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快速、无需基因隔离或扩增的无标记粪便中肠道病原体的基因检测。

Rapid, label-free genetic detection of enteropathogens in stool without genetic isolation or amplification.

机构信息

School of Biomedical Engineering, Science, and Health Systems, Drexel University, Philadelphia, PA 19104, USA.

Department of Materials Science and Engineering, Drexel University, PA 19104, USA.

出版信息

Biosens Bioelectron. 2019 Apr 1;130:73-80. doi: 10.1016/j.bios.2019.01.025. Epub 2019 Jan 21.

Abstract

Current genetic detection methods require gene isolation, gene amplification and detection with a fluorescent-tagged probe. They typically require sophisticated equipment and expensive fluorescent probes, rendering them not widely available for rapid acute infection diagnoses at the point of care to ensure timely treatment of the diseases. Here we report a rapid genetic detection method that can detect the bacterial gene directly from patient stools using a piezoelectric plate sensor (PEPS) in conjunction with a continuous flow system with two temperature zones. With stools spiked with sodium dodecyl sulfate (SDS) in situ bacteria lysing and DNA denaturation occurred in the high-temperature zone whereas in situ specific detection of the denatured DNA by the PEPS occurred in the lower-temperature zone. The outcome was a rapid genetic detection method that directly detected bacterial genes from stool in < 40 min without the need of gene isolation, gene amplification, or expensive fluorescent tag but with polymerase chain reaction (PCR) sensitivity. In 40 blinded patient stools, it detected the toxin B gene of Clostridium difficile with 95% sensitivity and 95% specificity. The all-electrical, label-free nature of the detection further supports its potential as a low-cost genetic test that can be used at the point of care.

摘要

目前的遗传检测方法需要基因分离、基因扩增和带有荧光标记探针的检测。它们通常需要复杂的设备和昂贵的荧光探针,因此无法在护理点快速进行急性感染诊断,以确保及时治疗疾病。在这里,我们报告了一种快速遗传检测方法,该方法可以使用压电板传感器 (PEPS) 与具有两个温度区的连续流系统结合,直接从患者粪便中检测细菌基因。通过在原位用十二烷基硫酸钠 (SDS) 处理粪便,高温区会发生细菌裂解和 DNA 变性,而在低温区,PEPS 会原位特异性检测变性 DNA。结果是一种快速遗传检测方法,无需基因分离、基因扩增或昂贵的荧光标记即可在<40 分钟内直接从粪便中检测细菌基因,但具有聚合酶链反应 (PCR) 敏感性。在 40 份盲法患者粪便中,该方法检测艰难梭菌毒素 B 基因的灵敏度为 95%,特异性为 95%。该检测的全电化、无标记性质进一步支持了其作为一种低成本基因检测方法在护理点使用的潜力。

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Comparison of five assays for detection of Clostridium difficile toxin.五种检测艰难梭菌毒素方法的比较。
J Mol Diagn. 2011 Jul;13(4):395-400. doi: 10.1016/j.jmoldx.2011.03.004. Epub 2011 Apr 29.

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