Transcriptional modulation of bacterial gene expression by subinhibitory concentrations of antibiotics

被引:391
作者
Goh, EB
Yim, G
Tsui, W
McClure, J
Surette, MG
Davies, J
机构
[1] Univ British Columbia, Dept Microbiol & Immunol, Vancouver, BC V6T 1Z3, Canada
[2] Univ Calgary, Dept Microbiol & Infect Dis, Calgary, AB T2N 4N1, Canada
关键词
D O I
10.1073/pnas.252607699
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Antibiotics such as erythromycin and rifampicin, at low concentrations, alter global bacterial transcription patterns as measured by the stimulation or inhibition of a variety of promoter-lux reporter constructs in a Salmonella typhimurium library. Analysis of a 6,500-clone library indicated that as many as 5% of the promoters may be affected, comprising genes for a variety of functions, as well as a significant fraction of genes with no known function. Studies of a selection of the reporter clones showed that stimulation varied depending on the nature of the antibiotic, the promoter, and what culture medium was used; the response differed on solid as compared with liquid media. Transcription was markedly reduced in antibiotic-resistant hosts, but the presence of mutations deficient in stress responses such as SOS or universal stress did not prevent antibiotic-induced modulation. The results show that small molecules may have contrasting effects on bacteria depending on their concentration: either the modulation of bacterial metabolism by altering transcription patterns or the inhibition of growth by the inhibition of specific target functions. Both activities could play important roles in the regulation of microbial communities. These studies indicate that the detection of pharmaceutically useful natural product inhibitors could be effectively achieved by measuring activation of transcription at low concentrations in high-throughput assays using appropriate bacterial promoter-reporter constructs.
引用
收藏
页码:17025 / 17030
页数:6
相关论文
共 27 条
[11]   Large-scale monitoring of pleiotropic regulation of gene expression by the prokaryotic nucleoid-associated protein, H-NS [J].
Hommais, F ;
Krin, E ;
Laurent-Winter, C ;
Soutourina, O ;
Malpertuy, A ;
Le Caer, JP ;
Danchin, A ;
Bertin, P .
MOLECULAR MICROBIOLOGY, 2001, 40 (01) :20-36
[12]   MAPPING AND SEQUENCING OF MUTATIONS IN THE ESCHERICHIA-COLI RPOB GENE THAT LEAD TO RIFAMPICIN RESISTANCE [J].
JIN, DJ ;
GROSS, CA .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 202 (01) :45-58
[13]   PHEROMONES, SOCIAL-BEHAVIOR AND THE FUNCTIONS OF SECONDARY METABOLISM IN BACTERIA [J].
KELL, DB ;
KAPRELYANTS, AS ;
GRAFEN, A .
TRENDS IN ECOLOGY & EVOLUTION, 1995, 10 (03) :126-129
[14]   IDENTIFICATION OF A CENTRAL REGULATOR OF STATIONARY-PHASE GENE-EXPRESSION IN ESCHERICHIA-COLI [J].
LANGE, R ;
HENGGEARONIS, R .
MOLECULAR MICROBIOLOGY, 1991, 5 (01) :49-59
[15]   SdiA of Salmonella enterica is a LuxR homolog that detects mixed microbial communities [J].
Michael, B ;
Smith, JN ;
Swift, S ;
Heffron, F ;
Ahmer, BMM .
JOURNAL OF BACTERIOLOGY, 2001, 183 (19) :5733-5742
[16]   Acyl-homoserine lactone quorum sensing in Gram-negative bacteria: A signaling mechanism involved in associations with higher organisms [J].
Parsek, MR ;
Greenberg, EP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (16) :8789-8793
[17]  
PIEPERSBERG W, 2001, MOL MED MICROBIOLOGY, V1, P561
[18]   A general definition of metabolic pathways useful for systematic organization and analysis of complex metabolic networks [J].
Schuster, S ;
Fell, DA ;
Dandekar, T .
NATURE BIOTECHNOLOGY, 2000, 18 (03) :326-332
[19]  
Storz G, 2000, BACTERIAL STRESS RESPONSES, P47
[20]  
Strohl W.R., 1997, Biotechnology of antibiotics