RPB0321

Pathogen Description

Target Pathogen Pathogen Name NCBI Taxonomy ID Order Family Genus Species Pathogen type
Streptococcus pyogenes M1 GAS Streptococcus pyogenes M1 GAS, Streptococcus pyogenes SF370, Streptococcus pyogenes ATCC 700294 160490 Lactobacillales Streptococcaceae Streptococcus Streptococcus pyogenes Bacterium

Primer Description

Primer Name Sequence(5'-3') Length(bp) Primer Final Concentration(μM) GC Content(%) Predicted Melting Temperature(℃) Molecular Weight(g/moles) Positions in GenBank accession number
speB-F CTTCTTCCGACTTGACGCACTAAACCCTTC 30 10 μM 50 62.79 9012.91 1608205-1607009
speB-R TTGATGCCTACAACAGCACTTTGATAACCG 30 10 μM 43.33 60.68 9150.02 1608205-1607009
P FITC-CTTCTTCCGACTTGACGCACTAATCCCTTC[THF]GCTCTTGATAATGGT-C3spacer 45 10 μM 46.67 67.89 13663.9 1608205-1607009

Gene Description

Target Gene GenBank ID
speB NZ_LS483338.1

Assay Description

Application Assay Primer Designing Software Reaction Time(min) Assay Temperature(℃) Readout System(s) Limit of Detection(LoD) Sensitivity(%) Specificity(%)
mproved RPA-LFS technique to realize the rapid and visual detection of Streptococcus pyogenes RPA-LFS Primer Premier 5 30 min 37°C LFS 0.908 ng 1 0.9926

Publication Description

Year of Publication Title Author(s) Journal PMID DOI
2024 Efficient detection of Streptococcus pyogenes based on recombinase polymerase amplification and lateral flow strip Xu-Zhu Gao,Yu-Die Cao,Yu-Zhi Gao,Juan Hu,Tuo Ji European Journal of Clinical Microbiology & Infectious Diseases 38361135 10.1007/s10096-024-04780-4

Efficient detection of Streptococcus pyogenes based on recombinase polymerase amplification and lateral flow strip

Author(s):

Xu-Zhu Gao,Yu-Die Cao,Yu-Zhi Gao,Juan Hu,Tuo Ji

Journal:

European Journal of Clinical Microbiology & Infectious Diseases

Year:

2024

Abstract:

Purpose: This article aims to establish a rapid visual method for the detection of Streptococcus pyogenes (GAS) based on recombinase polymerase amplification (RPA) and lateral flow strip (LFS). Methods: Utilizing speB of GAS as a template, RPA primers were designed, and basic RPA reactions were performed. To reduce the formation of primer dimers, base mismatch was introduced into primers. The probe was designed according to the forward primer, and the RPA-LFS system was established. According to the color results of the reaction system, the optimum reaction temperature and time were determined. Thirteen common clinical standard strains and 14 clinical samples of GAS were used to detect the selectivity of this method. The detection limit of this method was detected by using tenfold gradient dilution of GAS genome as template. One hundred fifty-six clinical samples were collected and compared with qPCR method and culture method. Kappa index and clinical application evaluation of the RPA-LFS were carried out. Results: The enhanced RPA-LFS method demonstrates the ability to complete the amplification process within 6 min at 33 °C. This method exhibits a high analytic sensitivity, with the lowest detection limit of 0.908 ng, and does not exhibit cross-reaction with other pathogenic bacteria. Conclusions: The utilization of RPA and LFS allows for efficient and rapid testing of GAS, thereby serving as a valuable method for point-of-care testing.