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本文引用的文献

1
Probing surface recombination velocities in semiconductors using two-photon microscopy.利用双光子显微镜探测半导体中的表面复合速度。
J Appl Phys. 2016 Mar;119(12). doi: 10.1063/1.4944597.
2
Specific in situ hepatitis B viral double mutation (HBVDM) detection in urine with 60 copies ml(-1) analytical sensitivity in a background of 250-fold wild type without DNA isolation and amplification.在无需DNA分离和扩增的情况下,于250倍野生型背景中对尿液进行特异性原位乙肝病毒双突变(HBVDM)检测,分析灵敏度达60拷贝/毫升。
Analyst. 2015 Mar 7;140(5):1590-8. doi: 10.1039/c4an01885k. Epub 2015 Jan 19.
3
DNA hybridization detection with 100 zM sensitivity using piezoelectric plate sensors with an improved noise-reduction algorithm.使用具有改进降噪算法的压电板传感器进行灵敏度为100 zM的DNA杂交检测。
Analyst. 2014 Jun 7;139(11):2754-63. doi: 10.1039/c4an00215f.
4
Folate receptor in adenocarcinoma and squamous cell carcinoma of the lung: potential target for folate-linked therapeutic agents.肺腺癌和肺鳞癌中的叶酸受体:叶酸偶联治疗药物的潜在靶点。
Arch Pathol Lab Med. 2013 Feb;137(2):241-4. doi: 10.5858/arpa.2012-0176-OA. Epub 2012 Sep 14.
5
Label-free Growth Receptor-2 Detection and Dissociation Constant Assessment in Diluted Human Serum Using a Longitudinal Extension Mode of a Piezoelectric Microcantilever Sensor.使用压电微悬臂梁传感器的纵向延伸模式在稀释人血清中进行无标记生长受体-2检测及解离常数评估
Sens Actuators B Chem. 2011 Dec 15;160(1):349-356. doi: 10.1016/j.snb.2011.07.060.
6
Evolution of testing algorithms at a university hospital for detection of Clostridium difficile infections.检测艰难梭菌感染的大学医院测试算法的演变。
J Clin Microbiol. 2012 Sep;50(9):3073-6. doi: 10.1128/JCM.00992-12. Epub 2012 Jun 20.
7
Antimicrobial stewardship: a collaborative partnership between infection preventionists and healthcare epidemiologists.抗菌药物管理:感染预防人员与医疗保健流行病学家之间的合作关系。
Infect Control Hosp Epidemiol. 2012 Apr;33(4):328-30. doi: 10.1086/665037.
8
Antimicrobial stewardship: a collaborative partnership between infection preventionists and health care epidemiologists.抗菌药物管理:感染预防专家和医疗保健流行病学家之间的合作关系。
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9
Detection of toxigenic Clostridium difficile: comparison of the cell culture neutralization, Xpert C. difficile, Xpert C. difficile/Epi, and Illumigene C. difficile assays.艰难梭菌毒素检测:细胞培养中和试验、Xpert C. difficile 检测、Xpert C. difficile/Epi 检测和 Illumigene C. difficile 检测的比较。
J Clin Microbiol. 2012 Apr;50(4):1331-5. doi: 10.1128/JCM.06597-11. Epub 2012 Jan 25.
10
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.

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.

DOI:10.1016/j.bios.2019.01.025
PMID:30731348
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6469511/
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。