RT Journal Article SR Electronic(1) A1 Franz, Martin A1 Eiden, Martin A1 Balkema-Buschmann, Anne A1 Greenlee, Justin A1 Schatzl, Hermann A1 Fast, Christine A1 Richt, Jürgen A1 Hildebrandt, Jan-Peter A1 Groschup, Martin H.YR 2012 T1 Detection of PrPSc in peripheral tissues of clinically affected cattle after oral challenge with bovine spongiform encephalopathy JF Journal of General Virology, VO 93 IS 12 SP 2740 OP 2748 DO https://doi.org/10.1099/vir.0.044578-0 PB Microbiology Society, SN 1465-2099, AB Bovine spongiform encephalopathy (BSE) is a fatal neurodegenerative prion disease that mainly affects cattle. Transmission of BSE to humans caused a variant form of Creutzfeldt–Jakob disease. Following infection, the protease-resistant, disease-associated isoform of prion protein (PrPSc) accumulates in the central nervous system and in other tissues. Many countries have defined bovine tissues that may contain prions as specified risk materials, which must not enter the human or animal food chains and therefore must be discarded. Ultrasensitive techniques such as protein misfolding cyclic amplification (PMCA) have been developed to detect PrPSc when present in minuscule amounts that are not readily detected by other diagnostic methods such as immunohistochemistry or Western blotting. This study was conducted to determine when and where PrPSc can be found by PMCA in cattle orally challenged with BSE. A total of 48 different tissue samples from four cattle infected orally with BSE at various clinical stages of disease were examined using a standardized PMCA protocol. The protocol used brain homogenate from bovine PrP transgenic mice (Tgbov XV) as substrate and three consecutive rounds of PMCA. Using this protocol, PrPSc was found in the brain, spinal cord, nerve ganglia, optic nerve and Peyer’s patches. The presence of PrPSc was confirmed in adrenal glands, as well as in mesenteric lymph nodes – a finding that was reported recently by another group. Interestingly, additional positive results were obtained for the first time in the oesophagus, abomasum, rumen and rectum of clinically affected cattle., UL https://www.microbiologyresearch.org/content/journal/jgv/10.1099/vir.0.044578-0