PI primers increase the efficacy of LAMP and RT-LAMP for SARS-CoV-2 and MS2 phage detection

被引:1
作者
Oscorbin, Igor P. [1 ]
Novikova, Lidiya M. [1 ]
Khrapov, Evgeniy A. [1 ]
Filipenko, Maxim L. [1 ]
机构
[1] Russian Acad Sci, Inst Chem Biol & Fundamental Med, Siberian Branch, Lab Pharmacogen, 8 Lavrentiev Ave, Novosibirsk 630090, Russia
关键词
LAMP; RT-LAMP; Additional primers; SARS-CoV-2; Inner primers; Reverse transcription; MEDIATED ISOTHERMAL AMPLIFICATION; DNA;
D O I
10.1016/j.diagmicrobio.2024.116449
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
LAMP (Loop-mediated isothermal amplification) is a popular method for the molecular diagnostics of numerous pathogens, specifically useful for point-of-care testing. However, the efficacy and sensitivity of LAMP still need to be maximised for the best performance in clinical settings. Adding a novel fourth primer pair is a promising way to accelerate the LAMP speed. Here, we report PI primers that are part of inner primers and can be used in LAMP without a specific design. PI primers were tested in quantitative LAMP detecting SARS-CoV-2 and MS2. The new primers have increased the speed and sensitivity of quantitative LAMP, RT-LAMP, and duplex LAMP with artificial templates and RNA samples from nasal swabs. Adding PI primers could become a valuable option for LAMP optimisation, especially when a desirable LAMP target is a highly variable DNA sequence with a few conservative sites for primers.
引用
收藏
页数:11
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