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      Oral vaccination as a potential strategy to manage chronic wasting disease in wild cervid populations

      review-article
      1 , 2 , , 3
      Frontiers in Immunology
      Frontiers Media S.A.
      chronic wasting disease, oral vaccine, wildlife, prion, cervid

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          Abstract

          Prion diseases are a novel class of infectious disease based in the misfolding of the cellular prion protein (PrP C) into a pathological, self-propagating isoform (PrP Sc). These fatal, untreatable neurodegenerative disorders affect a variety of species causing scrapie in sheep and goats, bovine spongiform encephalopathy (BSE) in cattle, chronic wasting disease (CWD) in cervids, and Creutzfeldt-Jacob disease (CJD) in humans. Of the animal prion diseases, CWD is currently regarded as the most significant threat due its ongoing geographical spread, environmental persistence, uptake into plants, unpredictable evolution, and emerging evidence of zoonotic potential. The extensive efforts to manage CWD have been largely ineffective, highlighting the need for new disease management tools, including vaccines. Development of an effective CWD vaccine is challenged by the unique biology of these diseases, including the necessity, and associated dangers, of overcoming immune tolerance, as well the logistical challenges of vaccinating wild animals. Despite these obstacles, there has been encouraging progress towards the identification of safe, protective antigens as well as effective strategies of formulation and delivery that would enable oral delivery to wild cervids. In this review we highlight recent strategies for antigen selection and optimization, as well as considerations of various platforms for oral delivery, that will enable researchers to accelerate the rate at which candidate CWD vaccines are developed and evaluated.

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          Most cited references108

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          Nobel Lecture: Prions

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            Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis.

            The mechanisms involved in prion neurotoxicity are unclear, and therapies preventing accumulation of PrPSc, the disease-associated form of prion protein (PrP), do not significantly prolong survival in mice with central nervous system prion infection. We found that depleting endogenous neuronal PrPc in mice with established neuroinvasive prion infection reversed early spongiform change and prevented neuronal loss and progression to clinical disease. This occurred despite the accumulation of extraneuronal PrPSc to levels seen in terminally ill wild-type animals. Thus, the propagation of nonneuronal PrPSc is not pathogenic, but arresting the continued conversion of PrPc to PrPSc within neurons during scrapie infection prevents prion neurotoxicity.
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              A general model of prion strains and their pathogenicity.

              Prions are lethal mammalian pathogens composed of aggregated conformational isomers of a host-encoded glycoprotein and which appear to lack nucleic acids. Their unique biology, allied with the public-health risks posed by prion zoonoses such as bovine spongiform encephalopathy, has focused much attention on the molecular basis of prion propagation and the "species barrier" that controls cross-species transmission. Both are intimately linked to understanding how multiple prion "strains" are encoded by a protein-only agent. The underlying mechanisms are clearly of much wider importance, and analogous protein-based inheritance mechanisms are recognized in yeast and fungi. Recent advances suggest that prions themselves are not directly neurotoxic, but rather their propagation involves production of toxic species, which may be uncoupled from infectivity.
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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                14 April 2023
                2023
                : 14
                : 1156451
                Affiliations
                [1] 1 Vaccine and Infectious Disease Organization, University of Saskatchewan , Saskatoon, SK, Canada
                [2] 2 Department of Biochemistry, Microbiology and Immunology, University of Saskatchewan , Saskatoon, SK, Canada
                [3] 3 Calgary Prion Research Unit, Faculty of Veterinary Medicine, University of Calgary , Calgary, AB, Canada
                Author notes

                Edited by: Brad Pickering, National Centre for Foreign Animal Disease (NCFAD), Canada

                Reviewed by: Julie Moreno, Colorado State University, United States; Kurt Zuelke, Texas A&M University, United States

                *Correspondence: Scott Napper, scott.napper@ 123456usask.ca

                This article was submitted to Vaccines and Molecular Therapeutics, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2023.1156451
                10140515
                af4e2901-aad4-42c3-a073-13a89ed5ede0
                Copyright © 2023 Napper and Schatzl

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 01 February 2023
                : 31 March 2023
                Page count
                Figures: 2, Tables: 0, Equations: 0, References: 109, Pages: 11, Words: 6386
                Funding
                Funded by: Alberta Conservation Association , doi 10.13039/100007583;
                Funded by: Ministry of Agriculture - Saskatchewan , doi 10.13039/100008921;
                Funded by: Alberta Environment and Parks , doi 10.13039/100012165;
                This work was supported by funding of the Alberta Conservation Association, Saskatchewan Fish and Wildlife Development Fund, and Alberta Environment and Parks. VIDO receives operational funding from the Government of Saskatchewan through Innovation Saskatchewan and the Ministry of Agriculture and from the Canada Foundation for Innovation through the Major Science Initiatives for its CL3 facility.
                Categories
                Immunology
                Review

                Immunology
                chronic wasting disease,oral vaccine,wildlife,prion,cervid
                Immunology
                chronic wasting disease, oral vaccine, wildlife, prion, cervid

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