Relationship between HBV/C subgenotypes and gene mutation of core promoter, precore/core region
Zuojiong Gong
Abstract
Zuojiong Gong
Abstract
Objective To study the core promoter, precore/core region mutation of HBV/C subgenotypes and to analyze the virological features. Methods A total of 79 sera of HBV/C genotype were chosen by the enzyme-linked immunosobent assay (ELISA). Then HBV/C strains were subtyped by polymerase chain reactioin and restricion fragment length polymporphism (PCR-RFLP), and their HBV DNA sequences bearing the core promoter, precore/core region were amplified by hemi-nested PCR, products thereof were directly sequenced. Results (1) Among 79 sera of HBV/C, 33 (41.8%) of subtype HBV/C1 and 46 (58.2%) of subtype HBV/C2 were detected. (2)The HBV/C1 was found only in patients from Southern China. (3) Prevalence of V1753 was higher in HBV/C1 strains (P0.04), A1898 was only found among HBV/C1. HBV/C2 distinguished by frequently found T1858 (90%) and A1896 (40%). T1762/A1764 was frequent in both subgenotypes. (3) Mutations associated with HCC in the present study were V1753 and T1762/A1764. Conclusions HBV/C1 and HBV/C2 have distinct geographic distribution in China. V1753 in addition to T1762/A1764 double mutation would be associated with HCC development, especially among patients with HBV/C1.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To study the core promoter, precore/core region mutation of HBV/C subgenotypes and to analyze the virological features. Methods A total of 79 sera of HBV/C genotype were chosen by the enzyme-linked immunosobent assay (ELISA). Then HBV/C strains were subtyped by polymerase chain reactioin and restricion fragment length polymporphism (PCR-RFLP), and their HBV DNA sequences bearing the core promoter, precore/core region were amplified by hemi-nested PCR, products thereof were directly sequenced. Results (1) Among 79 sera of HBV/C, 33 (41.8%) of subtype HBV/C1 and 46 (58.2%) of subtype HBV/C2 were detected. (2)The HBV/C1 was found only in patients from Southern China. (3) Prevalence of V1753 was higher in HBV/C1 strains (P0.04), A1898 was only found among HBV/C1. HBV/C2 distinguished by frequently found T1858 (90%) and A1896 (40%). T1762/A1764 was frequent in both subgenotypes. (3) Mutations associated with HCC in the present study were V1753 and T1762/A1764. Conclusions HBV/C1 and HBV/C2 have distinct geographic distribution in China. V1753 in addition to T1762/A1764 double mutation would be associated with HCC development, especially among patients with HBV/C1.
Key concepts: Virology, Hepatitis B virus, Genotype, Promoter, Mutation, Nested polymerase chain reaction, Polymerase chain reaction, Biology