Establishment of a droplet digital PCR method for the detection of hepatitis B virus covalently closed circular DNA
DOI:10.3969/j.issn.1001-5256.2021.08.013
- VernacularTitle:基于微滴数字PCR技术建立HBV共价闭合环状DNA的检测方法
- Author:
Yuan TIAN
1
;
Ling XU
;
Zihao FAN
;
Yaling CAO
;
Xiangying ZHANG
;
Yu CHEN
;
Zhongping DUAN
;
Feng REN
Author Information
1. Beijing YouAn Hospital, Capital Medical University, Beijing Institute of Hepatology, Beijing 100069, China
- Publication Type:Research Article
- Keywords:
Hepatitis B Virus;
DNA, Circular;
Droplet Digital PCR
- From:
Journal of Clinical Hepatology
2021;37(8):1806-1810.
- CountryChina
- Language:Chinese
-
Abstract:
ObjectiveTo establish a droplet digital PCR (ddPCR) method for detecting hepatitis B virus (HBV) covalently closed circular DNA (cccDNA). MethodsHBV cccDNA standard substance was constructed, and HBV cccDNA primers and probes were designed based on the structural differences between HBV cccDNA and relaxed circular DNA (rcDNA). HBV plasmid was amplified to obtain HBV cccDNA standard substance, and a ddPCR detection method was established with the standard substance after gradient dilution as the template for HBV cccDNA detection; the limit of detection and repeatability of this method were analyzed. Liver tissue samples were collected from 20 patients who attended Beijing YouAn Hospital, Capital Medical University, from June 2017 to October 2020, all of whom were diagnosed with HBV infection, and DNA of the samples was extracted and digested with plasmid-safe ATP-dependent DNA enzyme to obtain HBV cccDNA template; the ddPCR detection method was evaluated in clinical samples and was compared with the quantitative real-time PCR (qPCR) detection method. The chi-square test was used for comparison of categorical data between the two groups. ResultsThe HBV cccDNA detection method based on ddPCR was established, which accurately detected HBV cccDNA in standard substance after gradient dilution, with a limit of detection of 1 copy/μl, and the coefficients of variation of 1×103, 1×102, and 1×101 copies/μl standard substances were 441%, 3.98%, and 5.09%, respectively. HBV cccDNA was detected in the samples of 20 patients with HBV infection; the ddPCR detection method detected HBV cccDNA in 17 patients, with a positive rate of 85%, while the qPCR detection method detected HBV cccDNA in 11 patients, with a positive rate of 55%, and there was a significant difference between the two methods (χ2=4.286, P=0038). ConclusionThe established ddPCR method for detecting HBV cccDNA has a low limit of detection and good repeatability, which provides an effective tool for further clinical detection.
