Protein misfolding cyclic amplification as a rapid test for assessment of prion inactivation

• Published in: Biochemical and biophysical research communications Vol. 348; no. 2; pp. 758 - 762
• Main Authors: Murayama, Yuichi, Yoshioka, Miyako, Horii, Hiroko, Takata, Masuhiro, Yokoyama, Takashi, Sudo, Takashi, Sato, Koichi, Shinagawa, Morikazu, Mohri, Shirou
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 22-09-2006
• Subjects: Animals; Autoclaving; Bioassay; Biochemistry - methods; Cricetinae; Incineration; Mice; Prion inactivation; Protein Folding; Protein misfolding cyclic amplification; PrPSc Proteins - chemistry; PrPSc Proteins - pathogenicity; Protein misfolding cyclic amplification; Prion inactivation; Bioassay; Incineration; Autoclaving
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2006.07.130

Abnormal isoform of prion proteins (PrP
Sc), which are infectious agents associated with prion diseases, retain infectivity after undergoing routine sterilization processes. A sensitive method to detect the infectivity is a bioassay, and it has been used for assessing prion inactivation. However, the result is obtained after several hundred days. Here, protein misfolding cyclic amplification (PMCA) in which PrP
Sc can be amplified
in vitro was applied for assessing prion inactivation by dry heating and autoclaving. Scrapie-infected hamster brains were inactivated under various conditions, and residual infectivity and PrP
Sc were detected by the bioassay and PMCA, respectively. The PMCA results were in good agreement with those of the bioassay. In samples autoclaved at temperatures below 150
°C, while infected mice died in the bioassay, protease-resistant PrP (PrP
res) signals were detected in the second or third round of PMCA. Three rounds of PMCA require only 6 days, which means that the PMCA method is much faster than the bioassay.