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重型肝炎时乙型肝炎病毒基因型与基本核心启动子及前C区突变关系的研究
引用本文:许正锯,杨红,陈先礼,沈建坤,张启华,王崇国. 重型肝炎时乙型肝炎病毒基因型与基本核心启动子及前C区突变关系的研究[J]. 中华实验和临床病毒学杂志, 2006, 20(3): 229-231
作者姓名:许正锯  杨红  陈先礼  沈建坤  张启华  王崇国
作者单位:1. 362000,福建泉州,解放军第180医院南京军区临床肝病中心一病区
2. 362000,福建泉州,解放军第180医院肝病中心实验室
基金项目:志谢本课题部分工作在北京大学人民医院肝病研究所完成,杜绍财研究员给予大力支持和帮助.
摘    要:目的探讨重型肝炎(重肝)乙型肝炎病毒(HBV)基因型与基本核心启动子(BCP)及前C区突变的关系。方法采用聚合酶链反应(PCR)-限制性片段长度多态性分析技术(PCR-RFLP)对52例重肝和52例慢性乙肝(CHB)进行HBV基因分型。采用PCR产物直接测序技术,随机对15例B型和15例C型重肝患者的BCP区和前C区进行序列测定,分析HBV基因型与BCPT1762/A1764及前C区A1896突变的关系。结果泉州地区重肝的基因型以B型为主(48.08%),其次为C型(30.77%)和B/C混合型(17.31%),无A、E、F型存在。与CHB组比较,重肝组B型检出率明显降低,而C型和BIC混合型检出率明显升高。C型重肝患者BCPT1762/A1764双突变率显著高于B型(P〈0.05),而前C区A1896突变率在B、C型感染者中差异无统计学意义(P〉0.05)。结论C型感染易引起较重肝损伤,而B/C型混合感染可能是导致重肝发生的重要原因之一。C型重肝患者BCP T1762/A1764双突变率显著高于B型。

关 键 词:肝炎病毒 乙型 基因型 聚合酶链反应 多态性 限制性片段长度 启动区(遗传学) 突变
收稿时间:2005-04-29
修稿时间:2005-04-29

Relationship between hepatitis B virus genotypes and basic core promoter/precore mutations in patients with severe hepatitis
XU Zheng-ju,YANG Hong,CHEN Xian-li,SHEN Jian-kun,ZHANG Qi-hua,WANG Chong-guo. Relationship between hepatitis B virus genotypes and basic core promoter/precore mutations in patients with severe hepatitis[J]. Chinese journal of experimental and clinical virology, 2006, 20(3): 229-231
Authors:XU Zheng-ju  YANG Hong  CHEN Xian-li  SHEN Jian-kun  ZHANG Qi-hua  WANG Chong-guo
Affiliation:Clinical Liver Diseases Research Center of Nanjing Military Command, The No.180 Hospital of The People's Liberation Army, Quanzhou 362000, China. Corresponding author: XU Zheng-ju, E-mail: h180@163.com.
Abstract:Objective To investigate the relationship between hepatitis B virus genotypes and basic core promoter (BCP)/precore mutations in patients with severe hepatitis.Methods HBV genotypes were determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) in 52 patients with severe hepatitis and 52 cases with chronic hepatitis B (CHB). Eight samples of genotypes B and C were randomly selected and their S gene was directly sequenced, and then their phylogenetic trees were analyzed. Fifteen samples of each of genotypes B and C were randomly selected and their BCP and precore genes were directly sequenced with PCR, and then the relationship between genotypes and BCP(T1762/A1764)/precore (A1896)mutations were analyzed. Results Genotype B,C and mixed genotypes (B and C) were detected in patients with severe hepatitis in Quanzhou area. Genotype B was the majority with a proportion 48.08%,others had a proportion 30.77% and 17.31%,respectively. Genotype A, E and F were not detected. The percents of genotype C, mixed B and C in severe hepatitis were significantly higher than that in CHB. The double mutation in BCP (T1762/A1764) was significantly more frequent in severe hepatitis with genotype C than that in genotype B (P<0.05). However, there was no significant difference in the distribution of precore mutant with A1896 between genotype B and C patients (P>0.05).Conclusions Genotype C may induce more severe liver inflammation than that genotype B may do. Mixed genotypes B and C infection may be an important determinant of inducing severe hepatitis. The double mutation in BCP (T1762/A1764) was more common in severe hepatitis with genotype C than that with genotype B.
Keywords:Hepatitis B virus  Genotype  Polymerase chain reaction  Polymorphism  restriction fragment length  Promoter regions (Genetics)  Mutation
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