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Mildew Disease (mildew + disease)
Selected AbstractsDifferentiation of Two Pathogens of Powdery Mildew Disease in Flowering Dogwood (Cornus florida) by PCR-mediated Method Based on ITS SequencesJOURNAL OF PHYTOPATHOLOGY, Issue 5 2009Ainong Shi Abstract Two fungi, Phyllactinia guttata and Erysiphe pulchra were identified as the pathogens of powdery mildew of flowering dogwood (Cornus florida). The objective of this research was to identify and distinguish the two fungi by developing species-specific primers. The internal transcribed spacer (ITS) universal primers and a series of species-specific primers designed from the ITS regions were used to evaluate and validate the two fungi causing powdery mildew in dogwood. Four primer pairs showed specificity to P. guttata and three to E. pulchra. These species-specific primer pairs can be used as molecular markers to provide diagnostic tools for detection and differentiation of the two powdery mildew pathogens in flowering dogwood. [source] Peronospora belbahrii causing downy mildew disease on Agastache in the UK: a new host and location for the pathogenPLANT PATHOLOGY, Issue 4 2010B. Henricot No abstract is available for this article. [source] Pseudoperonospora cubensis causing downy mildew disease on Impatiens irvingii in Cameroon: a new host for the pathogenPLANT PATHOLOGY, Issue 2 2009H. Voglmayr No abstract is available for this article. [source] Mechanisms involved in control of Blumeria graminis f.sp. hordei in barley treated with mycelial extracts from cultured fungiPLANT PATHOLOGY, Issue 5 2002H. Haugaard Treatment with mycelial extracts, prepared from liquid cultures of Bipolaris oryzae, Pythium ultimum and Rhizopus stolonifer, protected barley (Hordeum vulgare) against powdery mildew disease caused by the fungus Blumeria graminis f.sp. hordei. The mechanisms of this protection were studied using histopathological methods and molecular analysis. Germination and appressorial formation of B. graminis were generally reduced after treatment with mycelial extracts. Although this reduction (between 12 and 62% depending on treatment and experiment) was inconsistent and only occasionally significantly different from the water-treated control, it indicated a direct antifungal effect of the extracts. In situations where the fungus succeeded in forming an appressorium, penetration efficiency and haustorium formation from these appressoria was not affected , no enhanced penetration resistance associated with papilla formation was detected. However, a post-penetration effect was observed, as B. graminis colonies on mycelial extract-treated leaves produced 50% fewer hyphae than on controls. Northern blot analyses showed earlier accumulation of defence-related gene transcripts following treatment with B. oryzae and P. ultimum mycelial extracts, and to a lesser extent R. stolonifer mycelial extract, compared with water-treated leaves. It is suggested that the protection mechanism of the mycelial extracts involves direct antifungal effects and possible induced resistance for the B. oryzae and P. ultimum mycelial extracts. [source] Sensitivity of Uncinula necator to quinoxyfen: evaluation of isolates selected using a discriminatory dose screenPEST MANAGEMENT SCIENCE (FORMERLY: PESTICIDE SCIENCE), Issue 6 2006Elizabeth A Green Abstract Quinoxyfen is a protectant fungicide that provides excellent control of many powdery mildew diseases. Prior to the launch of quinoxyfen in vines in 1998, a leaf disc sporulation assay was developed to assess the sensitivity of Uncinula necator (Schw) Burr to quinoxyfen. The distribution of EC50 values from 56 monoconidial U. necator isolates collected from six countries between 1993 and 1996 was found to range from less than 0.03 to 2.6 mg litre,1. Although this range of EC50 values was quite broad, the inability to establish a minimum inhibitory concentration (MIC) for the majority of these isolates, including some of the most sensitive isolates, was unexpected and suggested that the leaf disc sporulation assay may not reflect the true activity of quinoxyfen in the field. In 2002, following the detection of isolates resistant to quinoxyfen in Blumeria graminis Speer f. sp. tritici Marchal, a discriminatory dose screen was developed to test large populations of U. necator for rare individuals with significantly decreased sensitivity to quinoxyfen. The individual isolates selected by this method were tested with the leaf disc sporulation assay. Although a significant proportion were found to have EC50 values within the original distribution, a number of isolates with apparent reduced sensitivity to quinoxyfen were also detected. However, further examination of a subset of these isolates in a more quantitative germination/germ tube elongation inhibition assay suggested that the magnitude of the reduction in sensitivity for some of these isolates was much less than predicted by the sporulation assay. Thus, for an exclusively protectant fungicide such as quinoxyfen, a leaf disc sporulation assay may overestimate the frequency of isolates with significantly reduced sensitivity and the threat of decreased performance due to resistance. Copyright © 2006 Society of Chemical Industry [source] | ||||||||||