CRISPR-Cas-based diagnostics for point-of-care detection of sexually transmitted infections: a laboratory development and evaluation study

Low, SJ; O&#39;Neill, MT; Fernando, JA; Kerry, WJ; Prestedge, J; Wild, N; Chahal, S; Pollock, GL; Papadakis, G; Krysiak, M; Williams, E; Azzato, F; Tran, T; Fairley, C; Bradshaw, C; Chen, MY; Lim, CK; Williamson, DA; Pasricha, S

Author(s): Low, SJ; O'Neill, MT; Fernando, JA; Kerry, WJ; Prestedge, J; Wild, N; Chahal, S; Pollock, GL; Papadakis, G; Krysiak, M; Williams, E; Azzato, F; Tran, T; Fairley, C; Bradshaw, C; Chen, MY; Lim, CK; Williamson, DA; Pasricha, S;
Details: Publication Year 2026-04,Volume 7,Issue #4,Page 101289
Journal Title: Lancet Microbe
Abstract: BACKGROUND: Timely, point-of-care diagnosis of sexually transmitted infections (STIs) is crucial for enabling prompt treatment and reducing transmission. We aimed to develop a portable, multiplexed, CRISPR-based assay panel for the detection of Neisseria gonorrhoeae (including the ciprofloxacin resistance marker gyrA S91F), Chlamydia trachomatis, Treponema pallidum, and herpes simplex virus (HSV). METHODS: In this laboratory development and evaluation study, we developed and optimised four multiplexed, CRISPR-based, diagnostic STI assays for point-of-care use. The complete assay panel comprised a CRISPR TP-HSV (cTP-HSV) panel for the detection of T pallidum and pan-HSV, with reflex testing to distinguish HSV-1 from HSV-2, and a CRISPR NG-CT (cNG-CT) panel for the detection of N gonorrhoeae and C trachomatis, with reflex testing to detect N gonorrhoeae using two additional genome regions and to identify the gyrA S91F mutation. Each pathogen was targeted at two independent genomic regions by isothermal amplification and CRISPR-Cas reaction using Cas12a and Cas13a, each with distinct fluorescent reporters. Analytical specificity and limits of detection (LODs) were determined, and a retrospective, masked concordance study was conducted on genomic DNA from 900 clinical samples (400 for cTP-HSV and reflex testing and 500 for cNG-CT and reflex testing), using quantitative PCR as the reference standard. The diagnostic accuracy of the test was assessed by analysis of receiver operating characteristic curves. FINDINGS: The overall sensitivity of the TP-HSV CRISPR assay was 82·5% (95% CI 74·0-88·7) for T pallidum and 94·4% (90·2-97·0) for pan-HSV; LODs were 6·2 copies per μL for T pallidum and 7·8 copies per μL for HSV. Reflex testing gave sensitivities of 97·0% (91·1-99·3) for HSV-1 and 96·0% (89·7-98·7) for HSV-2. The NG-CT CRISPR assay had an overall sensitivity of 80·0% (74·0-84·9) for N gonorrhoeae and 73·0% (65·5-79·3) for C trachomatis, with a LOD of 3·9 copies per μL for both pathogens. Reflex testing for the detection of the gyrA S91F mutation in N gonorrhoeae showed an overall sensitivity of 63·1% (55·1-70·4); however, this was dependent on sample type, with a sensitivity of 85·7% (46·7-99·5) in genital samples and 61·2% (52·8-68·9) in extragenital samples. For all pathogens, assay sensitivity was positively correlated with pathogen load. Area under the curve (AUC) values were 0·90 for T pallidum and 0·99 for pan-HSV in the TP-HSV assay, with values of 0·99 for HSV-1 and 0·97 for HSV-2 obtained in the reflex HSV-1-HSV-2 assay. For the cNG-CT assay, AUC values were 0·90 for N gonorrhoeae and 0·85 for C trachomatis, with a value of 0·72 obtained for gyrA S91F in the reflex cNG-gyrA assay. INTERPRETATION: Our multiplexed, CRISPR-based, point-of-care platform achieved performance consistent with WHO target product profiles for N gonorrhoeae and T pallidum. Proof-of-concept detection of the gyrA S91F resistance marker highlights its potential for resistance-guided therapy. Although optimisation is required before large-scale deployment, this suite offers a promising approach for rapid, decentralised, and resistance-informed STI diagnosis, particularly in resource-limited settings. FUNDING: Victorian Government Department of Health, Australian Government Department of Health, Disability and Ageing and Aged Care, and Australian Research Council.
Publisher: Elsevier
Keywords: Humans; *CRISPR-Cas Systems; *Sexually Transmitted Diseases/diagnosis/microbiology; Neisseria gonorrhoeae/genetics/isolation & purification; Sensitivity and Specificity; Chlamydia trachomatis/genetics/isolation & purification; *Point-of-Care Systems; *Point-of-Care Testing; Treponema pallidum/genetics/isolation & purification; *Molecular Diagnostic Techniques/methods; Gonorrhea/diagnosis; Female; Nucleic Acid Amplification Techniques/methods; Simplexvirus/genetics/isolation & purification; Male; Chlamydia Infections/diagnosis
Research Division(s): Genetics and Gene Regulation
PubMed ID: 41791397
Publisher's Version: https://doi.org/10.1016/j.lanmic.2025.101289
Open Access at Publisher's Site: https://doi.org/10.1016/j.lanmic.2025.101289.
Terms of Use/Rights Notice: Refer to copyright notice on published article.

Creation Date: 2026-04-27 03:52:45

Last Modified: 2026-04-27 03:52:54