Hepatitis B virus resistance substitutions: long-term analysis by next-generation sequencing

被引:9
作者
Jones, Leandro R. [1 ,2 ]
Sede, Mariano [1 ,3 ]
Manrique, Julieta M. [1 ,2 ]
Quarleri, Jorge [1 ,3 ]
机构
[1] Consejo Nacl Invest Cient & Tecn, Ave Rivadavia 1917,C1083ACA, Buenos Aires, DF, Argentina
[2] Univ Nacl Patagonia San Juan Bosco, Lab Virol & Genet Mol, Fac Ciencias Nat Sede Trelew, 9 Julio & Begrano S-N, RA-9100 Trelew, Chubut, Argentina
[3] Univ Buenos Aires, Inst Invest Biomed Retrovirus & Sida INBIRS, Fac Med, Paraguay 2155-Piso 11,C1121ABG, Buenos Aires, DF, Argentina
关键词
MUTATIONS; HBV; LAMIVUDINE; INFECTION; VARIANTS; ADEFOVIR; THERAPY;
D O I
10.1007/s00705-016-2959-8
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
HBV phylogenetics and resistance-associated mutations (RAMs) were surveyed by next-generation sequencing of 21 longitudinal samples from seven patients entering antiviral therapy. The virus populations were dominated by a few abundant lineages that coexisted with substantial numbers of low-frequency variants. A few low-frequency RAMs were observed before treatment, but new ones emerged, and their frequencies increased during therapy. Together, these results support the idea that chronic HBV infection is dominated by a few virus lineages and that an accompanying plethora of diverse, low-frequency variants may function as a reservoir that potentially contribute to viral genetic plasticity, potentially affecting patient outcome.
引用
收藏
页码:2885 / 2891
页数:7
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