核酸
沙门氏菌
检出限
管(容器)
色谱法
核酸检测
肉眼
DNA
化学
核酸定量
DNA提取
重组酶聚合酶扩增
聚合酶链反应
纳米技术
材料科学
生物
细菌
环介导等温扩增
生物化学
基因
复合材料
遗传学
作者
Xiaoli Zhao,Qianyi Wan,Jian Zhang,Yake Duan,Yong Li,Jingrong Ma,Chao Shi,Cuiping Ma
标识
DOI:10.1007/s00216-022-03904-z
摘要
Herein, we developed an ultra-fast and visual single-tube nucleic acid detection approach, which combined the advantages of self-settling characteristics of chitosan-functionalized diatomaceous earth (CDE) and accelerated PCR (AC-PCR). DNA was rapidly extracted by CDE within 3 min for the next nucleic acid amplification based on the nucleic acid attached on the chitosan in pH = 5.0. Under the action of gravity, the DNA-enriched CDE self-sediments to the bottom of the tube could be directly used for AC-PCR to achieve single-tube extraction and amplification. Our method detected Salmonella culture fluids with a detection limit of 1 CFU/mL, which was 100-fold more sensitive than conventional method that have not undergone nucleic acid enrichment. Furthermore, it also displayed high specificity and sensitivity for a variety of spiked samples. The entire process could be completed within 17 min in a single tube, and in particular, the result was visualized by the naked eyes. Overall, it is an all-in-one detection strategy without the requirement of redundant procedure, which greatly improved the detection efficiency, and saved the time and the cost. With these advantages, the approach will supply a promising tool in the field of point-of-care testing for Salmonella and other foodborne pathogens.
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