Literature DB >> 17058178

Role of 2,4-diacetylphloroglucinol-producing fluorescent Pseudomonas spp. in the defense of plant roots.

D M Weller1, B B Landa, O V Mavrodi, K L Schroeder, L De La Fuente, S Blouin Bankhead, R Allende Molar, R F Bonsall, D V Mavrodi, L S Thomashow.   

Abstract

Plants have evolved strategies of stimulating and supporting specific groups of antagonistic microorganisms in the rhizosphere as a defense against diseases caused by soilborne plant pathogens owing to a lack of genetic resistance to some of the most common and widespread soilborne pathogens. Some of the best examples of natural microbial defense of plant roots occur in disease suppressive soils. Soil suppressiveness against many different diseases has been described. Take-all is an important root disease of wheat, and soils become suppressive to take-all when wheat or barley is grown continuously in a field following a disease outbreak; this phenomenon is known as take-all decline (TAD). In Washington State, USA and The Netherlands, TAD results from the enrichment during monoculture of populations of 2,4-diacetylphloroglucinol (2,4-DAPG)-producing Pseudomonas fluorescens to a density of 10 (5) CFU/g of root, the threshold required to suppress the take-all pathogen, Gaeumannomyces graminis var. tritici. 2,4-DAPG-producing P. fluorescens also are enriched by monoculture of other crops such as pea and flax, and evidence is accumulating that 2,4-DAPG producers contribute to the defense of plant roots in many different agroecosystems. At this time, 22 distinct genotypes of 2,4-DAPG producers (designated A - T, PfY and PfZ) have been defined by whole-cell repetitive sequence-based (rep)-PCR analysis, restriction fragment length polymorphism (RFLP) analysis of PHLD, and phylogenetic analysis of PHLD, but the number of genotypes is expected to increase. The genotype of an isolate is predictive of its rhizosphere competence on wheat and pea. Multiple genotypes often occur in a single soil and the crop species grown modulates the outcome of the competition among these genotypes in the rhizosphere. 2,4-DAPG producers are highly effective biocontrol agents against a variety of plant diseases and ideally suited for serving as vectors for expressing other biocontrol traits in the rhizosphere.

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Year:  2006        PMID: 17058178     DOI: 10.1055/s-2006-924473

Source DB:  PubMed          Journal:  Plant Biol (Stuttg)        ISSN: 1435-8603            Impact factor:   3.081


  49 in total

1.  Irrigation differentially impacts populations of indigenous antibiotic-producing pseudomonas spp. in the rhizosphere of wheat.

Authors:  Olga V Mavrodi; Dmitri V Mavrodi; James A Parejko; Linda S Thomashow; David M Weller
Journal:  Appl Environ Microbiol       Date:  2012-03-02       Impact factor: 4.792

2.  Comparison of barley succession and take-all disease as environmental factors shaping the rhizobacterial community during take-all decline.

Authors:  Karin Schreiner; Alexandra Hagn; Martina Kyselková; Yvan Moënne-Loccoz; Gerhard Welzl; Jean Charles Munch; Michael Schloter
Journal:  Appl Environ Microbiol       Date:  2010-06-04       Impact factor: 4.792

3.  Fluorescent Pseudomonads in the Phyllosphere of Wheat: Potential Antagonists Against Fungal Phytopathogens.

Authors:  Thomas Müller; Undine Behrendt; Silke Ruppel; Grit von der Waydbrink; Marina E H Müller
Journal:  Curr Microbiol       Date:  2015-12-21       Impact factor: 2.188

4.  Structural and functional analysis of the type III secretion system from Pseudomonas fluorescens Q8r1-96.

Authors:  Dmitri V Mavrodi; Anna Joe; Olga V Mavrodi; Karl A Hassan; David M Weller; Ian T Paulsen; Joyce E Loper; James R Alfano; Linda S Thomashow
Journal:  J Bacteriol       Date:  2010-10-22       Impact factor: 3.490

5.  Pseudomonas 2007.

Authors:  Joanna B Goldberg; Robert E W Hancock; Rebecca E Parales; Joyce Loper; Pierre Cornelis
Journal:  J Bacteriol       Date:  2007-12-28       Impact factor: 3.490

6.  Impact of antifungals producing rhizobacteria on the performance of Vigna radiata in the presence of arbuscular mycorrhizal fungi.

Authors:  Deepti Dwivedi; Bhavdish N Johri; Kurt Ineichen; Victor Wray; Andres Wiemken
Journal:  Mycorrhiza       Date:  2009-05-21       Impact factor: 3.387

7.  Assessment of DAPG-producing Pseudomonas fluorescens for Management of Meloidogyne incognita and Fusarium oxysporum on Watermelon.

Authors:  Susan L F Meyer; Kathryne L Everts; Brian McSpadden Gardener; Edward P Masler; Hazem M E Abdelnabby; Andrea M Skantar
Journal:  J Nematol       Date:  2016-03       Impact factor: 1.402

8.  Interaction between 2,4-Diacetylphloroglucinol- and Hydrogen Cyanide-Producing Pseudomonas brassicacearum LBUM300 and Clavibacter michiganensis subsp. michiganensis in the Tomato Rhizosphere.

Authors:  Mélanie M Paulin; Amy Novinscak; Carine Lanteigne; Vijay J Gadkar; Martin Filion
Journal:  Appl Environ Microbiol       Date:  2017-06-16       Impact factor: 4.792

Review 9.  Biotechnological utilization: the role of Zea mays rhizospheric bacteria in ecosystem sustainability.

Authors:  Emmanuel Edoghogho Imade; Olubukola Oluranti Babalola
Journal:  Appl Microbiol Biotechnol       Date:  2021-05-27       Impact factor: 4.813

10.  Evolutionary history of the phl gene cluster in the plant-associated bacterium Pseudomonas fluorescens.

Authors:  Jennifer A Moynihan; John P Morrissey; Eric R Coppoolse; Willem J Stiekema; Fergal O'Gara; E Fidelma Boyd
Journal:  Appl Environ Microbiol       Date:  2009-01-30       Impact factor: 4.792

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