Sequence polymorphisms in the Pneumocysits carinii cytochrome b gene and their association with atovaquone prophylaxis failure

被引:104
作者
Walker, DJ
Wakefield, AE
Dohn, MN
Miller, RE
Baughman, RP
Hossler, PA
Bartlett, MS
Smith, JW
Kazanjian, P
Meshnick, SR [1 ]
机构
[1] Univ Michigan, Sch Publ Hlth 1, Dept Epidemiol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Internal Med, Div Infect Dis, Ann Arbor, MI 48109 USA
[3] Univ Cincinnati, Coll Med, Dept Internal Med, Cincinnati, OH USA
[4] Indiana Univ, Med Ctr, Dept Pathol & Lab Med, Indianapolis, IN USA
[5] Univ Oxford, Inst Mol Med, Dept Paediat, Mol Infect Dis Grp, Oxford, England
[6] UCL, Sch Med, Dept Sexually Transmitted Dis, Div Pathol & Infect Dis, London W1N 8AA, England
来源
JOURNAL OF INFECTIOUS DISEASES | 1998年 / 178卷 / 06期
关键词
D O I
10.1086/314509
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Atovaquone (Mepron, 566c80) is an effective agent against Pneumocystis carinii, which probably acts by binding to cytochrome b and inhibiting electron transport, To assess the possibility that atovaquone resistance might be developing, the genes for the cytochrome b from P. carinii sp, f. carinii and P. carinii sp, f. hominis were partially sequenced. Eight of 10 patient isolates had cytochrome b genes with the same amino acid sequence, The P. carinii cytochrome b genes from 2 of 4 patients who had atovaquone prophylaxis failure contained mutations resulting in amino acid changes in one of the ubiquinone (coenzyme Q) binding sites (Q(o)), These mutations are homologous to mutations in other microorganisms that confer resistance to similar inhibitors. Variations in the sequence of the I! carinii cytochrome b gene suggest but do not prove the development of drug resistance.
引用
收藏
页码:1767 / 1775
页数:9
相关论文
共 39 条
[1]  
ALBERS B, 1989, MOL BIOL CELL
[2]   THE CLONING AND CHARACTERIZATION OF THE AROM GENE OF PNEUMOCYSTIS-CARINII [J].
BANERJI, S ;
WAKEFIELD, AE ;
ALLEN, AG ;
MASKELL, DJ ;
PETERS, SE ;
HOPKIN, JM .
JOURNAL OF GENERAL MICROBIOLOGY, 1993, 139 :2901-2914
[3]  
*CDCP, 1997, MMWR-MORBID MORTAL W, V46, P1
[4]   MUTATIONS CONFERRING RESISTANCE TO QUINOL OXIDATION (QZ) INHIBITORS OF THE CYT-BC1 COMPLEX OF RHODOBACTER-CAPSULATUS [J].
DALDAL, F ;
TOKITO, MK ;
DAVIDSON, E ;
FAHAM, M .
EMBO JOURNAL, 1989, 8 (13) :3951-3961
[5]   MITOCHONDRIAL CYTOCHROME-B - EVOLUTION AND STRUCTURE OF THE PROTEIN [J].
DEGLIESPOSTI, M ;
DEVRIES, S ;
CRIMI, M ;
GHELLI, A ;
PATARNELLO, T ;
MEYER, A .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1143 (03) :243-271
[6]  
DIRAGO JP, 1989, J BIOL CHEM, V264, P14543
[7]   SITE OF ACTION OF THE ANTIMALARIAL HYDROXYNAPHTHOQUINONE, 2-[TRANS-4-(4'-CHLOROPHENYL) CYCLOHEXYL]-3-HYDROXY-1,4-NAPHTHOQUINONE (566C80) [J].
FRY, M ;
PUDNEY, M .
BIOCHEMICAL PHARMACOLOGY, 1992, 43 (07) :1545-1553
[8]   INHIBITION OF RECOMBINANT PNEUMOCYSTIS-CARINII DIHYDROPTEROATE SYNTHETASE BY SULFA DRUGS [J].
HONG, YL ;
HOSSLER, PA ;
CALHOUN, DH ;
MESHNICK, SR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (08) :1756-1763
[9]   MUTATIONAL ANALYSIS OF THE MOUSE MITOCHONDRIAL CYTOCHROME-B GENE [J].
HOWELL, N ;
GILBERT, K .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 203 (03) :607-618
[10]   THE EFFECTS OF ANTIMALARIALS ON THE PLASMODIUM-FALCIPARUM DIHYDROOROTATE DEHYDROGENASE [J].
ITTARAT, I ;
ASAWAMAHASAKDA, W ;
MESHNICK, SR .
EXPERIMENTAL PARASITOLOGY, 1994, 79 (01) :50-56