R Nazari-Vanani, G H Tondro, R Dehdari Vais, M Haghkhah, H Heli, N Sattarahmady
MSc, Nanomedicine and Nanobiology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
PhD, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
J Biomed Phys Eng. 2020 Jun 1;10(3):307-318. doi: 10.31661/jbpe.v0i0.1912-1018. eCollection 2020 Jun.
(MTB) is a pathogen causing tuberculosis (TB) in human, and TB can cause enormous social and economic disruptions. Lateral flow test strips (LFTSs) are inexpensive, portable, disposable, rapid, and easy-to-use analytical tools.
LFTSs were prepared for the detection of MTB. LFTSs were fabricated using a new specific probe for MTB H37Rv, based on IS6110 sequence gene, and tailed with poly deoxyadenine (dA).
In this experimental study, to create test and control zones, streptavidin (STP) and a 150-mer dA were dotted on a nitrocellolose membrane. Gold nanoparticles (GNPs) were conjugated with poly deoxythymidine sequence and placed on the conjugate pad. The composition of immersion buffers for sample pad and conjugate pad, running solution, solutions of GNPs-S-dT150 and STP were introduced. DNA genome of MTB and in clinical samples was amplified with PCR, and then detected by the LFTSs. During the assay, samples were firstly hybridized in two steps and then placed on a conjugate pad in a manner that positive and negative samples provided two and one red lines, respectively, on the detection pad.
After PCR reaction with biotinylated primer, hybridization process with specific MTB probe-dA70-100 toke 10 min, and running process on the strip was performed within 5 min.
We showed that LFTS can discriminate a particular bacteria strain from others. The LFTSs can be redesigned for detection of other pathogenic genomes.
结核分枝杆菌(MTB)是导致人类结核病(TB)的病原体,结核病会造成巨大的社会和经济破坏。侧向流动试纸条(LFTSs)是廉价、便携、一次性、快速且易于使用的分析工具。
制备用于检测MTB的LFTSs。基于IS6110序列基因,使用针对MTB H37Rv的新型特异性探针制备LFTSs,并在其末端接上聚脱氧腺嘌呤(dA)。
在本实验研究中,为创建测试区和对照区,将链霉亲和素(STP)和150聚体dA点样于硝酸纤维素膜上。将金纳米颗粒(GNPs)与聚脱氧胸苷序列偶联,并置于结合垫上。介绍了样品垫和结合垫的浸泡缓冲液、运行液、GNPs-S-dT150和STP溶液的组成。用PCR扩增MTB的DNA基因组及临床样本中的DNA基因组,然后用LFTSs进行检测。在检测过程中,样品首先分两步进行杂交,然后以阳性和阴性样品在检测垫上分别产生两条和一条红线的方式置于结合垫上。
用生物素化引物进行PCR反应后,与特异性MTB探针-dA70-100的杂交过程耗时10分钟,试纸条上的运行过程在5分钟内完成。
我们证明了LFTSs可以区分特定的细菌菌株与其他菌株。LFTSs可以重新设计用于检测其他致病基因组。