Assessment and preliminary clinical application of a domestic nucleic acid detection reagent for hepatitis D virus
10.3760/cma.j.cn114452-20231130-00315
- VernacularTitle:国产丁型肝炎病毒核酸检测试剂的性能评估和初步临床应用
- Author:
Yongcong LI
1
;
Rongchen YUAN
;
Kuanhui XIANG
;
Guomin OU
;
Tianxun HUANG
;
Fangming CHENG
;
Zhenchao TIAN
;
Xiongwei LIU
;
Xiaozhong WANG
;
Feng GUO
;
Yahong MA
;
Jing ZHOU
;
Erhei DAI
;
Bangning CHENG
;
Tong LI
;
Tao SHEN
;
Chungen QIAN
Author Information
1. 北京大学-亚辉龙感染性疾病分子诊断联合实验室，北京 100191
- Keywords:
Hepatitis D virus;
RNA virus;
RT-qPCR;
Diagnosis;
Quality evaluation
- From:
Chinese Journal of Laboratory Medicine
2024;47(3):239-244
- CountryChina
- Language:Chinese
-
Abstract:
Objective:This study aims to evaluate the quality and explore the preliminary clinical applications of a domestically developed hepatitis D virus nucleic acid quantification reagent (abbreviated as"domestic HDV RNA reagent").Methods:The sensitivity and accuracy of the reagent were evaluated in accordance with the WHO HDV RNA international standard, employing the Bio-Rad CFX Opus 96 real-time fluorescence quantitative PCR analysis system. Serial dilutions of pseudo-viruses or cell culture-derived virus were used to determine the linear range of the domestic HDV RNA reagent. Specificity was assessed using positive samples of HAV, HBV, HCV infection, and HEV national reference materials. Precision was evaluated with samples at both high and low concentrations. In a comparative analysis, 30 HDV IgG positive samples were tested using both the domestic HDV RNA reagent and the RoboGene HDV RNA kit based on the ABI 7500 FAST DX system. The Pearson correlation coefficient (r) was used to examine the correlation between the two reagents.Results:The domestic HDV RNA reagent demonstrated a high sensitivity of up to 6 IU/ml, consistent with that of the comparator reagent. The calibration curve for WHO HDV RNA standards had a slope of -3.286, with an amplification efficiency of 101.6%. The linear detection range spanned from 10 to 10 8 IU/ml for eight HDV genotypes. The domestic HDV RNA reagent exhibited exceptional specificity, without cross-reactivity observed with HAV, HBV, HCV, or HEV. Accuracy assessments at five concentration levels met the required standards, with intra-assay precision coefficient of variation ( CV) ranging from 1.20% to 4.20%, and inter-assay precision CV from 1.20% to 7.90%. The detection results for HDV IgG positive samples were highly correlated with the comparator reagent ( r=0.984, P<0.001), achieving a diagnostic accuracy of 100% compared to sequencing results. Conclusion:In this study, the domestic HDV RNA reagent possesses excellent specificity, accuracy, precision, and a broad linear range, attaining a sensitivity level on par with international reagents of the same type.
