MECHANISM OF INHIBITION OF DUCK HEPATITIS-B VIRUS POLYMERASE BY (-)-BETA-L-2',3'-DIDEOXY-3'-THIACYTIDINE

被引:115
|
作者
SEVERINI, A [1 ]
LIU, XY [1 ]
WILSON, JS [1 ]
TYRRELL, DLJ [1 ]
机构
[1] UNIV ALBERTA,GLAXO HERITAGE RES INST,DEPT MED MICROBIOL & INFECT DIS,EDMONTON,AB T6G 2H7,CANADA
关键词
D O I
10.1128/AAC.39.7.1430
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We have used the endogenous reverse transcriptase reaction of viral core particles from duck liver to elucidate the mechanism of inhibition of duck hepatitis B virus (DHBV) replication by the nucleoside analog (-)-beta-L-2',3'-dideoxy-3'-thiacytidine (3TC), As is the case in human immunodeficiency virus replication, 3TC-5'-triphosphate (3TC-TP) acts as a chain terminator for the DNA polymerase activities, The results of several different experiments support this conclusion, which explains the potent activity of 3TC against the hepadnaviruses, In isolated DHBV core particles, 3TC-TP inhibited the reverse transcriptase in a manner that resembled competitive inhibition with respect to dCTP. However, the kinetics of inhibition was not linear on a double-reciprocal plot for the highest concentrations of 3TC-TP and the lowest concentration of dCTP. This anomaly would be expected if binding to the nucleotide site was followed by DNA chain termination. Calculations that used only the linear part of the curve yielded a K-i of 0.78 +/- 0.10 mu M 3TC-TP, The inhibition of core particles incubated in vitro with 3TC-TP was not reversed by removal of the free inhibitor, 3TC-TP inactivated the reverse transcriptase activity in a concentration-dependent manner. The K-m, of the chain termination reaction was calculated at 0.71 +/- 0.05 mu M. Similar competitive kinetics and irreversible inhibition were also obtained on the endogenous DNA polymerase from viral particles from serum, suggesting that 3TC-TP also acts as a chain terminator of the DNA-directed DNA polymerase of DHBV replication, Core particles purified from DHBV-infected hepatocytes treated with 3TC also showed irreversible inhibition of the endogenous reverse transcriptase activity, indicating that chain termination is the mechanism of inhibition in the presence of the normal deoxynucleotide pools within cells, Endogenous sequencing of duck liver viral core particles with 3TC-TP as a chain terminator shows a pattern of bands similar to that obtained with ddCTP, and [P-32]3TC-TP labeled the growing DNA chain at the C position.
引用
收藏
页码:1430 / 1435
页数:6
相关论文
共 50 条
  • [21] EFFECTS OF 2',3'-DIDEOXYNUCLEOSIDES ON DUCK HEPATITIS-B VIRUS
    MARTIN, P
    AOKI, S
    FORD, H
    KORENMAN, J
    KASSIANIDES, C
    HOOFNAGLE, JH
    BRODER, S
    MITSUYA, H
    AIDS RESEARCH AND HUMAN RETROVIRUSES, 1990, 6 (01) : 126 - 127
  • [22] INHIBITION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REPLICATION BY PHOSPHONOFORMATE AND PHOSPHONOACETATE-2',3'-DIDEOXY-3'-THIACYTIDINE CONJUGATES
    CHARVET, AS
    CAMPLO, M
    FAURY, P
    GRACIET, JC
    MOURIER, N
    CHERMANN, JC
    KRAUS, JL
    JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (14) : 2216 - 2223
  • [23] SYNTHESIS AND ANTIVIRAL ACTIVITY OF NEW CARBONYLPHOSPHONATE 2',3'-DIDEOXY-3'-THIACYTIDINE CONJUGATES
    CHARVET, AS
    TURIN, F
    FAURY, P
    HANTZ, O
    CAMPLO, M
    MOURIER, N
    BERTHILLON, P
    GRACIET, JC
    CHERMANN, JC
    TREPO, C
    KRAUS, JL
    ANTIVIRAL RESEARCH, 1994, 25 (02) : 161 - 168
  • [24] Pharmacodynamics of (-)-β-2′,3′-dideoxy-3′-thiacytidine in chronically virus-infected woodchucks compared to its pharmacodynamics in humans
    Hurwitz, SJ
    Tennant, BC
    Korba, BE
    Gerin, JL
    Schinazi, RF
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (11) : 2804 - 2809
  • [25] Theoretical study on the hydrolysis mechanism of N,N-dimethyl-N′-(2′,3′-dideoxy-3′-thiacytidine)formamidine
    ZHANG Chang1 & XUE Ying2? 1 College of Chemistry and Environment Protection Engineering
    2 College of Chemistry
    Science in China(Series B:Chemistry), 2008, (10) : 911 - 917
  • [26] Theoretical study on the hydrolysis mechanism of N,N-dimethyl-N′-(2′,3′-dideoxy-3′-thiacytidine)formamidine
    Chang Zhang
    Ying Xue
    Science in China Series B: Chemistry, 2008, 51 : 911 - 917
  • [27] 2',3'-DIDEOXY-BETA-L-5'-FLUOROCYTIDINE INHIBITS DUCK HEPATITIS-B VIRUS REVERSE TRANSCRIPTION AND SUPPRESSES VIRAL-DNA SYNTHESIS IN HEPATOCYTES
    ZOULIM, F
    DANNAOUI, E
    BOREL, C
    HANTZ, O
    LIN, TS
    LIU, SH
    TREPO, C
    CHENG, YC
    HEPATOLOGY, 1995, 22 (04) : 888 - 888
  • [28] Synthesis and Biological Evaluation of Fatty Acyl Ester Derivatives of (-)-2′,3′-Dideoxy-3′-thiacytidine
    Agarwal, Hitesh K.
    Chhikara, Bhupender S.
    Hanley, Michael J.
    Ye, Guofeng
    Doncel, Gustavo F.
    Parang, Keykavous
    JOURNAL OF MEDICINAL CHEMISTRY, 2012, 55 (10) : 4861 - 4871
  • [29] Synthesis and anti-HIV evaluation of new 2′,3′-dideoxy-3′-thiacytidine prodrugs
    Mourier, N
    Camplo, M
    Della Bruna, GS
    Pellacini, F
    Ungheri, D
    Chermann, JC
    Kraus, JL
    NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS, 2000, 19 (07): : 1057 - 1091
  • [30] Mutations at codon 184 in simian immunodeficiency virus reverse transcriptase confer resistance to the (-) enantiomer of 2',3'-dideoxy-3'-thiacytidine
    Cherry, E
    Slater, M
    Salomon, H
    Rud, E
    Wainberg, MA
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (12) : 2763 - 2765