VGRCOT: a one-tube visual detection method for group B <i>Streptococcus</i> combining RPA and CRISPR/Cas12a for point-of-care testing in reproductive health
Group B <i>Streptococcus</i> (GBS) is a significant pathogen that causes perinatal infections, seriously threatening the health of pregnant women and newborns. Prophylactic antibiotic treatment for pregnant women who screen positive for GBS can notably reduce the incidence and fatality of neonatal infections. Herein, we developed a <u>v</u>isual nucleic acid method for <u>G</u>BS that integrates <u>R</u>PA and <u>C</u>RISPR/Cas12a in a <u>o</u>ne-<u>t</u>ube setup, termed VGRCOT. The VGRCOT method achieved one-tube detection by adding the appropriate reagents to the bottom and lid of the EP tube, respectively. By rigorous optimization of ssDNA-FQ reporter concentration, crRNA concentration, RPA reaction time, and CRISPR/Cas12a cleavage time, VGRCOT can exhibit fluorescence under ultraviolet light, enabling visual detection. Under optimal conditions, VGRCOT has a satisfactory selectivity, and the detection limit was determined as 10<sup>1</sup> copies/reaction. Finally, VGRCOT also showed good performance comparable to qPCR in the actual detection of clinical specimens. Due to its ease of operation and convenient signal acquisition, VGRCOT shows promise for point-of-care testing in reproductive health.IMPORTANCEThis study presents a convenient, sensitive, and accurate visual detection method (VGRCOT) for GBS, combining RPA and CRISPR/Cas12a in a single reaction vessel. Through optimization of experimental conditions, VGRCOT enables detection within 60 min, with a minimum detection limit of 10<sup>1</sup> copies per reaction. VGRCOT offers several advantages by adding the appropriate reagents to the bottom and lid of the EP tube. The one-tube visualization method effectively prevents aerosol contamination, simplifies procedures, and enables visual detection without complex instruments, making it ideal for resource-limited environments. Additionally, its editable crRNA and the use of commonly available laboratory reagents allow for easy reprogramming to detect various pathogens, supporting scalable and low-cost batch production.
Authors
- T. T. Han (ORCID: https://orcid.org/0000-0003-1404-1578)
- Lisa W. Ru
- Yayun Jiang
- Gang Mai (ORCID: https://orcid.org/0000-0002-5843-2821)
- Caixia Ji
- Laibao Zheng (ORCID: https://orcid.org/0000-0003-0444-8163)
Institutions
- Changzhi Medical College (CN)
- Wenzhou Medical University (CN)
- Deyang Stomatological Hospital (CN)
- Zoucheng People's Hospital (CN)
- Shanxi Jincheng Anthracite Mining Group (China) (CN)
- Ministry of Education (KN)
- Anyang Hospital of Traditional Chinese Medicine (CN)
- Chengdu University of Traditional Chinese Medicine (CN)
Publication Details
- Journal
- Microbiology Spectrum
- Published
- 2025-08-14
- DOI
- https://doi.org/10.1128/spectrum.01395-25
- Citations
- 2
- Primary Topic
- Biosensors and Analytical Detection
- Type
- article
- Field-Weighted Citation Impact
- 1.35