Detection of and response to signals involved in host-microbe interactions by plant-associated bacteria

被引:241
作者
Brencic, A [1 ]
Winans, SC [1 ]
机构
[1] Cornell Univ, Dept Microbiol, Ithaca, NY 14853 USA
关键词
D O I
10.1128/MMBR.69.1.155-194.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Diverse interactions between hosts and microbes are initiated by the detection of host-released chemical signals. Detection of these signals leads to altered patterns of gene expression that culminate in specific and adaptive changes in bacterial physiology that are required for these associations. This concept was first demonstrated for the members of the family Rhizobiaceae and was later found to apply to many other plant-associated bacteria as well as to microbes that colonize human and animal hosts. The family Rhizobiaceae includes various genera of rhizobia as well as species of Agrobacterium. Rhizobia are symbionts of legumes, which fix nitrogen within root nodules, while Agrobacterium tumefaciens is a pathogen that causes crown gall tumors on a wide variety of plants. The plant-released signals that are recognized by these bacteria are low-molecular-weight, diffusible molecules and are detected by the bacteria through specific receptor proteins. Similar phenomena are observed with other plant pathogens, including Pseudomonas syringae, Ralstonia solanacearum, and Erwinia spp., although here the signals and signal receptors are not as well defined. In some cases, nutritional conditions such as iron limitation or the lack of nitrogen sources seem to provide a significant cue. While much has been learned about the process of host detection over the past 20 years, our knowledge is far from being complete. The complex nature of the plant-microbe interactions makes it extremely challenging to gain a comprehensive picture of host detection in natural environments, and thus many signals and signal recognition systems remain to be described.
引用
收藏
页码:155 / +
页数:41
相关论文
共 555 条
[1]   CHEMOTAXIS TOWARD SUGARS IN ESCHERICHIA-COLI [J].
ADLER, J ;
HAZELBAUER, GL ;
DAHL, MM .
JOURNAL OF BACTERIOLOGY, 1973, 115 (03) :824-847
[2]  
Agron PG, 1995, 2 COMPONENT SIGNAL T, P275
[3]  
AGUILAR JMM, 1988, J GEN MICROBIOL, V134, P2741
[4]   Mutations in the occQ operator that decrease OccR-induced DNA bending do not cause constitutive promoter activity [J].
Akakura, R ;
Winans, SC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (18) :15773-15780
[5]   Ralstonia solanacearum -: a plant pathogen in touch with its host:: Response [J].
Aldon, D ;
Genin, S .
TRENDS IN MICROBIOLOGY, 2000, 8 (11) :489-489
[6]   A bacterial sensor of plant cell contact controls the transcriptional induction of Ralstonia solanacearum pathogenicity genes [J].
Aldon, D ;
Brito, B ;
Boucher, C ;
Genin, S .
EMBO JOURNAL, 2000, 19 (10) :2304-2314
[7]  
Alfano JR, 1996, PLANT CELL, V8, P1683, DOI 10.1105/tpc.8.10.1683
[8]   The type III (Hrp) secretion pathway of plant pathogenic bacteria: trafficking harpins, Avr proteins, and death [J].
Alfano, JR ;
Collmer, A .
JOURNAL OF BACTERIOLOGY, 1997, 179 (18) :5655-5662
[9]   TEMPERATURE-SENSITIVE STEP IN TI PLASMID VIR-REGION INDUCTION AND CORRELATION WITH CYTOKININ SECRETION BY AGROBACTERIA [J].
ALTMOERBE, J ;
NEDDERMANN, P ;
VONLINTIG, J ;
WEILER, EW ;
SCHRODER, J .
MOLECULAR & GENERAL GENETICS, 1988, 213 (01) :1-8
[10]   The ecology and biogeography of microorganisms of plant surfaces [J].
Andrews, JH ;
Harris, RF .
ANNUAL REVIEW OF PHYTOPATHOLOGY, 2000, 38 :145-180