Department of Biomedical Engineering, University of Connecticut Health Center, 263 Farmington Avenue, Farmington, CT, 06030, USA.
Electrical and Computer Engineering, University of Texas at Austin, Austin, TX, 78712, USA.
Sci Rep. 2020 Nov 2;10(1):18819. doi: 10.1038/s41598-020-75795-y.
Fluorescence detection of nucleic acid isothermal amplification utilizing energy-transfer-tagged oligonucleotide probes provides a highly sensitive and specific method for pathogen detection. However, currently available probes suffer from relatively weak fluorescence signals and are not suitable for simple, affordable smartphone-based detection at the point of care. Here, we present a cleavable hairpin beacon (CHB)-enhanced fluorescence detection for isothermal amplification assay. The CHB probe is a single fluorophore-tagged hairpin oligonucleotide with five continuous ribonucleotides which can be cleaved by the ribonuclease to specifically initiate DNA amplification and generate strong fluorescence signals. By coupling with loop-mediated isothermal amplification (LAMP), the CHB probe could detect Borrelia burgdorferi (B. burgdorferi) recA gene with a sensitivity of 100 copies within 25 min and generated stronger specific fluorescence signals which were easily read and analysed by our programmed smartphone. Also, this CHB-enhanced LAMP (CHB-LAMP) assay was successfully demonstrated to detect B. burgdorferi DNA extracted from tick species, showing comparable results to real-time PCR assay. In addition, our CHB probe was compatible with other isothermal amplifications, such as isothermal multiple-self-matching-initiated amplification (IMSA). Therefore, CHB-enhanced fluorescence detection is anticipated to facilitate the development of simple, sensitive smartphone-based point-of-care pathogen diagnostics in resource-limited settings.
利用能量转移标记寡核苷酸探针的荧光检测核酸等温扩增提供了一种高度敏感和特异的病原体检测方法。然而,目前可用的探针具有相对较弱的荧光信号,不适合在简单、经济实惠的基于智能手机的即时检测中使用。在这里,我们提出了一种可切割发夹式 beacon(CHB)增强的荧光检测用于等温扩增分析。CHB 探针是一种带有 5 个连续核糖核苷酸的单荧光标记发夹寡核苷酸,可被核糖核酸酶切割,以特异性地启动 DNA 扩增并产生强烈的荧光信号。通过与环介导的等温扩增(LAMP)相结合,CHB 探针可以检测到伯氏疏螺旋体(B. burgdorferi)recA 基因,其灵敏度为 25 分钟内 100 个拷贝,并且产生的特异性荧光信号更强,可通过我们编程的智能手机轻松读取和分析。此外,该 CHB 增强的 LAMP(CHB-LAMP)检测已成功用于检测从蜱种中提取的伯氏疏螺旋体 DNA,与实时 PCR 检测结果相当。此外,我们的 CHB 探针与其他等温扩增方法兼容,如等温多重自匹配引发扩增(IMSA)。因此,CHB 增强的荧光检测有望促进在资源有限的环境中开发简单、灵敏的基于智能手机的即时检测病原体诊断方法。