Comparative analysis of drug resistant mutations in the reverse transcriptase domain of hepatitis B virus covalently closed circular DNA and the viral relax circle DNA.
- Author:
He-ling SU
1
;
Yong-ming LIU
;
Xiao-qiang REN
;
Dong-ping XU
;
Yan-wei ZHONG
Author Information
- Publication Type:Journal Article
- MeSH: DNA Primers; genetics; DNA, Circular; genetics; DNA, Viral; genetics; Drug Resistance, Viral; genetics; Genes, Viral; Hepatitis B virus; genetics; Hepatitis B, Chronic; virology; Humans; Mutation; Nucleic Acid Amplification Techniques; methods; Polymerase Chain Reaction; methods; RNA-Directed DNA Polymerase; genetics; Sequence Analysis, DNA
- From: Chinese Journal of Hepatology 2010;18(11):818-821
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo establish a method for detection of reverse transcriptase region of hepatitis B virus (HBV) covalently closed circular DNA (cccDNA), and to compare the pattern and frequency of drug-resistant mutations in the region between intrahepatic HBV cccDNA and serum HBV relax circle DNA (rcDNA).
METHODSHBV DNA were extracted from liver biopsy tissues of 20 patients with chronic hepatitis B. The RT region of HBV cccDNA was amplified by rolling circle amplification (RCA) followed by polymerase chain reaction (PCR) mediated by a pair of primers spanning across the gap region of HBV genome. The RT region of serum HBV rcDNA from the same patient was amplified by nested-PCR. The PCR products were directly sequenced and analyzed by Vector NTI Suite 8.0 and chromaslite 201 software. x2 test was used for statistical significance analysis of drug-resistant mutation occurrences between the HBV cccDNA and rcDNA.
RESULTSThe RT regions of HBV cccDNA were successfully amplified from liver tissues of all enrolled patients using the RCA plus PCR assay. Simultaneously, HBV the RT regions of rcDNA were amplified from these patients serum samples. Sequence analysis showed that the drug-resistant mutations were significantly more frequently detected in HBV rcDNA (40%) than in HBV cccDNA (10%) (P<0.05). Different mutational patterns were observed between the HBV cccDNA and rcDNA in a few cases.
CONCLUSIONThe RCA in combination with PCR is a practical method for the detection of drug-resistant mutation in the RT region of HBV cccDNA. Drug-resistant mutational patterns could be discrepant between HBV cccDNA and rcDNA.
