检出限
微流控
奇异变形杆菌
色谱法
分子信标
化学
细菌
大肠杆菌
锁核酸
杂交探针
核酸
DNA
分析化学(期刊)
微生物学
材料科学
纳米技术
生物
寡核苷酸
生物化学
遗传学
基因
作者
Yu‐Ting Kao,Silvia Calabrese,Nadine Borst,Michael Lehnert,Yu-Kai Lai,Franziska Schlenker,Peter Juelg,Roland Zengerle,Piotr Garstecki,Felix von Stetten
出处
期刊:Biosensors
[MDPI AG]
日期:2022-04-12
卷期号:12 (4): 237-237
被引量:4
摘要
We demonstrate detection and quantification of bacterial load with a novel microfluidic one-pot wash-free fluorescence in situ hybridization (FISH) assay in droplets. The method offers minimal manual workload by only requiring mixing of the sample with reagents and loading it into a microfluidic cartridge. By centrifugal microfluidic step emulsification, our method partitioned the sample into 210 pL (73 µm in diameter) droplets for bacterial encapsulation followed by in situ permeabilization, hybridization, and signal detection. Employing locked nucleic acid (LNA)/DNA molecular beacons (LNA/DNA MBs) and NaCl-urea based hybridization buffer, the assay was characterized with Escherichia coli, Klebsiella pneumonia, and Proteus mirabilis. The assay performed with single-cell sensitivity, a 4-log dynamic range from a lower limit of quantification (LLOQ) at ~3 × 103 bacteria/mL to an upper limit of quantification (ULOQ) at ~3 × 107 bacteria/mL, anda linearity R2 = 0.976. The total time-to-results for detection and quantification was around 1.5 hours.
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