scholarly journals Heat-dried sclerotia of Sclerotinia sclerotiorum myceliogenically germinate in water and are able to infect Brassica napus

2018 ◽  
Vol 69 (8) ◽  
pp. 765 ◽  
Author(s):  
D. W. Lane ◽  
L. G. Kamphuis ◽  
M. C. Derbyshire ◽  
M. Denton-Giles

The phytopathogenic fungus Sclerotinia sclerotiorum forms dormant structures (termed sclerotia) that germinate myceliogenically under certain environmental conditions. During myceliogenic germination, sclerotia produce hyphae, which can infect leaves or stems of host plants directly from the ground; this is termed basal infection. This study determined which abiotic conditions were most important for promoting myceliogenic germination of sclerotia in vitro. A high sclerotium hydration level and low incubation temperature (15°C) improved mycelial growth in the presence of a nutrient source. Sclerotia incubated without a nutrient source on moist sand, vigorously myceliogenically germinated most frequently (63%) when they had been previously imbibed and then conditioned at −20°C. By far the most consistent amount of vigorous myceliogenic germination (>75%) was produced when sclerotia were heat-dried before being submerged in water. The hyphae of these sclerotia were shown to infect and proliferate on leaves of intact Brassica napus plants. This research provides a better understanding of the abiotic conditions that are likely to increase the risk of basal infection by S. sclerotiorum.


2018 ◽  
Vol 69 (8) ◽  
pp. 765 ◽  
Author(s):  
Jana Jarošová ◽  
Jan Ripl ◽  
Jan Fousek ◽  
Jiban Kumar Kundu

The phytopathogenic fungus Sclerotinia sclerotiorum forms dormant structures (termed sclerotia) that germinate myceliogenically under certain environmental conditions. During myceliogenic germination, sclerotia produce hyphae, which can infect leaves or stems of host plants directly from the ground; this is termed basal infection. This study determined which abiotic conditions were most important for promoting myceliogenic germination of sclerotia in vitro. A high sclerotium hydration level and low incubation temperature (15°C) improved mycelial growth in the presence of a nutrient source. Sclerotia incubated without a nutrient source on moist sand, vigorously myceliogenically germinated most frequently (63%) when they had been previously imbibed and then conditioned at −20°C. By far the most consistent amount of vigorous myceliogenic germination (>75%) was produced when sclerotia were heat-dried before being submerged in water. The hyphae of these sclerotia were shown to infect and proliferate on leaves of intact Brassica napus plants. This research provides a better understanding of the abiotic conditions that are likely to increase the risk of basal infection by S. sclerotiorum.



2019 ◽  
Vol 48 (2) ◽  
pp. 85-91
Author(s):  
David Lane ◽  
Matthew Denton-Giles ◽  
Mark Derbyshire ◽  
Lars G. Kamphuis


2011 ◽  
Vol 46 (2) ◽  
pp. 137-142 ◽  
Author(s):  
Maurício Batista Fialho ◽  
Maria Heloisa Duarte de Moraes ◽  
Annelise Roberta Tremocoldi ◽  
Sérgio Florentino Pascholati

The objective of this work was to evaluate the potential of an artificial mixture of volatile organic compounds (VOCs), produced by Saccharomyces cerevisiae, to control Sclerotinia sclerotiorum in vitro and in bean seeds. The phytopathogenic fungus was exposed, in polystyrene plates, to an artificial atmosphere containing a mixture of six VOCs formed by alcohols (ethanol, 3-methyl-1-butanol, 2-methyl-1-butanol and phenylethyl alcohol) and esters (ethyl acetate and ethyl octanoate), in the proportions found in the atmosphere naturally produced by yeast. Bean seeds artificially contamined with the pathogen were fumigated with the mixture of VOCs in sealed glass flasks for four and seven days. In the in vitro assays, the compounds 2-methyl-1-butanol and 3-methyl-1-butanol were the most active against S. sclerotiorum, completely inhibiting its mycelial growth at 0.8 µL mL-1, followed by the ethyl acetate, at 1.2 µL mL-1. Bean seeds fumigated with the VOCs at 3.5 µL mL-1 showed a 75% reduction in S. sclerotiorum incidence after four days of fumigation. The VOCs produced by S. cerevisiae have potential to control the pathogen in stored seeds.



2021 ◽  
Author(s):  
Sergio E. Lemos da Silva ◽  
Kimberlly Soares Brito Bratifich ◽  
eloisa Teresa Corradini Santos

The Sclerotinia sclerotiorum is a phytopathogenic fungus that causes the White Mold of soybean, being responsible for losses of up to 100% in agricultural production. The objective of this work was to verify and analyze the effect of the raw aqueous extract (EBA) of ginger Zingiber officinalis on a strain of Sclerotinia Sclerotiorum isolated from soybean, cultivated and maintained in vitro in laboratory. The methodology consisted of a longitudinal study of the statistical analysis of the mycelial growth velocity index (MICV), after treatment of the mycelia with different concentrations of aqueous crude extract. The results showed a direct relationship between increasing concentration of EBA and a significant negative effect on the growth of scleroderia. It was possible to conclude that the antifungal activity of ginger EBA was able to inhibit the in vitro growth of Sclerotinia sclerotiorum, with potential protection of soybean crops; it can become a sustainable alternative in the control of this fungus, by decreasing the use of agrochemicals that cause damage to public health and environmental damage.



2005 ◽  
Vol 24 (3) ◽  
pp. 133-144 ◽  
Author(s):  
S. Liu ◽  
H. Wang ◽  
J. Zhang ◽  
B. D. L. Fitt ◽  
Z. Xu ◽  
...  


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Jefferson Allan ◽  
Roshan Regmi ◽  
Matthew Denton-Giles ◽  
Lars G. Kamphuis ◽  
Mark C. Derbyshire

AbstractSclerotinia sclerotiorum is a necrotrophic fungal pathogen that infects upwards of 400 plant species, including several economically important crops. The molecular processes that underpin broad host range necrotrophy are not fully understood. This study used RNA sequencing to assess whether S. sclerotiorum genes are differentially expressed in response to infection of the two different host crops canola (Brassica napus) and lupin (Lupinus angustifolius). A total of 10,864 of the 11,130 genes in the S. sclerotiorum genome were expressed. Of these, 628 were upregulated in planta relative to in vitro on at least one host, suggesting involvement in the broader infection process. Among these genes were predicted carbohydrate-active enzymes (CAZYmes) and secondary metabolites. A considerably smaller group of 53 genes were differentially expressed between the two plant hosts. Of these host-specific genes, only six were either CAZymes, secondary metabolites or putative effectors. The remaining genes represented a diverse range of functional categories, including several associated with the metabolism and efflux of xenobiotic compounds, such as cytochrome P450s, metal-beta-lactamases, tannases and major facilitator superfamily transporters. These results suggest that S. sclerotiorum may regulate the expression of detoxification-related genes in response to phytotoxins produced by the different host species. To date, this is the first comparative whole transcriptome analysis of S. sclerotiorum during infection of different hosts.



1989 ◽  
Vol 67 (5) ◽  
pp. 1387-1394 ◽  
Author(s):  
H. C. Huang ◽  
E. G. Kokko

While sclerotia of the normal strain of Sclerotinia sclerotiorum produced on potato-dextrose agar at 7, 16, and 30 °C were black, the color of sclerotia of the aberrant strain was light brown, brown or tan, and dark brown or greyish black under 7, 16, and 30 °C, respectively. In the normal strain, deposition of melanin substance was heavy both on the surface and inside the cell walls of the rind of black sclerotia formed at 16 and 30 °C, but in sclerotia formed at 7 °C, many of the rind cells were unmelanized or partially melanized. In sclerotia from the aberrant strain, an electron-dense material, smaller than the melanin particles of the black sclerotia, was present in trace amounts or absent in light-brown sclerotia formed at 7 °C, but it was more abundant in dark-brown or greyish black sclerotia formed at 30 °C. Despite marked differences in color, sclerotia of the aberrant strain produced at the three temperatures were capable of undergoing myceliogenic germination on moist sand. It is concluded that temperature affects cell wall melanization during sclerotial morphogenesis, and that myceliogenic germination of sclerotia of S. sclerotiorum was affected by the black pigment but was unaffected by the color intensity of the brown pigment.





2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Mariana Guilger-Casagrande ◽  
Taís Germano-Costa ◽  
Natália Bilesky-José ◽  
Tatiane Pasquoto-Stigliani ◽  
Lucas Carvalho ◽  
...  

Abstract Background Biogenic nanoparticles possess a capping of biomolecules derived from the organism employed in the synthesis, which contributes to their stability and biological activity. These nanoparticles have been highlighted for the control of phytopathogens, so there is a need to understand their composition, mechanisms of action, and toxicity. This study aimed to investigate the importance of the capping and compare the effects of capped and uncapped biogenic silver nanoparticles synthesized using the filtrate of Trichoderma harzianum against the phytopathogenic fungus Sclerotinia sclerotiorum. Capping removal, investigation of the composition of the capping and physico-chemical characterization of the capped and uncapped nanoparticles were performed. The effects of the nanoparticles on S. sclerotiorum were evaluated in vitro. Cytotoxicity and genotoxicity of the nanoparticles on different cell lines and its effects on nontarget microorganisms were also investigated. Results The capped and uncapped nanoparticles showed spherical morphology, with greater diameter of the uncapped ones. Functional groups of biomolecules, protein bands and the hydrolytic enzymes NAGase, β-1,3-glucanase, chitinase and acid protease from T. harzianum were detected in the capping. The capped nanoparticles showed great inhibitory potential against S. sclerotiorum, while the uncapped nanoparticles were ineffective. There was no difference in cytotoxicity comparing capped and uncapped nanoparticles, however higher genotoxicity of the uncapped nanoparticles was observed towards the cell lines. Regarding the effects on nontarget microorganisms, in the minimal inhibitory concentration assay only the capped nanoparticles inhibited microorganisms of agricultural importance, while in the molecular analysis of the soil microbiota there were major changes in the soils exposed to the uncapped nanoparticles. Conclusions The results suggest that the capping played an important role in controlling nanoparticle size and contributed to the biological activity of the nanoparticles against S. sclerotiorum. This study opens perspectives for investigations concerning the application of these nanoparticles for the control of phytopathogens.



1998 ◽  
Vol 76 (3) ◽  
pp. 494-499 ◽  
Author(s):  
H C Huang ◽  
C Chang ◽  
G C Kozub

A study was conducted to determine the effect of sclerotial dryness, temperature during sclerotia formation, and relative humiditiy during incubation on myceliogenic germination of sclerotia of two isolates of Sclerotinia sclerotiorum (Lib.) De Bary. In the absence of exogenous nutrients, sclerotia germinated more readily at 100% RH than at 95% RH or lower. Desiccation of sclerotia is an important factor affecting myceliogenic germination and hyphal growth. At high humidity, either in an atmosphere with 100% RH or on moist sand, desiccant-dried sclerotia germinated readily and produced vigorous hyphal growth that often developed into colonies. On the other hand, fresh, untreated sclerotia germinated less readily and produced limited growth of hyphae that rarely developed into colonies. There was generally no effect of temperature at which sclerotia formed on germination. The incidence of seed rot and seedling wilt of sunflower was significantly (p < 0.05) higher when desiccant-dried sclerotia were used as inoculum rather than fresh sclerotia.Key words: Sclerotinia sclerotionum, sclerotia, myceliogenic germination, sclerotinia wilt of sunflower, relative humidity.



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