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Research Paper

Exploration of genetic factors resulting in abnormal disease in cattle experimentally challenged with bovine spongiform encephalopathy

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Pages 1-11 | Received 29 Oct 2020, Accepted 22 Dec 2020, Published online: 04 Jan 2021

References

  • Wells GA, Scott A, Johnson C, et al. A novel progressive spongiform encephalopathy in cattle. Vet Rec. 1987;121(18):419–420.
  • Will RG, Ironside JW, Zeidler M, et al. A new variant of Creutzfeldt-Jakob disease in the UK. Lancet. 1996;347(9006):921–925.
  • Gray JG, Dudas S, Czub S. A study on the analytical sensitivity of 6 BSE tests used by the canadian BSE reference laboratory. Plos One. 2011;6(3):e17633.
  • Serra F, Dudas S, Torres JM, et al. Presumptive BSE cases with an aberrant prion protein phenotype in Switzerland, 2011: lack of prion disease in experimentally inoculated cattle and bovine prion protein transgenic mice. Transbound Emerg Dis. 2018;65(5):1348–1356.
  • Kaatz M, Fast C, Ziegler U, et al. Spread of classic BSE prions from the gut via the peripheral nervous system to the brain. Am J Pathol. 2012;181(2):515–524.
  • Buschmann A, Gretzschel A, Biacabe A-G, et al. Atypical BSE in Germany—proof of transmissibility and biochemical characterization. Vet Microbiol. 2006;117(2–4):103–116.
  • Franz M, Eiden M, Balkema-Buschmann A, et al. Detection of PrP(Sc) in peripheral tissues of clinically affected cattle after oral challenge with bovine spongiform encephalopathy. J Gen Virol. 2012;93(Pt 12):2740–2748.
  • Sigurdson CJ, Nilsson KPR, Hornemann S, et al. De novo generation of a transmissible spongiform encephalopathy by mouse transgenesis. Proc Natl Acad Sci U S A. 2009;106(1):304–309.
  • Browning SR, Mason GL, Seward T, et al. Transmission of prions from mule deer and elk with chronic wasting disease to transgenic mice expressing cervid PrP. J Virol. 2004;78(23):13345.
  • Cordier C, Bencsik A, Philippe S, et al. Transmission and characterization of bovine spongiform encephalopathy sources in two ovine transgenic mouse lines (TgOvPrP4 and TgOvPrP59). J Gen Virol. 2006;87(12):3763–3771.
  • Crozet C, Flamant F, Bencsik A, et al. Efficient transmission of two different sheep scrapie isolates in transgenic mice expressing the ovine PrP gene. J Virol. 2001;75(11):5328.
  • Lacroux C, Comoy E, Moudjou M, et al. Preclinical detection of variant CJD and BSE prions in blood. PLoS Pathog. 2014;10(6):e1004202. e1004202-e1004202
  • Ackermann I, Balkema-Buschmann A, Ulrich R, et al. Detection of PrP(BSE) and prion infectivity in the ileal peyer’s patch of young calves as early as 2 months after oral challenge with classical bovine spongiform encephalopathy. Vet Res. 2017;48(1):88.
  • Huor A, Espinosa JC, Vidal E, et al. The emergence of classical BSE from atypical/Nor98 scrapie. Proc Natl Acad Sci U S A. 2019;116(52):26853–26862.
  • Gambetti P, Dong Z, Yuan J, et al. A novel human disease with abnormal prion protein sensitive to protease. Ann Neurol. 2008;63(6):697–708.
  • Manson JC, Jamieson E, Baybutt H, et al. A single amino acid alteration (101L) introduced into murine PrP dramatically alters incubation time of transmissible spongiform encephalopathy. Embo J. 1999;18(23):6855–6864.
  • Zou W-Q, Puoti G, Xiao X, et al. Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein. Ann Neurol. 2010;68(2):162–172.
  • Aguilar-Calvo P, Fast C, Tauscher K, et al. Effect of Q211 and K222 PRNP polymorphic variants in the susceptibility of goats to oral infection with goat bovine spongiform encephalopathy. J Infect Dis. 2015;212(4):664–672.
  • Brunelle BW, Greenlee JJ, Seabury CM, et al. Frequencies of polymorphisms associated with BSE resistance differ significantly between Bos taurus, Bos indicus, and composite cattle. BMC Vet Res. 2008;4(1):36.
  • Sander P, Hamann H, Drögemüller C, et al. Bovine prion protein gene (PRNP) promoter polymorphisms modulate PRNP expression and may be Responsible for differences in bovine spongiform encephalopathy susceptibility. J Biol Chem. 2005;280(45):37408–37414.
  • Sander P, Hamann H, Pfeiffer I, et al. Analysis of sequence variability of the bovine prion protein gene (PRNP) in German cattle breeds. Neurogenetics. 2004;5(1):19–25.
  • Murdoch BM, Clawson ML, Yue S, et al. PRNP haplotype associated with classical BSE incidence in European Holstein cattle. PLoS One. 2010;5(9):e12786
  • Haase B, Doherr MG, Seuberlich T, et al. PRNP promoter polymorphisms are associated with BSE susceptibility in Swiss and German cattle. BMC Genet. 2007;8(1):15.
  • Ovelhey A, Beyerbach M, Schael J, et al. Risk factors for BSE-infections in Lower Saxony, Germany. Prev Vet Med. 2008;83(2):196–209.
  • Prusiner SB. Novel proteinaceous infectious particles cause scrapie. Science. 1982;216(4542):136–144.
  • Akanno EC, Chen L, Abo-Ismail MK, et al. Genomic prediction of breed composition and heterosis effects in Angus, Charolais, and Hereford crosses using 50K genotypes. Can J Anim Sci. 2017;97(3):431–438.
  • Buschmann A, Groschup MH. Highly bovine spongiform encephalopathy-sensitive transgenic mice confirm the essential restriction of infectivity to the nervous system in clinically diseased cattle. J Infect Dis. 2005;192(5):934–942.