Development of an accurate CRISPR/Cas13 diagnostic system for Wuchereria bancrofti
Background: Disease surveillance is critical for WHO’s Global Programme to Eliminate Lymphatic Filariasis (LF), but current field-ready diagnostics exhibit insufficient sensitivity and/or specificity in low-endemic settings. We aim to develop an ultra-sensitive and field-friendly CRISPR/Cas13-based SHERLOCK (Specific High-sensitivity Enzymatic Reporter unLOCKing) tool for point-of-care detection of Wuchereria bancrofti infection. Methods: The SHERLOCK assay was performed in two-step and one-pot formats with sensitivity compared to qPCR. Assays were validated using 149 pooled mosquito and 185 human blood samples from Samoa, which were previously tested for LF antigen using WHO-recommended Filariasis Test Strips (FTS) and microscopically examined for microfilariae (Mf). We also used lyophilised one-pot SHERLOCK master mix and assessed its thermostability after storage at 25°C, 4°C and -20°C. Findings: The W. bancrofti SHERLOCK assays achieved a detection limit of 0.1 fg/μL gBlock DNA and showed no cross-reaction with five other filarial species. For both mosquito and human samples, the two-step SHERLOCK assay reached 100% sensitivity and specificity, while one-pot SHERLOCK showed 94.0-96.4% sensitivity and 100% specificity. The lyophilised one-pot SHERLOCK mix maintained a detection limit of 10 fg/μL W. bancrofti gBlock after 10 days at 25°C, indicating reduced reliance on cold-chain for reagent storage and transport. However, when testing human blood samples with lyophilised SHERLOCK, reduced sensitivity (59.7%) was observed. Interpretation: This CRISPR-based platform offers a promising field-ready next-generation approach to LF diagnostics, potentially addressing current limitations, enhancing surveillance and elimination efforts.
Authors
- Hong You (ORCID: https://orcid.org/0000-0002-8790-7793)
- Skye R. MacGregor (ORCID: https://orcid.org/0009-0005-9937-8808)
- Patricia M. Graves (ORCID: https://orcid.org/0000-0002-5215-3901)
- Yuhai Bi (ORCID: https://orcid.org/0000-0002-5595-363X)
- Brady McPherson
- Beatris Mário Martin (ORCID: https://orcid.org/0000-0002-8264-0153)
- Helen J. Mayfield (ORCID: https://orcid.org/0000-0003-3462-4324)
- Satupaitea Viali (ORCID: https://orcid.org/0000-0002-4829-8403)
- Lisa Rigby (ORCID: https://orcid.org/0000-0002-2034-2396)
- Colleen L. Lau (ORCID: https://orcid.org/0000-0001-8288-4169)
- Richard S. Bradbury
- Malcolm K. Jones (ORCID: https://orcid.org/0000-0002-0035-6141)
- Robert E. Thomsen
- Vito Colella (ORCID: https://orcid.org/0000-0002-4903-1479)
- Shannon M. Hedtke (ORCID: https://orcid.org/0000-0002-7499-7662)
- Asrhyella Seeler (ORCID: https://orcid.org/0009-0009-0477-0823)
Institutions
- Federation University (AU)
- Queensland University of Technology (AU)
- The University of Queensland (AU)
- The University of Melbourne (AU)
- La Trobe University (AU)
- Chinese Academy of Sciences (CN)
- QIMR Berghofer Medical Research Institute (AU)
- National University of Samoa (WS)
- Australian Institute of Tropical Health and Medicine (AU)
- Australian Defence Force Malaria and Infectious Disease Institute (AU)
- James Cook University (AU)
Publication Details
- Journal
- Emerging Microbes & Infections
- Published
- 2026-11-06
- DOI
- https://doi.org/10.1080/22221751.2026.2761170
- Primary Topic
- Parasitic Diseases Research and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- QIMR Berghofer Medical Research Institute
- University of Queensland
- National Health and Medical Research Council