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Detection of Atypical H-Type Bovine Spongiform Encephalopathy and Discrimination of Bovine Prion Strains by Real-Time Quaking-Induced Conversion
Author(s) -
Kentaro Masujin,
Christina D. Orrú,
Kohtaro Miyazawa,
Bradley R. Groveman,
Lynne D. Raymond,
Andrew G. Hughson,
Byron Caughey
Publication year - 2016
Publication title -
journal of clinical microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.349
H-Index - 255
eISSN - 1070-633X
pISSN - 0095-1137
DOI - 10.1128/jcm.02731-15
Subject(s) - bovine spongiform encephalopathy , virology , recombinant dna , serial dilution , biology , prion protein , cerebrospinal fluid , proteinase k , microbiology and biotechnology , enzyme , medicine , pathology , genetics , biochemistry , gene , disease , alternative medicine , neuroscience
Prion diseases of cattle include the classical bovine spongiform encephalopathy (C-BSE) and the atypical H-type BSE (H-BSE) and L-type BSE (L-BSE) strains. Although the C- and L-BSE strains can be detected and discriminated by ultrasensitive real-time quaking-induced conversion (RT-QuIC) assays, no such test has yet been described for the detection of H-BSE or the discrimination of each of the major bovine prion strains. Here, we demonstrate an RT-QuIC assay for H-BSE that can detect as little as 10−9 dilutions of brain tissue and neat cerebrospinal fluid samples from clinically affected cattle. Moreover, comparisons of the reactivities with different recombinant prion protein substrates and/or immunoblot band profiles of proteinase K-treated RT-QuIC reaction products indicated that H-, L-, and C-BSE have distinctive prion seeding activities and can be discriminated by RT-QuIC on this basis.

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