Department of Sericulture, Raiganj University, North Dinajpur, Raiganj, West Bengal 733134, India.
Department of Microbiology, Raiganj University, North Dinajpur, Raiganj, West Bengal 733134, India.
ACS Appl Bio Mater. 2024 Aug 19;7(8):5740-5753. doi: 10.1021/acsabm.4c00833. Epub 2024 Aug 7.
The sericulture industry suffers severe crop losses due to various silkworm diseases, necessitating the development of further technologies for rapid pathogen detection. Here, we report an all-in-one portable biosensor that combines conjugated gold nanoparticles (Au NPs) with an aptamer-based lateral flow assay (LFA) platform for the real-time analysis of sp. and sp. Our platform enables sample-to-answer naked eye detection within 5 min without any cross-reactivity with other representatives of the silkworm pathogenic bacterial group. This assay was based on the sandwich-type format using a bacteria-specific primary aptamer (Apt1) conjugated with 23 nm ± 1.27 nm Au NPs as a signal probe and another bacteria-specific secondary aptamer (Apt2)-coated nitrocellulose membrane as a capture probe. The hybridization between the signal probe and the capture probe in the presence of bacteria develops a red band in the test line, whose intensity is directly proportional to the bacterial concentration. Under the optimal experimental conditions, the visual limit of detection of the strip for sp. and sp. was 1.5 × 10 CFU/mL and 1.5 × 10 CFU/mL, respectively. Additionally, the performance of the LFA device was validated by using a colorimetric assay, and the results from the colorimetric assay are consistent with those obtained from the LFA. Our findings indicate that the developed point-of-care diagnostic device has significant potential for providing a cost-effective, scalable alternative for the rapid detection of silkworm pathogens.
养蚕业因各种蚕病而遭受严重的作物损失,因此需要开发进一步的快速病原体检测技术。在这里,我们报告了一种一体式便携式生物传感器,该传感器结合了共轭金纳米粒子(Au NPs)和基于适配体的侧流分析(LFA)平台,用于实时分析 sp. 和 sp.。我们的平台可在 5 分钟内实现无需任何交叉反应即可实现肉眼检测,并且无需与蚕致病细菌组的其他代表进行交叉反应。该测定基于夹心型格式,使用与 23nm ± 1.27nm Au NPs 共轭的细菌特异性初级适配体(Apt1)作为信号探针,以及另一个细菌特异性次级适配体(Apt2)涂覆的硝酸纤维素膜作为捕获探针。在存在细菌的情况下,信号探针和捕获探针之间的杂交会在测试线上产生红色条带,其强度与细菌浓度成正比。在最佳实验条件下,用于 sp. 和 sp. 的条带的目视检测限分别为 1.5×10 CFU/mL 和 1.5×10 CFU/mL。此外,通过比色测定法验证了 LFA 设备的性能,并且比色测定法的结果与 LFA 的结果一致。我们的研究结果表明,开发的即时诊断设备具有提供具有成本效益的、可扩展的快速检测蚕病原体替代方法的巨大潜力。