RPB0427

Pathogen Description

Target Pathogen Pathogen Name NCBI Taxonomy ID Order Family Genus Species Pathogen type
Staphylococcus aureus Staphylococcus aureus, Micrococcus aureus, Staphylococcus pyogenes aureus 1280 Bacillales Staphylococcaceae Staphylococcus Staphylococcus aureus 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
LFD-Sau-F3 AATTACATAAAGAACCTGCGACTTTAATTA 30 10 µM 26.67 51.86 9181.08 \
LFD-Sau-R2 [biotin] ATGCACTTGCTTCAGGACCATATTTCTCTA 30 10 µM 40 59.06 9106.98 \
NFO-Sau [FAM]GCGATTGATGGTGATACGGTTAAATTAATG[THF]ACAAAGGTCAACCA[C3spacer] 44 10 µM 38.64 63.75 13651.95 \

Gene Description

Target Gene GenBank ID
Nuc \

Assay Description

Application Assay Primer Designing Software Reaction Time(min) Assay Temperature(℃) Readout System(s) Limit of Detection(LoD) Sensitivity(%) Specificity(%)
the advantages of simple equipment, rapid operation, and low cost. RPA-LFD \ 10 min 38℃ LFD 600 CFU\mL \ \

Publication Description

Year of Publication Title Author(s) Journal PMID DOI
2023 Development of a novel integrated isothermal amplification system for detection of bacteria-spiked blood samples Jin Li,Mei-Yun Shang,Shao-Li Deng,Min Li,Ning Su,Xiao-Dong Ren,Xian-Ge Sun,Wen-Man Li,Yu-Wei Li,Ruo-Xu Li,Qing Huang,Wei-Ping Lu AMB Express 38019349 10.1186/s13568-023-01643-7

Development of a novel integrated isothermal amplification system for detection of bacteria-spiked blood samples

Author(s):

Jin Li,Mei-Yun Shang,Shao-Li Deng,Min Li,Ning Su,Xiao-Dong Ren,Xian-Ge Sun,Wen-Man Li,Yu-Wei Li,Ruo-Xu Li,Qing Huang,Wei-Ping Lu

Journal:

AMB Express

Year:

2023

Abstract:

Bloodstream infection (BSI) caused by bacteria is highly pathogenic and lethal, and easily develops whole-body inflammatory state. Immediate identification of disease-causing bacteria can improve patient prognosis. Traditional testing methods are not only time-consuming, but such tests are limited to laboratories. Recombinase polymerase amplification combined with lateral flow dipstick (RPA-LFD) holds great promise for rapid nucleic acid detection, but the uncapping operation after amplification easily contaminates laboratories. Therefore, the establishment of a more effective integrated isothermal amplification system has become an urgent problem to be solved. In this study, we designed and fabricated a hermetically sealed integrated isothermal amplification system. Combining with this system, a set of RPA-LFD assays for detecting S. aureus, K. peneumoniae, P. aeruginosa, and H. influenza in BSI were established and evaluated. The whole process could be completed in less than 15 min and the results can be visualized by the naked eye. The developed RPA-LFD assays displayed a good sensitivity, and no cross-reactivity was observed in seven similar bacterial genera. The results obtained with 60 clinical samples indicated that the developed RPA-LFD assays had high specifcity and sensitivity for identifying S. aureus, K. peneumoniae, P. aeruginosa, and H. influenza in BSI. In conclusion, our results showed that the developed RPA-LFD assay is an alternative to existing PCR-based methods for detection of S. aureus, K. peneumoniae, P. aeruginosa, and H. influenza in BSI in primary hospitals.