Mutation Information
Mutation Site
|
S202G |
Mutation Type
|
Amino acid level |
Gene/Protein/Region Type
|
RT |
Combined Mutation
|
rt.L180M+rt.M204I+rt.S202G;rt.L180M+rt.M204I+rt.M204V+rt.S202G;rt.L180M+rt.M204V+rt.S202G+rt.T184L;rt.L180M+rt.M204V+rt.S202G+rt.T184L+rt.T184A;rt.L180M+rt.M204V+rt.S202G+rt.T184I;rt.M204V+rt.S202G+rt.T184I;rt.L180M+rt.M204V+rt.M250I+rt.S202G;rt.L180M+rt.M204V+rt.M250L+rt.S202G;rt.L180M+rt.M204V+rt.S202G+rt.T184A;rt.M204V+rt.S202G+rt.L180M;rt.M204V+rt.S202G+rt.A181C+rt.L180M |
Genotype/Subtype
|
C |
Relevant Drug
|
entecavir (ETV);lamivudine (LAM);adefovir dipivoxil (ADV);tenofovir (TDF) |
Country
|
China |
Literature Information
PubMed PMID
|
30866789
|
Disease
|
HBV infection
|
Published Year
|
2019 |
Journal
|
Emerging microbes & infections |
Title
|
Hepatitis B virus mutation pattern rtL180M+A181C+M204V may contribute to entecavir resistance in clinical practice. |
Author
|
Liu Y,Zhou Y,Li X,Niu M,Chen R,Shao J,Si L,Luo D,Lin Y,Li L,Zhang K,Xiao X,Xu Z,Liu M,Lu M,Zoulim F,Xu D |
Evidence
|
Patient-derived representative rtA181C-containing mutants, rtL180M+A181C+M204V, rtL180M+A181C+M204V+M250V, and rtL180M+A181C+S202G+M204V, exhibited 45.7%, 25.9%, and 25.0% replication capacity and 85.6-, 356.1-, and 307.1-fold decreased susceptibility to ETV respectively compared to the wild-type strain, while the three mutants remained sensitive to tenofovir (TDF).
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