Evolution of mutations conferring multidrug resistance during prophylaxis and therapy for cytomegalovirus disease

被引:122
作者
Chou, SW
Marousek, G
Guentzel, S
Follansbee, SE
Poscher, ME
Lalezari, JP
Miner, RC
Drew, WL
机构
[1] OREGON HLTH SCI UNIV, DIV INFECT DIS, PORTLAND, OR 97201 USA
[2] UNIV CALIF SAN FRANCISCO, RK DAVIES MED CTR, SAN FRANCISCO, CA 94143 USA
[3] UNIV CALIF SAN FRANCISCO, DEPT MED, SAN FRANCISCO, CA 94143 USA
[4] UNIV CALIF SAN FRANCISCO, DEPT CLIN MICROBIOL & INFECT DIS, MT ZION MED CTR, SAN FRANCISCO, CA 94143 USA
关键词
D O I
10.1086/517302
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In a human immunodeficiency virus-infected subject, cytomegalovirus (CMV) isolated 9 months after the patient began oral ganciclovir prophylaxis was resistant to ganciclovir and cidofovir and contained mutations in both UL97 and pol coding regions. At 1 year, retinitis developed, which progressed despite intravenous ganciclovir followed by foscarnet and then cidofovir. A subsequent buffy coat virus isolate was resistant to all three drugs and contained new mutations in UL97 and Pol. By individually transferring the observed mutations to laboratory strain AD169, it was shown that a mutation at codon 603 of UL97 conferred resistance to ganciclovir, a mutation at codon 412 of Pol conferred resistance to both ganciclovir and cidofovir, and a mutation at codon 802 of pol conferred resistance to ganciclovir and foscarnet. This case illustrates the development of multidrug resistance during prolonged exposure to antiviral therapy for CMV and cross-resistance arising from point mutations in the CMV Pol gene.
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页码:786 / 789
页数:4
相关论文
共 13 条
[1]   Single amino acid changes in the DNA polymerase confer foscarnet resistance and slow-growth phenotype, while mutations in the UL97-encoded phosphotransferase confer ganciclovir resistance in three double-resistant human cytomegalovirus strains recovered from patients with AIDS [J].
Baldanti, F ;
Underwood, MR ;
Stanat, SC ;
Biron, KK ;
Chou, SW ;
Sarasini, A ;
Silini, E ;
Gerna, G .
JOURNAL OF VIROLOGY, 1996, 70 (03) :1390-1395
[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, 1995, SCAND J INFECT DIS, P103
[4]   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
[5]   ANALYSIS OF THE UL97 PHOSPHOTRANSFERASE CODING SEQUENCE IN CLINICAL CYTOMEGALOVIRUS ISOLATES AND IDENTIFICATION OF MUTATIONS CONFERRING GANCICLOVIR RESISTANCE [J].
CHOU, SW ;
ERICE, A ;
JORDAN, MC ;
VERCELLOTTI, GM ;
MICHELS, KR ;
TALARICO, CL ;
STANAT, SC ;
BIRON, KK .
JOURNAL OF INFECTIOUS DISEASES, 1995, 171 (03) :576-583
[6]  
CRUMPACKER CS, 1996, J ACQUIRED IMMUNE S1, V12, pS1
[7]  
Drew W L, 1993, Clin Diagn Virol, V1, P179
[8]   Antiviral susceptibilities and analysis of UL97 and DNA polymerase sequences of clinical cytomegalovirus isolates from immunocompromised patients [J].
Erice, A ;
GilRoda, C ;
Perez, JL ;
Balfour, HH ;
Sannerud, KJ ;
Hanson, MN ;
Boivin, G ;
Chou, SW .
JOURNAL OF INFECTIOUS DISEASES, 1997, 175 (05) :1087-1092
[9]   NOVEL MUTATION IN THE UL97 GENE OF A CLINICAL CYTOMEGALOVIRUS STRAIN CONFERRING RESISTANCE TO GANCICLOVIR [J].
HANSON, MN ;
PREHEIM, LC ;
CHOU, SW ;
TALARICO, CL ;
BIRON, KK ;
ERICE, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (05) :1204-1205
[10]   POINT MUTATIONS IN THE DNA-POLYMERASE GENE OF HUMAN CYTOMEGALOVIRUS THAT RESULT IN RESISTANCE TO ANTIVIRAL AGENTS [J].
LURAIN, NS ;
THOMPSON, KD ;
HOLMES, EW ;
READ, GS .
JOURNAL OF VIROLOGY, 1992, 66 (12) :7146-7152