HBV mutation literature information.


  Drug-related mutational patterns in hepatitis B virus (HBV) reverse transcriptase proteins from Iranian treatment-naive chronic HBV patients.
 PMID: 23596461       2013       Hepatitis monthly
Result: Common and frequent lamivudine-related amino acid substitutions were found in this study incl
Discussion: Other compensatory mutations include the rtV173L and rtL80I changes.
Discussion: Recently, the GLOBE-Trial demonstrated that in vitro telbivudine resistance is conferred by either rtM204I or rtM204V+rtL180M and L80I/M204I but not by the rtM204V mutation alone, while in vivo telbivudine resistance is almost exclusively due to the presence of M204I.


  Characterization of antiviral resistance mutations among the Eastern Indian Hepatitis B virus infected population.
 PMID: 23409946       2013       Virology journal
Abstract: Notably, classical antiviral resistance mutations (rtL80I/V-rtI169T-rtV173L-rtL180M-rtA181T/V/S-rtT184A/S/G/C-rtA194T-rtS202C /G/I -rtM204V/I-rtN236T-rtM250V) were n


  Low-level persistence of drug resistance mutations in hepatitis B virus-infected subjects with a past history of Lamivudine treatment.
 PMID: 23114756       2013       Antimicrobial agents and chemotherapy
Abstract: Sanger sequencing identified >=1 LAM resistance mutations (rtL80I/V, rtM204I, and rtA181T) in samples from 5 (11%) of 46 LAM-experienced and none of 45 LAM-naive subjects (0%; P = 0.06).
Abstract: UDPS detected >=1 LAM resistance mutations (rtL80I/V, rtV173L, rtL180M, rtA181T, and rtM204I/V) in 10 (22%) of the 46 LAM-experienced subjects, including 5 in whom LAM resistance mutations were not identified by S


  rtL180M mutation of hepatitis B virus is closely associated with frequent virological resistance to adefovir dipivoxil therapy.
 PMID: 21777282       2012       Journal of gastroenterology and hepatology
Abstract: The rtL180M and rtL80V/I mutations were identified in 68% and 69%, respectively.
Abstract: There was no difference in the occurrence of VB with regard to types of YMDD mutation or rtL80V/I.


  Detection of mixed populations of wild-type and YMDD hepatitis B variants by pyrosequencing in acutely and chronically infected patients.
 PMID: 22672436       2012       BMC microbiology
Introduction: Compensatory mutations in the rt domain (rtL180M, rtV173L, rtL80I/V) that partially restore replication efficiency are often co-selected in HBV rt204 mutants.


  [Mutation analysis of the HBV reverse transcriptase in nucleos(t)ide-treated patients with chronic HBV infection].
 PMID: 23627028       2012       Zhonghua shi yan he lin chuang bing du xue za zhi
Abstract: RtM204 mutations were detected at the highest frequency among 63 mutants (40/63, 63.49%) and found to display 11 combination mutation patterns, in which rtM204I were associated with rtL80I/V and rtL180M, and rtM204V were associated with rtL1l80M, respectively.


  Clinical characteristics and chronicity of acute hepatitis B induced by lamivudine-resistant strains.
 PMID: 22930503       2012       Journal of medical virology
Abstract: Among these patients, six harbored the rtM204I mutation, two harbored the rtL180M + rtM204I mutations, one harbored the rtM204I + rtM204V mutations, one harbored the rtL80I + rtM204I mutations, and one harbored the rtV173L + rtL180M + rtM204V mutations.


  Frequency and mutation patterns of resistance in patients with chronic hepatitis B infection treated with nucleos(t)ide analogs in add-on and switch strategies.
 PMID: 22224083       2011       Hepatitis monthly
Introduction: Nine major mutation patterns associated with LAM resistance have been reported: (i) rtM204I/V + rtL180M; (ii) rtM204I; (iii) rtV173L + rtL180M + rtM204V; (iv) rtL80I + rtM204I; (v) rtQ215S + rtM204I/V +- rtL18


  Characterization of drug-resistance mutations in HBV D-genotype chronically infected patients, naive to antiviral drugs.
 PMID: 21920388       2011       Antiviral research
Abstract: HBV reverse-transcriptase (RT) region was sequenced and analyzed for 20 mutations, confirmed by in vitro studies as associated with resistance to nucleos(t)ide HBV-RT inhibitors (rtL80I/V-rtI169T-rtV173L-rtL180M-rtA181T/V/S-rtT184A/S/G/C-rtA194T-rtS202C/G/I-


  Role of hepatitis B virus genetic barrier in drug-resistance and immune-escape development.
 PMID: 21831732       2011       Digestive and liver disease
Abstract: rtL80I/V-rtL180M-rtV173L), whilst most primary mutations (including rtM204V-rtA181T/V-rtI169T-rtA194T) are associated with low genetic barrier.



Browser Board

 Co-occurred Entities




   Filtrator