Detection of drug resistance genes of mycobacterium tuberculosis by rolling circle amplification technique with multicolor fluorescent probes.
10.3760/cma.j.cn112150-20210813-00788
- VernacularTitle:多色荧光探针的滚环扩增技术检测结核分枝杆菌耐药基因
- Author:
Ke XIA
1
;
Meng Ya LI
1
;
Hui Yan TIAN
1
;
Guo Rong HUANG
1
;
Feng Xin XIE
1
;
Yang ZHANG
2
;
Wei Ling FU
1
Author Information
1. Department of Laboratory Medicine, First Affiliated Hospital, Army Medical University, Chongqing 400038, China.
2. Department of Laboratory Medicine, Chongqing University Cancer Hospital, Chongqing 400030, China.
- Publication Type:Journal Article
- MeSH:
Drug Resistance;
Fluorescent Dyes;
Humans;
Mycobacterium tuberculosis/genetics*;
Nucleic Acid Amplification Techniques
- From:
Chinese Journal of Preventive Medicine
2022;56(1):56-62
- CountryChina
- Language:Chinese
-
Abstract:
The aim of this study was to construct a simple, rapid and ultra-sensitive optical biosensing technique based on rolling circle amplification (RCA), and to apply it to multiple detection of drug-resistant genes of mycobacterium tuberculosis. The common mutation sites of isoniazid, rifampicin and streptomycin resistance genes are katG315 (AGC➝ACC), rpoB531 (CAC➝TAC) and rpsL43 (AAG➝AGG). For these three gene sites, from February 2020 to May 2021, in the Department of Laboratory Medicine of the First Affiliated Hospital of Army Military Medical University, the padlock probe (PLP), primers and capture probes were designed. And a solid-phase RCA constant temperature amplification reaction system based on magnetic beads was constructed and the experimental parameters were optimized. The RCA products were accurately captured by the multicolor fluorescent probes (Cy3/Cy5/ROX), and the single-tube multiple detection of three mutation genes was realized. The sensitivity, specificity and linear range of this method were further verified. The results showed that the response range of katG315 in the same reaction system ranged from 1.0 pmol/L to 0.1 nmol/L. The response range of rpoB531 and rpsL43 ranged from 1.0 pmol/L to 50.0 pmol/L and 1.0 pmol/L to 20.0 pmol/L, and the method had good specificity and sensitivity, and could accurately identify single base mutations in mixed targets, with the minimum detection limit as low as 1.0 pmol/L. The recoveries of simulated serum samples were 95.0%-105.2%. In conclusion, the constant temperature amplification multiple detection method constructed in this study can quickly realize the single-tube multiple detection of three drug resistance mutation sites. This technology is low-cost, simple and rapid, and does not rely on large equipment, providing a new analysis method for pathogen drug resistance gene detection.
