%0 Journal Article %A Murayama, Yuichi %A Masujin, Kentaro %A Imamura, Morikazu %A Ono, Fumiko %A Shibata, Hiroaki %A Tobiume, Minoru %A Yamamura, Tomoaki %A Shimozaki, Noriko %A Terao, Keiji %A Yamakawa, Yoshio %A Sata, Tetsutaro %T Ultrasensitive detection of PrPSc in the cerebrospinal fluid and blood of macaques infected with bovine spongiform encephalopathy prion %D 2014 %J Journal of General Virology, %V 95 %N 11 %P 2576-2588 %@ 1465-2099 %R https://doi.org/10.1099/vir.0.066225-0 %I Microbiology Society, %X Prion diseases are characterized by the prominent accumulation of the misfolded form of a normal cellular protein (PrPSc) in the central nervous system. The pathological features and biochemical properties of PrPSc in macaque monkeys infected with the bovine spongiform encephalopathy (BSE) prion have been found to be similar to those of human subjects with variant Creutzfeldt–Jakob disease (vCJD). Non-human primate models are thus ideally suited for performing valid diagnostic tests and determining the efficacy of potential therapeutic agents. In the current study, we developed a highly efficient method for in vitro amplification of cynomolgus macaque BSE PrPSc. This method involves amplifying PrPSc by protein misfolding cyclic amplification (PMCA) using mouse brain homogenate as a PrPC substrate in the presence of sulfated dextran compounds. This method is capable of amplifying very small amounts of PrPSc contained in the cerebrospinal fluid (CSF) and white blood cells (WBCs), as well as in the peripheral tissues of macaques that have been intracerebrally inoculated with the BSE prion. After clinical signs of the disease appeared in three macaques, we detected PrPSc in the CSF by serial PMCA, and the CSF levels of PrPSc tended to increase with disease progression. In addition, PrPSc was detectable in WBCs at the clinical phases of the disease in two of the three macaques. Thus, our highly sensitive, novel method may be useful for furthering the understanding of the tissue distribution of PrPSc in non-human primate models of CJD. %U https://www.microbiologyresearch.org/content/journal/jgv/10.1099/vir.0.066225-0