Evidence map›Paper›PMID 40230197›Full record

ArticleThe Journal of infectious diseases2025

Strain-Dependent Susceptibility to Prion Infection Encoded by Arg171 and Lys176 Sheep Prion Protein Polymorphic Variants.

Juan Carlos Espinosa, Natalia Fernández-Borges, Alba Marín-Moreno, Sara Canoyra, Patricia Aguilar-Calvo, Belén Pintado, Eva Pericuesta, Sylvie L Benestad, Romolo Nonno, Olivier Andréoletti and 1 more

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Article in The Journal of infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Juan Carlos EspinosaBiología Molecular y Celular de Priones, Centro de Investigación en Sanidad Animal, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria-Consejo Superior de Investigaciones Científicas, Madrid, Spain.ORCID 0000-0002-6719-9902
Natalia Fernández-BorgesBiología Molecular y Celular de Priones, Centro de Investigación en Sanidad Animal, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria-Consejo Superior de Investigaciones Científicas, Madrid, Spain.ORCID 0000-0001-6274-0096
Alba Marín-MorenoBiología Molecular y Celular de Priones, Centro de Investigación en Sanidad Animal, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria-Consejo Superior de Investigaciones Científicas, Madrid, Spain.
Sara CanoyraBiología Molecular y Celular de Priones, Centro de Investigación en Sanidad Animal, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria-Consejo Superior de Investigaciones Científicas, Madrid, Spain.ORCID 0000-0001-6371-8122
Patricia Aguilar-CalvoBiología Molecular y Celular de Priones, Centro de Investigación en Sanidad Animal, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria-Consejo Superior de Investigaciones Científicas, Madrid, Spain.ORCID 0000-0003-0166-9382
Belén PintadoTransgenesis Facility, Centro Nacional de Biotecnología-Universidad Autónoma de Madrid, Madrid, Spain.ORCID 0000-0002-8485-2520
Eva PericuestaDepartamento de Reproducción Animal, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria-Consejo Superior de Investigaciones Científicas, Madrid, Spain.
Sylvie L BenestadDepartment of Biohazard and Pathology, Norwegian Veterinary Institute, Ås, Norway.
Romolo NonnoDepartment of Food Safety, Nutrition and Veterinary Public Health, Istituto Superiore di Sanità, Rome, Italy.ORCID 0000-0001-7556-1564
Olivier AndréolettiUnité Mixte de Recherche, Institut National de la Recherche Agronomique-École Nationale Vétérinaire de Toulouse 1225, Interactions Hôtes Agents Pathogènes, Toulouse, France.
Juan María TorresBiología Molecular y Celular de Priones, Centro de Investigación en Sanidad Animal, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria-Consejo Superior de Investigaciones Científicas, Madrid, Spain.ORCID 0000-0003-0443-9232

Funding

Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria fellowship FPI-SGIT-2015-02Spanish Ministerio de Ciencia e Innovación, Ministerio de Economía y Competitividad AGL2009-11553-C02-02Spanish Ministerio de Ciencia e Innovación, Ministerio de Economía y Competitividad AGL2016-78054-RSpanish Ministerio de Ciencia e Innovación, Ministerio de Economía y Competitividad BES-2010-040922
6 · The paper itself

Abstract

backgroundClassical scrapie in sheep is caused by several different strains rather than a single strain, as is the case for epidemic classical bovine spongiform encephalopathy (BSE). Polymorphisms R171 and K176 located in the β2-α2 loop region of sheep prion protein (PrP) have been associated with potential protection for the propagation of classical scrapie.

methodsThe protective role of R171 and K176 polymorphic variants in susceptibility and resistance to different prion strains circulating in Europe was investigated using transgenic mouse lines expressing R171 or K176 sheep PrP in comparable levels (R171-Tg552 and K176-Tg570, respectively). Both lines were intracranially challenged with a panel of isolates representative of diverse prion strains, including at least 4 different classical scrapie strains. These isolates were previously characterized by transmission studies in ovine (Wt-OvPrP-Tg501) and bovine (BoPrP-Tg110) transgenic mice.

resultsR171-Tg552 and K176-Tg570 mouse lines succumbed after the inoculation of atypical scrapie isolates with 100% attack rates and long survival times. However, the propagation of all tested classical scrapie isolated was completely blocked in R171-Tg552 mice, whereas in K176-Tg570 mice the propagation of most of the classical scrapie isolates was highly restricted or completely blocked depending on the prion strain. BSE transmission to R171-Tg552 mice was only possible after its adaptation to sheep PrP while no infection could be detected in K176-Tg570 mice, even after passage in sheep.

conclusionsThese results indicate that the R171 and K176 polymorphic variants of the ovine PrP sequence restrict the propagation of prions in a strain-dependent manner and are useful tools for prion strain discrimination.

Indexed as

Polymorphism, GeneticPrion ProteinsPrionsScrapieAnimalsCattleDisease SusceptibilityGenetic Predisposition to DiseaseMiceMice, TransgenicSheepPrion ProteinsPrionsbovine spongiform encephalopathyprion strainPrP polymorphic variantsscrapietransmission barrier

Identifiers

PMID40230197
PMCPMC12308685

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.