Zhang Zhang, Guan Luhao, Zhang Yue, Yao Juan, Gu Shuo
Postdoctoral Research Workstation, Department of Neurosurgery, The First Affiliated Hospital of Hainan Medical University, Haikou, Hainan, 571199, People's Republic of China.
Department of Laboratory Medicine, Luzhou Traditional Chinese Medicine Hospital, Luzhou, 646000, People's Republic of China.
J Nanobiotechnology. 2025 Jul 5;23(1):490. doi: 10.1186/s12951-025-03581-x.
Dengue virus (DENV) and Zika virus (ZIKV) are mosquito-borne viruses that cause severe health problems upon infection, necessitating timely and accurate diagnostic testing for effective prevention and control of their transmission. In this study, a novel multiplex nucleic acids detection method was introduced based on ligation-based universal primer and probe loop-mediated isothermal amplification (LUPP-LAMP) for the simultaneous detection and genotyping of DENV and ZIKV. By employing ligation of universal primers and probes using splint DNA ligase, LUPP-LAMP simplifies primer design, eliminates primer dimer formation, and achieves high sensitivity and specificity at low temperatures, with a detection limit of 10 copies/reaction. The robustness of this strategy allows for precise differentiation even at low concentrations and in cases of co-infection, which is crucial for addressing early diagnostic challenges due to similar symptoms. LUPP-LAMP is further adapted for point-of-care testing (POCT) by integrating lateral flow test strips and fluorescence imaging, offering rapid and user-friendly results in resource-limited settings. This method is also applied to DENV genotyping (serotypes 1-4) using melting curve analysis (MCA) in cases of co-infection, aiding in epidemiological surveillance and intervention strategies. In summary, LUPP-LAMP represents a significant advancement in the detection and genotyping of DENV and ZIKV, offering a versatile tool for laboratory and POCT applications, thereby enhancing public health outcomes in the control of mosquito-borne diseases.
登革病毒(DENV)和寨卡病毒(ZIKV)是蚊媒病毒,感染后会引发严重的健康问题,因此需要进行及时准确的诊断检测,以有效预防和控制其传播。在本研究中,引入了一种基于连接通用引物和探针的环介导等温扩增(LUPP-LAMP)的新型多重核酸检测方法,用于同时检测DENV和ZIKV并进行基因分型。通过使用夹板DNA连接酶连接通用引物和探针,LUPP-LAMP简化了引物设计,消除了引物二聚体的形成,并在低温下实现了高灵敏度和特异性,检测限为10拷贝/反应。该策略的稳健性使得即使在低浓度和共感染情况下也能进行精确区分,这对于应对因症状相似而带来的早期诊断挑战至关重要。通过整合侧向流动试纸条和荧光成像,LUPP-LAMP进一步适用于即时检测(POCT),在资源有限的环境中提供快速且用户友好的结果。在共感染情况下,该方法还通过熔解曲线分析(MCA)应用于DENV基因分型(血清型1-4),有助于流行病学监测和干预策略。总之,LUPP-LAMP代表了DENV和ZIKV检测及基因分型方面的重大进展,为实验室和POCT应用提供了一种多功能工具,从而在控制蚊媒疾病方面提高公共卫生成果。