BMC Vet Res. 2010 Aug 4;6:41. doi: 10.1186/1746-6148-6-41.
In a recent paper written by Hilbe et al (BMC vet res, 2009), the nature and specificity of the prion protein deposition in the kidney of feline species affected with feline spongiform encephalopathy (FSE) were clearly considered doubtful. This article was brought to our attention because we published several years ago an immunodetection of abnormal prion protein in the kidney of a cheetah affected with FSE. At this time we were convinced of its specificity but without having all the possibilities to demonstrate it. As previously published by another group, the presence of abnormal prion protein in some renal glomeruli in domestic cats affected with FSE is indeed generally considered as doubtful mainly because of low intensity detected in this organ and because control kidneys from safe animals present also a weak prion immunolabelling. Here we come back on these studies and thought it would be helpful to relay our last data to the readers of BMC Vet res for future reference on this subject.Here we come back on our material as it is possible to study and demonstrate the specificity of prion immunodetection using the PET-Blot method (Paraffin Embedded Tissue--Blot). It is admitted that this method allows detecting the Proteinase K (PK) resistant form of the abnormal prion protein (PrPres) without any confusion with unspecific immunoreaction. We re-analysed the kidney tissue versus adrenal gland and brain samples from the same cheetah affected with TSE using this PET-Blot method. The PET-Blot analysis revealed specific PrPres detection within the brain, adrenal gland and some glomeruli of the kidney, with a complete identicalness compared to our previous detection using immunohistochemistry. In conclusion, these new data enable us to confirm with assurance the presence of specific abnormal prion protein in the adrenal gland and in the kidney of the cheetah affected with FSE. It also emphasizes the usefulness for the re-examination of any available tissue blocks with the PET-Blot method as a sensitive complementary tool in case of doubtful PrP IHC results.
在 Hilbe 等人最近发表的一篇论文中(BMC Vet Res,2009),猫传染性海绵状脑病(FSE)患猫肾脏中朊病毒蛋白沉积的性质和特异性被明确认为值得怀疑。这篇文章引起了我们的注意,因为我们几年前曾发表过一篇关于感染 FSE 的猎豹肾脏中异常朊病毒蛋白的免疫检测文章。当时,我们确信其具有特异性,但没有所有的可能性来证明这一点。正如另一组之前发表的那样,FSE 患家猫的一些肾小球中存在异常朊病毒蛋白通常被认为是可疑的,主要是因为在该器官中检测到的强度较低,而且来自安全动物的对照肾脏也存在微弱的朊病毒免疫标记。在这里,我们回顾了这些研究,并认为向 BMC Vet Res 的读者传达我们的最新数据将有助于将来参考这个主题。在这里,我们回顾了我们的材料,因为使用 PET-Blot 方法(Paraffin Embedded Tissue-Blot)研究和证明朊病毒免疫检测的特异性是可能的。人们承认,该方法允许在不与非特异性免疫反应混淆的情况下检测蛋白酶 K(PK)抗性形式的异常朊病毒蛋白(PrPres)。我们使用这种 PET-Blot 方法重新分析了同一只患有 TSE 的猎豹的肾脏组织与肾上腺和大脑样本。PET-Blot 分析显示,在大脑、肾上腺和肾脏的一些肾小球中特异性地检测到 PrPres,与我们之前使用免疫组织化学检测到的结果完全一致。总之,这些新数据使我们能够有把握地确认 FSE 患猎豹的肾上腺和肾脏中存在特异性异常朊病毒蛋白。它还强调了在怀疑 PrP IHC 结果的情况下,使用 PET-Blot 方法作为一种敏感的补充工具,重新检查任何可用的组织块的有用性。