as being susceptible to classical scrapie disease. The AHQ PrP allele was associated with the highest incidence of atypical scrapie (263 per 100 000 alleles), whilst VRQ was associated with the lowest incidence (10 per 100 000 alleles).

摘要

英国及其他地区在具有被认为对经典型羊瘙痒病具有遗传抗性的朊蛋白(PrP)基因型的绵羊中检测到了非典型羊瘙痒病感染。对英国非典型羊瘙痒病病例(n = 69)、经典羊瘙痒病病例(n = 59)和无羊瘙痒病对照(n = 138)的PrP基因进行DNA测序,以确定除三个已充分表征的多态密码子外,PrP变体是否会影响对非典型羊瘙痒病感染的易感性。检测到四个非同义变化,即M112T、M137T、L141F和P241S,它们很可能与A(136)R(154)Q(171)单倍型相关。仅发现氨基酸位置141处含有苯丙氨酸残基的PrP变体更常与非典型羊瘙痒病病例相关。除了与ARQ等位基因相关的单核苷酸多态性外,在九例ARR/ARR基因型的非典型羊瘙痒病病例中,有两例发现含有一个24 bp的插入片段,导致额外的八肽重复序列。就PrP遗传学而言,本研究中检测的英国羊瘙痒病病例的一种分类方法是,将携带ARR、AHQ或AF(141)RQ等位基因的任何纯合或杂合组合的动物,或与ARQ配对时这些等位基因中的任何一个,视为易患非典型羊瘙痒病感染;将VRQ杂合或纯合的动物或ARQ纯合的动物视为易患经典羊瘙痒病。AHQ PrP等位基因与非典型羊瘙痒病的最高发病率相关(每10万个等位基因中有263例),而VRQ与最低发病率相关(每10万个等位基因中有10例)。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验