Development of a Recombinase-Aided Amplification Assay for the Rapid Detection of Candida auris .
Junxia FengJinfeng ChenBing DuXiaohu CuiYuyan XiaGuanhua XueYanling FengYuehua KeHanqing ZhaoJinghua CuiChao YanLin GanZheng FanTongtong FuZiying XuYang YangZihui YuLijuan HuangShuo ZhaoZiyan TianZanbo DingYujie ChenZhoufei LiJing YuanPublished in: Analytical chemistry (2024)
Candida auris ( C. auris ) was first discovered in Japan in 2009 and has since spread worldwide. It exhibits strong transmission ability, high multidrug resistance, blood infectivity, and mortality rates. Traditional diagnostic techniques for C. auris have shortcomings, leading to difficulty in its timely diagnosis and identification. Therefore, timely and accurate diagnostic assays for clinical samples are crucial. We developed a novel, rapid recombinase-aided amplification (RAA) assay targeting the 18S rRNA, ITS1, 5.8S rRNA, ITS2, and 28S rRNA genes for C. auris identification. This assay can rapidly amplify DNA at 39 °C in 20 min. The analytical sensitivity and specificity were evaluated. From 241 clinical samples collected from pediatric inpatients, none were detected as C. auris -positive. We then prepared simulated clinical samples by adding 10-fold serial dilutions of C. auris into the samples to test the RAA assay's efficacy and compared it with that of real-time PCR. The assay demonstrated an analytical sensitivity of 10 copies/μL and an analytical specificity of 100%. The lower detection limit of the RAA assay for simulated clinical samples was 10 1 CFU/mL, which was better than that of real-time PCR (10 2 -10 3 CFU/mL), demonstrating that the RAA assay may have a better detection efficacy for clinical samples. In summary, the RAA assay has high sensitivity, specificity, and detection efficacy. This assay is a potential new method for detecting C. auris , with simple reaction condition requirements, thus helping to manage C. auris epidemics.
Keyphrases
- high throughput
- real time pcr
- loop mediated isothermal amplification
- cardiovascular disease
- dna methylation
- risk assessment
- drug delivery
- staphylococcus aureus
- label free
- genome wide
- candida albicans
- liquid chromatography
- cancer therapy
- climate change
- biofilm formation
- single cell
- single molecule
- transcription factor
- quantum dots