Unraveling the secret lives of bacteria: Use of in vivo expression technology and differential fluorescence induction promoter traps as tools for exploring niche-specific gene expression

被引:105
作者
Rediers, H
Rainey, PB
Vanderleyden, J
De Mot, R
机构
[1] Katholieke Univ Leuven, Ctr Microbial & Plant Genet, B-3001 Heverlee, Belgium
[2] De Nayer Inst, B-2860 St Katelijne Waver, Belgium
[3] Univ Auckland, Sch Biol Sci, Auckland, New Zealand
[4] Univ Oxford, Dept Plant Sci, Oxford, England
关键词
D O I
10.1128/MMBR.69.2.217-261.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A major challenge for microbiologists is to elucidate the strategies used by microorganisms to adapt to and thrive in highly complex and dynamic environments. In vitro studies, including those monitoring genomewide changes, have proven their value, but they, can, at best, mimic only a subset of the ensemble of abiotic and biotic stimuli that microorganisms experience in their natural habitats. The widely used gene-to-phenotype approach involves the identification of altered niche-related phenotypes on the basis of gene inactivation. However, many traits contributing to ecological performance that, upon inactivation, result in only subtle or difficult-to-score phenotypic changes are likely to be overlooked by this otherwise powerful approach. Based on the premise that many, if not most, of the corresponding genes will be induced or upregulated in the environment under study, ecologically significant genes can alternatively be traced using the promoter trap techniques differential fluorescence induction and in vivo expression technology (IVET). The potential anti limitations tire discussed fin. the different IVET selection strategies and system-specific variants thereof: Based on it compendium of genes that have emerged from these promoter-trapping studies, several functional groups have been distinguished, and their physiological relevance is illustrated with follow-up studies of selected genes. In addition to confirming results from largely, complementary approaches such as signature-tagged mutagenesis, some unexpected parallels as well as distinguishing features of microbial phenotypic acclimation in diverse environmental niches have surfaced. On the other hand, by the identification of a large proportion of genes with unknown function, these promoter-trapping studies underscore how little we know about the secret lives of bacteria and other microorganisms.
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页码:217 / +
页数:47
相关论文
共 306 条
[21]   CYCLIC BETA-GLUCANS OF MEMBERS OF THE FAMILY RHIZOBIACEAE [J].
BREEDVELD, MW ;
MILLER, KJ .
MICROBIOLOGICAL REVIEWS, 1994, 58 (02) :145-161
[22]   PHOSPHOTRANSACETYLASE ASSOCIATED WITH PYRUVATE DEHYDROGENASE COMPLEX FROM NITROGEN FIXING AZOTOBACTER-VINELANDII [J].
BRESTERS, TW ;
KRUL, J ;
VEEGER, C ;
SCHEEPENS, PC .
FEBS LETTERS, 1972, 22 (03) :305-+
[23]   Mig-14 is an inner membrane-associated protein that promotes Salmonella typhimurium resistance to CRAMP, survival within activated macrophages and persistent infection [J].
Brodsky, IE ;
Ghori, N ;
Falkow, S ;
Monack, D .
MOLECULAR MICROBIOLOGY, 2005, 55 (03) :954-972
[24]   Identification of Lactobacillus plantarum genes that are induced in the gastrointestinal tract of mice [J].
Bron, PA ;
Grangette, C ;
Mercenier, A ;
de Vos, WM ;
Kleerebezem, M .
JOURNAL OF BACTERIOLOGY, 2004, 186 (17) :5721-5729
[25]   Keys to symbiotic harmony [J].
Broughton, WJ ;
Jabbouri, S ;
Perret, X .
JOURNAL OF BACTERIOLOGY, 2000, 182 (20) :5641-5652
[26]   Ralstonia solanacearum genes induced during growth in tomato:: an inside view of bacterial wilt [J].
Brown, DG ;
Allen, C .
MOLECULAR MICROBIOLOGY, 2004, 53 (06) :1641-1660
[27]   Phages and the evolution of bacterial pathogens:: From genomic rearrangements to lysogenic conversion [J].
Brüssow, H ;
Canchaya, C ;
Hardt, WD .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2004, 68 (03) :560-+
[28]  
Buchanan BB., 2015, Biochemistry and Molecular Biology of Plants
[29]   THE PECKING ORDER OF FREE-RADICALS AND ANTIOXIDANTS - LIPID-PEROXIDATION, ALPHA-TOCOPHEROL, AND ASCORBATE [J].
BUETTNER, GR .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 300 (02) :535-543
[30]   Examination of Salmonella gene expression in an infected mammalian host using the green fluorescent protein and two-colour flow cytometry [J].
Bumann, D .
MOLECULAR MICROBIOLOGY, 2002, 43 (05) :1269-1283