Antonio D. Izzo

Mechanism of action and efficacy of seed meal-induced pathogen suppression differ in a brassicaceae species and time-dependent manner.

ABSTRACT The effect of seed meals derived from Brassica juncea, B. napus, or Sinapis alba on suppression of soilborne pathogens inciting replant disease of apple was evaluated in greenhouse trials. Regardless of plant source, seed meal amendment significantly improved apple growth in all orchard soils; however, relative differences in pathogen suppression were observed. All seed meals suppressed root infection by native Rhizoctonia spp. and an introduced isolate of Rhizoctonia solani AG-5, though B. juncea seed meal often generated a lower level of disease control relative to other seed meal types. When introduction of the pathogen was delayed until 4 to 8 weeks post seed meal amendment, disease suppression was associated with proliferation of resident Streptomyces spp. and not qualitative or quantitative attributes of seed meal glucosinolate content. Using the same experimental system, when soils were pasteurized prior to pathogen infestation, control of R. solani was eliminated regardless of seed meal type. In the case of B. juncea seed meal amendment, the mechanism of R. solani suppression varied in a temporal manner, which initially was associated with the generation of allylisothiocyanate and was not affected by soil pasteurization. Among those tested, only B. juncea seed meal did not stimulate orchard soil populations of Pythium spp. and infection of apple roots by these oomycetes. Although application of B. napus seed meal alone consistently induced an increase in Pythium spp. populations, no significant increase in Pythium spp. populations was observed in response to a composite B. juncea and B. napus seed meal amendment. Suppression of soil populations and root infestation by Pratylenchus spp. was dependent upon seed meal type, with only B. juncea providing sustained nematode control. Collectively, these studies suggest that use of a composite B. juncea and B. napus seed meal mixture can provide superior control of the pathogen complex inciting apple replant disease relative to either seed meal used alone.

Vegetation and ecological characteristics of mixed-conifer and Red Fir forests at the Teakettle Experimental Forest

References Anonymous. 1970. Recommendations for an international standard for a mapping method in bird census work.

Interaction of Brassicaceous Seed Meal and Apple Rootstock on Recovery of Pythium spp. and Pratylenchus penetrans from Roots Grown in Replant Soils

Pythium spp. and Pratylenchus penetrans are significant components of the diverse pathogen complex that incites apple replant disease in Washington State. The structure of the Pythium population differs among orchard soils but is composed of multiple pathogenic species. Studies were conducted to determine the effect of brassicaceous seed meals and apple rootstock on the activity and composition of these pathogen populations. Brassicaceous seed meals differed in capacity to suppress Pythium numbers and apple root infection, as well as differentially transformed composition of the population recovered from apple roots. Brassica juncea seed meal (SM) was the sole seed meal examined to suppress Pythium numbers and root infection; however, a persisting population was always detected in which Pythium irregulare existed as the dominant or co-dominant species. In general, the Geneva series rootstocks were less susceptible to root infection by native populations of Pythium, whereas M26, MM106, and MM111 were highly susceptible. Apple rootstocks from the Geneva series consistently supported lower populations of P. penetrans than did Malling or Malling-Merton rootstocks. B. juncea SM was superior to Brassica napus SM or Sinapis alba SM in suppressing lesion nematode populations. Significant rootstock × seed meal interaction was detected, and nematode suppression in response to B. napus or S. alba SM was only observed when used in concert with a tolerant rootstock, while B. juncea SM suppressed lesion nematode root populations irrespective of rootstock. These findings demonstrate that utilization of brassicaceous seed meal amendments for replant disease suppression must employ an appropriate rootstock in order to achieve optimal disease control.

Hybridization of an ITS-based macroarray with ITS community probes for characterization of complex communities of fungi and fungal-like protists.

The ability to characterize fungal community structure and dynamics in the environment is constantly challenged by the high levels of diversity that must be confronted. Large-scale oligonucleotide arrays for use in such analytical studies are currently under development; however, the implementation of this approach generally requires substantial time and financial resources. To address the need for a more accessible tool for fungal community profiling and broad diagnostics, we evaluated the potential utility of a reverse dot blot approach utilizing macroarray targets and probes that each consisted of a PCR product of the entire fungal ITS1-5.8S-ITS2 gene region. Samples used to generate the array targets included both culturable and non-culturable fungi and fungal-like protists representing a range of ecological functions. Tests performed using single-species probes within the genus Pythium demonstrated that taxonomic lineages could generally be distinguished when ITS DNA sequence similarity differed by greater than 5-10%. An artificially constructed community probe of known composition successfully detected eight of the 10 lineages contained on the array with only one clear false positive in 95 targets. The approach was also successfully applied to environmental samples. Taxa resident in the soil of a local orchard were identified using the array and matched those documented in previous studies. Closely related taxa from a previously uncharacterized and geographically distant orchard soil were also identified by the array and had affinities to Leptodontium, Cadophora, Zalerion, and Geomyces. These taxa were further confirmed to be present in the sample by cloning and DNA sequencing. A minority of lineages had DNA targets with low melting temperatures which were not detected on the arrays except under conditions that compromised specificity. Membrane-based ITS macroarrays coupled with community ITS probes possessed sufficient power to detect multiple genus-level lineages of fungi in complex samples and should have broad applications in the study of fungal communities.