scholarly journals Variations In Different Isolates Of Rhizoctonia Solani Based On Temperature And pH

1970 ◽  
Vol 36 (3) ◽  
pp. 389-396 ◽  
Author(s):  
BK Goswami ◽  
MM Rahaman ◽  
AKMA Hoque ◽  
K Bhuiyan ◽  
IH Mian
Keyword(s):  
Growth Factors ◽  
Rhizoctonia Solani ◽  
Radial Growth ◽  
Mycelial Growth ◽  
Potato Dextrose Agar ◽  
Optimum Temperature ◽  
Optimum Ph ◽  
Sclerotial Formation ◽  
Rates Of Growth ◽  
Different Levels

An experiment was conducted to find out variation in isolated Rhizoctonia solani based on radial mycelial growth and sclerotial production. Five isolates of Rhizoctonia solani representing five clusters group were selected and were grown at different levels of temperature and pH on potato dextrose agar (PDA). It was observed that optimum temperature and pH for growth and scierotial production varied among the isolates. The rates of growth and sclerotial formation were not uniform at the same levels of the two growth factors. The maximum mycelial growth of all isolates was found at 30°C. At 35°C, only GAZ-9 and GAZ-18 showed initiation of growth, but the rate was very slow. The optimum temperature for sclerotial production of the isolates GAZ-9, JES- 16, GAZ-18 SYL-26 was 30°C and for the isolate DIN-8 was 25°C. The optimum pH for maximum radial growth was 6 for DIN-8 and 7 for other four isolates. The maximum number of sclerotia was produced by DIN-8, GAZ-9, and SYL-30 at pH 8, 4, and 7, respectively. The optimum pH for sclerotia formation in JES-16 and GAZ-18 was pH 6. Keywords: Rhizoctonia solani; variations; temperature; pH. DOI: http://dx.doi.org/10.3329/bjar.v36i3.9267 BJAR 2011; 36(3): 389-396

scholarly journals Indian Mustard and Allyl Isothiocyanate Inhibit Sclerotium rolfsii

2002 ◽  
Vol 127 (1) ◽  
pp. 27-31 ◽  
Author(s):  
Stephanie G. Harvey ◽  
Heather N. Hannahan ◽  
Carl E. Sams
Keyword(s):  
Treatment Effect ◽  
Radial Growth ◽  
Mycelial Growth ◽  
Sclerotium Rolfsii ◽  
Indian Mustard ◽  
Allyl Isothiocyanate ◽  
Potato Dextrose Agar ◽  
Soilborne Pathogen ◽  
Low Concentrations ◽  
Sclerotial Germination

Allyl isothiocyanate (AITC) is the predominant isothiocyanate produced by damaged tissues of Indian mustard (Brassica juncea (L) Czerniak). This study investigated Indian mustard and AITC mediated suppression of mycelial growth and sclerotial germination of Sclerotium rolfsii Saccardo, a common soilborne pathogen. Indian mustard (IM) treatments of 0, 0.1, 0.2, 0.6, 1.0, 2.0, 4.1, 5.1, 10.2, 20.4, 40.8, 81.6, and 163.3 g·L-1 (weight of reconstituted mustard per liter of air) were evaluated for suppression of mycelial growth. Treatment effect was evaluated by measuring the radial growth of mycelia. Sclerotia were placed in culture tubes containing 18 g autoclaved soil and covered with an additional 5 g soil. AITC at concentrations of 0, 4.0, 16.0, 64.0, 256.0, 1024.0, or 4096.0 μmol·L-1 was injected into the tubes. Treated sclerotia were removed from tubes and plated on potato dextrose agar to determine viability. Mycelial growth was inhibited with IM treatments (P < 0.01). Inhibiting concentrations (IC) of IM for mycelial growth inhibition of 50% and 90% were 0.7 and 1.0 g·L-1, respectively, with death resulting with >2 g·L-1. Inhibition attributable to AITC alone was lower than that achieved by IM producing equivalent amounts of AITC. Germination of sclerotia was negatively correlated with AITC concentration (r = 0.96; P < 0.01). The IC50 and IC90, of AITC were 249.0 and 528.8 μmol·L-1, respectively, at 42 hours. The lethal concentration for sclerotia was not reached; only suppression occurred at the highest treatment concentrations. Sclerotium rolfsii mycelia were sensitive to the IM volatiles and were suppressed at low concentrations. Sclerotia were more resistant than the mycelia and required higher concentrations of AITC to suppress germination.

scholarly journals THE EFFECT OF CHITOSAN HYDROLYSATE ON THE FUNGI ALTERNARIA SOLANI, FUSARIUM SOLANI AND RHIZOCTONIA SOLANI IN VITRO

2021 ◽  
Vol 26 ◽  
pp. 200-209
Author(s):  
Balzhima Ts. Shagdarova ◽  
◽  
Natalia V. Karpova ◽  
Alla V. Il’ina ◽  
Valery P. Varlamov
Keyword(s):  
Molecular Weight ◽  
Nitric Acid ◽  
Rhizoctonia Solani ◽  
Fusarium Solani ◽  
Radial Growth ◽  
Alternaria Solani ◽  
Potato Dextrose Agar ◽  
Deacetylation Degree ◽  
Growth Experiments

Chitosan hydrolysate was obtained using nitric acid; the prevailing fraction had a molecular weight of 30 kDa and a deacetylation degree of 95%. The effect of chitosan hydrolysate when added to potato dextrose agar (PDA) in different concentrations (0.5, 1, 1.5, 2, 4, 6 and 8 mg/mL) was studied on the growth of the fungi Alternaria solani Sorauer, Fusarium solani (Mart.) Sacc. and Rhizoctonia solani J.G. Kühn. A. solani was the most sensitive to the addition of chitosan hydrolysate to PDA in radial growth experiments. On days 3 and 7 of incubation, the antifungal activity of the phytopathogen growth was 69%-92% and 69%-88%, respectively, in the concentration range of 0.5-2 mg/ml.

scholarly journals Rice Blast in Puerto Rico

1969 ◽  
Vol 62 (3) ◽  
pp. 290-300
Author(s):  
Lii-Jang Liu
Keyword(s):  
Puerto Rico ◽  
Rice Straw ◽  
Rice Blast ◽  
Mycelial Growth ◽  
Potato Dextrose Agar ◽  
Pyricularia Oryzae ◽  
In Vitro Tests ◽  
Optimum Temperature ◽  
Pathogenicity Tests

Rice blast, which had not been observed during the last six decades in Puerto Rico, reappeared recently in Manatí and in the Gurabo Substation, affecting Brazos, a cultivar introduced from Texas. Pathogenicity tests, as well as studies on the conidial morphology, showed that the fungus isolated from typical blast lesions is Pyricularia oryzae Cav. The physiology of the fungus and its sporulation on various media also were studied. The optimum temperature range, both for mycelial growth and for germination of conidia, was found to be between 24 to 28° C. Sporulation occurred satisfactorily on potato-dextrose agar enriched with coconut milk, and on steamed corn and barley, and rice-straw-decoction agars. In vitro tests with fungicides benomyl, pentachloronitrobenzene, mancozeb, chloroneb, and captan indicated that the first two compounds are the most effective in inhibiting mycelial growth of P. oryzae.

scholarly journals Stimulatory Effects of Boscalid on Virulence of Sclerotinia sclerotiorum Indicate Hormesis May Be Masked by Inhibitions

Plant Disease ◽  
2020 ◽  
Vol 104 (3) ◽  
pp. 833-840
Author(s):  
Simin Hu ◽  
Qianru Xu ◽  
Yuchao Zhang ◽  
Fuxing Zhu
Keyword(s):  
Sclerotinia Sclerotiorum ◽  
Negative Correlation ◽  
Plant Pathogen ◽  
Mycelial Growth ◽  
Molecular Mechanisms ◽  
Potato Dextrose Agar ◽  
Dosage Range ◽  
Expression Levels ◽  
The Future ◽  
Different Levels

Hormetic effects of fungicides on phytopathogens are of great importance for proper application of fungicides. The aim of the present study was to investigate the stimulatory effects of the fungicide boscalid on mycelial growth and virulence of the devastating plant pathogen Sclerotinia sclerotiorum. Boscalid in potato dextrose agar (PDA) at a dosage range from 0.0005 to 0.002 μg/ml exerted statistically significant (P ≤ 0.015) stimulations on mycelial growth of S. sclerotiorum, and the maximum stimulation magnitudes were 5.55 ± 0.73% (mean ± SD) for the four isolates tested. Boscalid in PDA at 0.02 μg/ml inhibited mycelial growth of isolates HLJ3H and HLJ4H by 15.0 and 8.9%, respectively. However, after the growth-inhibited mycelia were inoculated on rapeseed leaves, isolates HLJ3H and HLJ4H exhibited virulence stimulations of 8.7 and 17.8%, respectively, indicating that hormesis may be masked by inhibitions. Boscalid sprayed at 0.0001 to 0.1 μg/ml on detached rapeseed leaves had significant (P ≤ 0.041) stimulations on virulence of S. sclerotiorum, and the maximum stimulation magnitudes were 17.90 ± 5.94% (mean ± SD) for the four isolates tested. Experiments on 12 isolates with different levels of virulence showed there was a negative correlation (R = –0.663, P = 0.019) between the maximum virulence stimulation magnitude and virulence of S. sclerotiorum in the absence of fungicide. Boscalid at stimulatory concentrations had no significant effect on the expression levels of three virulence-associated genes that encode cutinase (SsCut), polygalacturonase (SsPG1), and oxaloacetate acetylhydrolase (SsOah1). The molecular mechanisms for hormetic effects of boscalid on S. sclerotiorum remain to be studied in the future.

scholarly journals Effect of Different Carbon and Nitrogen Sources on Sclerotium rolfsii sacc. Mycelial Growth and Sclerotial Development

2020 ◽  
Vol 9 (1) ◽  
pp. 17-27
Author(s):  
Fakher Ayed ◽  
Hayfa Jabnoun-Khiareddine ◽  
Rania Aydi-Ben Abdallah ◽  
Mejda Daami-Remadi
Keyword(s):  
Ammonium Chloride ◽  
Radial Growth ◽  
Mycelial Growth ◽  
Sodium Citrate ◽  
Ammonium Acetate ◽  
Sclerotium Rolfsii ◽  
N Source ◽  
Sclerotial Formation ◽  
Sclerotial Development ◽  
Sclerotial Germination

In vitro studies were conducted on Potato Dextrose Agar using different carbon (C) and nitrogen (N) sources to evaluate their effects on the mycelial growth, and the sclerotial development of three Tunisian Sclerotium rolfsii Sacc. isolates. Radial growth was optimum on basal medium supplemented with ammonium chloride (0.48 gram of nitrogen per liter (g of N.L-1)) as N source but was restricted on L-Arginine and completely inhibited on ammonium acetate amended media (0.48 g N.L-1). Sclerotial initiation occurred from the 3rd to the 12th day of incubation for all tested isolates. Potassium nitrate was the most suitable N source for sclerotial formation whereas sclerotial development was completely inhibited on ammonium acetate amended medium. Optimal sclerotial germination was recorded using L-Arginine (78-80%) followed by L-Asparagine (46-94%) and ammonium chloride (46-88%) as N sources. Nevertheless, the lowest sclerotial germination rate was noted on sodium nitrate and ammonium acetate amended media. As for C sources (16 gram of carbon per liter (g of C.L-1)), optimal radial growth occurred using D-mannitol for Sr1 and Sr2 isolates and maltose for Sr3, but no mycelial growth was recorded using sodium citrate for all isolates. All C sources tested, except sodium citrate, were suitable for sclerotial formation, production, and germination. Mature sclerotia became brownish after 6 to 12 days of incubation and sclerotial production was highest using D-mannitol, maltose, and D-glucose, depending on isolates used, as C sources. Optimal germination of sclerotia was noted using D-glucose, D-mannitol and maltose for Sr1 isolate, maltose for Sr2 and D-glucose and maltose for Sr3. It was concluded that N and C sources are both important factors for the growth of S. rolfsii and its survival.

scholarly journals Development of Sclerotia and Apothecia of Sclerotinia sclerotiorum from Infected Soybean Seed and Its Control by Fungicide Seed Treatment

Plant Disease ◽  
1999 ◽  
Vol 83 (12) ◽  
pp. 1113-1115 ◽  
Author(s):  
D. S. Mueller ◽  
G. L. Hartman ◽  
W. L. Pedersen
Keyword(s):  
Sclerotinia Sclerotiorum ◽  
Radial Growth ◽  
Mycelial Growth ◽  
Seed Treatment ◽  
Soybean Seed ◽  
Potato Dextrose Agar ◽  
Field Soil ◽  
Laboratory Studies ◽  
Infected Seed ◽  
Seed Coats

Field and laboratory studies were done to evaluate the development of sclerotia and apothecia of Sclerotinia sclerotiorum from soybeans and its control with fungicide seed treatment. Soybean seed infected with S. sclerotiorum produced mycelia on both seed coats and cotyledons after 48 h on potato dextrose agar (PDA). Obviously infected soybean seed also were placed in aluminum pans containing field soil and placed in soybean fields near Urbana, Illinois and Clinton, Wisconsin. In 1997, a total of 553 sclerotia, 20 stipes, and 10 apothecia were produced from 500 infected seeds. In 1998, 201 sclerotia and 22 stipes were produced, but no apothecia were observed from the 500 infected seeds. Fludioxonil was the most effective fungicide for reducing radial growth of S. sclerotiorum on PDA plates and suppressed 99% of the radial growth at 0.1 μg a.i./ml. S. sclerotiorum was recovered from 2% of soybean seed lots containing infected seed. When this seed lot was treated with several fungicides, captan + pentachloronitrobenzene + thiabendazole and fludioxonil completely inhibited mycelial growth from infected seed; thiram and thiabendazole each reduced recovery of S. sclerotiorum by 90%. In the field, 754 sclerotia and 10 apothecia were produced from 1,000 infected seeds over a two-year period. When evaluating fungicide control in the field, thiram, fludioxonil, and captan + pentachloronitrobenzene + thiabendazole reduced sclerotia formation from infected seed by more than 98%.

scholarly journals First Report of Rhizoctonia solani AG-4-HG-II on Garden Pink in Buenos Aires, Argentina

Plant Disease ◽  
2001 ◽  
Vol 85 (12) ◽  
pp. 1287-1287
Author(s):  
E. R. Wright ◽  
M. C. Rivera ◽  
K. Asciutto ◽  
L. Gasoni
Keyword(s):  
Rhizoctonia Solani ◽  
Mycelial Growth ◽  
Buenos Aires ◽  
Morphological Characteristics ◽  
Anastomosis Group ◽  
Potato Dextrose Agar ◽  
Stem Rot ◽  
American Phytopathological Society ◽  
Basal Stem Rot ◽  
First Report

During 2001, basal stem rot, wilt, and plant death were observed on 30% of the plants in a crop of Dianthus plumarius L. ‘Telstar’ in Buenos Aires. Pieces of diseased stems ≈1 cm long were surface-disinfested in 2% NaOCl for 1 min and cultured on 2% potato dextrose agar (PDA), pH 7, at 22 to 24°C. After 7 days, an identical fungus was consistently isolated from pieces of infected tissue. Colonies initially were white, turned brown after 2 to 3 days, and eventually formed irregularly shaped sclerotia. Cultures exhibited morphological characteristics typical of Rhizoctonia solani Kühn (2) and were identified with known anastomosis group tester isolates (1). Positive anastomosis was observed with tester strains of R. solani AG-4-HG-II. One isolate was tested for pathogenicity by placing two pieces of PDA (1 cm2) containing 7-day-old mycelial growth ≈0.5 cm from the base of healthy 2-month-old plants. Control plants were treated with sterile pieces of PDA using the same procedures. Ten replicate plants were used for each treatment. Plants were maintained at 22 to 24°C under 95 to 100% relative humidity and a 12-h light/dark photoperiod. After 7 days, symptoms developed that were similar to those originally observed, and Koch's postulates were satisfied by reisolating the fungus. To our knowledge, this is the first report of R. solani AG4-HG-II causing disease on D. plumarius in Argentina. References: (1) B. Sneh et al. Identification of Rhizoctonia Species. The American Phytopathological Society, St. Paul, MN, 1991. (2) C. C. Tu and J. W. Kimbrough. Mycologia 65:941, 1973.

STUDIES IN FOREST PATHOLOGY: XXIV. POLYPORUS TOMENTOSUS FR. AS A MAJOR FACTOR IN STAND-OPENING DISEASE OF WHITE SPRUCE

1962 ◽  
Vol 40 (12) ◽  
pp. 1631-1658 ◽  
Author(s):  
R. D. Whitney
Keyword(s):  
Competitive Advantage ◽  
Rhizoctonia Solani ◽  
Disease Development ◽  
Forest Pathology ◽  
Phytophthora Cactorum ◽  
Optimum Temperature ◽  
Root Tips ◽  
Root Decay ◽  
Dead Trees ◽  
Optimum Ph

Stand-opening disease in Saskatchewan spruce forests is characterized by the occurrence of patches, often of an acre or more, of declining and dead trees. Polyporus tomentosus Fr. is a major cause of the disease, which develops slowly, with 20 to 30 years elapsing between initiation of attack and death of the trees. Extensive root decay develops before the above-ground symptoms become apparent. Inoculation experiments have shown that P. tomentosus grows about 1.5 in. per year, and that the fungus is parasitic on white spruce.Polyporus tomentosus may enter healthy roots at a point of contact with infected roots; no evidence was found that it entered through root tips or directly from the soil. The fungus remains viable in infected roots for at least 16 years. The disease is commonly associated with injury caused by root-tunnelling weevils in the genus Hylobius. Host vigor did not appear to influence infection or disease development. In culture, the optimum temperature for P. tomentosus was 20 °C and the optimum pH was 4.5. At lower temperatures P. tomentosus appeared to have a competitive advantage over fungi isolated from dying rootlets. Small seedlings grown in agar with P. tomentosus were killed in 8 months. Under these conditions P. tomentosus was much less virulent than Rhizoctonia, solani Kühn and Phytophthora cactorum L. and C. Schroet.

Peanut Web Blotch: I. Cultural Characteristics and Identity of Causal Fungus1

1984 ◽  
Vol 11 (2) ◽  
pp. 109-114 ◽  
Author(s):  
R. A. Taber ◽  
R. E. Pettit ◽  
G. L. Philley
Keyword(s):  
South Africa ◽  
Cultural Studies ◽  
Mycelial Growth ◽  
Fungal Species ◽  
Optimum Temperature ◽  
Cultural Characteristics ◽  
Foliar Disease ◽  
The Usa

Abstract A foliar disease of peanuts, previously unreported in the USA, was found in Texas in 1972. The pathogen was identified as a species of Ascochyta. Further cultural studies have revealed this fungus to be Phoma arachidicola Marasas, Pauer, and Boerema. Pycnidia form profusely at 20 C and 25 C. Pycnidiospores are borne on short pycnidiosphores and are predominantly one-celled in culture. Spores produced in pycnidia on infected leaflets become 1 septate. Large 1-septate spores, as well as an occasional 2-septate spore, may form in culture. Optimum temperature for mycelial growth in 20 C; little or no growth occurs at 5 C or above 30 C. The teleomorphic state develops in the field on fallen leaflets and can be induced to form in the laboratory on sterilized peanut leaflets between 15 and 20 C. Cultures derived from single ascospores form pseudothecia. Pycnidiospores, ascospores, and chlamydospores are all infective units. Because this fungus produces hyaline ascospores and pseudoparaphyses, it has been transferred to the genus Didymella as Didymella arachidicola (Choch.) comb. nov. Comparisons with 15 isolates causing web blotch of peanut in the USA, Argentina, and South Africa indicate that web blotch symptoms are produced by the same fungal species.

scholarly journals Effects of Long-Wave UV Light on Monilinia Growth and Identification of Species

Plant Disease ◽  
1999 ◽  
Vol 83 (1) ◽  
pp. 62-65 ◽  
Author(s):  
A. De Cal ◽  
P. Melgarejo
Keyword(s):  
Short Distance ◽  
Mycelial Growth ◽  
Uv Light ◽  
Dark Period ◽  
Morphological Characteristics ◽  
Potato Dextrose Agar ◽  
Long Wave ◽  
The World ◽  
Identification Of Species ◽  
Respective Species

The effect of long-wave UV/dark period on mycelial growth of 46 isolates of Monilinia sp. collected in Spain and 16 isolates collected from other parts of the world was investigated. Typical isolates of M. laxa, M. fructigena, and M. fructicola were grown in the dark and identified by morphological characteristics. Long-wave UV/dark conditions reduced the growth rates of M. laxa, M. fructigena, and M. fructicola on potato dextrose agar. All isolates of M. fructigena grew more slowly than those of M. fructicola. Typical and atypical isolates of M. fructigena and M. fructicola were placed in their respective species based on long-wave UV/dark growth rate data. M. laxa isolates were readily distinguished by the short distance from their conidium to the first germ tube branch. The involvement of different photoreceptors in photoresponses by M. fructicola and M. fructigena is discussed. Differences in mycelial growth under long-wave UV may be a useful tool to identify Monilinia spp.

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