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
Table: A181T/V
Discussion: Adefovir resistance has been associated with a primary mutation in the D domain at rtN236T and rtA181T/Vin the B domain.
Discussion: The rtA181T change has been reported to occur in the absence of rtM204I/V and is considered a primary resistance mutation.


  Quasispecies and pre-existing drug-resistant mutations of hepatitis B virus in patients with chronic hepatitis B.
 PMID: 23710315       2013       Gut and liver
Discussion: In addition to classical ADV resistance mutations such as rtN236S or rtA181T, a few other related-variants including rtV84I/S, rtL84S, and rtQ215H were identified before VB in patient 1, 3, 4, and 6.
Discussion: In our sequencing data, rtI169L mutation was present in 8%, 1%, and 1% of 100 colonies in patient 1, 3, and 4, as well as rtA181V/T ADV resistance mutations in patient 1 and 4.
Discussion: Regarding HBV quasispecies associated with ADV resistance, the  PMID: 23796863       2013       The Journal of infection
Abstract: Indeed, rtS78T (prevalence: 1.1% in drug-naive and 12.2% in adefovir-failing patients) decreased the RT-affinity for adefovir more than the classical adefovir-resistance mutations rtA181 T/V (WT:-9.63 kcal/mol, rtA181T:-9.30 kcal/mol, rtA181V:-7.96 kcal/mol, rtS78T:-7.37 kcal/mol).


  Mutation analysis of hepatitis B virus reverse transcriptase region among untreated chronically infected patients in Ahvaz city (South-West of Iran).
 PMID: 24064642       2013       Indian journal of medical microbiology
Abstract: Of these, 3 (6.6%) patients had primary resistance mutation (rtM204I, rtA181T and rtA181S) and 20 (44.4%) patients had secondary resistance mutations.


  Profile of hepatitis B virus resistance mutations against nucleoside/nucleotide analogue treatment in Chinese patients with chronic hepatitis B.
 PMID: 24160943       2013       Virology journal
Introduction: According to previously studies, the patterns of genotypic resistance in the HBV polymerase can be categorized into five specific evolutionary pathways, inc
Result: In this cohort, HBV rtA181T/V mutation was observed in 19.3% (22/114) of patients with LAM/LdT-based therapies and 23.9% (11/46) of patients with ADV-based therapies.
Result: Our findings suggested that rtA181T/V mutations were common among patients with NAs resistance, and it should be regularly monitored in real clinical practice.


  Substitution rtq267h of hepatitis B virus increases the weight of replication and Lamivudine resistance.
 PMID: 24348637       2013       Hepatitis monthly
Introduction: Substitution rtA181V/T and/or rtN236T can reduce the anti-HBV effect of ADV, rtN238R, rtT240Y and rtN248H of HBV were newly reported to decrease susceptibility to ADV (8).


  Hepatitis B virus genotype C encoding resistance mutations that emerge during adefovir dipivoxil therapy: in vitro replication phenotype.
 PMID: 26201776       2013       Hepatology international
Abstract: CONCLUSIONS: The identification of secretion-defective HBV in the setting of ADV therapy for HBV genotype C, and to a lesser extent HBV genotype B, has major implications for the diagnosis and treatment of HBV in the Asia-Pacific region, as it is likely that quantitative HBsAg and viral load testing of serum from patients infected with HBV encoding rtA181T and rtN236T substitutions may not accurately reflect the level of replication within hepatocytes.
Abstract: Importantly, less HBsAg was detected in the cells transfected with the rtA181T resistance mutants, and the overlapping sW172stop mutation ablated secretion of


  An improved reverse dot hybridization for simple and rapid detection of adefovir dipivoxil-resistant hepatitis B virus.
 PMID: 22290465       2012       Genetics and molecular research
Abstract: Wedeveloped an improved reverse dot hybridization test for simple and rapiddetection of the rtA181V/T and rtN236T mutations associated with adefovirdipivoxil resistance in chronic hepatitis B patients.


  Decreased infectivity of nucleoside analogs-resistant hepatitis B virus mutants.
 PMID: 22314422       2012       Journal of hepatology
Abstract: METHODS: HBV-resistant mutants (rtL180M+M204V, rtV173L+L180M+M204V, rtM204I, rtL180M+M204I, rtN236T, rtA181V, rtA181V+rtN236T, rtA181T+N236T, and rt


  Treatment response and evolution of HBV resistance during lamivudine plus adefovir or entecavir therapy in patients with adefovir-resistant mutants.
 PMID: 22358132       2012       Antiviral therapy
Abstract: In the LAM+ADV group, patients with single rtN236T resistant mutation had higher rates of undetectable HBV DNA than those with the double mutant rtA181T/V+rtN236T at months 3-18 of therapy.
Abstract: LAM+ADV were less effective in patients with the double mutant rtA181T/V+rtN236T than the single rtN236T mutation.
Abstract: No virological breakthrough occurred except for one patient with rtN236T resistant mutation who experienced virological and biochemical breakthrough a



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