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Fast and ultrasensitive method for quantitating prion infectivity titer

机译:快速超灵敏定量病毒感染性滴度的方法

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摘要

Bioassay by end-point dilution has been employed for decades for routine determination of prion infectivity titer. Here we show that the new Protein Misfolding Cyclic Amplification with Teflon beads (PMCAb) can be used to estimate titers of the misfolded version of the prion protein (PrPSc) with a higher level of precision and in 3 to 6 days as opposed to two years, when compared with bioassay. For two hamster strains 263K and SSLOW, median infective doses (ID50) determined by PCMAb (PMCAb50) were found to be 1012.8 and 1012.2 per gram of brain tissue, which are 160- and 4,000-fold higher than the corresponding ID50 values measured by bioassay. These 102-103-fold differences could be attributed to a large excess of PMCAb-reactive prion protein seeds with little or no infectivity. Alternatively, the differences between ID50 and PMCAb50 could be due to higher rate of clearance of PrPSc seeds in animals versus PMCAb reactions. A well calibrated PMCAb reaction can be an efficient and cost effective method for the estimation of PrPSc titer.
机译:通过终点稀释的生物测定已被用于常规测定determination病毒感染性滴度。在这里,我们证明了使用特氟隆珠子(PMCAb)进行的新的蛋白质错误折叠循环扩增可用于估算the蛋白的错误折叠形式(PrP Sc )的滴定度,其准确度更高,并且在3中与生物测定法相比,从2年减少到6天,而不是2天。对于两种仓鼠菌株263K和SSLOW,发现每克脑组织的PCMAb(PMCAb50)测定的中位感染剂量(ID50)为10 12.8 和10 12.2 。比通过生物测定法测得的相应ID50值分别高160倍和4,000倍。这些10 2 -10 3 倍的差异可能归因于PMCAb反应性病毒蛋白种子大量过量,几乎没有或没有传染性。另外,ID50和PMCAb50之间的差异可能是由于动物中PrP Sc 种子的清除率高于PMCAb反应。校准良好的PMCAb反应可能是估算PrP Sc 效价的有效方法。

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