Growth and susceptibility of evergreen Rhododendron ‘English Roseum’, ‘Cunningham’s White’, and ‘Compact P.J.M.’ to Phytophthora ramorum in response to biweekly nitrogen (N) fertilizer application at rates of 25, 75, and 150 mg N per 11.4-L container was evaluated during two growing seasons. At the end of both growing seasons, horticultural evaluation of the different plants showed that 150 mg N-fertilized cultivars had superior shoot growth, visual quality, leaf color, and the highest leaf N concentration, whereas the 25-mg N cultivars were inferior for these characteristics. Plants fertilized with the 75-mg N rate were typically intermediate to the 150- and 25-mg N plants for the measured characteristics. During the first growing season, the number of flower buds on ‘Cunningham’s White’ and ‘English Roseum’ was not influenced by N rate but the second season bud numbers increased with increasing N fertilizer. Foliar susceptibility to P. ramorum was influenced by N fertilizer application rates in the most susceptible cultivars, ‘English Roseum’ and ‘Cunningham’s White’, in which lesion size and infection frequency both increased at higher N rates. The results were variable in ‘Compact P.J.M.’, the most resistant cultivar.
Gray bulb rot of tulips and bulbous iris is caused by the soil-borne fungal pathogen, Rhizoctonia tuliparum (Rtul). Sclerotia present in infected bulbs, as well as overwintering sclerotia in soil and field debris, are the primary sources of infection. A method for accurate and sensitive detection of Rtul from soil and infected bulbs, and estimation of inoculum threshold levels, is needed for the management of disease caused by this pathogen. We designed a unique set of primers targeting the ITS2 region of the Rtul genome and developed a highly sensitive quantitative PCR (qPCR)-based method for Rtul identification using these primers, where the threshold of detection was approximately 1 fg Rtul DNA. The assay was more sensitive with sclerotia collected from the field (natural) than with those grown in the lab, and more sensitive with natural-light than natural-dark sclerotia. Also, the detection method was more sensitive when sclerotia were extracted from soil than from bulb tissue. The qPCR method was highly specific, as no PCR amplification was detected when genomic DNA from 62 non-Rtul Rhizoctonia isolates from a wide range of anastomosis groups were tested. To understand the evolutionary relationships and genomic diversity of Rtul, we performed phylogenetics of the ITS1-5.8S-ITS2 region and ITS2-molecular morphometric characterization (MMC) of Rtul isolates. The three Rtul isolates whose ITS sequences were available in GenBank formed a distinct phylogenetic clade with Ceratobasidium anceps as the nearest relative. Furthermore, MMC analysis revealed genetic divergence among these three Rtul isolates.
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