Yajima Shuto, Koto Ayako, Koda Maho, Sakamoto Hiroaki, Takamura Eiichiro, Suye Shin-Ichiro
Department of Frontier Fiber Technology and Science, Graduate School of Engineering, University of Fukui, 3-9-1, Bunkyo, Fukui 910-8507, Japan.
Department of Advanced Interdisciplinary Science and Technology, Graduate School of Engineering, University of Fukui, 3-9-1, Bunkyo, Fukui 910-8507, Japan.
ACS Omega. 2022 Apr 6;7(15):12701-12706. doi: 10.1021/acsomega.1c07012. eCollection 2022 Apr 19.
Polymerase chain reaction (PCR) assays are used to diagnose various infectious diseases such as Coronavirus disease 2019 by detecting the nucleic acids of the pathogen. However, in practice, the yield of the extraction process and the inhibition of the reverse transcription reaction and PCR by foreign substances reduce the sensitivity and may yield false negative results. The sensitivity of the PCR test can be improved by using technologies that can reliably capture the target nucleic acid and remove foreign substances. In this study, we developed photo-cross-linkable probe-modified magnetic particles (PPMPs) for the sequence-specific recovery of target nucleic acids using photo-cross-linkable artificial nucleic acid probes and magnetic particles. Nucleic acid probes modified with photo-cross-linkable artificial nucleic acids can hybridize with the target nucleic acids in a sequence-specific manner and then securely capture the target nucleic acids by UV irradiation-mediated covalent bonding. Then the target nucleic acid is detected by trapping the target-bound probe on the surface of the magnetic particles and subjecting these collected magnetic particles to PCR. Recovery of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) N gene pseudo-DNA (120 bp) was performed using PPMPs. We confirmed that the PPMPs captured the target consistently even after washes were done with denaturing agents and surfactants. Even in the presence of foreign DNA fragments, PPMPs were able to specifically recover the target DNA. This method allows for a more accurate detection by recovering only the target DNA for PCR. Hence, PPMPs can be successfully used for PCR-mediated detection of SARS-CoV-2 and other pathogens whose nucleic acid sequences are known.
聚合酶链反应(PCR)检测法通过检测病原体的核酸来诊断各种传染病,如2019冠状病毒病。然而,在实际操作中,提取过程的产量以及外源物质对逆转录反应和PCR的抑制会降低灵敏度,并可能产生假阴性结果。使用能够可靠捕获目标核酸并去除外源物质的技术,可以提高PCR检测的灵敏度。在本研究中,我们利用可光交联的人工核酸探针和磁性颗粒,开发了用于序列特异性回收目标核酸的可光交联探针修饰磁性颗粒(PPMPs)。用可光交联人工核酸修饰的核酸探针能够以序列特异性方式与目标核酸杂交,然后通过紫外线照射介导的共价键合牢固地捕获目标核酸。然后,通过将与目标结合的探针捕获在磁性颗粒表面,并对这些收集的磁性颗粒进行PCR来检测目标核酸。使用PPMPs对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)N基因假DNA(120 bp)进行了回收。我们证实,即使在用变性剂和表面活性剂洗涤后,PPMPs仍能持续捕获目标。即使存在外源DNA片段,PPMPs也能够特异性地回收目标DNA。该方法通过仅回收用于PCR的目标DNA,实现了更准确的检测。因此,PPMPs可成功用于PCR介导的SARS-CoV-2及其他核酸序列已知的病原体的检测。