Effects of a foliar fertilizer containing boron on the development of Sclerotinia stem rot ( Sclerotinia sclerotiorum ) on canola ( Brassica napus L.) leaves

2019 ◽  
Vol 168 (1) ◽  
pp. 47-55 ◽  
Author(s):  
Li Ni ◽  
Zamir K. Punja
Sensors ◽  
2018 ◽  
Vol 18 (6) ◽  
pp. 1764 ◽  
Author(s):  
Wenwen Kong ◽  
Chu Zhang ◽  
Feng Cao ◽  
Fei Liu ◽  
Shaoming Luo ◽  
...  

2021 ◽  
Author(s):  
Andreas von Tiedemann ◽  
Birger Koopmann ◽  
Kerstin Hoech

Sclerotinia stem rot (SSR) is an economically and globally significant disease in oilseed rape (Brassica napus L.) caused by the necrotrophic ascomycete Sclerotinia sclerotiorum. This study explored the role of cell wall reinforcement by lignin as a relevant factor for effective plant defence against attack of this pathogen. Expression of key genes in the phenylpropanoid pathway and the induced synthesis of lignin in infected stem tissues were investigated in a study comparing a susceptible (Loras) and a moderately resistant cultivar (Zhongyou 821, ZY821). Data revealed an earlier and more rapid defence activation in ZY821 through up-regulation of transcript levels of genes related to key steps in the phenylpropanoid pathway associated with enhanced lignin deposition in the resistant B. napus genotype. Expression level of BnCAD5, encoding a cinnamyl alcohol dehydrogenase, responsible for conversion of monolignol to lignin, was more rapidly up-regulated in ZY821 than Loras. The similar expression pattern of BnCAD5 and the gene BnF5H, encoding for the ferulate-5-hydroxylase which catalyses the synthesis of syringyl (S) lignin precursors, suggests that BnCAD5 is involved in the S lignin formation. Histological observations confirmed these results, showing an earlier increase of S lignin deposition in the infected resistant genotype. Deposition of guaiacyl (G) lignin was detected in both genotypes and is thus considered a component of basal, cultivar-independent defence response of B. napus to stem rot. The results indicate the importance of cell wall modification for quantitative stem rot resistance by responses in the phenylpropanoid metabolism generating distinct lignin types on different temporal scales.


2011 ◽  
Vol 12 (1) ◽  
pp. 15 ◽  
Author(s):  
S. D. Khot ◽  
V. N. Bilgi ◽  
L. E. del Río ◽  
C. A. Bradley

A collection of Brassica napus plant introduction (PI) lines was evaluated in a series of research trials to identify lines with resistance to Sclerotinia sclerotiorum, causal agent of Sclerotinia stem rot of canola. Five PI lines (169080, 286418, 436554, 458940, and 633119) were identified that consistently had SSR resistance levels equal to or greater than the partially resistant check cultivar Hyola 357. In addition, two of these lines (436554 and 458940) were found to exhibit SSR field resistance levels similar to Hyola 357. The PI lines identified from our research studies could be used in canola breeding programs to develop cultivars with improved resistance to S. sclerotiorum. Accepted for publication 21 February 2011. Published 22 April 2011.


Plant Disease ◽  
2016 ◽  
Vol 100 (5) ◽  
pp. 984-990 ◽  
Author(s):  
B. R. Ziesman ◽  
T. K. Turkington ◽  
U. Basu ◽  
S. E. Strelkov

Sclerotinia stem rot, caused by Sclerotinia sclerotiorum, is an economically important disease of canola (Brassica napus) commonly managed by routine application of fungicides. Petal infestation has been demonstrated to be an important stage of the disease cycle in canola and has been the focus of previously developed Sclerotinia stem rot risk assessment methods. Quantitative polymerase chain reaction (qPCR) analysis can provide a more rapid and accurate assessment of petal infestation levels. Primers and a hydrolysis probe were designed to amplify a 70-bp region of an S. sclerotiorum-specific gene, SS1G_00263. A hydrolysis probe-based qPCR assay was developed that had a detection limit of 8.0 × 10−4 ng of S. sclerotiorum DNA and only amplified S. sclerotiorum DNA. Evaluation of petals collected at five sampling points in each of 10 commercial canola fields on each of two sampling dates (corresponding to 20 to 30% bloom and 40 to 50% bloom) revealed S. sclerotiorum DNA infestation levels of 0 to 3.3 × 10−1 ng/petal. This qPCR assay can be used to reliably quantify petal infestation and, with further research, has the potential to serve as the basis for a Sclerotinia stem rot risk assessment tool or as a means to study Sclerotinia stem rot epidemiology.


Plant Disease ◽  
2008 ◽  
Vol 92 (10) ◽  
pp. 1473-1473 ◽  
Author(s):  
G. T. Tziros ◽  
G. A. Bardas ◽  
J. T. Tsialtas ◽  
G. S. Karaoglanidis

Oilseed rape (Brassica napus L.) was recently introduced into Greece for the production of biofuels. During May of 2007, symptoms typical of stem rot were observed on oilseed rape plants in three commercial fields in the area of Galatades-Pella, Central Macedonia, Greece. Approximately 30% of the plants were affected. Symptoms began as a chlorotic wilt on the foliage and developed into necrosis of basal stems. In the advanced stages of the disease, stems and branches became bleached and eventually died. White, as well as black, mycelium and irregularly shaped sclerotia (2 to 5 mm in diameter) were produced abundantly on and inside the affected stems. To isolate the pathogen, 20 symptomatic 6-month-old plants were collected from each field. Sclerotia were dipped in 70% ethanol, surface sterilized in 1% sodium hypochlorite for 1 min, and rinsed in sterile water. Sclerotia placed on potato dextrose agar (PDA) were incubated in the dark at 25°C for 10 days. Sclerotinia sclerotiorum (Lib.) de Bary was identified on the basis of morphological characteristics (2). To conduct pathogenicity tests, 10 6-week-old oilseed rape plants (cv. Titan) were each inoculated with a 5-mm-diameter colonized PDA disk placed in wounds made in the basal stem with a sterile scalpel. Five control plants were treated similarly except that the agar disk did not contain mycelium. Plants were then covered with a plastic bag to maintain high humidity. After 72 h, the bags were removed and the plants were maintained in a growth chamber at 23 to 25°C with a 12-h photoperiod and 75% relative humidity. Pathogenicity tests were repeated three times. Symptoms identical to those observed in the field developed within 12 days after inoculation; control plants remained healthy. The fungus was reisolated from all inoculated plants, confirming Koch's postulates. S. sclerotiorum has been reported on oilseed rape in Argentina, Australia, Brazil, Canada, the United States, and New Zealand (1). To our knowledge, this is the first report of Sclerotinia stem rot of oilseed rape in Greece. References: (1) D. F. Farr et al. Fungal Databases. Systematic Botany and Mycology Laboratory. Online publication. ARS, USDA, 2008. (2) L. M. Kohn. Phytopathology 69:881, 1979.


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