A tiered molecular surveillance framework linking rapid dengue detection to genomic epidemiology in Senegal - Scorecard - MDSpire
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A Multilevel Molecular Monitoring System Connecting Swift Dengue Identification to Genomic Epidemiology in Senegal

  • By

  • Amy Gaye

  • Varun Vaidya

  • Mariama Toure

  • Ibrahima Mbaye Ndiaye

  • Sebastian Gallon

  • Mamadou Samb Yade

  • Bassirou Ngom

  • Djiby Sow

  • Ndeye Coumba Diop

  • Ousmane Kebe

  • Yaye Die Ndiaye

  • Mamadou Alpha Diallo

  • Aita Sene

  • Abdoulaye Tine

  • Awa Bineta Deme

  • Younousse Diedhiou

  • Abdoulaye Kane Dia

  • Aida S. Badiane

  • Mouhamad Sy

  • Daouda Ndiaye

  • August 25, 2026

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Clinical Scorecard: A Multilevel Molecular Monitoring System Connecting Swift Dengue Identification to Genomic Epidemiology in Senegal

At a Glance

Category

Detail

Condition

Dengue, Zika, and chikungunya virus infections

Key Mechanisms

Tiered surveillance combining multiplex RT-qPCR, RT-RPA dengue serotyping, and genomic sequencing

Target Population

Individuals presenting with febrile or nonfebrile illness in 4 regions of Senegal

Care Setting

Participating clinical surveillance sites in Diourbel, Touba, Thiès, and Kédougou

Key Highlights

  • The observational surveillance study included 367 participants between September and December 2025.

  • Multiplex RT-qPCR provided evidence of concurrent DENV, ZIKV, and CHIKV circulation.

  • Forty-three samples from Touba were tested individually; the remaining specimens were analyzed in 108 pools of 3.

  • DENV-1-4 NS1-specific IgM was detected in 15 participants (4.1%), supporting recent dengue transmission.

  • All serotyped DENV-positive samples were identified as DENV-2; the study did not detect DENV-1, DENV-3, or DENV-4.

  • Targeted amplicon sequencing recovered near-complete DENV-2 genomes more frequently than metagenomic sequencing.

Guideline-Based Recommendations

This observational surveillance study did not establish clinical guidelines for diagnosing, treating, or monitoring individual patients.

Diagnosis

  • Multiplex RT-qPCR was used to detect DENV, ZIKV, and CHIKV simultaneously.

  • RT-RPA provided rapid DENV-1-4 serotyping and was completely concordant with RT-qPCR within the tested subset.

  • Pool-level RT-qPCR positivity should not be interpreted as individual-level prevalence.

  • Routine malaria rapid tests were negative in all participants, although metagenomic sequencing detected Plasmodium falciparum reads in 3 samples.

Management

  • The study evaluated a surveillance workflow rather than clinical treatment or patient-management strategies.

  • Positive RT-qPCR or RT-RPA samples were prioritized for genomic sequencing.

  • The tiered design reduced the number of samples requiring more resource-intensive sequencing.

  • The study did not evaluate whether the workflow improved treatment decisions or clinical outcomes.

Monitoring & Follow-up

  • DENV serology provided additional evidence of recent transmission in the sampled population.

  • Phylogenetic analysis characterized the detected DENV-2 genotype and lineage.

  • Longer surveillance periods are needed to capture seasonal variation.

  • Genomic characterization of the detected ZIKV and CHIKV was not performed.

Risks

  • Overlapping clinical syndromes may contribute to under-recognition of arboviral infections.

  • Pooled testing may underestimate infection burden and prevents calculation of individual prevalence.

  • Exclusive DENV-2 detection among serotyped samples does not establish the absence of other serotypes throughout Senegal.

  • The short surveillance period limits conclusions about seasonal transmission patterns.

Patient & Prescribing Data

The study included 367 individuals presenting with febrile or nonfebrile illness across 4 Senegalese regions. Of these specimens, 43 were tested individually and the remainder were screened in 108 pools containing 3 samples each.

The study did not evaluate medications, prescribing practices, antiviral treatment, or clinical outcomes.

Clinical Best Practices

  • Interpret pooled RT-qPCR findings as surveillance signals rather than individual prevalence estimates.

  • Use RT-RPA as a triage step for rapid dengue serotyping and selection of samples for sequencing.

  • Combine molecular findings with serologic and genomic evidence when characterizing arbovirus circulation.

  • Use targeted amplicon sequencing to improve DENV-2 genome recovery from selected positive samples.

  • Apply the findings cautiously because surveillance was conducted over a short period and sequencing was limited to DENV-2.

Related Resources & Content

A Tiered Molecular Surveillance Framework Linking Rapid Dengue Detection to Genomic Epidemiology in Senegal — Gaye A, Vaidya V, Toure M, et al. International Journal of Infectious Diseases. 2026;171:109009. doi:10.1016/j.ijid.2026.109009.

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