Development of a new method for detecting a mutation in the gene encoding hepatitis B virus reverse transcriptase active site (YMDD motif)

被引:27
作者
Kobayashi, S
Shimada, K
Suzuki, H
Tanikawa, K
Sata, M
机构
[1] Kurume Univ, Sch Med, Dept Med 2, Fukuoka 8300011, Japan
[2] Sumitomo Met Ind Ltd, Div Biomed, Med Business Dept, Diagnost Sect, Hasaki, Ibaraki 3140255, Japan
[3] Kurume Res Ctr, Int Inst Liver Res, Fukuoka 8390861, Japan
关键词
hepatitis B virus (HBV); lamivudine; mutation;
D O I
10.1016/S1386-6346(99)00061-3
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
It is a developing problem that long-term treatment with lamivudine, which is a therapeutic drug for chronic hepatitis B under clinical study, causes mutation in the region encoding the YMDD motif in the HBV DNA polymerase gene, inducing lamivudine-resistant HBV in some cases. Therefore, we developed a new method of detecting gene mutation using the mini-sequencing method. Serum samples collected from patients with HBV infection (60 cases untreated with lamivudine and four cases treated with lamivudine) were examined for gene mutation by this method. As a result, while there were no mutations detected in lamivudine-untreated cases, a mutation from YMDD to YVDD or YIDD was detected in cases with lamivudine administration. In cases in which the mutation was detected, HBV gene obtained from the serum was subcloned and sequenced to detect the mutation, confirming that this method is appropriate for detecting gene mutations. This method may be a rapid, simple, and reliable method of detecting resistant virus that can process a number of serum samples that will be necessary to be tested when lamivudine is approved and administration to chronic hepatitis B patients is initiated. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:31 / 42
页数:12
相关论文
共 11 条
[1]   Association of mutations in the core promoter and precore region of hepatitis virus with fulminant and severe acute hepatitis in Japan [J].
Aritomi, T ;
Yatsuhashi, H ;
Fujino, T ;
Yamasaki, K ;
Inoue, O ;
Koga, M ;
Kato, Y ;
Yano, M .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1998, 13 (11) :1125-1132
[2]   Hepatitis-B-virus resistance to lamivudine given for recurrent infection after orthotopic liver transplantation [J].
Bartholomew, MM ;
Jansen, RW ;
Jeffers, LJ ;
Reddy, KR ;
Johnson, LC ;
Bunzendahl, H ;
Condreay, LD ;
Tzakis, AG ;
Schiff, ER ;
Brown, NA .
LANCET, 1997, 349 (9044) :20-22
[3]   HIGH-LEVEL RESISTANCE TO (-) ENANTIOMERIC 2'-DEOXY-3'-THIACYTIDINE IN-VITRO IS DUE TO ONE AMINO-ACID SUBSTITUTION IN THE CATALYTIC SITE OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REVERSE-TRANSCRIPTASE [J].
BOUCHER, CAB ;
CAMMACK, N ;
SCHIPPER, P ;
SCHUURMAN, R ;
ROUSE, P ;
WAINBERG, MA ;
CAMERON, JM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (10) :2231-2234
[4]   Emergence and takeover of YMDD motif mutant hepatitis B virus during long-term lamivudine therapy and re-takeover by wild type after cessation of therapy [J].
Chayama, K ;
Suzuki, Y ;
Kobayashi, M ;
Kobayashi, M ;
Tsubota, A ;
Hashimoto, M ;
Miyano, Y ;
Koike, H ;
Kobayashi, M ;
Koida, I ;
Arase, Y ;
Saitoh, S ;
Murashima, N ;
Ikeda, K ;
Kumada, H .
HEPATOLOGY, 1998, 27 (06) :1711-1716
[5]   INHIBITION OF THE REPLICATION OF HEPATITIS-B VIRUS INVITRO BY 2',3'-DIDEOXY-3'-THIACYTIDINE AND RELATED ANALOGS [J].
DOONG, SL ;
TSAI, CH ;
SCHINAZI, RF ;
LIOTTA, DC ;
CHENG, YC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (19) :8495-8499
[6]   Generation of duck hepatitis B virus polymerase mutants through site-directed mutagenesis which demonstrate resistance to lamivudine [(-)-beta-L-2',3'-dideoxy-3'-thiacytidine] in vitro [J].
Fischer, KP ;
Tyrrell, DLJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (08) :1957-1960
[7]   Naturally occurring hepatitis B virus genomes bearing the hallmarks of retroviral G->A hypermutation [J].
Gunther, S ;
Sommer, G ;
Plikat, U ;
Iwanska, A ;
WainHobson, S ;
Will, H ;
Meyerhans, A .
VIROLOGY, 1997, 235 (01) :104-108
[8]   CRYSTAL-STRUCTURE AT 3.5 ANGSTROM RESOLUTION OF HIV-1 REVERSE-TRANSCRIPTASE COMPLEXED WITH AN INHIBITOR [J].
KOHLSTAEDT, LA ;
WANG, J ;
FRIEDMAN, JM ;
RICE, PA ;
STEITZ, TA .
SCIENCE, 1992, 256 (5065) :1783-1790
[9]   Selection of mutations in the hepatitis B virus polymerase during therapy of transplant recipients with lamivudine [J].
Ling, R ;
Mutimer, D ;
Ahmed, N ;
Boxall, EH ;
Elias, E ;
Dusheiko, GM ;
Harrison, TJ .
HEPATOLOGY, 1996, 24 (03) :711-713
[10]  
TANIGAWA K, 1997, KAN TAN SUI, V35, P529