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Suppressive Soil (suppressive + soil)

Distribution by Scientific Domains

Life Sciences	100%

Selected Abstracts

Impact of soil suppressiveness on various population densities of Heterodera schachtii

ANNALS OF APPLIED BIOLOGY, Issue 3 2001
A WESTPHAL
Summary Infectivity of second-stage juvenile (J2) populations of Heterodera schachtii was assayed with radish. The numbers of J2 in three-day-old seedlings were proportional to the numbers of J2 in two differently textured soils. In a microplot trial with a known H.schachtii-supprcssivc soil, half of the plots contained untreated suppressive soil, the other half contained the same soil, but methyl iodide-fumigated and therefore conducive. Both soils were infested with cysts introducing the equivalents of 0, 30, 60 or 120 H.schachtii eggs g- 1 soil, kept moist for 2 months, and then planted to Swiss chard. The numbers of J2 in radish roots were proportional to the numbers of H.schachtii eggs introduced into the microplots, at a low level of detection in suppressive soil and at a high level in conducive soil.Growth of Swiss chard was not different at increasing infestation levels in suppressive soil, but growth was reduced in conducive soil proportionally to increasing nematode infestation level. [source]

Immunological quantification of the nematode parasitic bacterium Pasteuria penetrans in soil

FEMS MICROBIOLOGY ECOLOGY, Issue 3 2001
S Fould
Abstract Currently, the abundance of Pasteuria penetrans in soils, an unculturable bacterial parasite of root-knot nematodes (Meloidogyne spp.), is estimated by the percentage of nematode juveniles infected with bacteria and the number of spores attached to their cuticle. Indirect immunofluorescence led to detection of free spores directly in soil suspensions using UV light and polyclonal antibodies raised against two P. penetrans populations (ORS-21414-Sen and PP1). Three extraction methods were compared in order to improve spore recovery. A gentle shaking/sieving method recovered more than 90% of the spores inoculated in soils and was more efficient and simple than aqueous two-phase partitioning and polyethylene glycol extractions. All the spores inoculated in sandy or sandy,clay soils were detected with immunofluorescence microscopy. The quantification of the spores was improved using an ELISA technique that showed a good correlation between optical density and spore concentration in inoculated soils. Specific antibodies provide a suitable method to quantify P. penetrans and may be used to follow the evolution of the real pool of bacteria either in native suppressive soils or in inoculated ones. [source]

Role of 2,4-Diacetylphloroglucinol-Producing Fluorescent Pseudomonas spp. in the Defense of Plant Roots

PLANT BIOLOGY, Issue 1 2007
D. M. Weller
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 105 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. [source]