Quantitative Detection and Biological Propagation of Scrapie Seeding Activity In Vitro Facilitate Use of Prions as Model Pathogens for Disinfection
Authors:
Open Access
- 27 May 2011
- journal article
- research article
- Published by Public Library of Science (PLoS) in PLOS ONE
- Vol. 6 (5) , e20384
Abstract
Prions are pathogens with an unusually high tolerance to inactivation and constitute a complex challenge to the re-processing of surgical instruments. On the other hand, however, they provide an informative paradigm which has been exploited successfully for the development of novel broad-range disinfectants simultaneously active also against bacteria, viruses and fungi. Here we report on the development of a methodological platform that further facilitates the use of scrapie prions as model pathogens for disinfection. We used specifically adapted serial protein misfolding cyclic amplification (PMCA) for the quantitative detection, on steel wires providing model carriers for decontamination, of 263K scrapie seeding activity converting normal protease-sensitive into abnormal protease-resistant prion protein. Reference steel wires carrying defined amounts of scrapie infectivity were used for assay calibration, while scrapie-contaminated test steel wires were subjected to fifteen different procedures for disinfection that yielded scrapie titre reductions of ≤101- to ≥105.5-fold. As confirmed by titration in hamsters the residual scrapie infectivity on test wires could be reliably deduced for all examined disinfection procedures, from our quantitative seeding activity assay. Furthermore, we found that scrapie seeding activity present in 263K hamster brain homogenate or multiplied by PMCA of scrapie-contaminated steel wires both triggered accumulation of protease-resistant prion protein and was further propagated in a novel cell assay for 263K scrapie prions, i.e., cerebral glial cell cultures from hamsters. The findings from our PMCA- and glial cell culture assays revealed scrapie seeding activity as a biochemically and biologically replicative principle in vitro, with the former being quantitatively linked to prion infectivity detected on steel wires in vivo. When combined, our in vitro assays provide an alternative to titrations of biological scrapie infectivity in animals that substantially facilitates the use of prions as potentially highly indicative test agents in the search for novel broad-range disinfectants.Keywords
This publication has 46 references indexed in Scilit:
- Highly Efficient Protein Misfolding Cyclic AmplificationPLOS Pathogens, 2011
- Rapid End-Point Quantitation of Prion Seeding Activity with Sensitivity Comparable to BioassaysPLOS Pathogens, 2010
- Generating a Prion with Bacterially Expressed Recombinant Prion ProteinScience, 2010
- Highly sensitive, quantitative cell-based assay for prions adsorbed to solid surfacesProceedings of the National Academy of Sciences, 2009
- Resistance of Bovine Spongiform Encephalopathy (BSE) Prions to InactivationPLOS Pathogens, 2008
- Scrapie Agent (Strain 263K) Can Transmit Disease via the Oral Route after Persistence in Soil over YearsPLOS ONE, 2007
- Cell-free formation of misfolded prion protein with authentic prion infectivityProceedings of the National Academy of Sciences, 2006
- Novel methods for disinfection of prion-contaminated medical devicesThe Lancet, 2004
- Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cells.Journal of Cell Biology, 1990
- Novel Proteinaceous Infectious Particles Cause ScrapieScience, 1982