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基于椭偏测量法的新型DNA生物传感器,用于无标记实时检测副百日咳博德特氏菌。

Ellipsometric-based novel DNA biosensor for label-free, real-time detection of Bordetella parapertussis.

作者信息

Rafique S, Idrees M, Bokhari H, Bhatti A S

机构信息

Department of Physics, Air University, PAF Complex, E-9, Islamabad, 44000, Pakistan.

Department of Microbiology, COMSATS Institute of Information Technology, Islamabad, 44000, Pakistan.

出版信息

J Biol Phys. 2019 Sep;45(3):275-291. doi: 10.1007/s10867-019-09528-2. Epub 2019 Aug 2.

Abstract

Pertussis (or whooping cough) is a contagious disease mainly affecting infants and children and predominantly caused by Bordetella pertussis followed by Bordetella parapertussis. B. parapertussis causes a milder cough but usually symptomatically appears like B. pertussis infection. Thus the epidemiology of illness caused by B. parapertussis is not well understood. In this study, a sensitive and specific method for the rapid diagnosis of B. parapertussis is presented. The covalent immobilization of thiol-terminated DNA oligonucleotides (ss DNA SAM) on a silicon surface by disulfide bond formation is investigated with atomic force microscopy (AFM) and ellipsometry. The measurements indicated an average layer thickness of 5 ± 0.84 nm for 2 μg/μl concentration and 24 h incubation time. This thickness changed to 8.4 ± 0.92 nm for the same concentration (2 μg/μl) by altering the incubation time to 48 h. Ellipsometric data recorded before and after hybridization of B. parapertussis revealed an increase in mean grain area from 91 nm to 227 nm and a change in the refractive index from 1.489 to 1.648 for 2 μg/μl B. parapertussis, respectively. This change in the refractive index was used to evaluate the amount of adsorbed molecules and their density. The results showed that the density of adsorbed molecules increased from 0.2 to 0.97 g/cm after B. parapertussis attachment, respectively. To confirm the hybridization of B. parapertussis to ss DNA SAM, the ds DNA SAM was denatured and the ss DNA SAM surface was reproduced with an average height variation of 6.42 ± 0.75 nm. This showed the stability of the DNA film that can be tuned by varying the concentration and incubation time, thus providing a robust method for the label-free detection of B. parapertussis other than routinely used PCR detection.

摘要

百日咳(或百日咳)是一种主要影响婴幼儿的传染病,主要由百日咳博德特氏菌引起,其次是副百日咳博德特氏菌。副百日咳博德特氏菌引起的咳嗽较轻,但通常在症状上与百日咳博德特氏菌感染相似。因此,由副百日咳博德特氏菌引起的疾病的流行病学尚不完全清楚。在本研究中,提出了一种快速诊断副百日咳博德特氏菌的灵敏且特异的方法。通过原子力显微镜(AFM)和椭偏仪研究了通过二硫键形成将巯基末端DNA寡核苷酸(单链DNA自组装单分子层)共价固定在硅表面的情况。测量结果表明,对于浓度为2μg/μl且孵育时间为24小时的情况,平均层厚度为5±0.84nm。通过将孵育时间改为48小时,对于相同浓度(2μg/μl),该厚度变为8.4±0.92nm。副百日咳博德特氏菌杂交前后记录的椭偏数据显示,对于2μg/μl的副百日咳博德特氏菌,平均颗粒面积从91nm增加到227nm,折射率从1.489变为1.648。折射率的这种变化用于评估吸附分子的数量及其密度。结果表明,副百日咳博德特氏菌附着后,吸附分子的密度分别从0.2增加到0.97g/cm。为了确认副百日咳博德特氏菌与单链DNA自组装单分子层的杂交,双链DNA自组装单分子层被变性,单链DNA自组装单分子层表面被重现,平均高度变化为6.42±0.75nm。这表明DNA膜的稳定性可以通过改变浓度和孵育时间来调节,从而提供了一种除常规使用的PCR检测之外用于副百日咳博德特氏菌无标记检测的可靠方法。

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