Wang Yi, Li Hui, Wang Yan, Zhang Lu, Xu Jianguo, Ye Changyun
State Key Laboratory of Infectious Disease Prevention and Control, National Institute for Communicable Disease Control and Prevention, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention Beijing, China.
State Key Laboratory of Infectious Disease Prevention and Control, National Institute for Communicable Disease Control and Prevention, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and PreventionBeijing, China; Department of Microbiology, GuiZhou Medical UniversityGuiyang, China.
Front Microbiol. 2017 Feb 10;8:192. doi: 10.3389/fmicb.2017.00192. eCollection 2017.
The report describes a simple, rapid and sensitive assay for visual and multiplex detection of and based on multiple loop-mediated isothermal amplification (mLAMP) and lateral flow biosensor (LFB). Detection and differentiation of the gene (-specific gene) and gene (-specific gene) were determined using fluorescein (FITC)-and digoxin-modified primers in the mLAMP process. In the presence of biotin- and FITC-/digoxin-modified primers, the mLAMP yielded numerous biotin- and FITC-/digoxin-attached duplex products, which were detected by LFB through biotin/streptavidin interaction (biotin on the duplex and streptavidin on the gold nanoparticle) and immunoreactions (FITC/digoxin on the duplex and anti-FITC/digoxin on the LFB test line). The accumulation of gold nanoparticles generated a characteristic red line, enabling visual and multiplex detection of target pathogens without instrumentation. The limit of detection (LoD), analytical specificity and feasibility of LAMP-LFB technique were successfully examined in pure culture and blood samples. The entire procedure, including specimen (blood samples) processing (30 min), isothermal reaction (40 min) and result reporting (within 2 min), could be completed within 75 min. Thus, this assay offers a simple, rapid, sensitive and specific test for multiplex detection of and strains. Furthermore, the LAMP-LFB strategy is a universal technique, which can be extended to detect various target sequences by re-designing the specific LAMP primers.
该报告描述了一种基于多重环介导等温扩增(mLAMP)和侧向流动生物传感器(LFB)的用于可视化和多重检测[具体物质1]和[具体物质2]的简单、快速且灵敏的检测方法。在mLAMP过程中,使用荧光素(FITC)和地高辛修饰的引物来确定[基因1]([具体物质1]特异性基因)和[基因2]([具体物质2]特异性基因)的检测与区分。在生物素以及FITC/地高辛修饰引物存在的情况下,mLAMP产生大量附着有生物素以及FITC/地高辛的双链产物,这些产物通过LFB利用生物素/链霉亲和素相互作用(双链上的生物素与金纳米颗粒上的链霉亲和素)以及免疫反应(双链上的FITC/地高辛与LFB检测线上的抗FITC/地高辛)进行检测。金纳米颗粒的积累产生一条特征性红线,无需仪器即可实现对目标病原体的可视化和多重检测。LAMP-LFB技术的检测限(LoD)、分析特异性和可行性在纯培养物和血液样本中得到了成功验证。整个过程,包括样本(血液样本)处理(30分钟)、等温反应(40分钟)和结果报告(2分钟内),可在75分钟内完成。因此,该检测方法为[具体物质1]和[具体物质2]菌株的多重检测提供了一种简单、快速、灵敏且特异的测试。此外,LAMP-LFB策略是一种通用技术,通过重新设计特异性LAMP引物可扩展用于检测各种目标序列。