A Sensitive, Specific and Fast Electrochemical-based Nanobiosensor Diagnostic for Xanthomonas albilineans, the Cause of Sugarcane Leaf Scald Disease

Moutoshi Chakraborty, Shamsul Arafin Bhuiyan, Simon Strachan, Muhammad J.A. Shiddiky, Nam-Trung Nguyen, Narshone Soda, Rebecca Ford
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Abstract

Leaf scald (LS) caused by Xanthomonas albilineans (Xalb), is a major bacterial disease of sugarcane. The unreliable symptom expressions make traditional visual detection challenging. The molecular methods of detection require expensive equipment, labor-intensive, and time-consuming. This study proposes a novel electrochemical (EC)-approach, that is relatively easy to use and less expensive to detect Xalb DNA in LS-infected sugarcane leaves, meristematic tissue, and xylem sap samples. This method involves three key steps: i) DNA isolation from sugarcane samples via boiling lysis; ii) magnetic purification of target sequences from the lysate using magnetic bead-bound capture probes; and iii) EC detection of the target DNA. The method shows excellent detection sensitivity (10 cells µL−1), reproducibility (Standard deviation, SD <5%, for n = 3), and a wide linear dynamic range (1 nM–1 fM or 106–10° copies µL−1, r = 0.99). The EC assay has a strong negative correlation with quantitative polymerase chain reaction (qPCR) results (r = −0.95–0.97, n = 24, p < 0.001), and weak or no correlation with the varietal resistance ratings. This EC-based assay can be a commercially viable alternative, providing a DNA isolation/purification-free solution, and can potentially be adapted into a handheld device for on-farm detection and quantification of the LS-causing pathogen.

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一种灵敏、特异、快速的电化学纳米生物传感器诊断甘蔗叶片烫伤病病原菌白脂黄单胞菌
甘蔗叶片烫伤(LS)是由白叶黄单胞菌(Xanthomonas albilineans, Xalb)引起的甘蔗主要细菌性病害。不可靠的症状表达给传统的视觉检测带来了挑战。分子检测方法需要昂贵的设备,劳动密集,耗时。本研究提出了一种新的电化学(EC)方法,该方法相对容易使用且成本较低,可用于检测ls感染的甘蔗叶片,分生组织和木质部汁液样品中的Xalb DNA。该方法包括三个关键步骤:1)通过煮沸裂解从甘蔗样品中分离DNA;Ii)利用磁珠结合捕获探针从裂解物中对目标序列进行磁纯化;iii)靶DNA的EC检测。该方法具有良好的检测灵敏度(10个细胞µL−1)、重复性(标准偏差,SD <5%, n = 3)和宽线性动态范围(1 nM-1 fM或106-10°拷贝µL−1,r = 0.99)。EC检测与定量聚合酶链反应(qPCR)结果呈显著负相关(r = - 0.95-0.97, n = 24, p <;0.001),与品种抗性等级的相关性较弱或无相关性。这种基于ec的检测方法是一种商业上可行的替代方法,它提供了一种无需DNA分离/纯化的解决方案,并且有可能被改编成一种手持式设备,用于农场检测和定量ls引起的病原体。
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