用于快速柑橘组织裂解和核酸提取的3d打印手持设备

IF 6.5 Q1 CHEMISTRY, ANALYTICAL
Chia-Wei Liu , Brent Kalish , Sohrab Bodaghi , Georgios Vidalakis , Hideaki Tsutsui
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引用次数: 0

摘要

开发了一种3d打印手持设备,用于快速高效的样品制备,从柑橘叶片中提取病原体总核酸,用于下游分子分析。凭借其高速电机,用于快速样品裂解的滚花裂解室,以及使用纤维素纸盘(Whatman CHR1)的快速核酸提取,该设备可以在12分钟内产生即用型DNA和RNA。除了电机,线路和纸盘外,所有组件都使用PolyJet带有光敏树脂的3D打印机进行内部打印。通过评估操作电压和腔室特征,通过使用量子比特荧光仪测量DNA和RNA浓度以及通过qPCR分析获得的定量周期(Cq)值,对该装置进行了优化,以实现最大的样品裂解。结果表明,内置滚花的裂解室和在7.5 V下工作的马达足以在1 min内有效裂解样品,其RNA浓度达到杵臼研磨的87.6%。利用NanoDrop分光光度计和qPCR对纸盘洗涤和洗脱条件进行了优化,其中两次1分钟洗涤和100µL洗脱量可获得最高纯度和最低Cq值。优化后的手持设备在柑橘源感染柑橘tristeza病毒(CTV)和柑橘螺旋体(S. citri)的柑橘源中进行了验证,显示出较高的检测准确率(100%)和较低的检测变异(CV <;3.8%)。基于这些成功的结果,该装置有望广泛应用于影响植物的类似病毒和细菌病原体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A 3D-printed handheld device for quick citrus tissue lysis and nucleic acid extraction

A 3D-printed handheld device for quick citrus tissue lysis and nucleic acid extraction
A 3D-printed handheld device has been developed for rapid and efficient sample preparation, extracting pathogen total nucleic acids from citrus leaves for downstream molecular analysis. With its high-speed motor, knurled lysis chamber for rapid sample lysis, and quick nucleic acid extraction using cellulose paper disks (Whatman CHR1), this device can yield ready-to-use DNA and RNA in just 12 min. All components, except for the motor, wiring, and paper disks, were printed in-house using a PolyJet 3D printer with photosensitive resins. The device was optimized for maximum sample lysis by evaluating operation voltages and chamber features, as measured by DNA and RNA concentrations using a Qubit fluorometer and quantification cycle (Cq) values obtained through qPCR assays. The results showed that the lysis chamber with internal knurling and the motor operated at 7.5 V was sufficient for effective sample lysis in 1 min, achieving RNA concentrations up to 87.6 % of those obtained with mortar-and-pestle grinding. Paper disk washing and elution conditions were also optimized using a NanoDrop spectrophotometer and qPCR assays, where two 1-minute washes and a 100 µL elution volume resulted in the highest purity and lowest Cq value. The optimized handheld device was validated with citrus sources infected with Citrus tristeza virus (CTV) and Spiroplasma citri (S. citri), demonstrating high detection accuracy (100 %) and low assay variation (CV < 3.8 %) in qPCR-based analysis. Based on these successful results, this device is expected to be broadly applicable to similar viral and bacterial pathogens affecting plants.
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CiteScore
3.50
自引率
0.00%
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