Differences in sequences between HBV-relaxed circular DNA and covalently closed circular DNA

被引:9
|
作者
Rybicka, Magda [1 ,2 ]
Woziwodzka, Anna [1 ,2 ]
Romanowski, Tomasz [1 ,2 ]
Stalke, Piotr [3 ]
Dreczewski, Marcin [1 ,2 ]
Bielawski, Krzysztof Piotr [1 ,2 ]
机构
[1] Univ Gdansk, Intercollegiate Fac Biotechnol, Dept Mol Diagnost, Abrahama 58, PL-80307 Gdansk, Poland
[2] Med Univ Gdansk, Abrahama 58, PL-80307 Gdansk, Poland
[3] Med Univ Gdansk, Dept Infect Dis, Smoluchowskiego 18, PL-80214 Gdansk, Poland
关键词
cccDNA; HBV; MALDI-TOF MS; polymorphism; RCDNA; DRUG-RESISTANCE; PERSISTENCE; TIME;
D O I
10.1038/emi.2017.41
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The hepatitis B virus (HBV) genome exists in two forms: circular covalently closed DNA (cccDNA) and relaxed circular DNA (RCDNA). Here, we investigated the presence of differences in the sequences of both forms in paired samples of serum and liver tissue. The serum and liver biopsy samples were collected at the same time from 67 chronically infected patients. The genotyping of the RCDNA and cccDNA was performed using mass spectrometry analysis. The HBV mutations located in the HBV pol (P) and the HBV basal core promoter/pre-core (BCP/PC) regions were included. The BCP/PC and P sequences of the RCDNA extracted from liver and blood samples were different in 39% and 16% of patients, respectively. Differences were also found between RCDNA and cccDNA extracted from the same liver specimen. Moreover, the cccDNA BCP/PC region sequence had an impact on various virological and clinical parameters. We demonstrated that there are differences between the RCDNA and cccDNA sequences that were extracted from the same liver tissue. However, further investigations are needed to analyze whether the mutations in the cccDNA are conserved and whether cccDNA serves as a `mutation storage' pool for HBV. This result could have profound implications for the subsequent therapy choices for treatment-experienced patients.
引用
收藏
页数:7
相关论文
共 50 条
  • [21] Rebound of HBV DNA after cessation of nucleos/tide analogues in chronic hepatitis B patients with undetectable covalently closed circular DNA
    Lai, Ching-Lung
    Wong, Danny Ka-Ho
    Wong, Gerald Tsz-Yau
    Seto, Wai-Kay
    Fung, James
    Yuen, Man-Fung
    JHEP REPORTS, 2020, 2 (03)
  • [22] Research progress on detection methods for hepatitis B virus covalently closed circular DNA
    Sun, Fenglan
    Xia, Wei
    Ouyang, Yaoling
    JOURNAL OF VIRAL HEPATITIS, 2023, 30 (05) : 366 - 373
  • [23] A Novel Mouse Model Harboring Hepatitis B Virus Covalently Closed Circular DNA
    Xu, Zaichao
    Zhao, Li
    Zhong, Youquan
    Zhu, Chengliang
    Zhao, Kaitao
    Teng, Yan
    Cheng, Xiaoming
    Chen, Qiang
    Xia, Yuchen
    CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY, 2022, 13 (04): : 1001 - 1017
  • [24] Covalently closed-circular hepatitis B virus DNA reduction with entecavir or lamivudine
    Bowden, Scott
    Locarnini, Stephen
    Chang, Ting-Tsung
    Chao, You-Chen
    Han, Kwang-Hyub
    Gish, Robert G.
    de Man, Robert A.
    Yu, Miao
    Llamoso, Cyril
    Tang, Hong
    WORLD JOURNAL OF GASTROENTEROLOGY, 2015, 21 (15) : 4644 - 4651
  • [25] Cellular DNA Topoisomerases Are Required for the Synthesis of Hepatitis B Virus Covalently Closed Circular DNA
    Sheraz, Muhammad
    Cheng, Junjun
    Tang, Liudi
    Chang, Jinhong
    Guo, Ju-Tao
    JOURNAL OF VIROLOGY, 2019, 93 (11)
  • [26] Impact of Intrahepatic Hepatitis B DNA and Covalently Closed Circular DNA on Survival After Hepatectomy in HBV-Associated Hepatocellular Carcinoma Patients
    Wang, Qin
    Fiel, M. Isabel
    Luan, Wei
    Blank, Sima
    Kadri, Hena
    Kim, Ki Won
    Hiotis, Spiros P.
    ANNALS OF SURGICAL ONCOLOGY, 2013, 20 (12) : 3761 - 3770
  • [27] Epigenetic regulation and its therapeutic potential in hepatitis B virus covalently closed circular DNA
    Ren, Jihua
    Cheng, Shengtao
    Ren, Fang
    Gu, Huiying
    Wu, Daiqing
    Yao, Xinyan
    Tan, Ming
    Huang, Ailong
    Chen, Juan
    GENES & DISEASES, 2025, 12 (01)
  • [28] DNA Polymerase κ Is a Key Cellular Factor for the Formation of Covalently Closed Circular DNA of Hepatitis B Virus
    Qi, Yonghe
    Gao, Zhenchao
    Xu, Guangwei
    Peng, Bo
    Liu, Chenxuan
    Yan, Huan
    Yao, Qiyan
    Sun, Guoliang
    Liu, Yang
    Tang, Dingbin
    Song, Zilin
    He, Wenhui
    Sun, Yinyan
    Guo, Ju-Tao
    Li, Wenhui
    PLOS PATHOGENS, 2016, 12 (10)
  • [29] Detection of the hepatitis B virus (HBV) covalently-closed-circular DNA (cccDNA) in mice transduced with a recombinant AAV-HBV vector
    Lucifora, Julie
    Salvetti, Anna
    Marniquet, Xavier
    Mailly, Laurent
    Testoni, Barbara
    Fusil, Floriane
    Inchauspe, Aurore
    Michelet, Maud
    Michel, Marie-Louise
    Levrero, Massimo
    Cortez, Pierre
    Baumert, Thomas F.
    Cosset, Francois-Loic
    Challier, Cecile
    Zoulim, Fabien
    Durantel, David
    ANTIVIRAL RESEARCH, 2017, 145 : 14 - 19
  • [30] Droplet digital PCR technique is ultrasensitive for the quantification of covalently closed circular DNA in the blood of chronic HBV-infected patients
    Singh, Ravinder
    Ramakrishna, Gayatri
    Sharma, Manoj Kumar
    Kumar, Rahul
    Gupta, Ekta
    Rastogi, Archana
    Tanwar, Pranay
    Sarin, Shiv Kumar
    Trehanpati, Nirupama
    CLINICS AND RESEARCH IN HEPATOLOGY AND GASTROENTEROLOGY, 2025, 49 (03)