Zhu Afang, Ahmad Waqas, Xu Yi, Wei Wenya, Jiao Tianhui, Ouyang Qin, Chen Quansheng
School of Food and Biological Engineering, Jiangsu University, Zhenjiang 212013, PR China.
College of Ocean Food and Biological Engineering, Jimei University, Xiamen 361021, PR China.
Talanta. 2025 May 1;286:127458. doi: 10.1016/j.talanta.2024.127458. Epub 2024 Dec 26.
Staphylococcus aureus (S. aureus) has been identified as a indicator of food contamination. In this study, a sensitive and accurate biosensor strategy for S. aureus through rolling circle amplification-assisted surface-enhanced Raman scattering (RCA-assisted-SERS), has been established. The work relies on the interaction between the aptamer and its partial complementary DNA strands fabricated on the surface of gold and silver-assisted magnetic microspheres and the subsequent detachment to trigger the activation of the RCA process. In RCA, template DNA, T4 DNA ligase, and Phi29 DNA polymerase were assembled to form long single-stranded DNA containing repetitive sequences. The gold core encapsulated with a layer of 4-nitrothiophenol and further covered with a silica shell was employed as the SERS nanoprobe (Au@NTP@SiO). Subsequently, the output and amplification of SERS signal were performed by hybridizing ssDNA functionalized Au@NTP@SiO to realize the quantitative detection of S. aureus. Under the optimal conditions, S. aureus sensing was monitored (36.0-3.6 × 10 cfu/mL) with a limit of detection of 2.0 cfu/mL. This strategy was further validated for S. aureus recognition in spiked real samples with favorable recoveries (94.0-103.4 %) at p > 0.05. The suggested RCA-assisted SERS approach exhibits potential for multiple foodborne pathogens in both food safety and biomedical investigations.
金黄色葡萄球菌已被确定为食品污染的一个指标。在本研究中,通过滚环扩增辅助表面增强拉曼散射(RCA辅助-SERS)建立了一种用于检测金黄色葡萄球菌的灵敏且准确的生物传感器策略。这项工作依赖于适配体与其在金和银辅助磁性微球表面构建的部分互补DNA链之间的相互作用以及随后的分离,以触发RCA过程的激活。在RCA中,模板DNA、T4 DNA连接酶和Phi29 DNA聚合酶组装形成含有重复序列的长单链DNA。以包裹有一层4-硝基硫酚并进一步覆盖有二氧化硅壳的金核作为SERS纳米探针(Au@NTP@SiO)。随后,通过将功能化的单链DNA与Au@NTP@SiO杂交来进行SERS信号的输出和放大,以实现对金黄色葡萄球菌的定量检测。在最佳条件下,监测金黄色葡萄球菌的检测范围为(36.0 - 3.6×10 cfu/mL),检测限为2.0 cfu/mL。该策略在加标的实际样品中对金黄色葡萄球菌的识别进一步得到验证,在p > 0.05时回收率良好(94.0 - 103.4%)。所提出的RCA辅助SERS方法在食品安全和生物医学研究中对多种食源性病原体具有应用潜力。