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
  • [1] Detection of HBV Covalently Closed Circular DNA
    Li, Xiaoling
    Zhao, Jinghua
    Yuan, Quan
    Xia, Ningshao
    VIRUSES-BASEL, 2017, 9 (06):
  • [2] Covalently closed circular DNA: The ultimate therapeutic target for curing HBV infections
    Martinez, Maria Guadalupe
    Boyd, Anders
    Combe, Emmanuel
    Testoni, Barbara
    Zoulim, Fabien
    JOURNAL OF HEPATOLOGY, 2021, 75 (03) : 706 - 717
  • [3] Serum HBcrAg is better than HBV RNA and HBsAg in reflecting intrahepatic covalently closed circular DNA
    Chen, En-Qiang
    Wang, Meng-Lan
    Tao, Ya-Chao
    Wu, Dong-Bo
    Liao, Juan
    He, Min
    Tang, Hong
    JOURNAL OF VIRAL HEPATITIS, 2019, 26 (05) : 586 - 595
  • [4] INTRAHEPATIC HBV DNA AND COVALENTLY CLOSED CIRCULAR DNA (CCCDNA) LEVELS IN PATIENTS POSITIVE FOR ANTI-HBC AND NEGATIVE FOR HBSAG
    Chaiteerakij, Roongruedee
    Komolmit, Piyawat
    Sa-nguanmoo, Pattaratida
    Poovorawan, Yong
    SOUTHEAST ASIAN JOURNAL OF TROPICAL MEDICINE AND PUBLIC HEALTH, 2010, 41 (04) : 867 - 875
  • [5] Untying relaxed circular DNA of hepatitis B virus by polymerase reaction provides a new option for accurate quantification and visualization of covalently closed circular DNA
    Kamiya, Naohiro
    Sugimoto, Takahiko
    Abe-Chayama, Hiromi
    Akiyama, Rie
    Tsuboi, Yasunori
    Mogami, Akira
    Imamura, Michio
    Hayes, C. Nelson
    Chayama, Kazuaki
    JOURNAL OF GENERAL VIROLOGY, 2022, 103 (02)
  • [6] Quantatitative assays for covalently closed circular DNA of hepatitis B virus
    Shi, Tianshu
    Cao, Jiali
    Yang, Yinan
    Yuan, Quan
    CHINESE SCIENCE BULLETIN-CHINESE, 2020, 65 (16): : 1529 - 1545
  • [7] Cre/LoxP-HBV plasmids generating recombinant covalently closed circular DNA genome upon transfection
    Kruse, Robert L.
    Legras, Xavier
    Barzi, Mercedes
    VIRUS RESEARCH, 2021, 292
  • [8] The role of host DNA ligases in hepadnavirus covalently closed circular DNA formation
    Long, Quanxin
    Yan, Ran
    Hu, Jieli
    Cai, Dawei
    Mitra, Bidisha
    Kim, Elena S.
    Marchetti, Alexander
    Zhang, Hu
    Wang, Soujuan
    Liu, Yuanjie
    Huang, Ailong
    Guo, Haitao
    PLOS PATHOGENS, 2017, 13 (12)
  • [9] HBV covalently closed circular DNA minichromosomes in distinct epigenetic transcriptional states differ in their vulnerability to damage
    Wang, Yang
    Li, Yumeng
    Zai, Wenjing
    Hu, Kongying
    Zhu, Yuanfei
    Deng, Qiang
    Wu, Min
    Li, Yaming
    Chen, Jieliang
    Yuan, Zhenghong
    HEPATOLOGY, 2022, 75 (05) : 1275 - 1288
  • [10] Recent advances in the study of hepatitis B virus covalently closed circular DNA
    Ji, Mengying
    Hu, Kanghong
    VIROLOGICA SINICA, 2017, 32 (06) : 454 - 464