# CRISPR-Based Detection of Viral Hemorrhagic Fevers at the Point of Care

**Authors:** Kylene Wupori, Lauren Garnett, Alexander Bello, James E. Strong

PMC · DOI: 10.3390/v18020218 · Viruses · 2026-02-07

## TL;DR

This paper reviews CRISPR-based point-of-care tests for detecting viral hemorrhagic fevers, highlighting their potential for rapid and accurate diagnosis during outbreaks.

## Contribution

The paper provides a comprehensive review of CRISPR-based point-of-care tests for specific viral hemorrhagic fever pathogens.

## Key findings

- CRISPR-based tests offer high sensitivity and specificity for diagnosing viral hemorrhagic fevers.
- Current CRISPR-based tests are paired with isothermal amplification methods like LAMP and RPA.
- There is limited research on CRISPR-based point-of-care tests for viral hemorrhagic fevers.

## Abstract

Viral hemorrhagic fevers (VHFs) are highly lethal diseases that often present non-specific, influenza-like symptoms in their early stages, making clinical recognition and differentiation from other febrile illnesses difficult. This overlap underscores the critical need for diagnostic tests that are both sensitive and specific. Point-of-care (POC) diagnostic tests are an invaluable tool for detecting and controlling the spread of pathogens that threaten public health, such as VHFs, as these require fast, accurate diagnostics to ensure biosafety and appropriate mobilization of resources during outbreaks. Current molecular and serological diagnostic tests, while efficient and effective, lack the characteristics required of a POC test (POCT) to quickly and easily respond to a VHF outbreak while maintaining a low cost. Clustered regularly interspaced short palindromic repeats (CRISPR)-based diagnostic tests have gained popularity as POCTs due to their inherent attractive qualities, including high sensitivity and specificity, adaptability, low cost, quick turnaround time, and ease of use. However, studies on the development of CRISPR-based POC diagnostic tests for VHFs are limited. This review summarizes the current CRISPR-based POCTs for VHFs, including Ebola virus (EBOV), Lassa virus (LASV), Dengue virus (DENV), and Crimean–Congo hemorrhagic fever virus (CCHF). The isothermal pre-amplification methods commonly paired with CRISPR-based tests, such as loop-mediated isothermal amplification (LAMP) and recombinase polymerase amplification (RPA), are also discussed.

## Full-text entities

- **Genes:** BCAR1 (BCAR1 scaffold protein, Cas family member) [NCBI Gene 9564] {aka CAS, CAS1, CASS1, CRKAS, P130Cas}, IVNS1ABP (influenza virus NS1A binding protein) [NCBI Gene 10625] {aka ARA3, FLARA3, HSPC068, IMD70, KLHL39, ND1}, GDF10 (growth differentiation factor 10) [NCBI Gene 2662] {aka BIP, BMP-3b, BMP3B}, LAMP3 (lysosome associated membrane protein 3) [NCBI Gene 27074] {aka CD208, DC LAMP, DC-LAMP, DCLAMP, LAMP, LAMP-3}, RPA1 (replication protein A1) [NCBI Gene 6117] {aka HSSB, MST075, PFBMFT6, REPA1, RF-A, RP-A}, USF2 (upstream transcription factor 2, c-fos interacting) [NCBI Gene 7392] {aka FIP, bHLHb12}
- **Diseases:** chills (MESH:D023341), infection (MESH:D007239), deaths (MESH:D003643), infectious diseases (MESH:D003141), CCHF (MESH:D006479), Yellow Fever (MESH:D015004), LASV (MESH:D007835), HUDSON (MESH:D018883), malaria (MESH:D008288), myalgia (MESH:D063806), sickle cell disease (MESH:D000755), cancer (MESH:D009369), flu (MESH:D007251), injury to (MESH:D014947), Ebola (MESH:D019142), VHF (MESH:D006482), febrile illnesses (MESH:D005334), acute (MESH:D000208), diarrhea (MESH:D003967), hemorrhaging (MESH:D006470), DENV infection (MESH:D003715)
- **Chemicals:** urea (MESH:D014508), Cas12a (-), ATP (MESH:D000255), methicillin (MESH:D008712), sodium dodecyl sulfate (MESH:D012967)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rift Valley fever virus (no rank) [taxon 11588], Staphylococcus aureus (species) [taxon 1280], Dothidea sp. ENV1 (species) [taxon 154308], Brevibacillus sp. (species) [taxon 1882945], West Nile virus (no rank) [taxon 11082], LASV [taxon 11620], CCHF [taxon 1980519], Human papillomavirus 16 (serotype) [taxon 333760], Dengue virus (no rank) [taxon 12637], Alicyclobacillus acidoterrestris (species) [taxon 1450], Human papillomavirus (species) [taxon 10566], EBOV [taxon 186536], Ebola virus (no rank) [taxon 1570291], Zika virus (no rank) [taxon 64320], Bacillus subtilis (species) [taxon 1423], Escherichia coli (E. coli, species) [taxon 562], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Marburg virus [taxon 186537]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12944878/full.md

## References

112 references — full list in the complete paper: https://tomesphere.com/paper/PMC12944878/full.md

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Source: https://tomesphere.com/paper/PMC12944878