2017
DOI: 10.5376/mpb.2017.08.0005
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Pathogen Identification of Clubroot Disease in Chinese Cabbage from Yuanyang County, Henan Province

Abstract: To clarify the causal agent of clubroot disease in Chinese cabbage from Yuanyang experimental base, the isolate YY was collected from the clubroot for further research. After morphological, cytological observation and pathogenicity identification, the pathogen was preliminary inferred as Plasmodiophora brassicae. In order to quickly detect the pathogen, specific primers were designed according to D85819 and Pro1 gene, respectively, and used to amplify the expected fragment from the template DNA of target patho… Show more

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Cited by 3 publications
(4 citation statements)
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“…Root gall samples from Chinese cabbage plants were collected from Xinye, Henan province, and the pathogen was identified and reported as race 4 [ 20 , 21 , 22 ]. Inoculation and resistance testing were performed using our previously described method [ 23 ].…”
Section: Methodsmentioning
confidence: 99%
“…Root gall samples from Chinese cabbage plants were collected from Xinye, Henan province, and the pathogen was identified and reported as race 4 [ 20 , 21 , 22 ]. Inoculation and resistance testing were performed using our previously described method [ 23 ].…”
Section: Methodsmentioning
confidence: 99%
“…The Yuanyang terraces (YYT; Yunnan, China) were shaped by the agricultural practices of the Hani ethnic group [7]; they were classified by UNESCO in 2013 as a Cultural Landscape and are known for being home to a wide range of rice landraces [8]. Quite importantly, the available records indicate that the YYT only suffer 1% losses caused by disease [9], a striking feature compared to the well-documented 32% losses at the global level [10]. High genetic diversity of some YYT landraces has been documented in previous reports using a limited number of molecular markers [11][12][13], suggesting they resemble composite populations.…”
Section: Introductionmentioning
confidence: 99%
“…Development of race-specific markers would enable more effective and precise detection of this pathogen. Such molecular markers have been used effectively in plant disease diagnostics for many years, including limited methods in P. brassicae based on PCR amplification of DNA from galls or resting spores ( Faggian and Strelkov, 2009 ; Ito et al, 1997 , 2008 ; Li et al, 2017 ; Wallenhammar and Arwidsson, 2001 ; Yang et al, 2002 ). Ito et al (1997) cloned and sequenced 1.4 kb DNA fragment from 19 different Japanese P. brassicae isolates and found that the markers covering that sequence do not amplify fungi and bacterial DNA they studied.…”
mentioning
confidence: 99%
“…The authors, however, found that isolates from two different countries had variation in 18s and ITS1 (inter-transcribed spacer 1) regions indicating that those markers are unable to differentiate any isolate specific variations. In a recent study in China, Li et al (2017) successfully detected an unknown P. brassicae isolate after targeting D85819 and Pro1 gene-specific primers. However, none of those PCR based methods could distinguish between the different P. brassicae isolates.…”
mentioning
confidence: 99%