An extraction‐free method for rapid detection of CYP2C19 * 2/3/17 polymorphisms in one tube using melting curve analysis

Author:

Guo Jianguang1,You Weixin1,Lin Kangfeng1,Li Qinghan1,Guo Xiangju1,Wang Shuai1,Bian Ya1,Ren Wenjing1,Zhang Rui2,Wang Yanping3,Li Boan1

Affiliation:

1. State Key Laboratory of Cellular Stress Biology Innovation Center for Cell Signaling Network and Engineering Research Center of Molecular Diagnostics of the Ministry of Education School of Life Sciences Xiamen University Xiamen Fujian China

2. Xiamen Cell Therapy Research Center The First Affiliated Hospital of Xiamen, University, School of Medicine, Xiamen University Xiamen China

3. Emergency Department HuBei ProvinciaI HospitaI Of TCM Wuhan China

Abstract

AbstractDrug‐metabolizing enzymes play an important role in the metabolism of drugs in vivo. Their activity is an important factor affecting the rate of drug metabolism, which directly determines the intensity and persistence of drug action. Patients taking medication can be divided into different metabolic types through detection of CYP2C19 drug‐metabolizing enzyme gene polymorphisms, which can then be used for medication guidance for clopidogrel. Here, we describe a detection method based on real‐time polymerase chain reaction (PCR). This method uses multicolor melting curve analysis to accurately identify different mutation sites and genotypes of CYP2C19 * 2, CYP2C19 * 3, and CYP2C19 * 17.The detection limit of plasmid samples was 1 copies μL−1; that of genomic samples was 0.1 ng μL−1. The system can detect nine types of CYP2C19 * 2/3/17 at three sites in one tube, quickly achieving detection within 1 h. Combined with the sample release agent, sample extraction was completed in 5 s, achieving rapid diagnosis without extraction for timely diagnosis and treatment. Furthermore, the system is not limited to blood samples and can also be applied to oropharyngeal and saliva samples, increasing sampling diversity and convenience. When using clinical blood samples (n = 93), the detection system we established was able to quickly and accurately identify different genotypes, and the accuracy and effectiveness of the detection were confirmed by Sanger sequencing.Due to its accuracy, rapidity, simple operation, and low cost, detection technology based on real‐time polymerase amplification combined with melting curve analysis is expected to become a powerful tool for detecting and guiding clopidogrel use in countries with limited resources.

Publisher

Wiley

Subject

Molecular Medicine,Applied Microbiology and Biotechnology,General Medicine

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