Pseudomonas fluorescens strain CHAO suppresses Thielaviopsis basicola-induced black root rot of tobacco and Gaeumannomyces graminis var. tritici-induced take-all of wheat. Strain CHAO produces 2,4-diacetylphloroglucinol, a metabolite with antifungal, antibacterial, and phytotoxic activity. The role of this compound in disease suppression was tested under gnotobiotic conditions. A P. fluorescens mutant, obtained by Tn5 insertion, did not produce 2,4-diacetylphloroglucinol, showed diminished inhibition of T. basicola and of G. g. var. tritici in vitro, and had a reduced suppressive effect on tobacco black root rot and on take-all of wheat, compared with wild-type CHAO. Complementation of the mutant with an 11-kb DNA fragment from a genomic library of wild-type CHAO largely restored production of the metabolite, inhibition of the fungal pathogens in vitro and disease suppression. The Tn5 insertion was physically mapped using a 5.8-kb complementing fragment as a probe. 2,4-Diacetylphloroglucinol was shown to be produced in the rhizosphere of wheat by strain CHAO and by the complemented mutant, but not by the mutant defective in 2,4-diacetylphloroglucinol synthesis. These results support the importance of 2,4-diacetylphloroglucinol production by strain CHAO in the suppression of soilborne plant pathogens in the rhizosphere.

The antimicrobial metabolite 2,4-diacetylphloroglucinol (2,4-DAPG) contributes to the capacity of Pseudomonas fluorescens strain CHA0 to control plant diseases caused by soilborne pathogens. A 2,4-DAPG-negative Tn5 insertion mutant of strain CHA0 was isolated, and the nucleotide sequence of the 4-kb genomic DNA region adjacent to the Tn5 insertion site was determined. Four open reading frames were identified, two of which were homologous to phlA, the first gene of the 2,4-DAPG biosynthetic operon, and to the phlF gene encoding a pathway-specific transcriptional repressor. The Tn5 insertion was located in an open reading frame, tentatively named phlH, which is not related to known phl genes. In wild-type CHA0, 2,4-DAPG production paralleled expression of a phlA-lacZ translational fusion, reaching a maximum in the late exponential growth phase. Thereafter, the compound appeared to be degraded to monoacetylphloroglucinol by the bacterium. 2,4-DAPG was identified as the active compound in extracts from culture supernatants of strain CHA0 specifically inducing phlA-lacZ expression about sixfold during exponential growth. Induction by exogenous 2,4-DAPG was most conspicuous in a phlA mutant, which was unable to produce 2,4-DAPG. In a phlF mutant, 2,4-DAPG production was enhanced severalfold and phlA-lacZ was expressed at a level corresponding to that in the wild type with 2,4-DAPG added. The phlF mutant was insensitive to 2,4-DAPG addition. A transcriptional phlA-lacZ fusion was used to demonstrate that the repressor PhlF acts at the level of transcription. Expression of phlA-lacZ and 2,4-DAPG synthesis in strain CHA0 was strongly repressed by the bacterial extracellular metabolites salicylate and pyoluteorin as well as by fusaric acid, a toxin produced by the pythopathogenic fungus Fusarium. In the phlF mutant, these compounds did not affect phlA-lacZ expression and 2,4-DAPG production. PhlF-mediated induction by 2,4-DAPG and repression by salicylate of phlA-lacZ expression was confirmed by using Escherichia coli as a heterologous host. In conclusion, our results show that autoinduction of 2,4-DAPG biosynthesis can be countered by certain bacterial (and fungal) metabolites. This mechanism, which depends on phlF function, may help P. fluorescens to produce homeostatically balanced amounts of extracellular metabolites.Certain root-associated strains of fluorescent Pseudomonas spp. produce and excrete metabolites that are inhibitory to soilborne plant pathogens (13, 24, 52). Among these metabolites, 2,4-diacetylphloroglucinol (2,4-DAPG) has received particular attention because of its production by a wide range of pseudomonads used for the biological control of root diseases (13,26,50,52). 2,4-DAPG is a phenolic compound with broadspectrum antifungal, antibacterial, antihelminthic, and phytotoxic activity (13,25,52). A 2,4-DAPG biosynthetic gene cluster is conserved among numerous 2,4-DAPG-producing pseudomonads isolated from soils that are naturally suppressive to take-all of wheat, black root rot of tobacco, and tomat...

Pseudomonas fluorescens CHA0 colonizes plant roots, produces several secondary metabolites in stationary growth phase, and suppresses a number of plant diseases, including Thielaviopsis basicola-induced black root rot of tobacco. We discovered that mutations in a P. fluorescens gene named gacA (for global antibiotic and cyanide control) pleiotropically block the production of the secondary metabolites 2,4-diacetylphloroglucinol (Phl), HCN, and pyoluteorin. The gacA mutants of strain CHA0 have a drastically reduced ability to suppress black root rot under gnotobiotic conditions, supporting the previous observations that the antibiotic Phl and HCN individually contribute to the suppression of black root rot. The gacA gene is directly followed by a uvrC gene. Double gacA-uvrC mutations render P. fluorescens sensitive to UV irradiation. The gacA-uvrC cluster is homologous to the orf-2 (= uvrY)-uvrC operon of Escherichia coli. The gacA gene specifies a trans-active 24-kDa protein. Sequence data indicate that the GacA protein is a response regulator in the FixJ/DegU family of two-component regulatory systems. Expression of the gacA gene itself was increased in stationary phase. We propose that GacA, perhaps activated by conditions of restricted growth, functions as a global regulator of secondary metabolism in P. fluorescens.

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Pseudomonas fluorescens CHA0 and the related strain Pf-5 are well-characterized representatives of rhizosphere bacteria that have the capacity to protect crop plants from fungal root diseases, mainly by releasing a variety of exoproducts that are toxic to plant pathogenic fungi. Here, we report that the two plant-beneficial pseudomonads also exhibit potent insecticidal activity. Anti-insect activity is linked to a novel genomic locus encoding a large protein toxin termed Fit (for P. fluorescensinsecticidal toxin) that is related to the insect toxin Mcf (Makes caterpillars floppy) of the entomopathogen Photorhabdus luminescens, a mutualist of insect-invading nematodes. When injected into the haemocoel, even low doses of P. fluorescens CHA0 or Pf-5 killed larvae of the tobacco hornworm Manduca sexta and the greater wax moth Galleria mellonella. In contrast, mutants of CHA0 or Pf-5 with deletions in the Fit toxin gene were significantly less virulent to the larvae. When expressed from an inducible promoter in a non-toxic Escherichia coli host, the Fit toxin gene was sufficient to render the bacterium toxic to both insect hosts. Our findings establish the Fit gene products of P. fluorescens CHA0 and Pf-5 as potent insect toxins that define previously unappreciated anti-insect properties of these plant-colonizing bacteria.

Bacteria of the genus Pseudomonas occupy diverse environments. The Pseudomonas fluorescens group is particularly well-known for its plant-beneficial properties including pathogen suppression. Recent observations that some strains of this group also cause lethal infections in insect larvae, however, point to a more versatile ecology of these bacteria. We show that 26 P. fluorescens group strains, isolated from three continents and covering three phylogenetically distinct sub-clades, exhibited different activities toward lepidopteran larvae, ranging from lethal to avirulent. All strains of sub-clade 1, which includes Pseudomonas chlororaphis and Pseudomonas protegens, were highly insecticidal regardless of their origin (animals, plants). Comparative genomics revealed that strains in this sub-clade possess specific traits allowing a switch between plant-and insect-associated lifestyles. We identified 90 genes unique to all highly insecticidal strains (sub-clade 1) and 117 genes common to all strains of sub-clade 1 and present in some moderately insecticidal strains of sub-clade 3. Mutational analysis of selected genes revealed the importance of chitinase C and phospholipase C in insect pathogenicity. The study provides insight into the genetic basis and phylogenetic distribution of traits defining insecticidal activity in plant-beneficial pseudomonads. Strains with potent dual activity against plant pathogens and herbivorous insects have great potential for use in integrated pest management for crops.

Certain strains of fluorescent pseudomonads can effectively colonize plant roots and protect plants from diseases caused by a variety of root pathogens. Such beneficial or plant health-promoting strains are emerging as promising biocontrol agents. They are suited as soil inoculants either individually or in combination and may be compatible with current chemical pesticides (1, 2, 3, 4, 5, 6, 7, 8). In our biocontrol studies, we have focused on Pseudomonasfluorescens strain CHAO, an isolate from a suppressive soil in the western part of Switzerland (9). This strain was originally shown to colonize tobacco roots and to suppress black root rot, which is caused by the fungus Thielaviopsis basicola (9, 10). Subsequent work has established that disease suppression by strain CHAO displays little specificity with respect to the host plant and the pathogen. Protected plants include wheat, cucumber, sugar beet, cotton, flax, corn, and cress. Pathogenic action of at least the following fungal pathogens can be reduced by strain CHAO: Pythium ultimum, Gaeumannomyces graminis var. tritici (Ggt), Fusarium oxysporum f.s p. cucurbitaceae, Phomopsis sclerotioides, and Rhizoctonia solani (11, 12, 13, 14, 15; our unpublished data). Since the interactions between I! fluorescens, other organisms and the soil environment are extremely complex, it became important to develop reproducible methods that allow us to monitor the plant-beneficial effects of strain CHAO reliably and to analyze the traits that make it an effective biocontrol agent. In section 6.2 we will review some of our approaches to investigate the mechanisms by which strain CHAO achieves biological control.We are using strain CHAO as a model organism to study not only the mechanisms of disease suppression but also the ecological impact of introduced plant-beneficial bacteria (see section 6.3). In a parallel approach, we are investigating the potential applications of biological control agents to improve the yields of protected crops. We are testing a variety of strains, singly and in combination, for the development of greenhouse applications. A brief account of this work is presented in section 6.4. 68Disease Suppression by I! Fluorescens CHAO Mechanistic Studies on Biocontrol m i t s of Pseudomonas Fluorescens CHAO Chemical Identification of Extracellular MetabolitesMetabolites produced and excreted by I? fluorescens are assumed to be important biotic factors in the biological control of root diseases (2, 5, 16, 17, 18, 19, 20, 21). Until now, about a dozen low molecular weight compounds have been identified in culture supernatants of Rfluorescens CHAO ( Table 1). These products can be broadly classified into two groups: siderophores and secondary metabolites. The siderophores (e. g. , iron chelators) pyoverdine (pseudobactin), salicylate and pyochelin are all produced by I? fluorexens CHAO (22, 23 ; our unpublished results) and by other fluorescent pseudomonads when these bacteria are grown under ironlimiting conditions (24; reviewed by Loper & Buyer [20] and O'Sullivan...

Insects are an important and probably the most challenging pest to control in agriculture, in particular when they feed on belowground parts of plants. The application of synthetic pesticides is problematic owing to side effects on the environment, concerns for public health and the rapid development of resistance. Entomopathogenic bacteria, notably Bacillus thuringiensis and Photorhabdus/Xenorhabdus species, are promising alternatives to chemical insecticides, for they are able to efficiently kill insects and are considered to be environmentally sound and harmless to mammals. However, they have the handicap of showing limited environmental persistence or of depending on a nematode vector for insect infection. Intriguingly, certain strains of plant root-colonizing Pseudomonas bacteria display insect pathogenicity and thus could be formulated to extend the present range of bioinsecticides for protection of plants against root-feeding insects. These entomopathogenic pseudomonads belong to a group of plant-beneficial rhizobacteria that have the remarkable ability to suppress soil-borne plant pathogens, promote plant growth, and induce systemic plant defenses. Here we review for the first time the current knowledge about the occurrence and the molecular basis of insecticidal activity in pseudomonads with an emphasis on plant-beneficial and prominent pathogenic species. We discuss how this fascinating Pseudomonas trait may be exploited for novel root-based approaches to insect control in an integrated pest management framework.