Cytomegalovirus UL97 phosphotransferase mutations that affect susceptibility to ganciclovir

被引:139
作者
Chou, S
Waldemer, RH
Senters, AE
Michels, KS
Kemble, GW
Miner, RC
Drew, WL
机构
[1] Vet Adm Med Ctr, Med Serv, Portland, OR 97201 USA
[2] Vet Adm Med Ctr, Res Serv, Portland, OR 97201 USA
[3] Oregon Hlth Sci Univ, Div Infect Dis, Portland, OR 97201 USA
[4] Aviron, Mt View, CA USA
[5] Univ Calif San Francisco, Mt Zion Med Ctr, Dept Lab Med, San Francisco, CA 94120 USA
[6] Univ Calif San Francisco, Mt Zion Med Ctr, Dept Med, San Francisco, CA 94120 USA
关键词
D O I
10.1086/338362
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Most ganciclovir (GCV)-resistant cytomegalovirus (CMV) isolates contain UL97 gene mutations at codon 460 or 520 or between codons 590 and 607, where an increasing variety of mutations have been detected, including deletions. To determine their phenotypic effect, 9 UL97 mutations not previously studied were transferred to drug-sensitive laboratory CMV strains that contained unique restriction sites developed for this purpose. Deletion of the entire codon range 591-607 conferred a 6-fold increase in GCV resistance, with little effect on viral replication. Some mutations found in clinical isolates, including C592G and A594T, conferred only 2-3-fold decreases in GCV susceptibility. For C592G, this phenotype was confirmed by transfer to different CMV strains and by restoration of full drug susceptibility after removal of the mutation. Low drug levels resulting from oral GCV therapy may predispose the virus to the initial selection of these low-grade UL97 resistance mutations and to later accumulation of other mutations and greater resistance.
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页码:162 / 169
页数:8
相关论文
共 34 条
[1]  
Baldanti F, 1998, ANTIMICROB AGENTS CH, V42, P444
[2]   A 3-NUCLEOTIDE DELETION IN THE UL97 OPEN READING FRAME IS RESPONSIBLE FOR THE GANCICLOVIR RESISTANCE OF A HUMAN CYTOMEGALOVIRUS CLINICAL ISOLATE [J].
BALDANTI, F ;
SILINI, E ;
SARASINI, A ;
TALARICO, CL ;
STANAT, SC ;
BIRON, KK ;
FURIONE, M ;
BONO, F ;
PALU, G ;
GERNA, G .
JOURNAL OF VIROLOGY, 1995, 69 (02) :796-800
[3]  
Baldanti F., 1998, AIDS (London), V12, P816
[4]   Cloning of the human cytomegalovirus (HCMV) genome as an infectious bacterial artificial chromosome in Escherichia coli:: a new approach for construction of HCMV mutants [J].
Borst, EM ;
Hahn, G ;
Koszinowski, UH ;
Messerle, M .
JOURNAL OF VIROLOGY, 1999, 73 (10) :8320-8329
[5]  
Bowen EF, 1999, J MED VIROL, V58, P402, DOI 10.1002/(SICI)1096-9071(199908)58:4&lt
[6]  
402::AID-JMV13&gt
[7]  
3.0.CO
[8]  
2-5
[9]  
Chou S, 1999, Transpl Infect Dis, V1, P105, DOI 10.1034/j.1399-3062.1999.010204.x
[10]   FREQUENCY OF UL97 PHOSPHOTRANSFERASE MUTATIONS RELATED TO GANCICLOVIR RESISTANCE IN CLINICAL CYTOMEGALOVIRUS ISOLATES [J].
CHOU, SW ;
GUENTZEL, S ;
MICHELS, KR ;
MINER, RC ;
DREW, WL .
JOURNAL OF INFECTIOUS DISEASES, 1995, 172 (01) :239-242