Xenotropic murine leukemia virus-related virus is susceptible to AZT

被引:37
作者
Sakuma, Ryuta [2 ]
Sakuma, Toshie [2 ]
Ohmine, Seiga [2 ]
Silverman, Robert H. [1 ]
Ikeda, Yasuhiro [2 ]
机构
[1] Lerner Res Inst, Cleveland Clin, Dept Canc Biol, Cleveland, OH 44195 USA
[2] Mayo Clin, Dept Mol Med, Rochester, MN 55906 USA
关键词
XMRV; AZT; 3TC; Tenofovir; D4T; Ritonavir; Indinavir; Saquinavir; 118-D-24; Efavirenz; HUMAN-IMMUNODEFICIENCY-VIRUS; TYPE-1; REVERSE-TRANSCRIPTASE; NUCLEOSIDE ANALOG RESISTANCE; RETROVIRAL DISEASE; INHIBITOR; MUTATIONS; PROTEASE; REPLICATION; TELOMERASE; CANCER;
D O I
10.1016/j.virol.2009.11.013
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The xenotropic murine leukemia virus-related virus (XMRV) is a human retrovirus, recently isolated from tissues of prostate cancer patients with impaired RNase L activity. In this study, we evaluated 10 licensed anti-HIV-1 compounds for their activity against XMRV, including protease inhibitors (PI), nucleoside reverse transcriptase (RT) inhibitors (NRTI), non-nucleoside RT inhibitors (NNRTI) and an integrase inhibitor. No PI affected XMRV production: even high concentrations of Ritonavir failed to inhibit the maturation of XMRV Gag polyproteins. Among the NRTI, NNRTI and integrase inhibitors used in this study, only AZT blocked XMRV infection and replication through inhibition of vital reverse transcription. This sensitivity of XMRV to AZT may be explained by the modest homology in the motif D sequences of HIV-1 and XMRV reverse transcriptases. If XMRV becomes established as an etiological agent for prostate cancer or other diseases, AZT may be useful for preventing or treating XMRV infections in humans. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 6
页数:6
相关论文
共 52 条
[1]   Haploinsufficiency of telomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita [J].
Armanios, M ;
Chen, JL ;
Chang, YPC ;
Brodsky, RA ;
Hawkins, A ;
Griffin, CA ;
Eshleman, JR ;
Cohen, AR ;
Chakravarti, A ;
Hamosh, A ;
Greider, CW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (44) :15960-15964
[2]   A human cell-surface receptor for xenotropic and polytropic murine leukemia viruses: Possible role in G protein-coupled signal transduction [J].
Battini, JL ;
Rasko, JEJ ;
Miller, AD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (04) :1385-1390
[3]   YADD mutants of human immunodeficiency virus type 1 and Moloney murine leukemia virus reverse transcriptase are resistant to lamivudine triphosphate (3TCTP) in vitro [J].
Boyer, PL ;
Gao, HQ ;
Clark, PK ;
Sarafianos, SG ;
Arnold, E ;
Hughes, SH .
JOURNAL OF VIROLOGY, 2001, 75 (14) :6321-6328
[4]   Nucleoside analog resistance caused by insertions in the fingers of human immunodeficiency virus type 1 reverse transcriptase involves ATP-mediated excision [J].
Boyer, PL ;
Sarafianos, SG ;
Arnold, E ;
Hughes, SH .
JOURNAL OF VIROLOGY, 2002, 76 (18) :9143-9151
[5]   Selective excision of AZTMP by drug-resistant human immunodeficiency virus reverse transcriptase [J].
Boyer, PL ;
Sarafianos, SG ;
Arnold, E ;
Hughes, SH .
JOURNAL OF VIROLOGY, 2001, 75 (10) :4832-4842
[6]   The motif D loop of human immunodeficiency virus type 1 reverse transcriptase is critical for nucleoside 5′-triphosphate selectivity [J].
Canard, B ;
Chowdhury, K ;
Sarfati, R ;
Doublié, S ;
Richardson, CC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (50) :35768-35776
[7]   RNASEL Arg462Gln variant is implicated in up to 13% of prostate cancer cases [J].
Casey, G ;
Neville, PJ ;
Plummer, SJ ;
Xiang, Y ;
Krumroy, LM ;
Klein, EA ;
Catalona, WJ ;
Nupponen, N ;
Carpten, JD ;
Trent, JM ;
Silverman, RH ;
Witte, JS .
NATURE GENETICS, 2002, 32 (04) :582-583
[8]   THE SEPARATED ENANTIOMERS OF 2'-DEOXY-3'-THIACYTIDINE (BCH-189) BOTH INHIBIT HUMAN-IMMUNODEFICIENCY-VIRUS REPLICATION INVITRO [J].
COATES, JAV ;
CAMMACK, N ;
JENKINSON, HJ ;
MUTTON, IM ;
PEARSON, BA ;
STORER, R ;
CAMERON, JM ;
PENN, CR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (01) :202-205
[9]   An infectious retrovirus susceptible to an IFN antiviral pathway from human prostate tumors [J].
Dong, Beihua ;
Kim, Sanggu ;
Hong, Seunghee ;
Das Gupta, Jaydip ;
Malathi, Krishnamurthy ;
Klein, Eric A. ;
Ganem, Don ;
DeRisi, Joseph L. ;
Chow, Samson A. ;
Silverman, Robert H. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (05) :1655-1660
[10]   Leukemogenesis by Moloney murine leukemia virus: A multistep process [J].
Fan, H .
TRENDS IN MICROBIOLOGY, 1997, 5 (02) :74-82