Literature DB >> 18754377

Persistence of pathogenic prion protein during simulated wastewater treatment processes.

Glen T Hinckley1, Christopher J Johnson, Kurt H Jacobson, Christian Bartholomay, Katherine D McMahon, Debbie McKenzie, Judd M Aiken, Joel A Pedersen.   

Abstract

Transmissible spongiform encephalopathies (TSEs, prion diseases) are a class of fatal neurodegenerative diseases affecting a variety of mammalian species including humans. A misfolded form of the prion protein (PrP(TSE)) is the major, if not sole, component of the infectious agent. Prions are highly resistant to degradation and to many disinfection procedures suggesting that, if prions enter wastewater treatment systems through sewers and/or septic systems (e.g., from slaughterhouses, necropsy laboratories, rural meat processors, private game dressing) or through leachate from landfills that have received TSE-contaminated material, prions could survive conventional wastewater treatment. Here, we report the results of experiments examining the partitioning and persistence of PrPTSE during simulated wastewater treatment processes including activated and mesophilic anaerobic sludge digestion. Incubation with activated sludge did not result in significant PrPTSE degradation. PrPTSE and prion infectivity partitioned strongly to activated sludge solids and are expected to enter biosolids treatment processes. A large fraction of PrPTSE survived simulated mesophilic anaerobic sludge digestion. The small reduction in recoverable PrPTSE after 20-d anaerobic sludge digestion appeared attributable to a combination of declining extractability with time and microbial degradation. Our results suggest that if prions were to enter municipal wastewater treatment systems, most would partition to activated sludge solids, survive mesophilic anaerobic digestion, and be present in treated biosolids.

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Year:  2008        PMID: 18754377      PMCID: PMC3087203          DOI: 10.1021/es703186e

Source DB:  PubMed          Journal:  Environ Sci Technol        ISSN: 0013-936X            Impact factor:   9.028


  38 in total

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  13 in total

1.  Inactivation of template-directed misfolding of infectious prion protein by ozone.

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Authors:  Qi Yuan; Glenn Telling; Shannon L Bartelt-Hunt; Jason C Bartz
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Authors:  Christopher J Johnson; P U P A Gilbert; Debbie McKenzie; Joel A Pedersen; Judd M Aiken
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