Home LiteratureArticle Details
PMID: 11607544 Published · ppublish English Journal Article

Molecular mechanisms of defense by rhizobacteria against root disease.

Cook RJ, Thomashow LS, Weller DM, Fujimoto D, Mazzola M, Bangera G, Kim DS

Abstract

Genetic resistance in plants to root diseases is rare, and agriculture depends instead on practices such as crop rotation and soil fumigation to control these diseases. "Induced suppression" is a natural phenomenon whereby a soil due to microbiological changes converts from conducive to suppressive to a soilborne pathogen during prolonged monoculture of the susceptible host. Our studies have focused on the wheat root disease "take-all," caused by the fungus Gaeumannomyces graminis var. tritici, and the role of bacteria in the wheat rhizosphere (rhizobacteria) in a well-documented induced suppression (take-all decline) that occurs in response to the disease and continued monoculture of wheat. The results summarized herein show that antibiotic production plays a significant role in both plant defense by and ecological competence of rhizobacteria. Production of phenazine and phloroglucinol antibiotics, as examples, account for most of the natural defense provided by fluorescent Pseudomonas strains isolated from among the diversity of rhizobacteria associated with take-all decline. There appear to be at least three levels of regulation of genes for antibiotic biosynthesis: environmental sensing, global regulation that ties antibiotic production to cellular metabolism, and regulatory loci linked to genes for pathway enzymes. Plant defense by rhizobacteria producing antibiotics on roots and as cohabitants with pathogens in infected tissues is analogous to defense by the plant's production of phytoalexins, even to the extent that an enzyme of the same chalcone/stilbene synthase family used to produce phytoalexins is used to produce 2,4-diacetylphloroglucinol. The defense strategy favored by selection pressure imposed on plants by soilborne pathogens may well be the ability of plants to support and respond to rhizosphere microorganisms antagonistic to these pathogens.

Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Cook R J
United States Department of Agriculture, Agricultural Research Service, Root Disease and Biological Control Research, Washington State University, Pullman, WA 99164-6430, USA.
Thomashow L S
Weller D M
Fujimoto D
Mazzola M
Bangera G
Kim D S
References (16)
16 references, click to expand
  1. Isolation of 2,4-diacetylphloroglucinol from a fluorescent pseudomonad and investigation of physiological parameters influencing its production.
    Appl Environ Microbiol. 1992 Jan;58(1):353-8 PMID: 16348633
  2. Production of the antibiotic phenazine-1-carboxylic Acid by fluorescent pseudomonas species in the rhizosphere of wheat.
    Appl Environ Microbiol. 1990 Apr;56(4):908-12 PMID: 16348176
  3. Salicylic Acid: a likely endogenous signal in the resistance response of tobacco to viral infection.
    Science. 1990 Nov 16;250(4983):1002-4 PMID: 17746925
  4. Extracellular protease and phospholipase C are controlled by the global regulatory gene gacA in the biocontrol strain Pseudomonas fluorescens CHA0.
    FEMS Microbiol Lett. 1994 Feb 15;116(2):155-60 PMID: 8150259
  5. Zwittermicin A-producing strains of Bacillus cereus from diverse soils.
    Appl Environ Microbiol. 1994 Dec;60(12):4404-12 PMID: 7811080
  6. Global regulation of expression of antifungal factors by a Pseudomonas fluorescens biological control strain.
    Mol Plant Microbe Interact. 1994 Jul-Aug;7(4):455-63 PMID: 8075420
  7. Iron metabolism in Pseudomonas: salicylic acid, a siderophore of Pseudomonas fluorescens CHAO.
    Biofactors. 1992 Dec;4(1):23-7 PMID: 1292472
  8. Cloning and heterologous expression of the phenazine biosynthetic locus from Pseudomonas aureofaciens 30-84.
    Mol Plant Microbe Interact. 1992 Jul-Aug;5(4):330-9 PMID: 1325219
  9. Contribution of phenazine antibiotic biosynthesis to the ecological competence of fluorescent pseudomonads in soil habitats.
    Appl Environ Microbiol. 1992 Aug;58(8):2616-24 PMID: 1514808
  10. Genetic analysis of the antifungal activity of a soilborne Pseudomonas aureofaciens strain.
    Appl Environ Microbiol. 1991 Oct;57(10):2928-34 PMID: 1660695
  11. Relative importance of fluorescent siderophores and other factors in biological control of Gaeumannomyces graminis var. tritici by Pseudomonas fluorescens 2-79 and M4-80R.
    Appl Environ Microbiol. 1991 Nov;57(11):3270-7 PMID: 1838240
  12. Global control in Pseudomonas fluorescens mediating antibiotic synthesis and suppression of black root rot of tobacco.
    Proc Natl Acad Sci U S A. 1992 Mar 1;89(5):1562-6 PMID: 1311842
  13. Exploitation of gene(s) involved in 2,4-diacetylphloroglucinol biosynthesis to confer a new biocontrol capability to a Pseudomonas strain.
    Appl Environ Microbiol. 1992 Dec;58(12):3873-8 PMID: 1476431
  14. Role of a phenazine antibiotic from Pseudomonas fluorescens in biological control of Gaeumannomyces graminis var. tritici.
    J Bacteriol. 1988 Aug;170(8):3499-508 PMID: 2841289
  15. [Effect of bacterial antagonists on the development of wheat root rot].
    Mikrobiol Zh. 1974 Sep-Oct;36(5):599-602 PMID: 4465699
  16. [Antibiotic action of bacteria of the genus Pseudomonas on phytopathogenic fungi].
    Mikrobiol Zh. 1974 Feb-Mar;36(2):197-202 PMID: 4465652
Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1995-05-09
Pages
4197-201
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC41910
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com