Reverse transcription loop-mediated isothermal amplification (RT-LAMP) primer design based on Indonesia SARS-CoV-2 RNA sequence

IF 3.5 Q3 Biochemistry, Genetics and Molecular Biology Journal of Genetic Engineering and Biotechnology Pub Date : 2023-12-18 DOI:10.1186/s43141-023-00580-z
Irsyad Ibadurrahman, Suryani, Desriani
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Abstract

The COVID-19 pandemic has highlighted the importance of tracking cases by using various methods such as the Reverse transcription loop-mediated isothermal amplification (RT-LAMP) which is a fast, simple, inexpensive, and accurate mass tracker. However, there have been no reports about the development of RT-LAMP primer designs that use genome sequences of viruses from Indonesia. Therefore, this study aimed to design an RT-LAMP primer using SARS-CoV-2 genome sequences from Indonesia and several other countries representing five continents in the world, as well as genomes from five Variants of Concern (VOC). The results showed that the consensus sequence of 70 SARS-CoV-2 virus sequences was obtained with a length of 29,982 bases. The phylogenetic test confirmed that the consensus sequence had a close kinship with the SARS-CoV-2 Wuhan Isolate. Furthermore, the SimPlot analysis showed that there was a high genetic diversity of sequences from the Coronaviridae tribal virus at base sequences of 1,500–5,000, 6,500–7,500, and 23,300–25,500. A total of 139 sets of primers were obtained from the primer design with 4 sets namely T1_6, T1_9, T4_7, and T4_52 having the best characteristics. Based on the secondary structure analysis test on 4 sets of primers, T1_6 and T1_9 were predicted not to form secondary structures at RT-LAMP operational temperatures. The primer set T1_9 showed better specificity in BLAST NCBI and eLAMP BLAST tests. This study obtained a primer set of T1_9 with base sequence F3: CACTGAGACTCATTGATGCTATG, B3: CCAACCGTCTCTAAGAAACTCT, F2: GTTCACATCTGATTTGGCTACT, F1c: GAAGTCAACTGAACAACACCACCT, B2: CCTTCCTTAAACTTCTCTTCAAGC, B1c: GTGGCTAACTAACATCTTTGGCACT, LB: TGAAAACAAACCCGCCGTCCTTG, which meets the ideal parameters and has the best specificity. Therefore, it is recommended for use in further tests to recognize SARS-CoV-2 from Indonesia, other five continents, as well as five VOCs, including the new Omicron sub-variant.
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基于印度尼西亚 SARS-CoV-2 RNA 序列的反转录环介导等温扩增 (RT-LAMP) 引物设计
COVID-19 大流行凸显了使用各种方法追踪病例的重要性,例如反转录环介导等温扩增法(RT-LAMP),这是一种快速、简单、廉价且准确的大规模追踪方法。然而,目前还没有关于利用印度尼西亚病毒基因组序列开发 RT-LAMP 引物设计的报道。因此,本研究旨在利用来自印度尼西亚和代表世界五大洲的其他几个国家的 SARS-CoV-2 基因组序列以及五个关注变体(VOC)的基因组设计 RT-LAMP 引物。结果显示,70 个 SARS-CoV-2 病毒序列的共识序列长度为 29 982 个碱基。系统进化检验证实,该共识序列与 SARS-CoV-2 武汉样本具有近缘关系。此外,SimPlot分析表明,冠状病毒科部落病毒序列的遗传多样性较高,碱基序列分别为1,500-5,000、6,500-7,500和23,300-25,500。引物设计共获得 139 组引物,其中 4 组引物(即 T1_6、T1_9、T4_7 和 T4_52)具有最佳特性。根据对 4 组引物的二级结构分析测试,预测 T1_6 和 T1_9 在 RT-LAMP 操作温度下不会形成二级结构。在 BLAST NCBI 和 eLAMP BLAST 测试中,引物组 T1_9 显示出更好的特异性。本研究得到的 T1_9 引物集的碱基序列为:F3:CACTGAGACTCATTGATGCTATG、B3:CCAACCGTCTCTAAGAAACTCT、F2:GTTCACATCTGATTTGGCTACT、F1c:GAAGTCAACTGAACAACACCACCT、B2:CCTTCCTTAAACTTCTCTTCAAGC、B1c:GTGGCTAACTAACATCTTTGGCACT、LB:TGAAAACAAACCCGCCGTCCTTG,符合理想参数,特异性最好。因此,建议将其用于进一步的检测,以识别来自印度尼西亚、其他五大洲以及包括新的 Omicron 亚变异体在内的五种 VOC 的 SARS-CoV-2 病毒。
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来源期刊
Journal of Genetic Engineering and Biotechnology
Journal of Genetic Engineering and Biotechnology Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
5.70
自引率
5.70%
发文量
159
审稿时长
16 weeks
期刊介绍: Journal of genetic engineering and biotechnology is devoted to rapid publication of full-length research papers that leads to significant contribution in advancing knowledge in genetic engineering and biotechnology and provide novel perspectives in this research area. JGEB includes all major themes related to genetic engineering and recombinant DNA. The area of interest of JGEB includes but not restricted to: •Plant genetics •Animal genetics •Bacterial enzymes •Agricultural Biotechnology, •Biochemistry, •Biophysics, •Bioinformatics, •Environmental Biotechnology, •Industrial Biotechnology, •Microbial biotechnology, •Medical Biotechnology, •Bioenergy, Biosafety, •Biosecurity, •Bioethics, •GMOS, •Genomic, •Proteomic JGEB accepts
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