RPB0390

Pathogen Description

Target Pathogen Pathogen Name NCBI Taxonomy ID Order Family Genus Species Pathogen type
Mycobacterium Mycobacterium 1763 Corynebacteriales Mycobacteriaceae Mycobacterium 0 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
F ATGCTCACCACCCGGCTGGTCGTGTTGTAG 30 \ 60 69.84 9189.99 \
R GCTTCGCTATCGTTTGCGTGCCCTGATTGA 30 \ 53.33 66.65 9170.98 \

Gene Description

Target Gene GenBank ID
CARDS LR214945.1

Assay Description

Application Assay Primer Designing Software Reaction Time(min) Assay Temperature(℃) Readout System(s) Limit of Detection(LoD) Sensitivity(%) Specificity(%)
simple, rapid, portable and highly sensitive method to diagnose MP infection, which can be used as a promising tool in a variety of settings including clinical, field, and resource-limited aeras. RPA- CRISPR-Cas12a Primer Premier 5.0 30 min 37°C CRISPR-Cas12b 5 fg 1 1

Publication Description

Year of Publication Title Author(s) Journal PMID DOI
2023 Rapid, ultrasensitive and highly specific diagnosis of Mycoplasma pneumoniae by a CRISPR-based detection platform Juan Zhou,Fei Xiao,Jin Fu,Nan Jia,Xiaolan Huang,Chunrong Sun,Zheng Xu,Yu Zhang,Dong Qu,Yi Wang Frontiers in Cellular and Infection Microbiology 37577370 10.3389/fcimb.2023.1147142

Rapid, ultrasensitive and highly specific diagnosis of Mycoplasma pneumoniae by a CRISPR-based detection platform

Author(s):

Juan Zhou,Fei Xiao,Jin Fu,Nan Jia,Xiaolan Huang,Chunrong Sun,Zheng Xu,Yu Zhang,Dong Qu,Yi Wang

Journal:

Frontiers in Cellular and Infection Microbiology

Year:

2023

Abstract:

Mycoplasma pneumoniae (MP) is an important causative agent of morbidity and mortality among all age groups, especially among patients of extreme ages. Improved and readily available tests for accurate, sensitive and rapid diagnosis of MP infection is sorely needed. Here, we developed a CRISPR-Cas12b-based detection platform on the basis of recombinase polymerase amplification (RPA) for rapid, simple, and accurate diagnosis of MP infection, named MP-RPA-CRISPR. The RPA was employed for amplifying the community-acquired respiratory distress syndrome (CARDS) toxin gene of MP strains at the optimal reaction temperature 37°C. The resulting amplicons were decoded by the CRISPR-Cas12b-based detection platform, which was interpreted by real-time PCR system and by naked eye under blue light. The MP-RPA-CRISPR can detected down to 5 fg of genomic DNA templates of MP strains and accurately distinguish MP strains from non-MP strains without any cross-reactivity. A total of 96 bronchoalveolar lavage fluid (BALF)samples collected from patients suspected of respiratory infection were used to evaluate the clinical performance of the MP-RPA-CRISPR assay. As a result, our assay accurately diagnosed 45 MP-infected samples and 51 non-MP infected sample, and the results obtained from MP-RPA-CRISPR were consistent with microfluidic chip technology. In conclusion, our MP-RPA-CRISPR assay is a simple, rapid, portable and highly sensitive method to diagnose MP infection, which can be used as a promising tool in a variety of settings including clinical, field, and resource-limited aeras.