SYNTHESIS OF HETEROKARYONS IN RHIZOCTONIA SOLANI KÜHN

1963 ◽  
Vol 41 (6) ◽  
pp. 879-886 ◽  
Author(s):  
H. S. Whitney ◽  
J. R. Parmeter Jr.
Keyword(s):  
Rhizoctonia Solani ◽  
Single Spore ◽  
Wide Range ◽  
Cultural Types

The single-spore progeny of an isolate of Rhizoctonia solani showed a wide range of cultural types. When these progeny were paired by plating on opposite sides of Petri plates or by mixing semiliquid cultures, certain combinations gave rise to heterokaryons. The heterokaryons originated from hyphal anastomoses and were culturally distinct from either of the contributing homokaryons. Observations suggested a bipolar coaipatibility mechanism among the homokaryons. Some homokaryotic strains fruited, yielding culturally indistinguishable progeny. These homothallic lines also formed heterokaryons with other homothallic lines. The progeny of these heterokaryons showed a wide range of cultural types, indicating that some homokaryons could fruit either homothallically or heterothallically.

scholarly journals In situ Impact of the Antagonistic Fungal Strain, Trichoderma gamsii T30 on the Plant Pathogenic Fungus, Rhizoctonia solani in Soil

2019 ◽  
Vol 68 (2) ◽  
pp. 211-216
Author(s):  
MUHAMMAD ANEES ◽  
MUHAMMAD ABID ◽  
SOBIA CHOHAN ◽  
MUHAMMAD JAMIL ◽  
NADEEM AHMED ◽  
...  
Keyword(s):  
Population Density ◽  
Rhizoctonia Solani ◽  
Pathogenic Fungus ◽  
Suppressive Effect ◽  
Fungal Strain ◽  
Soil Microbiome ◽  
Target Dna ◽  
Wide Range ◽  
First Time

Rhizoctonia solani is a soil-borne fungus causing a wide range of plants diseases. Trichoderma gamsii strain T30 has previously been reported as antagonistic against R. solani. Although there are a few studies about the influence of Trichoderma strains on the R. solani densityin a pathosystem in the presence of plant hosts, this report for the first time comprehensively describes in situ effects of a T. gamsii strain on the population density of R. solani in the soil microcosmic conditions. The population dynamics of R. solani were followed in the autoclaved and non-autoclaved soils in artificially prepared microcosms up to day 25 after co-inoculation with T. gamsii in the variable ratios (R1/T1; R1/T0.1; R1/T0.01 of R. solani/T. gamsii). The population density of R. solani was evaluated by qPCR. In the autoclaved soil, target DNA copies of R. solani increased in the control samples from 1 × 105 to 6.5 × 106. At R1/T0.01, the number of target DNA copies were not significantly changed until day 11; however, it decreased by around five times at day 25. At R1/T0.1 and R1/T1, the number of DNA copies was reduced to 2.1 × 106 and 7.6 × 105 at day 11, respectively and the reduction was as much as 17 times at day 25. In the non-autoclaved soil, the number of the fungal cells decreased at day 25 whether inoculated or not with Trichoderma indicating a general suppression by the soil microbiome. In brief, T. gamsii significantly inhibited the growth of R. solani in the soil in situ and there was a general suppressive effect of the natural microbiome.

scholarly journals Droplet-based microfluidics platform for antifungal analysis against filamentous fungi

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Sehrish Iftikhar ◽  
Aurélie Vigne ◽  
Julia Elisa Sepulveda-Diaz
Keyword(s):  
Fungal Pathogens ◽  
Antimicrobial Agents ◽  
Pearson Correlation ◽  
Hyphal Growth ◽  
Bulk Analysis ◽  
Single Spore ◽  
Microfluidic Platform ◽  
Viability Assay ◽  
Wide Range ◽  
Potential Applications

AbstractFungicides are extensively used in agriculture to control fungal pathogens which are responsible for significant economic impact on plant yield and quality. The conventional antifungal screening techniques, such as water agar and 96-well plates, are based on laborious protocols and bulk analysis, restricting the analysis at the single spore level and are time consuming. In this study, we present a droplet-based microfluidic platform that enables antifungal analysis of single spores of filamentous fungus Alternaria alternata. A droplet-based viability assay was developed, allowing the germination and hyphal growth of single A. alternata spores within droplets. The viability was demonstrated over a period of 24 h and the antifungal screening was achieved using Kunshi/Tezuma as antifungal agent. The efficacy results of the droplet-based antifungal analysis were compared and validated with the results obtained from conventional protocols. The percentage inhibitions assessed by the droplet-based platform were equivalent with those obtained by the other two methods, and the Pearson correlation analysis showed high correlation between the three assays. Taken together, this droplet-based microfluidic platform provides a wide range of potential applications for the analysis of fungicide resistance development as well as combinatorial screening of other antimicrobial agents and even antagonistic fungi.

Molecular and physiological comparison ofAzospirillumspp. isolated fromRhizoctonia solanimycelia, wheat rhizosphere, and human skin wounds

2004 ◽  
Vol 50 (4) ◽  
pp. 291-297 ◽  
Author(s):  
Michael F Cohen ◽  
Xiang Y Han ◽  
Mark Mazzola
Keyword(s):  
Rhizoctonia Solani ◽  
Azospirillum Brasilense ◽  
Type Strain ◽  
Apple Orchard ◽  
Rrna Gene ◽  
Bacterial Strains ◽  
Free Living ◽  
Root Pathogen ◽  
Wide Range ◽  
Orchard Soil

Four phenotypically similar bacterial strains isolated from fungal, plant, and human sources were identified as Azospirillum species. Strains RC1 and LOD4 were isolated from the mycelium of the apple root pathogen Rhizoctonia solani AG 5 and from the rhizosphere of wheat grown in apple orchard soil, respectively. Strains C610 and F4626 isolated from human wounds were previously misclassified as Roseomonas genomospecies 3 and 6. All four strains demonstrated close similarities in 16S rRNA gene sequences, having [Formula: see text]97% identity to Azospirillum brasilense type strain ATCC 29145 and <90% identity to Roseomonas gilardii, the Roseomonas type strain. Extensive phenotypic similarities among the four strains included the ability of free-living cells to fix N2. Cells of strains RC1, LOD4, and C610 but not of strain F4626 could be induced to flocculate by incubation with 10 mmol·L–1glycerol or fructose in medium containing 0.5 mmol·L–1NO3–. Our results indicate a wide range of potential sources for Azospirillum spp. with the isolation of Azospirillum spp. from human wounds warranting further investigation.Key words: Azospirillum brasilense, Roseomonas fauriae, flocculation, Rhizoctonia solani.

scholarly journals Temperature, Moisture, and Seed Treatment Effects on Rhizoctonia solani Root Rot of Soybean

Plant Disease ◽  
2003 ◽  
Vol 87 (5) ◽  
pp. 533-538 ◽  
Author(s):  
A. E. Dorrance ◽  
M. D. Kleinhenz ◽  
S. A. McClure ◽  
N. T. Tuttle
Keyword(s):  
Soil Moisture ◽  
Rhizoctonia Solani ◽  
Root Rot ◽  
Seed Treatment ◽  
Anastomosis Group ◽  
Control Measures ◽  
Root Weight ◽  
Wide Range ◽  
Plant Stand ◽  
Growth Chamber Studies

The effects of temperature and soil moisture on infection and disease development by Rhizoctonia solani on soybean were studied individually. In addition, the anastomosis group of R. solani isolates recovered from soybean from 35 fields in 15 counties was determined. All of the 44 isolates recovered in this study were AG-2-2 IIIB. Five isolates of R. solani were able to infect and colonize soybean roots and hypocotyls at 20, 24, 28, and 32°C in growth chamber studies. The temperatures evaluated in this study were not limiting to the isolates tested. In greenhouse studies, nine R. solani isolates and a noninoculated control were evaluated at 25, 50, 75, and 100% soil moisture holding capacity (MHC). Root weights were greater and percent stand averages higher at 50 and 75% than at 25 or 100% MHC; however, as percentage of control, the main effect on percent moisture for percent stand, plant height, or root weight was not significant. There were significant differences among the isolates for the percent stand, root rot rating, and root fresh weight of soybean in each study. In both temperature and moisture studies, the R. solani isolates could be separated as predominantly causing (i) seed rot, as detected by greatly reduced plant stand; (ii) root rot generally having no effect on plant stand but a high root rot rating and low root weight; or (iii) hypocotyl lesions, having no effect on plant stand, a low root rot score, and a high number of red lesions on the hypocotyl. In the greenhouse seed treatment evaluations of five fungicides, there was no fungicide by isolate interaction using these pathogenic types of R. solani. None of the seed treatments evaluated in this study provided 100% control of the four isolates tested. Due to the wide range of environmental factors that permit R. solani infection and disease on soybeans, other control measures that last all season, such as host resistance, should be emphasized.

Barcoded microbial system for high-resolution object provenance

Science ◽  
2020 ◽  
Vol 368 (6495) ◽  
pp. 1135-1140 ◽  
Author(s):  
Jason Qian ◽  
Zhi-xiang Lu ◽  
Christopher P. Mancuso ◽  
Han-Ying Jhuang ◽  
Rocío del Carmen Barajas-Ornelas ◽  
...  
Keyword(s):  
Food Safety ◽  
Nucleic Acid ◽  
High Resolution ◽  
Human Health ◽  
Nucleic Acid Detection ◽  
Single Spore ◽  
Detection Assay ◽  
Wide Range ◽  
Fundamental Challenge ◽  
Microbial System

Determining where an object has been is a fundamental challenge for human health, commerce, and food safety. Location-specific microbes in principle offer a cheap and sensitive way to determine object provenance. We created a synthetic, scalable microbial spore system that identifies object provenance in under 1 hour at meter-scale resolution and near single-spore sensitivity and can be safely introduced into and recovered from the environment. This system solves the key challenges in object provenance: persistence in the environment, scalability, rapid and facile decoding, and biocontainment. Our system is compatible with SHERLOCK, a Cas13a RNA-guided nucleic acid detection assay, facilitating its implementation in a wide range of applications.

Phylogenetic grouping of cultural types of Rhizoctonia solani AG 2–2 based on ribosomal ITS sequences

Mycologia ◽  
2000 ◽  
Vol 92 (3) ◽  
pp. 505-509
Author(s):  
Oscar Salazar ◽  
María C. Julián ◽  
Mitsuro Hyakumachi ◽  
Victor Rubio
Keyword(s):  
Rhizoctonia Solani ◽  
Its Sequences ◽  
Phylogenetic Grouping ◽  
Cultural Types

Phylogenetic Grouping of Cultural Types of Rhizoctonia solani AG 2-2 Based on Ribosomal ITS Sequences

Mycologia ◽  
2000 ◽  
Vol 92 (3) ◽  
pp. 505 ◽  
Author(s):  
Oscar Salazar ◽  
Maria C. Julian ◽  
Mitsuro Hyakumachi ◽  
Victor Rubio
Keyword(s):  
Rhizoctonia Solani ◽  
Its Sequences ◽  
Phylogenetic Grouping ◽  
Cultural Types

SURVIVAL OF SINGLE-BASIDIOSPORE ISOLATES OF RHIZOCTONIA PRATICOLA AND RHIZOCTONIA SOLANI

1964 ◽  
Vol 10 (5) ◽  
pp. 739-746 ◽  
Author(s):  
George C. Papavizas
Keyword(s):  
Organic Matter ◽  
Rhizoctonia Solani ◽  
High Tolerance ◽  
Single Spore ◽  
Time Rate ◽  
Unamended Soil ◽  
Parent Culture ◽  
Oat Straw ◽  
Rhizoctonia Praticola ◽  
Rate Of Decline

Twenty randomly selected single-basidiospore isolates from each of Rhizoctonia praticola and R. solani differed considerably in their tolerance to CO2, competitive saprophytic activity, and ability to survive within precolonized substrate segments incubated in soils with or without pentachloronitrobenzene (PCNB) or oat straw. With a few exceptions, isolates possessing high saprophytic activity also possessed high tolerance to CO2 and high surviving ability in precolonized substrate. Several single-spore isolates of R. solani possessed higher ability for saprophytic survival in organic matter and lower CO2-sensitivity than their parent culture. Survival of single-basidiospore isolates in precolonized substrate segments was greater in unamended soil or soil amended with oat straw than in soil treated with PCNB. Mature oat straw reduced surviving ability of several isolates, whereas it increased surviving ability of others above that observed in unamended soil. The isolates whose surviving ability was increased by oat straw were mostly those possessing high saprophytic activity in unamended soil. Saprophytic activity and virulence of all isolates tested declined with time. Rate of decline of virulence was much more rapid for weak than strong saprophytes.

scholarly journals Rapid Determination of Rice Cultivar Responses to the Sheath Blight Pathogen Rhizoctonia solani Using a Micro-Chamber Screening Method

Plant Disease ◽  
2007 ◽  
Vol 91 (5) ◽  
pp. 485-489 ◽  
Author(s):  
Y. Jia ◽  
F. Correa-Victoria ◽  
A. McClung ◽  
L. Zhu ◽  
G. Liu ◽  
...  
Keyword(s):  
Rhizoctonia Solani ◽  
Field Experiments ◽  
Rapid Determination ◽  
Selection Process ◽  
Screening Method ◽  
Sheath Blight ◽  
Field Conditions ◽  
Economic Losses ◽  
Transparent Plastic ◽  
Wide Range

An accurate greenhouse screening method has not been developed previously to identify host response to sheath blight disease caused by Rhizoctonia solani Kühn that causes significant economic losses in rice yield worldwide. The unavailability of a robust screening system in the greenhouse has made it difficult to quantify disease reactions to R. solani, and has hampered studies on the genetics of resistance and plant breeding efforts to improve resistance. In an effort to develop a standardized laboratory micro-chamber screening method to quantify resistance to R. solani in rice, five rice cultivars, representing a wide range of observed disease reactions under field conditions, were examined in a blind inoculation test at three locations (Arkansas, Texas, and Colombia). Rice seedlings were inoculated at the three- to four-leaf stage with potato dextrose agar plugs containing mycelium and then covered with a 2- or 3-liter transparent plastic bottle for maintaining high humidity after inoculation. Two cultivars, Jasmine 85 and Lemont, that consistently have shown the highest and lowest levels of resistance, respectively, in previous field and greenhouse studies, were used as standards. Concurrent field experiments in Arkansas and Texas also were performed to compare the greenhouse disease ratings with those observed under field conditions. Overall, the relative disease ratings of the seven test cultivars were consistent between test locations and with field evaluations. Thus, the micro-chamber screening method can be used as an effective approach to accurately quantify resistance to the sheath blight pathogen under controlled greenhouse conditions and should help expedite the selection process to improve resistance to this important pathogen.

Sign in / Sign up

Export Citation Format

Share Document