Transcriptional response of Enterococcus faecalis V583 to erythromycin

被引:63
作者
Aakra, Å
Vebo, H
Snipen, L
Hirt, H
Aastveit, A
Kapur, V
Dunny, G
Murray, B
Nes, IF
机构
[1] Norwegian Univ Life Sci, Lab Microbial Gene Technol, N-1432 As, Norway
[2] Norwegian Univ Life Sci, Sect Bioinformat & Data Anal, N-1432 As, Norway
[3] Norwegian Univ Life Sci, Dept Chem Biotechnol & Food Sci, N-1432 As, Norway
[4] Univ Minnesota, Sch Med, Dept Microbiol, Minneapolis, MN 55455 USA
[5] Univ Minnesota, Dept Vet Pathobiol, Biomed Genom Ctr, St Paul, MN 55108 USA
[6] Univ Texas, Sch Med, Ctr Study Emerging & Reemerging Pathogens, Houston, TX 77030 USA
关键词
D O I
10.1128/AAC.49.6.2246-2259.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A transcriptional profile of Enterococcus faecalis V583 (V583) treated with erythromycin is presented. This is the first study describing a complete transcriptional profile of Enterococcus. E. faecalis is a common and nonvirulent bacterium in many natural environments, but also an important cause of nosocomial infections. We have used a genome-wide microarray based on the genome sequence of V583 to study gene expression in cells exposed to erythromycin. V583 is resistant to relatively high concentrations of erythromycin, but growth is retarded by the treatment. The effect of erythromycin treatment on V583 was studied by a time course experiment; samples were extracted at five time points over a period of 90 min. A drastic change in gene transcription was seen with the erythromycin-treated cells compared to the untreated cells. Altogether, 260 genes were down-regulated at one or more time points, while 340 genes were up-regulated. Genes encoding hypothetical proteins and genes encoding transport and binding proteins were the two most dominating groups of differentially expressed genes. The gene encoding ermB (EFA0007) was expressed, but not differentially, which indicated that other genes are important for the survival and growth maintenance of V583 treated with erythromycin. One of these genes is a putative MsrC-like protein, which was up-regulated at all time points studied. Other specific genes that were found to be up-regulated were genes encoding ABC transporters and two-component regulatory systems, and these may be genes that are important for the specific response of V583 to erythromycin.
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页码:2246 / 2259
页数:14
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