Effect of temperature on melanization and myceliogenic germination of sclerotia of Sclerotinia sclerotiorum

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.


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.



1989 ◽  
Vol 67 (5) ◽  
pp. 1395-1401 ◽  
Author(s):  
H. C. Huang ◽  
S. K. Sun

Tan-colored sclerotia of Sclerotium rolfsii and of an aberrant strain of Sclerotinia sclerotiorum that were freshly harvested from 5-week-old cultures on potato dextrose agar or stored at room temperature in paper bags for 4 weeks germinated myceliogenically on moist field soil without exogenous nutrients. A comparative study by time-lapse photomicroscopy revealed similarity in the mode of myceliogenic germination of sclerotia of the two species. The germination appeared to be of the hyphal type in both species and was characterized by the emergence of individual hyphae through the rind. There was no evidence of eruptive type of germination in any of the strains tested. Although several hyphae often emerged through the same spot of the rind, these hyphae emerged singly, and the time-lapse photomicrographs showed no evidence of eruptive germination. While most of the germinated sclerotia of S. rolfsii developed into colonies within 4 days of incubation on moist soil, the development of colonies from germinating sclerotia of S. sclerotiorum appeared to be slow, taking up to 28 days. Results of the inoculation studies showed that mycelia from the germinated sclerotia of S. rolfsii were able to infect and cause seed rot and damping-off of canola and alfalfa, which were planted near the soil surface at a distance of at least 15 mm from the sclerotium, without providing exogenous nutrients.



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.



1993 ◽  
Vol 71 (12) ◽  
pp. 1631-1638 ◽  
Author(s):  
H. C. Huang ◽  
E. G. Kokko

Among sclerotia of Sclerotinia sclerotiorum collected from diseased bean plants in a field near Lethbridge in 1987 and 1988, 30 and 16%, respectively, were contaminated by Trichothecium roseum. Laboratory studies showed that T. roseum is a mycoparasite of S. sclerotiorum, able to infect and destroy sclerotia in dual cultures on potato dextrose agar. Among sclerotia inoculated with spores of T. roseum and incubated for 4 weeks on moist sand, 54 and 43% were infected and killed by the isolates TR-4 and TR-6, respectively. Transmission electron microscopic studies of infected sclerotia revealed that hyphae of T. roseum entered the rind tissue by penetrating the melanized cell walls or via junctions between cells. Lysis of host cell walls occurred at penetration sites. Hyphae of T. roseum ramified in cortical and medullary tissues, destroying the sclerotium. In sclerotia with light infections of T. roseum, numerous cortical and (or) medullary cells showed cytoplasmic granulation and vacuolization without direct association with the mycoparasitic hyphae. Key words: biocontrol, hyperparasite, mycoparasitism.



1974 ◽  
Vol 140 (1) ◽  
pp. 47-55 ◽  
Author(s):  
David Jones ◽  
Alex. H. Gordon ◽  
John S. D. Bacon

1. Two fungi, Coniothyrium minitans Campbell and Trichoderma viride Pers. ex Fr., were grown on autoclaved crushed sclerotia of the species Sclerotinia sclerotiorum, which they parasitize. 2. in vitro the crude culture filtrates would lyse walls isolated from hyphal cells or the inner pseudoparenchymatous cells of the sclerotia, in which a branched β-(1→3)-β-(1→6)-glucan, sclerotan, is a major constituent. 3. Chromatographic fractionation of the enzymes in each culture filtrate revealed the presence of several laminarinases, the most active being an exo-β-(1→3)-glucanase, known from previous studies to attack sclerotan. Acting alone this brought about a limited degradation of the glucan, but the addition of fractions containing an endo-β-(1→3)-glucanase led to almost complete breakdown. A similar synergism between the two enzymes was found in their lytic action on cell walls. 4. When acting alone the endo-β-(1→3)-glucanase had a restricted action, the products including a trisaccharide, tentatively identified as 62-β-glucosyl-laminaribiose. 5. These results are discussed in relation to the structure of the cell walls and of their glucan constituents.



Plant Disease ◽  
2014 ◽  
Vol 98 (10) ◽  
pp. 1364-1370 ◽  
Author(s):  
Feng Zhou ◽  
Hong-Jie Liang ◽  
Ya-Li Di ◽  
Hong You ◽  
Fu-Xing Zhu

Growth and virulence stimulations of sublethal doses of fungicides on plant-pathogenic fungi and oomycetes have been reported and the stimulatory effects are potentially relevant to plant disease management. Sclerotinia sclerotiorum is one of the most devastating and economically important necrotrophic fungal phytopathogens, capable of infecting more than 400 species of plants worldwide. In order to study stimulatory effects of sublethal doses of fungicides on S. sclerotiorum, 55 dimethachlon-sensitive isolates and 3 dimethachlon-resistant isolates of S. sclerotiorum were assayed to determine effects of sublethal doses of dimethachlon on mycelial growth rate on potato dextrose agar (PDA) media and virulence on oilseed rape plants. Results showed that all 3 dimethachlon-resistant isolates and 13 of the 55 sensitive isolates exhibited stimulatory responses to sublethal doses of dimethachlon. Dimethachlon-resistant isolates grew significantly (P < 0.05) faster on PDA media amended with dimethachlon at 0.5 to 4 μg/ml than on fungicide-free PDA media. As for virulence on detached leaves of oilseed rape plants, lesion diameters of dimethachlon-resistant isolates after growth on PDA media amended with dimethachlon at 0.5 to 2 μg/ml were significantly larger (P < 0.05) than the control. The maximum stimulatory effects were 42.40 to 59.80%. In pot experiments, for both dimethachlon-sensitive and -resistant isolates, significant (P < 0.05) virulence stimulations were observed after spraying with dimethachlon at a concentration of 2 μg/ml. After growing on dimethachlon-amended PDA media, H2O2 sensitivity of S. sclerotiorum decreased significantly (P < 0.05) compared with the nonamended PDA control.



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.



2007 ◽  
Vol 58 (12) ◽  
pp. 1198 ◽  
Author(s):  
C. X. Li ◽  
Hua Li ◽  
A. B. Siddique ◽  
K. Sivasithamparam ◽  
P. Salisbury ◽  
...  

Sclerotinia stem rot (SSR) is a significant agricultural problem worldwide. Finding sources of resistance is crucial to the ongoing search for better management of this disease. Brassica germplasm from Australia, China and India was screened for resistance to SSR under Western Australian field conditions following stem inoculation, application of a spray of mycelial suspension, or as a consequence of myceliogenic germination originating from sclerotia resident in soil. Significant differences in response were observed among 53 genotypes using each of the three screening methods. There was a variable impact of the time of inoculation on the disease level depending upon time of assessment post-stem inoculation. However, this impact could be reduced to an insignificant level provided the assessment after stem inoculation was delayed until 3 weeks post-inoculation. The results of these studies indicate that the use of appropriate inoculation and assessment methods could significantly reduce variability in the responses commonly observed in screening for resistance in crop plants against Sclerotinia sclerotiorum.



2010 ◽  
Vol 132 (2) ◽  
Author(s):  
Xi Liu ◽  
Jiantao Zheng ◽  
Suresh K. Sitaraman

The thermal efficacy of thermal interface material (TIM) is highly dependent on its ability to adhere to the surfaces of interest. Any delamination of the TIM from the die or the lid will increase the local thermal resistance and, thus, will reduce the overall effectiveness of the TIM. Although significant amount of work has been done on understanding the thermal and moisture effects of various polymer materials used in microelectronic package assemblies, very limited work has been done to study the effect of temperature and moisture on TIM delamination. In this paper, a sequential hygro-thermal-mechanical finite-element model has been developed to mimic the loadsteps associated with package assembly as well as moisture soaking under 85°C/85RH over 500 h. The predictions from the models have been validated with a wide range of experimental data including laser Moiré data for thermomechanical loading and digital image correlation data for hygro-thermo-mechanical loading. Weight gain and coordinate-measurement machine have been used to characterize moisture diffusivity and moisture expansion coefficient of various polymer materials in the package assembly. The developed models show the evolution of normal strain in TIM during various loadsteps and provide important insight into the potential for TIM delamination under package assembly process and moisture soaking. Thus, the models can be used for developing various designs and process steps for reducing the chances for TIM delamination.



1986 ◽  
Vol 64 (12) ◽  
pp. 2909-2915 ◽  
Author(s):  
V. N. Tariq ◽  
P. Jeffries

The infection of leaf and stem tissues of Phaseolus by Sclerotinia sclerotiorum was studied using electron microscopy. Direct entry of the intact plant surface was achieved by hyphae from simple or compound appressoria. A closely appressed hyphal tip developed an electron-lucent region at the apex, in which a plasmalemmal invagination formed. This invagination surrounded a region of extracytoplasmic vesicular material which penetrated the cuticle during invasion. Penetration occurred by a narrow infection peg which passed through the cuticle via a narrow pore and caused little change in cuticle integrity. Once the cuticle was breached, a walled subcuticular vesicle developed from which infection hyphae spread laterally. Destruction of the epidermal cell walls was both rapid and extensive. Leaf and stem colonization occurred by intercellular growth of undifferentiated hyphae accompanied by cellular necrosis in advance of the mycelial front.



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