Moutoshi Chakraborty, Shamsul Arafin Bhuiyan, Simon Strachan, Muhammad J.A. Shiddiky, Nam-Trung Nguyen, Narshone Soda, Rebecca Ford
{"title":"A Sensitive, Specific and Fast Electrochemical-based Nanobiosensor Diagnostic for Xanthomonas albilineans, the Cause of Sugarcane Leaf Scald Disease","authors":"Moutoshi Chakraborty, Shamsul Arafin Bhuiyan, Simon Strachan, Muhammad J.A. Shiddiky, Nam-Trung Nguyen, Narshone Soda, Rebecca Ford","doi":"10.1002/adsr.202400103","DOIUrl":null,"url":null,"abstract":"<p>Leaf scald (LS) caused by <i>Xanthomonas albilineans</i> (<i>Xalb</i>), 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 <i>Xalb</i> 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<sup>−1</sup>), reproducibility (Standard deviation, SD <5%, for <i>n</i> = 3), and a wide linear dynamic range (1 nM–1 fM or 10<sup>6</sup>–10° copies µL<sup>−1</sup>, <i>r</i> = 0.99). The EC assay has a strong negative correlation with quantitative polymerase chain reaction (qPCR) results (<i>r</i> = −0.95–0.97, <i>n</i> = 24, <i>p <</i> 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.</p>","PeriodicalId":100037,"journal":{"name":"Advanced Sensor Research","volume":"4 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/adsr.202400103","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Sensor Research","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/adsr.202400103","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
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.