Classical BSE prions emerge from asymptomatic pigs challenged with atypical/Nor98 scrapie

• Published in: Scientific reports Vol. 11; no. 1; pp. 17428 - 8
• Main Authors: Marín, Belén, Otero, Alicia, Lugan, Séverine, Espinosa, Juan Carlos, Marín-Moreno, Alba, Vidal, Enric, Hedman, Carlos, Romero, Antonio, Pumarola, Martí, Badiola, Juan J., Torres, Juan María, Andréoletti, Olivier, Bolea, Rosa
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 31-08-2021; Nature Publishing Group; Nature Portfolio
• Subjects: 631/378/1689; 692/699/255; Animals; Bioassays; Bovine spongiform encephalopathy; Brain - metabolism; Brain - pathology; Cattle; Chronic wasting disease; Disease Susceptibility; Disease transmission; Encephalopathy, Bovine Spongiform - metabolism; Encephalopathy, Bovine Spongiform - pathology; Encephalopathy, Bovine Spongiform - transmission; Enzyme immunoassay; Female; Humanities and Social Sciences; Immunohistochemistry; Inoculation; Life Sciences; Male; Mice; multidisciplinary; Prion protein; Prions - physiology; Protein folding; PrPSc Proteins - metabolism; Science; Science (multidisciplinary); Scrapie; Scrapie - metabolism; Scrapie - pathology; Scrapie - transmission; Swine; Swine, Miniature; Transmissible spongiform encephalopathy; Western blotting
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-021-96818-2

Pigs are susceptible to infection with the classical bovine spongiform encephalopathy (C-BSE) agent following experimental inoculation, and PrP
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 accumulation was detected in porcine tissues after the inoculation of certain scrapie and chronic wasting disease isolates. However, a robust transmission barrier has been described in this species and, although they were exposed to C-BSE agent in many European countries, no cases of natural transmissible spongiform encephalopathies (TSE) infections have been reported in pigs. Transmission of atypical scrapie to bovinized mice resulted in the emergence of C-BSE prions. Here, we conducted a study to determine if pigs are susceptible to atypical scrapie. To this end, 12, 8–9-month-old minipigs were intracerebrally inoculated with two atypical scrapie sources. Animals were euthanized between 22- and 72-months post inoculation without clinical signs of TSE. All pigs tested negative for PrP
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 accumulation by enzyme immunoassay, immunohistochemistry, western blotting and bioassay in porcine PrP mice. Surprisingly, in vitro protein misfolding cyclic amplification demonstrated the presence of C-BSE prions in different brain areas from seven pigs inoculated with both atypical scrapie isolates. Our results suggest that pigs exposed to atypical scrapie prions could become a reservoir for C-BSE and corroborate that C-BSE prions emerge during interspecies passage of atypical scrapie.