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Author Spotlight: Development of a Smartphone-Enhanced Paper-Based Device for Rapid Dengue NS1 Detection
Published on: January 26, 2024
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Diagnostic biologique de la dengue
Fatiha Najioullah1, Florent Viron1, Laure Paturel1
1CHU de Fort-de-France et EA 4537, université des Antilles et de la Guyane, laboratoire de virologie, pôle de biologie-pathologie, BP632, 97261 Fort-de-France Cedex, France.
Virologie (Montrouge, France)
|October 17, 2020
Summary
Rapid diagnosis of dengue virus is crucial due to lack of treatments. Viral detection by reverse transcription-polymerase chain reaction (RT-PCR) is the best clinical tool for severe dengue infections.
Area of Science:
- * Arbovirology
- * Infectious Diseases
- * Medical Diagnostics
Background:
- * Dengue is a significant arboviral disease with a wide spectrum of clinical presentations, ranging from asymptomatic to fatal outcomes.
- * The absence of effective antiviral treatments or vaccines underscores the critical need for accurate and timely diagnosis.
- * Effective dengue diagnosis is essential for both clinical management and public health surveillance.
Purpose of the Study:
- * To evaluate diagnostic methods for dengue virus infection based on the timing of clinical sign appearance.
- * To identify the most effective diagnostic tool for severe dengue cases in clinical settings.
Main Methods:
- * Review of diagnostic methods including RT-PCR, serology (EIA), NS1 antigen detection, and viral isolation.
- * Assessment of diagnostic accuracy, specificity, sensitivity, and serotype identification capabilities.
- * Consideration of the time-dependency of diagnostic test performance relative to disease onset.
Main Results:
- * Direct tests, particularly RT-PCR, are preferred within the first seven days of fever for sensitive and specific viral serotype identification.
- * Real-time PCR is expected to supersede conventional RT-PCR with the availability of standardized assays for all four serotypes.
- * Serology (EIA) is useful after seven days but lacks serotype discrimination and exhibits high cross-reactivity; NS1 antigen detection has limited clinical sensitivity.
Conclusions:
- * Viral detection via RT-PCR remains the optimal method for rapid diagnosis of severe dengue infections in clinical settings.
- * Despite necessary improvements, RT-PCR offers the best balance of speed, sensitivity, and specificity for early dengue diagnosis.
- * Continued development of standardized real-time PCR assays is recommended for comprehensive serotype identification.

