Yu Qing, Li Jiaxuan, Zheng Shuai, Hu Yajin, Tian Benshun, Lu Meirou, Gu Bing, Wang Chongwen
Department of Clinical Laboratory Medicine, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, 510006, China.
School of Medicine, South China University of Technology, Guangzhou, Guangdong, 510000, China.
Adv Sci (Weinh). 2025 Aug;12(31):e2502574. doi: 10.1002/advs.202502574. Epub 2025 May 8.
Rapid, sensitive, and accurate detection of respiratory pathogens is essential yet challenging. Here, this study presents a universal nanozyme immunochromatographic assay (ICA) that utilizes the broad binding capacity of 4-mercaptophenylboronic acid (MPBA) for glycosylated molecules on bacterial and viral surfaces, along with the colorimetric-catalytic dual enhancement capability of multi-tentacle magnetic nanozyme (FeAu@AuIr), to achieve ultrasensitive, wide-range, and simultaneous detection of multiple respiratory pathogens. The virus-like biomimetic FeAu@AuIr with multi-tentacle shell is prepared by sequentially assembling a layer of large Au nanoparticles and a layer of highly catalytic 5 nm AuIr nanoparticles on 160 nm FeO surface, greatly enhancing the universal capture/detection capability of detection system for both bacteria and virus. By simultaneously detecting two significant respiratory bacteria (Streptococcus pneumoniae and Pseudomonas aeruginosa) and one respiratory virus (Severe Acute Respiratory Syndrome Coronavirus 2), this study demonstrates that combination of FeAu@AuIr-MPBA probe and antibody-modified ICA strips can achieve ultrasensitive and highly specific detection of different respiratory pathogens, with sensitivity and detection range improved by more than 238 times compared to existing colorimetric ICA methods. Moreover, the practical utility of the FeAu@AuIr-based ICA is validated through testing 170 positive clinical respiratory samples, underscoring its considerable potential for real-time pathogen detection in both clinical and field settings.
快速、灵敏且准确地检测呼吸道病原体至关重要但具有挑战性。在此,本研究提出了一种通用的纳米酶免疫层析检测法(ICA),该方法利用4-巯基苯硼酸(MPBA)对细菌和病毒表面糖基化分子的广泛结合能力,以及多触角磁性纳米酶(FeAu@AuIr)的比色催化双重增强能力,实现对多种呼吸道病原体的超灵敏、宽范围和同时检测。通过在160nm的FeO表面依次组装一层大尺寸金纳米颗粒和一层高催化活性的5nm AuIr纳米颗粒,制备出具有多触角外壳的病毒样仿生FeAu@AuIr,大大增强了检测系统对细菌和病毒的通用捕获/检测能力。通过同时检测两种重要的呼吸道细菌(肺炎链球菌和铜绿假单胞菌)和一种呼吸道病毒(严重急性呼吸综合征冠状病毒2),本研究表明FeAu@AuIr-MPBA探针与抗体修饰的ICA试纸条相结合,能够实现对不同呼吸道病原体的超灵敏和高特异性检测,与现有的比色ICA方法相比,灵敏度和检测范围提高了238倍以上。此外,通过对170份临床呼吸道阳性样本进行检测,验证了基于FeAu@AuIr的ICA的实际应用价值,突出了其在临床和现场环境中实时病原体检测的巨大潜力。