Core Promoter and Pre-Core Variants of the Hepatitis B Virus (HBV) Are Frequent in Chronic Hepatitis B HBeAg-Negative Patients Infected by Genotypes A and D

被引:0
|
作者
Reuter, Tania [1 ,2 ]
Gomes-Gouvea, Michele Soares [2 ]
Chuffi, Samira [2 ]
Duque, Ulisses Horst [1 ]
Perini, Waltesia [1 ]
Azevedo, Raymundo Soares [3 ]
Pinho, Joao Renato Rebello [2 ,4 ,5 ]
Lewis-Ximenez, Lia L.
Villar, Livia Melo
Espul, Carlos Alberto
Pujol, Flor H.
Roman, Sonia
机构
[1] Univ Fed Espirito Santo, Univ Hosp Cassiano Antonio de Moraes, Hlth Sci Ctr, Internal Med Dept, BR-29041295 Vitoria, ES, Brazil
[2] Univ Sao Paulo, Sch Med, Inst Trop Med, Dept Gastroenterol,LIM 07, BR-05403907 Sao Paulo, SP, Brazil
[3] Univ Sao Paulo, Sch Med, Dept Pathol, BR-01246903 Sao Paulo, SP, Brazil
[4] Hosp Israelita Albert Einstein, Clin Lab, BR-05652900 Sao Paulo, SP, Brazil
[5] Univ Sao Paulo, Clin Hosp, Sch Med, Cent Labs Div,LIM 03, BR-05403000 Sao Paulo, SP, Brazil
来源
VIRUSES-BASEL | 2023年 / 15卷 / 12期
关键词
chronic hepatitis B; HBV; pre core mutations; basal core promoter mutations; BCP and PC variants; MUTATIONS; BRAZIL;
D O I
10.3390/v15122339
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In Brazil, hepatitis B virus endemicity is low, moderate, or high in some areas, such as Espirito Santo State in the southeast region. In this study, we intend to characterize the basal core promoter (BCP) and pre-core region (PC) variants and their association with clinical/epidemiological disease patterns in patients infected with genotypes A and D. The study included 116 chronic hepatitis B patients from Espirito Santo State, Southeast Brazil, infected with genotypes A and D. Basal core promoter (BCP) and pre-core mutations were analyzed in these patients. The frequency of BCP and PC mutations was compared with age, HBeAg status, HBV genotype and subgenotype, HBV-DNA level, clinical classification, and transmission route. HBeAg-negative status was found in 101 (87.1%) patients: 87 (75.0%) were infected with genotype A (A1 = 85; A2 = 2) and 29 (25.0%) were infected with genotype D (D3 = 24; D4 = 3; D2 = 2). BCP + PC variants altogether were more frequent (48.1%) in genotype D than in genotype A strains (6.0%) (p < 0.001). When this evaluation was performed considering the cases that presented only the A1762T and/or G1764A (BCP) mutations, it was observed that the frequency was higher in genotype A (67.5%) compared to genotype D (7.4%) (p < 0.001). On the other hand, considering the samples with mutations only in positions G1896A and/or G1899A (PC), the frequency was higher in genotype D (75.8%) than in genotype A (6.9%) (p < 0.001). Interestingly, HBV DNA was lower than 2000 IU/mL especially when both BCP/PC mutations were present (p < 0.001) or when only PC mutations were detected (p = 0.047), reinforcing their role in viral replication.
引用
收藏
页数:11
相关论文
共 50 条
  • [11] Hepatitis B Virus Core Promoter Mutations in Patients With Chronic Hepatitis B and Hepatocellular Carcinoma in Bucharest, Romania
    Constantinescu, Ileana
    Dinu, Andrei-Antoniu
    Boscaiu, Voicu
    Niculescu, Marius
    HEPATITIS MONTHLY, 2014, 14 (10)
  • [12] Treatment of HBeAg-negative chronic hepatitis B
    Hadziyannis, SJ
    Papatheodoridis, GV
    Vassilopoulos, D
    SEMINARS IN LIVER DISEASE, 2003, 23 (01) : 81 - 88
  • [13] Diagnosis and management of pre-core mutant chronic hepatitis B
    Papatheodoridis, GV
    Hadziyannis, SJ
    JOURNAL OF VIRAL HEPATITIS, 2001, 8 (05) : 311 - 321
  • [14] Clinical and virological aspects of core and pre-core mutations in three generations of chronic hepatitis B virus patients
    Naderi, Malihe
    Hosseini, Seyed Masoud
    Besharat, Sima
    Behnampour, Naser
    Shahramian, Iraj
    Moradi, Abdolvahab
    FUTURE VIROLOGY, 2023, 18 (06) : 349 - 358
  • [15] Precore/Core promoter variants to predict significant fibrosis in both HBeAg positive and negative chronic hepatitis B
    Lapalus, Martine
    Laouenan, Cedric
    Cardoso, Ana-Carolina
    Estrabaud, Emilie
    Carvalho-Filho, Roberto J.
    Zhang, Qian
    Lada, Olivier
    Appourchaux, Kevin
    Mouri, Feryel
    Boyer, Nathalie
    Bedossa, Pierre
    Asselah, Tarik
    Martinot-Peignoux, Michelle
    Marcellin, Patrick
    LIVER INTERNATIONAL, 2015, 35 (09) : 2082 - 2089
  • [16] Pre-Core/Basal-Core Promoter and Reverse Transcriptase Mutations in Chronic HBV Infected-Patients
    Xu, Lu
    Chen, En-Qiang
    Lei, Jun
    Liu, Li
    Zhou, Tao-You
    Gao, Zhan
    Tang, Hong
    HEPATO-GASTROENTEROLOGY, 2012, 59 (113) : 212 - 215
  • [17] Deep sequencing of hepatitis B virus basal core promoter and precore mutants in HBeAg-positive chronic hepatitis B patients
    Yan, Linlin
    Zhang, Henghui
    Ma, Hui
    Liu, Di
    Li, Wei
    Kang, Yulin
    Yang, Ruifeng
    Wang, Jianghua
    He, Gaixia
    Xie, Xingwang
    Wang, Hao
    Wei, Lai
    Lu, Zuhong
    Shao, Qixiang
    Chen, Hongsong
    SCIENTIFIC REPORTS, 2015, 5
  • [18] Hepatitis B virus (HBV) genotypes/subgenotypes in China: Mutations in core promoter and precore/core and their clinical implications
    Yuan, Jing
    Zhou, Boping
    Tanaka, Yasuhito
    Kurbanov, Fulat
    Orito, Etsuro
    Gong, Zuojiong
    Xu, Liumei
    Lu, Jian
    Jiang, Xiaoling
    Lai, Weizhen
    Mizokami, Masashi
    JOURNAL OF CLINICAL VIROLOGY, 2007, 39 (02) : 87 - 93
  • [19] Comparison of Serum Hepatitis B Virus DNA and HBsAg Levels Between HBeAg-Negative and HBeAg-Positive Chronic Hepatitis B Patients
    Keshvari, Maryam
    Alavian, Seyed Moayed
    Sharafi, Heidar
    JUNDISHAPUR JOURNAL OF MICROBIOLOGY, 2015, 8 (03)
  • [20] Detection of Hepatitis B Virus Covalently Closed Circular DNA in the Plasma of Iranian HBeAg-Negative Patients With Chronic Hepatitis B
    Tajik, Zahra
    Keyvani, Hossein
    Bokharaei-Salim, Farah
    Zolfaghari, Mohammad Reza
    Fakhim, Shahin
    Keshvari, Maryam
    Alavian, Seyed Moayed
    HEPATITIS MONTHLY, 2015, 15 (09)