28
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Novel Strain of the Chronic Wasting Disease Agent Isolated From Experimentally Inoculated Elk With LL132 Prion Protein

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Chronic wasting disease (CWD) is a fatal, progressive disease that affects cervid species, including Rocky mountain elk ( Cervus elaphus nelsoni). There are 2 allelic variants in the elk prion protein gene: L132 (leucine) and M132 (methionine). Following experimental oral challenge with the CWD agent incubation periods are longest in LL132 elk, intermediate in ML132 elk, and shortest in MM132 elk. In order to ascertain whether such CWD-infected elk carry distinct prion strains, groups of Tg12 mice that express M132 elk prion protein were inoculated intracranially with brain homogenate from individual CWD-infected elk of various genotypes (LL132, LM132, or MM132). Brain samples were examined for microscopic changes and assessment of the biochemical properties of disease-associated prion protein (PrP Sc). On first passage, mice challenged with LL132 elk inoculum had prolonged incubation periods and greater PrP Sc fibril stability compared to mice challenged with MM132 or LM132 inoculum. On second passage, relative incubation periods, western blot profiles, and neuropathology were maintained. These results suggest that the CWD prion isolated from LL132 elk is a novel CWD strain and that M132 PrP C is able to propagate some biophysical properties of the L132 PrP Sc conformation.

          Related collections

          Most cited references29

          • Record: found
          • Abstract: found
          • Article: not found

          A test for Creutzfeldt-Jakob disease using nasal brushings.

          Definite diagnosis of sporadic Creutzfeldt-Jakob disease in living patients remains a challenge. A test that detects the specific marker for Creutzfeldt-Jakob disease, the prion protein (PrP(CJD)), by means of real-time quaking-induced conversion (RT-QuIC) testing of cerebrospinal fluid has a sensitivity of 80 to 90% for the diagnosis of sporadic Creutzfeldt-Jakob disease. We have assessed the accuracy of RT-QuIC analysis of nasal brushings from olfactory epithelium in diagnosing sporadic Creutzfeldt-Jakob disease in living patients.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication.

            Transgenic (Tg) mice expressing both Syrian hamster (Ha) and mouse (Mo) prion protein (PrP) genes were used to probe the mechanism of scrapie prion replication. Four Tg lines expressing HaPrP exhibited distinct incubation times ranging from 48 to 277 days, which correlated inversely with HaPrP mRNA and HaPrPC. Bioassays of Tg brain extracts showed that the prion inoculum dictates which prions are synthesized de novo. Tg mice inoculated with Ha prions had approximately 10(9) ID50 units of Ha prions per gram of brain and less than 10 units of Mo prions. Conversely, Tg mice inoculated with Mo prions synthesized Mo prions but not Ha prions. Similarly, Tg mice inoculated with Ha prions exhibited neuropathologic changes characteristic of hamsters with scrapie, while Mo prions produced changes similar to those in non-Tg mice. Our results argue that species specificity of scrapie prions resides in the PrP sequence and prion synthesis is initiated by a species-specific interaction between PrPSc in the inoculum and homologous PrPC.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy.

              The molecular basis of strain variation in scrapie diseases is unknown. The only identified component of the agent is the posttranslationally modified host prion protein (PrPSc). The biochemical and physical properties of PrP from two strains of transmissible mink encephalopathy (TME), called hyper (HY) and drowsy (DY), were compared to investigate if PrP heterogeneity could account for strain diversity. The degradation rate of PrPTME digested with proteinase K was found to be strain specific and correlated with inactivation of the TME titer. Edman protein sequencing revealed that the major N-terminal end of HY PrPTME commenced at least 10 amino acid residues prior to that of DY PrPTME after digestion with proteinase K. Analysis of the brain distribution of PrPTME exhibited a strain-specific pattern and localization of PrPTME to the perikarya of specific neuron populations. Our findings are consistent with HY and DY PrPTME having distinct protein conformations and/or strain-specific ligand interactions that influence PrPTME properties. We propose that PrPTME conformation could play a role in targeting TME strains to different neuron populations in which strain-specific formation occurs. These data are consistent with the idea that PrPTME protein structure determines the molecular basis of strain variation.
                Bookmark

                Author and article information

                Contributors
                justin.greenlee@usda.gov
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                21 February 2020
                21 February 2020
                2020
                : 10
                : 3148
                Affiliations
                [1 ]ISNI 0000 0004 0404 0958, GRID grid.463419.d, USDA, Agricultural Research Service, National Animal Disease Center, Virus and Prion Research Unit, ; Ames, 50010 USA
                [2 ]ISNI 0000 0004 1936 7312, GRID grid.34421.30, Iowa State University, Department of Biomedical Sciences, ; Ames, 50010 USA
                [3 ]ISNI 0000 0001 2164 3847, GRID grid.67105.35, Case Western Reserve University, Departments of Pathology and Neurology, ; Cleveland, 44106 USA
                Author information
                http://orcid.org/0000-0002-6622-0044
                http://orcid.org/0000-0003-0298-5264
                http://orcid.org/0000-0003-2202-3054
                Article
                59819
                10.1038/s41598-020-59819-1
                7035384
                32081886
                99a65226-7d64-4eae-9c8f-4659dcb3ead8
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 11 November 2018
                : 4 February 2020
                Categories
                Article
                Custom metadata
                © The Author(s) 2020

                Uncategorized
                neurodegeneration,prion diseases
                Uncategorized
                neurodegeneration, prion diseases

                Comments

                Comment on this article