Aguilar-Calvo Patricia, Espinosa Juan Carlos, Pintado Belén, Gutiérrez-Adán Alfonso, Alamillo Elia, Miranda Alberto, Prieto Irene, Bossers Alex, Andreoletti Olivier, Torres Juan María
Centro de Investigación en Sanidad Animal (CISA-INIA), Valdeolmos, Madrid, Spain.
J Virol. 2014 Mar;88(5):2670-6. doi: 10.1128/JVI.02074-13. Epub 2013 Dec 18.
The prion protein-encoding gene (prnp) strongly influences the susceptibility of small ruminants to transmissible spongiform encephalopathies (TSEs). Hence, selective breeding programs have been implemented to increase sheep resistance to scrapie. For goats, epidemiological and experimental studies have provided some association between certain polymorphisms of the cellular prion protein (PrP(C)) and resistance to TSEs. Among them, the Q/K polymorphism at PrP(C) codon 222 (Q/K222) yielded the most promising results. In this work, we investigated the individual effects of the K222-PrP(C) variant on the resistance/susceptibility of goats to TSEs. For that purpose, we generated two transgenic mouse lines, expressing either the Q222 (wild type) or K222 variant of goat PrP(C). Both mouse lines were challenged intracerebrally with a panel of TSE isolates. Transgenic mice expressing the wild-type (Q222) allele were fully susceptible to infection with all tested isolates, whereas transgenic mice expressing similar levels of the K222 allele were resistant to all goat scrapie and cattle BSE isolates but not to goat BSE isolates. Finally, heterozygous K/Q222 mice displayed a reduced susceptibility to the tested panel of scrapie isolates. These results demonstrate a highly protective effect of the K222 variant against a broad panel of different prion isolates and further reinforce the argument supporting the use of this variant in breeding programs to control TSEs in goat herds.
The objective of this study was to determine the role of the K222 variant of the prion protein (PrP) in the susceptibility/resistance of goats to transmissible spongiform encephalopathies (TSEs). Results showed that transgenic mice expressing the goat K222-PrP polymorphic variant are resistant to scrapie and bovine spongiform encephalopathy (BSE) agents. This protective effect was also observed in heterozygous Q/K222 animals. Therefore, the single amino acid exchange from Q to K at codon 222 of the cellular prion protein provides resistance against TSEs. All the results presented here support the view that the K222 polymorphic variant is a good candidate for selective breeding programs to control and eradicate scrapie in goat herds.
朊病毒蛋白编码基因(prnp)对小型反刍动物感染传染性海绵状脑病(TSEs)的易感性有强烈影响。因此,已实施选择性育种计划以提高绵羊对羊瘙痒病的抵抗力。对于山羊,流行病学和实验研究已表明细胞朊病毒蛋白(PrP(C))的某些多态性与对TSEs的抵抗力之间存在一定关联。其中,PrP(C)密码子222处的Q/K多态性(Q/K222)产生了最有前景的结果。在本研究中,我们调查了K222-PrP(C)变体对山羊感染TSEs的抵抗力/易感性的个体影响。为此,我们构建了两个转基因小鼠品系,分别表达山羊PrP(C)的Q222(野生型)或K222变体。两个小鼠品系均经脑内接种一组TSE分离株。表达野生型(Q222)等位基因的转基因小鼠对所有测试分离株均完全易感,而表达相似水平K222等位基因的转基因小鼠对所有山羊瘙痒病和牛海绵状脑病(BSE)分离株具有抗性,但对山羊BSE分离株无抗性。最后,杂合的K/Q222小鼠对测试的一组瘙痒病分离株的易感性降低。这些结果表明K222变体对多种不同的朊病毒分离株具有高度保护作用,并进一步支持在育种计划中使用该变体来控制山羊群中TSEs的观点。
本研究的目的是确定朊病毒蛋白(PrP)的K222变体在山羊对传染性海绵状脑病(TSEs)的易感性/抵抗力中的作用。结果表明,表达山羊K222-PrP多态性变体的转基因小鼠对瘙痒病和牛海绵状脑病(BSE)病原体具有抗性。在杂合的Q/K222动物中也观察到了这种保护作用。因此,细胞朊病毒蛋白密码子222处从Q到K 的单个氨基酸交换赋予了对TSEs的抗性。此处呈现的所有结果均支持以下观点,即K222多态性变体是用于控制和根除山羊群中瘙痒病的选择性育种计划的良好候选者。