Evolution of a vancomycin-intermediate Staphylococcus aureus strain in vivo:: Multiple changes in the antibiotic resistance phenotypes of a single lineage of methicillin-resistant S-aureus under the impact of antibiotics administered for chemotherapy

被引:106
作者
Sieradzki, K
Leski, T
Dick, J
Borio, L
Tomasz, A
机构
[1] Rockefeller Univ, New York, NY 10021 USA
[2] Johns Hopkins Med Inst, Baltimore, MD 21287 USA
关键词
D O I
10.1128/JCM.41.4.1687-1693.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A number of methicillin-resistant Staphylococcus aureus (MRSA) isolates were recovered over a period of several weeks from blood samples and from the heart valve of a patient who underwent extensive vancomycin chemotherapy for persistent S. aureus bacteremia. Consecutive isolates showed gradually decreasing growth rates during in vitro cultivation and increasing vancomycin MICs, from an MIC of 1 mug/ml for the initial isolate to an MIC of 8 mug/ml for the final MRSA isolates, which also became tolerant to vancomycin. Major changes were observed in the oxacillin resistance phenotype of several of the isolates-apparently related to in vivo exposure to imipenem, which was also used during a period of chemotherapy. Both the gradually increasing vancomycin MICs and the changes in oxacillin resistance could be reproduced by appropriate exposure of the initial MRSA isolate to antibiotics in vitro. All isolates had the same pulsed-field gel electrophoresis pattern, spaA type, and multilocus sequence type (MLST), which was identified as a single-locus variant of STS, the MLST characteristic of previously characterized MRSA isolates with reduced susceptibility to vancomycin in the United States and Japan.
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页码:1687 / 1693
页数:7
相关论文
共 21 条
[1]  
AUSUBEL FM, 1995, CURRENT PROTOCOLS MO, P241
[2]  
Centers for Disease Control and Prevention (CDC), 1997, MMWR Morb Mortal Wkly Rep, V46, P813
[3]   Molecular typing of methicillin-resistant Staphylococcus aureus by pulsed-field gel electrophoresis:: Comparison of results obtained in a multilaboratory effort using identical protocols and MRSA strains [J].
Chung, M ;
De Lencastre, H ;
Matthews, P ;
Tomasz, A ;
Adamsson, I ;
De Sousa, MA ;
Camou, T ;
Cocuzza, C ;
Corso, A ;
Couto, I ;
Dominguez, A ;
Gniadkowski, M ;
Goering, R ;
Gomes, A ;
Kikuchi, K ;
Marchese, A ;
Mato, R ;
Melter, O ;
Oliveira, D ;
Palacio, R ;
Sá-Leao, R ;
Sanches, IS ;
Song, JH ;
Tassios, PT ;
Villari, P .
MICROBIAL DRUG RESISTANCE-MECHANISMS EPIDEMIOLOGY AND DISEASE, 2000, 6 (03) :189-198
[4]   EVALUATION OF THE BACTERICIDAL ACTIVITY OF BETA-LACTAM ANTIBIOTICS ON SLOWLY GROWING BACTERIA CULTURED IN THE CHEMOSTAT [J].
COZENS, RM ;
TUOMANEN, E ;
TOSCH, W ;
ZAK, O ;
SUTER, J ;
TOMASZ, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1986, 29 (05) :797-802
[5]   The evolution of methicillin resistance in Staphylococcus aureus:: Similarity of genetic backgrounds in historically early methicillin-susceptible and -resistant isolates and contemporary epidemic clones [J].
Crisóstomo, MI ;
Westh, H ;
Tomasz, A ;
Chung, M ;
Oliveira, DC ;
de Lencastre, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (17) :9865-9870
[6]   Similarity of antibiotic resistance patterns and molecular typing properties of methicillin-resistant Staphylococcus aureus isolates widely spread in hospitals in New York City and in a hospital in Tokyo, Japan [J].
De Sousa, MA ;
De Lencastre, H ;
Sanches, IS ;
Kikuchi, K ;
Totsuka, K ;
Tomasz, A .
MICROBIAL DRUG RESISTANCE-MECHANISMS EPIDEMIOLOGY AND DISEASE, 2000, 6 (03) :253-258
[7]   BACTERICIDAL EFFECTS OF ANTIBIOTICS ON SLOWLY GROWING AND NONGROWING BACTERIA [J].
ENG, RHK ;
PADBERG, FT ;
SMITH, SM ;
TAN, EN ;
CHERUBIN, CE .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (09) :1824-1828
[8]   Multilocus sequence typing for characterization of methicillin-resistant and methicillin-susceptible clones of Staphylococcus aureus [J].
Enright, MC ;
Day, NPJ ;
Davies, CE ;
Peacock, SJ ;
Spratt, BG .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (03) :1008-1015
[9]   Methicillin-resistant Staphylococcus aureus clinical strain with reduced vancomycin susceptibility [J].
Hiramatsu, K ;
Hanaki, H ;
Ino, T ;
Yabuta, K ;
Oguri, T ;
Tenover, FC .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 40 (01) :135-136
[10]  
NCCLS, 2000, PERF STAND ANT DISK