Full TGIF Record # 302908
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DOI:10.1094/PDIS-01-18-0165-RE
Web URL(s):https://apsjournals.apsnet.org/doi/full/10.1094/PDIS-01-18-0165-RE
    Last checked: 12/13/2018
    Access conditions: Item is within a limited-access website
https://apsjournals.apsnet.org/doi/pdf/10.1094/PDIS-01-18-0165-RE
    Last checked: 12/13/2018
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Publication Type:
i
Refereed
Author(s):Giordano, Paul R.; Wang, Jie; Vargas, Joseph M.; Jacobs, Janette; Chilvers, Martin I.; Zeng, Quan
Author Affiliation:Giordano, Wang, Vargas, Jacobs, and Chilvers: Department of Plant, Soil and Microbial Sciences, Michigan State University, East Lansing; Zeng: Department of Plant Pathology and Ecology, The Connecticut Agricultural Experiment Station, New Haven
Title:Using a genome-based PCR primer prediction pipeline to develop molecular diagnostics for the turfgrass pathogen Acidovorax avenae
Section:Research
Other records with the "Research" Section
Source:Plant Disease. Vol. 102, No. 11, November 2018, p. 2224-2232.
Publishing Information:[Washington, D.C.]: Bureau of Plant Industry, U.S. Dept. of Agriculture
# of Pages:9
Related Web URL:https://apsjournals.apsnet.org/doi/abs/10.1094/PDIS-01-18-0165-RE
    Last checked: 12/13/2018
    Notes: Abstract only
Keywords:TIC Keywords: Acidovorax avenae; Disease identification; Etiolation; Genomes; Polymerase chain reaction
Abstract/Contents:"Acidovorax avenae is the causal agent of bacterial etiolation and decline (BED) of creeping bentgrass, a poorly understood and often misdiagnosed disease that can result in considerable aesthetic and functional damage to golf course putting greens. Current diagnostics of BED are based on laborious culture-based methods. In this work, we employed a novel alignment-free primer prediction pipeline to design diagnostic primers for turfgrass-pathogenic A. avenae using 15 draft genomes of closely related target and nontarget Acidovorax spp. as input. Twenty candidate primer sets specific to turfgrass-pathogenic A. avenae were designed. The specificity and sensitivity of these primer sets were validated via a traditional polymerase chain reaction (PCR) and a real-time PCR assay. Primer sets 0017 and 0019 coupled with an internal oligo probe showed optimal sensitivity and specificity when evaluated with the target pathogen, closely related bacterial species, and microorganisms that inhabit the same host and soil environment. Finally, the accuracy of the newly developed real-time PCR assay was evaluated to detect BED pathogens from BED-symptomatic and asymptomatic turfgrass samples. The diagnostic results produced by the real-time PCR assay were consistent with results of a cultural-based method. This assay will allow quicker and more effective detection of the BED pathogen, thus potentially reducing misdiagnoses and unnecessary usage of fungicides."
Language:English
References:38
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ASA/CSSA/SSSA Citation (Crop Science-Like - may be incomplete):
Giordano, P. R., J. Wang, J. M. Vargas, J. Jacobs, M. I. Chilvers, and Q. Zeng. 2018. Using a genome-based PCR primer prediction pipeline to develop molecular diagnostics for the turfgrass pathogen Acidovorax avenae. Plant Disease. 102(11):p. 2224-2232.
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DOI: 10.1094/PDIS-01-18-0165-RE
Web URL(s):
https://apsjournals.apsnet.org/doi/full/10.1094/PDIS-01-18-0165-RE
    Last checked: 12/13/2018
    Access conditions: Item is within a limited-access website
https://apsjournals.apsnet.org/doi/pdf/10.1094/PDIS-01-18-0165-RE
    Last checked: 12/13/2018
    Requires: PDF Reader
    Access conditions: Item is within a limited-access website
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MSU catalog number: b2191617
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