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Establishment and Evaluation of a Novel Method Based on Loop-Mediated Isothermal Amplification for the Rapid Diagnosis of Thalassemia Genes

机译:基于环介导等温扩增的新型方法的建立与评价,以便快速诊断炎基因

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Purpose: Currently, thalassemia is commonly detected using gap-polymerase chain reaction (PCR) and deoxyribonucleic acid (DNA) reverse dot blot, which have high requirements of space, instruments, and personnel. Therefore, it is necessary to develop a new method for thalassemia detection with high sensitivity, low cost, and simple and fast operation. In this study, we aimed to design and evaluate a new method for detecting three α-thalassemia genes including –Southeast Asian (SEA), -α 3.7, and -α 4.2 and five β-thalassemia genes including 654M, 41/42M, ? 28M, 17M, and 27/28M based on loop-mediated isothermal amplification (LAMP). Methods: Primer sequences were designed using Primer Explorer V4 software. Blood samples (5 mL) were collected from all participants in EDTA. DNA was extracted using Chelex 100 and was subjected to LAMP. LAMP products were detected by fluorescence development in ultraviolet light. Results: We found that LAMP assays for positive samples of thalassemia reached a plateau before 60 minutes, whereas the negative control samples entered the plateau after 70 minutes or showed no amplification. The concentration range of positive reactions was between 20– 60 pg/μL and 20– 60 ng/μL. Additionally, there were no cross-reactivities among 8 thalassemia subtypes. For clinical samples, the positive sample tube showed strong green fluorescence, whereas the negative tube showed light green fluorescence. According to these results, the LAMP method has high sensitivity for detecting thalassemia (252/254). However, 43 false-positive results were obtained in the LAMP test. The LAMP assay was also?of low cost and with simple and fast operation. Conclusion: The novel LAMP assay can be completed within 60 min using a heating block or a water bath, and the result can be read visually based on color change to detect thalassemia. The LAMP assay fulfills the requirements of field application and resource-limited areas, especially those with primary hospitals and rural areas.
机译:目的:目前,使用间隙聚合酶链式反应(PCR)和脱氧核糖核酸(DNA)反向点印迹通常检测地月地血症,其具有高要求的空间,仪器和人员。因此,有必要开发一种具有高灵敏度,低成本和简单和快速运行的新血症检测方法。在这项研究中,我们旨在设计和评估一种检测三个α-zhalassemia基因的新方法,包括-soutound亚洲(海洋),-α3.7,-α4.2和5β-zhalassemia基因,包括654m,41 / 42m,?基于环介导的等温扩增(灯)28M,17M和27 / 28M。方法:使用Primer Explorer V4软件设计底漆序列。从EDTA的所有参与者收集血样(5mL)。使用Chelex 100提取DNA并进行灯。紫外光荧光发育检测到灯产品。结果:我们发现,在60分钟之前达到高原的阳性样本的灯测定,而阴性对照样品在70分钟后进入高原或没有扩增。阳性反应的浓度范围为20-60pg /μl和20-60ng /μl。另外,8个月的亚型亚型中没有交叉反射症。对于临床样品,正样管显示出强大的绿色荧光,而负管显示浅绿色荧光。根据这些结果,灯法具有高灵敏度,用于检测地中海贫血(252/254)。但是,在灯测试中获得了43种假阳性结果。灯泡测定也是多少?低成本,操作简单,操作简单。结论:新型灯测定可以使用加热块或水浴在60分钟内完成,结果可以基于颜色变化来视觉读取以检测到亚血症。灯泡测定满足现场应用和资源有限的领域的要求,尤其是有小医院和农村地区的要求。

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