Bacterial blotch is a group of economically important diseases of the common button mushroom (). Once the pathogens are introduced to a farm, mesophilic growing conditions (that are optimum for mushroom production) result in severe and widespread secondary infections. Efficient, timely and quantitative detection of the pathogens is hence critical for the design of localized control strategies and prediction of disease risk. This study describes the development of real-time TaqMan assays that allow molecular diagnosis of three currently prevalent bacterial blotch pathogens: " and (as yet uncharacterized) strains (belonging to ). For each pathogen, assays targeting specific DNA markers on two different loci, were developed for primary detection and secondary verification. All six developed assays showed high diagnostic specificity and sensitivity when tested against a panel of 63 strains and 40 other plant pathogenic bacteria. The assays demonstrated good analytical performance indicated by linearity across calibration curve (>0.95), amplification efficiency (>90%) and magnitude of amplification signal (>2.1). The limits of detection were optimized for efficient quantification in bacterial cultures, symptomatic tissue, infected casing soil and water samples from mushroom farms. Each target assay was multiplexed with two additional assays. was detected as an extraction control, to account for loss of DNA during sample processing. And the total population was detected, to quantify the proportion of pathogenic to beneficial in the soil. This ratio is speculated to be an indicator for blotch outbreaks. The multiplexed assays were successfully validated and applied by routine testing of diseased mushrooms, peat sources, casing soils, and water from commercial production units.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261844 | PMC |
http://dx.doi.org/10.3389/fmicb.2020.00989 | DOI Listing |
Fungal Biol
December 2024
Department of Plant Pathology and Environmental Microbiology, The Pennsylvanian State University, University Park, PA, USA.
Productive cultivation of the button mushroom (Agaricus bisporus) relies on the use of selective substrates and effective disease management. In extending our previous work on manipulating the developmental microbiome (devome), this study employs the strategy of substrate passaging to explore its effects on crop outcomes and disease dynamics. Here we subjected the casing substrate to ten cycles of passaging.
View Article and Find Full Text PDFPlant Pathol J
December 2024
Microbial Safety Division, National Institute of Agricultural Sciences, Rural Develop-ment Administration, Wanju 55365, Korea.
Bacterial fruit blotch (BFB) caused by Paracidovorax citrulli is a devastating disease in cucurbit hosts such as watermelon. P. citrulli is a seed-borne pathogen, and contaminated seeds are the primary inoculum.
View Article and Find Full Text PDFPlant Pathol J
December 2024
Eco-Friendly New Materials Research Center, Korea Research Institute of Chemical Technology, Daejeon 34114, Korea.
Acidovorax citrulli is a causative pathogen for bacterial fruit blotch (BFB) in Cucurbitaceae, including watermelon. The most effective method to control this plant disease is to cultivate resistant cultivars. Herein, this study aimed to establish an efficient screening method to determine the resistance of watermelon cultivars against A.
View Article and Find Full Text PDFFoods
November 2024
Tianjin Key Laboratory of Food Quality and Health, College of Food Science and Engineering, Tianjin University of Science & Technology, Tianjin 300457, China.
Carvacrol (CAR), a naturally occurring phenolic monoterpene compound, has recently received attention for its potential use in food preservation. However, whether it is effective in controlling brown blotch disease caused by in edible mushrooms is unknown. The results of this study showed that CAR effectively inhibits and kills in vitro by disrupting cell membrane integrity and causing the leakage of cellular components.
View Article and Find Full Text PDFPlant Dis
November 2024
Qujing Normal University, Qujing Normal University Sanjiang Avenue, Qujing, China, 650011;
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