Saá Paula, Cervenakova Larisa
Transmissible Diseases Department, American National Red Cross, Biomedical Services, Holland Laboratory, 15601 Crabbs Branch Way, Rockville, MD 20855, United States.
Transmissible Diseases Department, American National Red Cross, Biomedical Services, Holland Laboratory, 15601 Crabbs Branch Way, Rockville, MD 20855, United States.
Virus Res. 2015 Sep 2;207:47-61. doi: 10.1016/j.virusres.2014.11.007. Epub 2014 Nov 13.
Transmissible spongiform encephalopathies (TSEs) most commonly known as prion diseases are invariably fatal neurological disorders that affect humans and animals. These disorders differ from other neurodegenerative conformational diseases caused by the accumulation in the brain of misfolded proteins, sometimes with amyloid properties, in their ability to infect susceptible species by various routes. While the infectious properties of amyloidogenic proteins, other than misfolded prion protein (PrP(TSE)), are currently under scrutiny, their potential to transmit from cell to cell, one of the intrinsic properties of the prion, has been recently shown in vitro and in vivo. Over the decades, various cell culture and laboratory animal models have been developed to study TSEs. These assays have been widely used in a variety of applications but showed to be time consuming and entailed elevated costs. Novel economic and fast alternatives became available with the development of in vitro assays that are based on the property of conformationally abnormal PrP(TSE) to recruit normal cellular PrP(C) to misfold. These include the cell-free conversion assay, protein misfolding cyclic amplification (PMCA) and quaking induced conversion assay (QuIC), of which the PMCA has been the only technology shown to generate infectious prions. Moreover, it allows indefinite amplification of PrP(TSE) with strain-specific biochemical and biological properties of the original molecules and under certain conditions may give rise to new spontaneously generated prions. The method also allows addressing the species barrier phenomena and assessing possible risks of animal-to-animal and animal-to-human transmission. Additionally, its unprecedented sensitivity has made possible the detection of as little as one infectious dose of PrP(TSE) and the biochemical identification of this protein in different tissues and biological fluids, including blood, cerebral spinal fluid (CSF), semen, milk, urine and saliva during the pre-clinical and clinical phases of the disease. The mechanistic similarities between TSEs and other conformational disorders have resulted in the adaptation of the PMCA to the amplification and detection of various amyloidogenic proteins. Here we provide a compelling discussion of the different applications of this technology to the study of TSEs and other neurodegenerative diseases.
传染性海绵状脑病(TSEs),通常被称为朊病毒疾病,是一类总是致命的神经紊乱疾病,会影响人类和动物。这些疾病与其他由错误折叠的蛋白质在大脑中积累(有时具有淀粉样蛋白特性)引起的神经退行性构象疾病不同,它们能够通过各种途径感染易感物种。虽然除了错误折叠的朊病毒蛋白(PrP(TSE))之外,淀粉样蛋白的传染性目前正在研究中,但它们从细胞到细胞传播的潜力,作为朊病毒内在特性之一,最近已在体外和体内得到证实。几十年来,人们开发了各种细胞培养和实验动物模型来研究TSEs。这些检测方法已广泛应用于各种领域,但显示出耗时且成本高昂。随着基于构象异常的PrP(TSE)招募正常细胞PrP(C)进行错误折叠特性的体外检测方法的发展,出现了新的经济且快速的替代方法。这些方法包括无细胞转化检测、蛋白质错误折叠循环扩增(PMCA)和颤抖诱导转化检测(QuIC),其中PMCA是唯一被证明能产生传染性朊病毒的技术。此外,它允许以原始分子的菌株特异性生化和生物学特性无限扩增PrP(TSE),并且在某些条件下可能产生新的自发产生的朊病毒。该方法还可以解决物种屏障现象,并评估动物之间以及动物到人类传播的潜在风险。此外,其前所未有的灵敏度使得在疾病的临床前和临床阶段能够检测到低至一个感染剂量的PrP(TSE),并在不同组织和生物流体(包括血液、脑脊液(CSF)、精液、牛奶、尿液和唾液)中对该蛋白进行生化鉴定。TSEs与其他构象疾病之间的机制相似性导致PMCA被用于各种淀粉样蛋白的扩增和检测。在此,我们对该技术在TSEs和其他神经退行性疾病研究中的不同应用进行了有说服力的讨论。