Evaluation of molecular inhibitors of loop-mediated isothermal amplification (LAMP)

被引:24
作者
Nwe, May Khat [1 ]
Jangpromma, Nisachon [2 ,3 ]
Taemaitree, Lapatrada [1 ]
机构
[1] Khon Kaen Univ, Fac Sci, Dept Integrated Sci, Forens Sci Program, Khon Kaen 40002, Thailand
[2] Khon Kaen Univ, Fac Sci, Prot & Prote Res Ctr Commercial & Ind Purposes Pro, Khon Kaen 40002, Thailand
[3] Khon Kaen Univ, Fac Sci, Dept Biochem, Khon Kaen 40002, Thailand
来源
SCIENTIFIC REPORTS | 2024年 / 14卷 / 01期
关键词
Loop-mediated isothermal amplification; Human DNA; Inhibitors; Forensics; REAL-TIME PCR; POLYMERASE-CHAIN-REACTION; IMMUNOGLOBULIN-G; HUMAN DNA; CALCIUM; MECHANISMS; ACID; IDENTIFICATION; URINE; BLOOD;
D O I
10.1038/s41598-024-55241-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Loop-mediated isothermal amplification (LAMP) is a cost-effective and easy-to-perform assay that enables the direct detection of DNA. Its use in point-of-care diagnostic tests is growing, while it has the potential to be used in presumptive on-the-field forensic tests. Samples are often collected from complex matrices that contain high levels of contaminants. Herein, we evaluate the effect of seven common DNA amplification inhibitors on LAMP - bile salts, calcium chloride, hematin, humic acid, immunoglobulin G, tannic acid and urea. We study the effect of each inhibitor individually in real-time detection systems coupled with end-point measurements to delineate their inhibitory effects from the matrix in which they may be found. Our studies show LAMP inhibitors generally delay the onset of amplicon formation and quench fluorescence at similar or higher concentrations compared to PCR, but that end-point measurements of LAMP amplicons are unaffected. This is important as LAMP amplicons can be detected in non-fluorometric ways thus contributing to the assertions that LAMP is more robust to inhibitors than PCR.
引用
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页数:10
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