ArticleJournal of clinical microbiology2026
High sensitivity of the Bionote Anigen Rapid Rabies Antigen Test in detection of diverse rabies virus variants suggests utility for global rabies control.
Article in Journal of clinical microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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31 authors.
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Abstract
Point-of-care, immunochromatographic tests have not reliably detected the rabies virus and have not utilized a consistent diagnostic protocol. International diagnostic standards established by the World Organization for Animal Health require strategic and large-scale validation studies prior to widespread use. The United States (US) Centers for Disease Control and Prevention, National Rabies Reference Laboratory, undertook a large-scale validation of the BioNote Anigen Rapid Rabies Antigen Test in collaboration with eight US public health laboratories and three international laboratories. Modifications were made according to the manufacturer's instructions to maximize antigen concentration in the test diluent. A total of 1,399 samples underwent paired testing with one of three US gold standard tests, consisting of 31 types of animals and 9 rabies virus variants (RVVs). Test sensitivity and specificity were 97.11% (CI: 95.21%-98.27%) and 99.89% (CI: 99.36%-99.98%). Fourteen samples resulted in false-negative results, primarily impacting dogs that were euthanized early or shown to have a low viral load. Limit-of-detection studies found that false-negative results often occurred when the sample had a PCR Ct value
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