Transmission of CJD from nasal brushings but not spinal fluid or RT‐QuIC product. Issue 6 (15th June 2020)

• Record Type: Journal Article
• Authors: Raymond, Gregory J.; Race, Brent; Orrú, Christina D.; Raymond, Lynne D.; Bongianni, Matilde; Fiorini, Michele; Groveman, Bradley R.; Ferrari, Sergio; Sacchetto, Luca; Hughson, Andrew G.; Monaco, Salvatore; Pocchiari, Maurizio; Zanusso, Gianluigi; Caughey, Byron
• Is Part Of: Annals of clinical and translational neurology. Volume 7:Issue 6(2020)
• Page Start: 932
• Page End: 944
• Publication Date: 2020-06-15
• Subjects: Nervous system -- Diseases -- Periodicals; Neurology -- Periodicals; 616.8005
• DOI: 10.1002/acn3.51057
• Languages: English
• ISSNs: 2328-9503

Abstract

Abstract: Objective: The detection of prion seeding activity in CSF and olfactory mucosal brushings using real‐time quaking‐induced conversion assays allows highly accurate clinical diagnosis of sporadic Creutzfeldt–Jakob disease. To gauge transmission risks associated with these biospecimens and their testing, we have bioassayed prion infectivity levels in patients' brain tissue, nasal brushings, and CSF, and assessed the pathogenicity of amplified products of real‐time quaking‐induced conversion assays seeded with Creutzfeldt–Jakob disease prions. Methods: We obtained olfactory mucosal brushings and CSF from patients with a final diagnosis of sporadic Creutzfeldt–Jakob disease subtype MM1 (n = 3). Samples were inoculated intracerebrally into Tg66 transgenic mice that overexpress the homologous human 129M prion protein. The mice were evaluated for clinical, neuropathological, and biochemical evidence of prion infection. Results: Patients' brain tissue at 10 2 to 10 5 fold dilutions affected 47/48 Tg66 mice. In contrast, maximum acutely tolerable doses of insoluble pellets from their olfactory mucosa brushings caused evidence of prion disease in only 4/28 inoculated mice, and no effects were seen with 10‐fold dilutions. No clinical prion disease was observed in mice inoculated with antemortem CSF samples or prion‐seeded real‐time quaking‐induced conversion assay products. Interpretation: Pellets from patients' olfactory mucosa brushings had ≥10, 000‐fold lower infectivity per unit volume than brain tissue, while CSF lacked detectable infectivity. Nonetheless, the results suggest that appropriate precautions may be warranted in surgical interventions involving the olfactory areas. The lack of pathogenic infectivity in the real‐time quaking‐induced conversion assay products provides evidence that the assay does not replicate biohazardous prions in vitro.