Emerging infectious diseases · 2013 · 25 citations · 29 references
Incubation PeriodCreutzfeldt-jakob DiseasePathologyPrion DiseaseIncubation PeriodsNeuropathologyHealth SciencesVeterinary EpidemiologyNeurological AssessmentFood SafetyMedical DiagnosticsFoodborne TransmissionRodent-borne DiseasesAnimal ScienceZoonotic DiseasePathogenesisVeterinary ScienceIncubation TimesAnimal Disease PreventionMedicine
Risk for human exposure to bovine spongiform encephalopathy (BSE)-inducing agent was estimated in a nonhuman primate model. To determine attack rates, incubation times, and molecular signatures, we orally exposed 18 macaques to 1 high dose of brain material from cattle with BSE. Several macaques were euthanized at regular intervals starting at 1 year postinoculation, and others were observed until clinical signs developed. Among those who received ≥5 g BSE-inducing agent, attack rates were 100% and prions could be detected in peripheral tissues from 1 year postinoculation onward. The overall median incubation time was 4.6 years (3.7-5.3). However, for 3 macaques orally exposed on multiple occasions, incubation periods were at least 7-10 years. Before clinical signs were noted, we detected a non-type 2B signature, indicating the existence of atypical prion protein during the incubation period. This finding could affect diagnosis of variant Creutzfeldt-Jakob disease in humans and might be relevant for retrospective studies of positive tonsillectomy or appendectomy specimens because time of infection is unknown.
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A new variant of Creutzfeldt-Jakob disease in the UK
Robert Will, James W. Ironside, Martin Zeidler et al. · The Lancet · 1996 · 2.7K citations
Creutzfeldt-jakob Disease, Neurological Disorder, New Variant +6
Transmissions to mice indicate that ‘new variant’ CJD is caused by the BSE agent
M. E. Bruce, Robert Will, James W. Ironside et al. · Nature · 1997 · 2K citations
Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD
John Collinge, Katie Sidle, Julie Meads et al. · Nature · 1996 · 1.7K citations
Creutzfeldt-jakob Disease, Prion Strain Variation, Genetics +7