School of Chemical Engineering, Clean Energy Research Center, Jeonbuk National University, 567 Baekje-daero, Deokjin-gu, Jeonju-si 54896, Jeollabuk-do, Republic of Korea.
Department of Bioprocess Engineering, Jeonbuk National University, 567 Baekje-daero, Deokjin-gu, Jeonju-si 54896, Jeollabuk-do, Republic of Korea.
Biosensors (Basel). 2024 Jan 2;14(1):26. doi: 10.3390/bios14010026.
In the context of virus outbreaks, the need for early and accurate diagnosis has become increasingly urgent. In addition to being crucial for effective disease control, timely and precise detection of viral infections is also necessary for the implementation of essential public health measures, especially during pandemics. Among these measures, point-of-care testing (POCT) stands out as a powerful approach with the potential to revolutionize the landscape of viral diagnosis. In this study, we developed a one-pot clustered regularly interspaced short palindromic repeats (CRISPR)-Cas12a-based viral DNA detection system tailored for POCT; this method utilizes multi-enzyme-modified Au@FeO nanoparticles. As an alternative to nucleic acid amplification, our method uses single-stranded DNA elongation to facilitate multi-enzyme modification; this guarantees heightened sensitivity and expedites the diagnostic process. We achieved a satisfactory limit of detection of 0.25 nM, demonstrating the remarkable sensitivity of the method without the need for sophisticated equipment. The incorporation of Au@FeO magnetic nanoparticles facilitates sample separation, further streamlining the workflow and reinforcing the simplicity of our method. This integrated approach offers a practical solution for sensitive viral DNA detection in POCT scenarios, advancing the field of rapid and accurate diagnostics.
在病毒爆发的背景下,早期和准确的诊断变得越来越紧迫。除了对有效疾病控制至关重要外,及时准确地检测病毒感染对于实施基本公共卫生措施也很必要,特别是在大流行期间。在这些措施中,即时检测(POCT)作为一种强大的方法脱颖而出,有可能彻底改变病毒诊断的格局。在这项研究中,我们开发了一种针对 POCT 的基于一锅簇状规律间隔短回文重复序列(CRISPR)-Cas12a 的病毒 DNA 检测系统;该方法利用了多酶修饰的 Au@FeO 纳米颗粒。作为核酸扩增的替代方法,我们的方法使用单链 DNA 延伸来促进多酶修饰;这保证了更高的灵敏度并加快了诊断过程。我们实现了令人满意的 0.25 nM 检测限,证明了该方法的出色灵敏度,而无需复杂的设备。Au@FeO 磁性纳米颗粒的掺入促进了样品分离,进一步简化了工作流程并增强了我们方法的简便性。这种集成方法为 POCT 场景中的敏感病毒 DNA 检测提供了实用的解决方案,推动了快速准确诊断领域的发展。