Full TGIF Record # 263842
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Web URL(s):http://turf.rutgers.edu/research/abstracts/symposium2015.pdf#page=43
    Last checked: 08/04/2015
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Publication Type:
i
Report
Author(s):Zhao, Shuang; Zhang, Lisa; Clarke, Bruce B.; Zhang, Ning
Author Affiliation:Zhao, Clark and Zhang, N.: Deaprtment of Plant Biology and Pathology, Rutgers University; Zhang, L.: Yale University, New Haven, CT
Title:Development and application of a TaqMan real-time PCR assay for rapid detection of the summer patch pathogen of turfgrass
Section:Poster presentations
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Meeting Info.:New Brunswick, New Jersey: January 16, 2015
Source:Proceedings of the Twenty-Fourth Annual Rutgers Turfgrass Symposium. 2015, p. 42.
Publishing Information:New Brunswick, New Jersey: The Center for Turfgrass Science, Rutgers, The State University of New Jersey
# of Pages:1
Keywords:TIC Keywords: Application methods; Disease control; Disease identification; Magnaporthe poae; Pathogens; Polymerase chain reaction; Summer patch
Abstract/Contents:"In North America, one of the most important root diseases of Poa and Festuca turf is summer patch, caused by Magnaporthiopsis poae (=Magnaporthe poae). Detection and identification of M. poae in infected roots by conventional culture-based methods is difficult and time consuming. In turfgrass breeding and management evaluation studies, an important question to address is whether the better performance of some grasses is simply because of the absence of the pathogen in certain plots. In this study, a culture-independent TaqMan real-time PCR assay has been developed for M. poae that enables pathogen detection from the field samples within a few hours. The assay was validated with the target pathogen, closely related fungal species, and a number of other microorganisms that inhabit the same host and soil environment. This TaqMan real-time PCR assay is more sensitive (detecting as little as 3.88 pg genomic DNA of M. poae), rapid, and accurate compared to direct microscopic observation and isolation on a selective medium. The real-time PCR detection results correspond closely to visual assessments of disease severity in the field. Utilization of this assay in diagnostic laboratories will enable turfgrass managers to more quickly and effectively detect and potentially reduce fungicide usage through early and accurate identification of the pathogen."
Language:English
References:0
Note:This item is an abstract only!
ASA/CSSA/SSSA Citation (Crop Science-Like - may be incomplete):
Zhao, S., L. Zhang, B. B. Clarke, and N. Zhang. 2015. Development and application of a TaqMan real-time PCR assay for rapid detection of the summer patch pathogen of turfgrass. Proc. Rutgers Turfgrass Symp. p. 42.
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Web URL(s):
http://turf.rutgers.edu/research/abstracts/symposium2015.pdf#page=43
    Last checked: 08/04/2015
    Requires: PDF Reader
    Notes: Item is within a single large file
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