Using microarray gene signatures to elucidate mechanisms of antibiotic action and resistance

被引:100
作者
Brazas, MD [1 ]
Hancock, REW [1 ]
机构
[1] Univ British Columbia, Ctr Microbial Dis & Immun Res, Vancouver, BC V6T 1Z4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
D O I
10.1016/S1359-6446(05)03566-X
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Microarray analyses reveal global changes in gene expression in response to environmental changes and, thus, are well suited to providing a detailed picture of bacterial responses to antibiotic treatment. These responses are represented by patterns of gene expression, termed expression signatures, which provide insight into the mechanism of action of antibiotics as well as the general physiological responses of bacteria to antibiotic-related stresses. The complexity of such signatures is challenging the notion that antibiotics act on single targets and this is consistent with the concept that there are multiple targets coupled with common stress responses. A more detailed knowledge of how known antibiotics act should reveal new strategies for antimicrobial drug discovery.
引用
收藏
页码:1245 / 1252
页数:8
相关论文
共 48 条
[1]   Peptide deformylase as an antibacterial drug target:: Target validation and resistance development [J].
Apfel, CM ;
Locher, H ;
Evers, S ;
Takács, B ;
Hubschwerlen, C ;
Pirson, W ;
Page, MGP ;
Keck, W .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (04) :1058-1064
[2]   Proteomic approach to understanding antibiotic action [J].
Bandow, JE ;
Brötz, H ;
Leichert, LIO ;
Labischinski, H ;
Hecker, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (03) :948-955
[3]   Antibiotic resistance - what can we do? [J].
Bax, RP ;
Anderson, R ;
Crew, J ;
Fletcher, P ;
Johnson, T ;
Kaplan, E ;
Knaus, B ;
Kristinsson, K ;
Malek, M ;
Strandberg, L .
NATURE MEDICINE, 1998, 4 (05) :545-546
[4]   Signature gene expression profiles discriminate between isoniazid-, thiolactomycin-, and triclosan-treated Mycobacterium tuberculosis [J].
Betts, JC ;
McLaren, A ;
Lennon, MG ;
Kelly, FM ;
Lukey, PT ;
Blakemore, SJ ;
Duncan, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (09) :2903-2913
[5]   Minimum information about a microarray experiment (MIAME) - toward standards for microarray data [J].
Brazma, A ;
Hingamp, P ;
Quackenbush, J ;
Sherlock, G ;
Spellman, P ;
Stoeckert, C ;
Aach, J ;
Ansorge, W ;
Ball, CA ;
Causton, HC ;
Gaasterland, T ;
Glenisson, P ;
Holstege, FCP ;
Kim, IF ;
Markowitz, V ;
Matese, JC ;
Parkinson, H ;
Robinson, A ;
Sarkans, U ;
Schulze-Kremer, S ;
Stewart, J ;
Taylor, R ;
Vilo, J ;
Vingron, M .
NATURE GENETICS, 2001, 29 (04) :365-371
[6]   ArrayExpress - a public repository for microarray gene expression data at the EBI [J].
Brazma, A ;
Parkinson, H ;
Sarkans, U ;
Shojatalab, M ;
Vilo, J ;
Abeygunawardena, N ;
Holloway, E ;
Kapushesky, M ;
Kemmeren, P ;
Lara, GG ;
Oezcimen, A ;
Rocca-Serra, P ;
Sansone, SA .
NUCLEIC ACIDS RESEARCH, 2003, 31 (01) :68-71
[7]   Taking inventory: antibacterial agents currently at or beyond Phase 1 [J].
Bush, K ;
Macielag, M ;
Weidner-Wells, M .
CURRENT OPINION IN MICROBIOLOGY, 2004, 7 (05) :466-476
[8]   Computing prokaryotic gene ubiquity: Rescuing the core from extinction [J].
Charlebois, RL ;
Doolittle, WF .
GENOME RESEARCH, 2004, 14 (12) :2469-2477
[9]   The future challenges facing the development of new antimicrobial drugs [J].
Coates, A ;
Hu, YM ;
Bax, R ;
Page, C .
NATURE REVIEWS DRUG DISCOVERY, 2002, 1 (11) :895-910
[10]   Gene Expression Omnibus: NCBI gene expression and hybridization array data repository [J].
Edgar, R ;
Domrachev, M ;
Lash, AE .
NUCLEIC ACIDS RESEARCH, 2002, 30 (01) :207-210