结核分枝杆菌耐药基因变异检测的pHEAA/pMA-DNA水凝胶传感平台

IF 4.6 Q1 CHEMISTRY, ANALYTICAL
ACS Measurement Science Au Pub Date : 2025-09-04 eCollection Date: 2025-10-15 DOI:10.1021/acsmeasuresciau.5c00057
Tingting Sun, Shuhang Li, Brij Mohan, Yuanhua Yu, Wei Sun
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引用次数: 0

摘要

结核分枝杆菌耐药基因的突变给临床用药带来了挑战。传统的耐药基因检测需要进行细胞培养和药敏试验,耗时1-2周。本研究开发了一种dna敏感水凝胶(pHEAA/pMA-DNA),具有核酸结合能力、保水能力和耐高温能力,可在105℃下正常工作。分子动力学模拟已被用来获得必要的物理化学参数。该dna敏感水凝胶可作为检测结核分枝杆菌耐利福平和异烟肼基因突变的新型生物传感器。微阵列传感器的检测范围在109 ~ 101个拷贝/ml之间,稳定变异系数(CV)为2.424%。研究表明,凝胶晶格中不存在相互干扰。此外,在实际核酸样品上进行的实验也能准确检测出菌株和耐药基因突变。回归曲线符合核酸扩增动力学特征,呈s型曲线。采用四参数Logistic回归(4PL)方程进行拟合,获得了良好的决定系数(R2 = 0.99791 bb0 0.99)。该方法能够在耐多药结核分枝杆菌中并行检测微阵列生物传感器。该传感器在检测结核分枝杆菌对利福平和异烟肼的耐药突变位点方面表现出较高的效率,为研究人员在体外检测领域设计不同的探针铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
pHEAA/pMA-DNA Hydrogel Sensing Platform for Detecting Drug-Resistant Gene Variants in Mycobacterium tuberculosis.

Mutations in the drug-resistant gene ofMycobacterium tuberculosiscan make it challenging to use drugs in clinical practice. Traditional genetic testing for resistance requires cell culture and susceptibility testing, which take 1-2 weeks. In this study, a DNA-sensitive hydrogel (pHEAA/pMA-DNA) has been developed with nucleic acid binding ability, water retention capacity, and high-temperature resistance, allowing it to work normally at 105 °C. Molecular dynamics simulations have been used to obtain the necessary physicochemical parameters. The DNA-sensitive hydrogel acts as a novel biosensor for detecting rifampicin- and isoniazid-resistant gene mutations in Mycobacterium tuberculosis. The microarray sensor's detection range is between 109 copies/ml and 101 copies/mL, and its stability coefficient of variation (CV) is 2.424%. The study demonstrates that there is no mutual interference in the gel lattice. In addition, experiments on actual nucleic acid samples reveal accurate detection of bacterial strains and drug-resistant gene mutations. The regression curve conforms to the kinetic characteristics of nucleic acid amplification, exhibiting a sigmoidal shape. The Four-Parameter Logistic Regression (4PL) equation was employed for fitting, achieving an excellent coefficient of determination (R2 = 0.99791 > 0.99). The method enables parallel detection of microarray biosensors in multidrug-resistant Mycobacterium tuberculosis. The sensors show high efficiency in detecting resistance mutation sites of Mycobacterium tuberculosis to rifampicin and isoniazid, paving the way for researchers to design different probes in in vitro detection fields.

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来源期刊
ACS Measurement Science Au
ACS Measurement Science Au 化学计量学-
CiteScore
5.20
自引率
0.00%
发文量
0
期刊介绍: ACS Measurement Science Au is an open access journal that publishes experimental computational or theoretical research in all areas of chemical measurement science. Short letters comprehensive articles reviews and perspectives are welcome on topics that report on any phase of analytical operations including sampling measurement and data analysis. This includes:Chemical Reactions and SelectivityChemometrics and Data ProcessingElectrochemistryElemental and Molecular CharacterizationImagingInstrumentationMass SpectrometryMicroscale and Nanoscale systemsOmics (Genomics Proteomics Metabonomics Metabolomics and Bioinformatics)Sensors and Sensing (Biosensors Chemical Sensors Gas Sensors Intracellular Sensors Single-Molecule Sensors Cell Chips Arrays Microfluidic Devices)SeparationsSpectroscopySurface analysisPapers dealing with established methods need to offer a significantly improved original application of the method.
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