Mycelial Compatibility Groups Research Articles

Molecular, morphological and pathogenic diversity of Sclerotinia sclerotiorum isolates from common bean (Phaseolus vulgaris) fields in Argentina

White mould, caused by Sclerotinia sclerotiorum, is one of the most threatening fungal diseases occurring across major bean production regions worldwide. In Argentina, under favourable weather conditions, up to 100% seed yield losses occur on susceptible common bean cultivars. The aim of this study was to characterize the diversity of S. sclerotiorum isolates from six dry bean fields in the main production area of Argentina by means of molecular, morphological (mycelium colour, number and pattern of sclerotia distribution) and pathogenic approaches. Among 116 isolates analysed, high genotypic and morphological variability was observed. A total of 52 mycelial compatibility groups (MCGs) and 59 URPs (universal rice primers) molecular haplotypes were found. All the MCGs were location specific, while only 12% of the URP haplotypes were shared among locations. The molecular analysis of variance revealed a significant differentiation among populations, with higher genetic variability within the populations analysed than among them. The aggressiveness of the isolates towards bean seedlings was assessed in the greenhouse. Most of the isolates were highly aggressive, while no variation among locations was observed. The information generated in the present study provides, for the first time, information on the variability of S. sclerotiorum associated with white mould in the main common bean production area in Argentina. In addition, the findings suggest the occurrence of both clonal and sexual reproduction in the populations analysed. This work contributes to the development of sustainable management strategies in bean production aimed to minimize yield losses due to white mould.

Mycelial compatibility group and genetic variation of sunflower Sclerotinia sclerotiorum in Northeast China

Sunflower is an economically important crop, particularly for oil production in Northeast China. Sclerotinia sclerotiorum, a fungal pathogen can cause severe yield loss of several crop species, including sunflower. In the present study, mycelial compatibility groups (MCGs) were investigated among a total of 115 isolates of Sclerotinia sclerotiorum from sunflower fields in different regions of Northeast China. A total of 35 different MCGs were identified, with 1–12 isolates within each group. There were nine MCGs with only one representative isolate. Additionally, simple sequence repeats (SSRs, i.e., microsatellite loci) method was employed to assess the genetic variation among the 115 isolates. The clustering based on SSRs suggested that most isolates that were geographically close were grouped in the same cluster or a close cluster. The clustering results of all 115 isolates suggested that the clusters based on microsatellite loci were highly consistent with the MCGs results. Our findings add value to the current knowledge base on the population structure and genetic diversity of S. sclerotiorum, specifically in the context of sunflower cultivation in Northeast China, and may provide valuable information for breeding of sunflower stocks with enhanced resistance towards S. sclerotiorum.

Population structure and phenotypic variation of Sclerotinia sclerotiorum from dry bean (Phaseolus vulgaris) in the United States.

The ascomycete pathogen Sclerotinia sclerotiorum is a necrotrophic pathogen on over 400 known host plants, and is the causal agent of white mold on dry bean. Currently, there are no known cultivars of dry bean with complete resistance to white mold. For more than 20 years, bean breeders have been using white mold screening nurseries (wmn) with natural populations of S. sclerotiorum to screen new cultivars for resistance. It is thus important to know if the genetic diversity in populations of S. sclerotiorum within these nurseries (a) reflect the genetic diversity of the populations in the surrounding region and (b) are stable over time. Furthermore, previous studies have investigated the correlation between mycelial compatibility groups (MCG) and multilocus haplotypes (MLH), but none have formally tested these patterns. We genotyped 366 isolates of S. sclerotiorum from producer fields and wmn surveyed over 10 years in 2003–2012 representing 11 states in the United States of America, Australia, France, and Mexico at 11 microsatellite loci resulting in 165 MLHs. Populations were loosely structured over space and time based on analysis of molecular variance and discriminant analysis of principal components, but not by cultivar, aggressiveness, or field source. Of all the regions tested, only Mexico (n = 18) shared no MLHs with any other region. Using a bipartite network-based approach, we found no evidence that the MCGs accurately represent MLHs. Our study suggests that breeders should continue to test dry bean lines in several wmn across the United States to account for both the phenotypic and genotypic variation that exists across regions.

Monitoring Fungicide Sensitivity Levels and Mycelial Compatibility Groupings of Sclerotium rolfsii Isolates from Florida Peanut Fields

ABSTRACT Sclerotium rolfsii, the causal agent of peanut stem rot, is a diverse pathogen that has exhibited decreases in sensitivity to fungicides in areas where they are frequently applied. To better understand this pathogen's diversity and its response to various fungicides in Florida, a monitoring survey was done to examine isolates from several peanut producing areas using morphological characteristics, mycelial compatibility groupings and fungicide sensitivity profiles. A high level of morphological diversity was observed among a small number (N = 15) of isolates which was affirmed by both Shannon-Weiner (E = 0.812) and Simpson's (D = 0.280) indices. However, despite this high level of diversity, fungicide sensitivity of these isolates to flutolanil (EC50 = 0.031 ppm) and tebuconazole (EC50 = 0.008 ppm) appears to remain relatively unchanged when compared to a previous baseline study. Utilizing a small number of isolates, this monitoring survey indicated the EC50 values for the products azoxystrobin (EC50 = 0.050 ppm), prothioconazole (EC50 = 0.213 ppm), penthiopyrad (EC50 = 0.016 ppm) and solatenol (EC50 = 0.005 ppm). A trend for hormesis was also noted in this survey (e.g. flutolanil), but further research is necessary to better understand sub-lethal fungicide dose effects on increasing mycelial growth. It is apparent from these results that despite the high levels of phenotypic diversity in S. rolfsii populations, current fungicide management practices should remain effective for disease control.

Independently founded populations of Sclerotinia sclerotiorum from a tropical and a temperate region have similar genetic structure.

Sclerotinia sclerotiorum populations from tropical agricultural zones have been suggested to be more variable compared to those from temperate zones. However, no data were available comparing populations from both zones using the same set of markers. In this study, we compared S. sclerotiorum populations from the United States of America (USA, temperate) and southeast Brazil (tropical) using the frequency of mycelial compatibility groups (MCGs) and 13 microsatellite (SSR) markers. Populations were sourced from diseased plants within leguminous crops in New York, USA (NY; n = 78 isolates), and Minas Gerais State, Brazil (MG; n = 109). Twenty MCGs were identified in NY and 14 were previously reported in MG. The effective number of genotypes based on Hill’s number of order 0, which corresponded to the number of multilocus genotypes (MLGs) were 22 (95% CI = 15.6–28.4) and 24 (95% CI = 18.9–29.1) in NY and MG, respectively. Clonal fractions of MLGs were 71.8% (NY) and 78.0% (MG). The effective number of genotypes based on Hill’s number of orders 1 and 2 in NY were 8.9 (95% CI = 5.2–12.6) and 4.4 (95% CI = 2.6–6.1), respectively. For MG these indices were 11.4 (95% CI = 8.7–14.1) and 7.1 (95% CI = 5.1–9.0), respectively. There were no significant differences of allelic richness, private allelic richness, gene diversity, effective number of alleles and genotype evenness between the NY and MG populations. The populations were differentiated, with 29% of total variance attributed to differences between them and G''ST and Jost’s D indices higher than 0.50. Cluster analysis revealed dissimilarity higher than 80% among most MLGs from both populations. Different alleles segregated in the populations but both had similar levels of genotypic variability.

Mycelial compatibility in Valsa malicola, the causal agent of canker disease in Iran

Mycelial compatibility of 62 isolates of Valsa malicola from different hosts and areas of Iran were investigated on potato dextrose agar (PDA) and oat meal agar (OMA). Four mycelial compatibility groups (MCGs) on PDA, 1–4, including three single membered (1–3) and a 58 membered (4) were identified. However, 8 MCGs, 1–8, consisting of 6 single membered (1–3, 5, 6 and 8), a 6 membered (4) and a 50 membered (7) were identified on OMA. On PDA, the number of groups and the time to achieve results were less than on OMA as well as the barrage zones were clearer on PDA than OMA. There was no correlation between groups and host or geographical origins of the isolates. The low number of identified MCGs on both culture media revealed low genetic diversity of investigated isolates of V. malicola.

Are Sclerotinia sclerotiorum populations from the tropics more variable than those from subtropical and temperate zones?

The genetic variability of Sclerotinia sclerotiorum populations has been investigated in many countries and, consequently, under different ecological conditions. The first studies were conducted to gather information about the genetic structure of populations sampled in temperate climate areas. Based on DNA fingerprinting analysis of restriction fragment length polymorphism (RFLP) data and mycelial compatibility groups, most studies revealed a clonal population structure. Later, using DNA sequences, populations from subtropical regions of North America were reported to be more variable than those from temperate regions. In the past few years, new analyses in temperate, sub-tropical and tropical areas were conducted using microsatellite (SSR) markers. Most studies using SSR reported both high variability and evidence of outcrossing in S. sclerotiorum populations, but evidence of clonality has also been found. Some authors argue that populations from subtropical and tropical areas are more diverse. We argue that the reports of high variability of S. sclerotiorum in tropical or subtropical regions may be due to an increase in the number of studies performed with SSR markers in these regions and in some cases due to inappropriate interpretations of the results.

Characterization of the Mycelial Compatibility Groups and Mating Type Alleles in Populations of Sclerotinia minor in Central China.

Ninety-five single-sclerotium isolates were obtained from lettuce and weeds in three counties in central China. They were identified belonging to Sclerotinia minor based on colony morphology and the S. minor-specific DNA marker. Mycelial compatibility groups (MCGs) and the mating type (MAT) alleles in these isolates were determined using the methods of paired cultures and specific PCR, respectively, and the MCG data were used to calculate Shannon's H index (H) and Simpson index (S), thereby evaluating diversity of S. minor. Eight MCGs (MCG1 to MCG8) and two MAT alleles (Inv+, Inv-) were identified in these isolates. Low diversity was detected for the total 95 isolates (H = 1.748, S = 0.786). Isolates of different MCGs or with different MAT alleles did not significantly differ (P > 0.05) in mycelial growth rate on potato dextrose agar (PDA, 20°C) or lesion diameter on lettuce leaves (20°C), but slightly differed in the number of sclerotia produced on PDA (20°C). Furthermore, this study reported five new host plants of S. minor in China, including Capsella bursa-pastoris, Oenanthe javanica, Fragaria gracilis, Ranunculus ternatus, and Salvia plebeia, and identified three hypovirulent isolates. These results broaden our understanding about the population biology of S. minor.

Characterization of Alternaria isolates and reaction of potato genotypes to early blight

ABSTRACT: Early blight is one of the most important fungal diseases of potato. The objective of this study was to evaluate the in vitro reaction of potato genotypes to the severity of early blight and compare the species Alternaria solani and Alternaria grandis , etiologic agents of disease, through the evaluation of physiological characteristics. Twenty-two genotypes of the Potato Breeding Program at UFLA, two cultivars, Aracy and Bintje, patterns of resistance and susceptibility, respectively were evaluated. For inoculation, three isolates of A. grandis and two isolates of A. solani were used. Plantlets obtained in vitro were inoculated with a 5mm diameter mycelial disk of isolates Alternaria spp. of. These were incubated in severity and classified according to the rating scale. Isolates of Alternaria spp. were evaluated for mycelial growth index (MGI) and for formation of mycelial compatibility groups (MCG). The methodology for evaluating the in vitro reaction of genotypes to severity of early blight was efficient for both isolates. The isolates of A. solani and A. grandis were similar in their aggressiveness. The isolates of A. grandis MGI's had higher, and therefore mycelium grew faster when compared to those isolated from A. solani . The occurrence of mycelial compatibility among isolates of A. solani and A. grandis indicated the possible occurrence of parasexual cycle.

Analysis of genetic diversity of Sclerotinia sclerotiorum from eggplant by mycelial compatibility, random amplification of polymorphic DNA (RAPD) and simple sequence repeat (SSR) analyses

ABSTRACTThe genetic diversity and pathogenicity/virulence among 60 eggplant Sclerotinia sclerotiorum isolates collected from six different geographic regions of Turkey were analysed using mycelial compatibility groupings (MCGs), random amplified polymorphic DNA (RAPD) and simple sequence repeat (SSR) polymorphism. By MCG tests, the isolates were classified into 22 groups. Out of 22 MCGs, 36% were represented each by a single isolate. The isolates showed great variability for virulence regardless of MCG and geographic origin. Based on the results of RAPD and SSR analyses, 60 S. sclerotiorum isolates representing 22 MCGs were grouped in 2 and 3 distinct clusters, respectively. Analyses using RAPD and SSR markers illustrated that cluster groupings or genetic distance of S. sclerotiorum populations from eggplant were not distinctly relative to the MCG, geographical origin and virulence diversity. The patterns obtained revealed a high heterogeneity of genetic composition and suggested the occurrence of clonal and sexual reproduction of S. sclerotiorum on eggplant in the areas surveyed.

GENETIC DIVERSITY OF SCLEROTINIA SCLEROTIORUM WITHIN A SINGLE SUNFLOWER FIELD IN WENQUAN, XINJIANG PROVINCE, CHINA

To unravel the genetic diversity of Sclerotinia sclerotiorum, 90 isolates collected from a single sunflower field in Wenquan of Xinjiang were studied using the method of mycelial compatibility grouping (MCG). Meanwhile, the oxalic acid (OA) secretion ability, polygalacturonases (PG) enzymatic activity and pathogenicity of the isolates within the same and between different MCGs were studied. The distribution of inversion minus (Inv-) and inversion plus (Inv+) isolates of S. sclerotiorum at MAT locus within the same MCGs and also in the whole population were identified using specific PCR primers. The sensitivity of S. sclerotiorum isolates to both carbendazim and dimethachlon fungicides were also tested in this study. The results suggested that the 90 isolates from a single sunflower field in Wenquan, Xinjiang region, can be grouped into 15 MCGs. MCG1, the biggest group, contained 34 isolates, representing 37.8% of all the tested isolates; 6 MCGs contained only a single isolate; 8 MCGs include 2 to 13 isolates each. The dramatically variation on OA level, PG enzyme activities and pathogenicity was observed among isolates from the same and between different MCGs, and no obvious positive correlation was detected between OA, PG and pathogenicity. For mating type distribution ratio, 17:17 (1:1) ratio of Inv+ and Inv- isolates at mating type locus (MAT) was observed only in MCG1, however, 12:1, 7:2 and 9:1 of Inv+ to Inv- ratio at MAT locus was detected in MCG2, MCG4 and MCG6, respectively. The distribution ratio of Inv+ and Inv- in the whole population is 56:34, which is deviated from the 1:1 steady state. The results of fungicide sensitivity test within MCG1 and MCG2 suggested that 84% of isolates is more sensitive to dimethachlon than to carbendazim. Seven isolates, three from MCG1 and four from MCG2, showed the opposite tendency of sensitivity to both fungicides. Three isolates, one from MCG1 and two from MCG2, showed the same sensitivity to both fungicides. Based on above results, we concluded that dramatic genetic diversity do exist within S. sclerotiorum population collected from a single sunflower field in Wenquan of Xinjiang.

Similar Aggressiveness of Phenotypically and Genotypically Distinct Isolates of Sclerotinia sclerotiorum.

Understanding how Sclerotinia sclerotiorum aggressiveness varies among isolates may be useful for breeding programs aimed at developing common bean cultivars resistant to white mold. The aggressiveness of 20 S. sclerotiorum isolates collected in common bean fields from four Brazilian states was tested against two common bean genotypes (Pérola and A195) using two inoculation methods. The isolates were characterized using 10 microsatellite (SSR) loci, mycelial compatibility groups (MCGs), partial sequences of the oxaloacetate acetylhydrolase (OAH) gene, and morphological traits. Twenty SSR and seven OAH haplotypes, 10 MCGs, and high variability in colony morphology were found. One isolate was more aggressive when inoculated on plants of the genotype A195, but all other isolates had similar aggressiveness. Aggressiveness was not related with MCGs, SSR, OAH haplotypes, mycelial pigmentation, growth rate, or sclerotia production.

Effect of some fungicides against the growth inhibition of Sclerotinia sclerotiorum mycelial compatibility groups

Abstract Sclerotinia sclerotiorum (Lib.) de Bary, the causal agent of Sclerotinia stem rot, is one of the most important pathogens of Brassica napus L. in northern Iran. In this study, 13 mycelial compatibility groups (MCGs) of the fungus were identified among 31 isolates sampled from four regions of Mazandaran province, Iran. Effective fungicides are useful in the integrated management of the disease. So, the effect of tebuconazole, propiconazole, cyproconazole, and Rovral-TS at five doses (0.0001, 0.001, 0.01, 0.1, and 1 ppm) was studied on the growth inhibition of S. sclerotiorum as in vitro tests. Maximum inhibition (100%) of S. sclerotiorum mycelial growth was obtained by the highest dose (1 ppm) of all tested fungicides, as well as by the doses of 0.1 and 0.01 ppm of propiconazole, cyproconazole, and tebuconazole. In this investigation, the reaction of S. sclerotiorum isolates belonging to different MCGs was evaluated against tebuconazole, propiconazole, cyproconazole, and Rovral-TS at their EC50 ranges. The results revealed that there was high variation of S. sclerotiorum MCGs against different fungicides. The inhibition percentage varied between 4.29% and 71.72%.

Genetic Variation of Sclerotinia sclerotiorum from Multiple Crops in the North Central United States.

Sclerotinia sclerotiorum is an important pathogen of numerous crops in the North Central region of the United States. The objective of this study was to examine the genetic diversity of 145 isolates of the pathogen from multiple hosts in the region. Mycelial compatibility groups (MCG) and microsatellite haplotypes were determined and analyzed for standard estimates of population genetic diversity and the importance of host and distance for genetic variation was examined. MCG tests indicated there were 49 different MCGs in the population and 52 unique microsatellite haplotypes were identified. There was an association between MCG and haplotype such that isolates belonging to the same MCG either shared identical haplotypes or differed at no more than 2 of the 12 polymorphic loci. For the majority of isolates, there was a one-to-one correspondence between MCG and haplotype. Eleven MCGs shared haplotypes. A single haplotype was found to be prevalent throughout the region. The majority of genetic variation in the isolate collection was found within rather than among host crops, suggesting little genetic divergence of S. sclerotiorum among hosts. There was only weak evidence of isolation by distance. Pairwise population comparisons among isolates from canola, dry bean, soybean and sunflower suggested that gene flow between host-populations is more common for some crops than others. Analysis of linkage disequilibrium in the isolates from the four major crops indicated primarily clonal reproduction, but also evidence of genetic recombination for isolates from canola and sunflower. Accordingly, genetic diversity was highest for populations from canola and sunflower. Distribution of microsatellite haplotypes across the study region strongly suggest that specific haplotypes of S. sclerotiorum are often found on multiple crops, movement of individual haplotypes among crops is common and host identity is not a barrier to gene flow for S. sclerotiorum in the north central United States.

Low genetic variability in Sclerotinia sclerotiorum populations from common bean fields in Minas Gerais State, Brazil, at regional, local and micro‐scales

Sclerotinia sclerotiorum, causal agent of white mould, is the most destructive and widely distributed soilborne pathogen of common bean during the autumn–winter season in Brazil. Nevertheless, little is known about the genetic structure of the pathogen population. Microsatellite (SSR) markers and mycelial compatibility groups (MCGs) were used to characterize 118 isolates collected from 20 bean fields located in the most important growing regions of Minas Gerais State (MG). Additionally, the genetic variability among 10 isolates obtained from a single sclerotium was investigated in 10 different sclerotia. Seventy SSR haplotypes and 14 MCGs were identified among the 118 isolates. The genetic differences within bean growing areas accounted for most of the genetic variation (72%). Despite the relatively high genotypic diversity, the SSR loci were at linkage disequilibrium. Moreover, 70% of the isolates were assigned to only two MCGs, and haplotypes of a given MCG were closely related. The discriminant analysis of principal components revealed five groups. There was strong genetic differentiation between isolates collected in one municipality in southern MG when compared to other regions. Common bean resistance to white mould should be assessed with representative isolates of the five genetic groups and, if possible, of the different MCGs detected in the present study. One to five haplotypes were detected among the 10 isolates obtained from a single sclerotium. Therefore, in order to ensure genetic identity of an isolate, hyphal tip or monoascosporic isolates should be used.

English

Sclerotinia sclerotiorum , infection of bean fields, has increased in Brazil. Fungicides application is the control strategy used due to lack of cultivars with complete disease resistance. To guide the use of isolates in resistance screening 25 S. sclerotiorum isolates from Brazilian dry bean fields were characterized using microsatellite markers, mycelial compatibility groups (MCGs) and aggressiveness. Microsatellite primer pairs were used to identify polymorphisms among the S. sclerotiorum isolates and MCGs were determined from interaction of all isolates grown side-by-side. Aggressiveness was derived from a straw test where fungal mycelium was placed over a cut bean stem and rated for disease progress. Data from microsatellite profiles grouped the 25 isolates into four clusters and seven MCGs were identified. No association among host cultivar and cluster or MCG of isolates was observed. For MCGs, 57% contained isolates sampled frequently over multiple locations and 43% contained isolates unique to locations. There were significant differences among isolates in aggressiveness within and between MCGs. The most aggressive isolates in resistance screening will be helpful in the identification of higher levels of resistance in bean germplasm/lines.

Evaluation of the virulence of Sclerotium rolfsii isolates on Arachis hypogaea and screening for resistant genotypes in greenhouse conditions

Summary Sclerotium rolfsii is a soil borne pathogen responsible for root and stem rot on a wide range of crops. This study was conducted to identify the virulence of different S. rolfsii isolates on a susceptible local peanut germplasm and determine the resistance of 20 peanut genotypes to the most virulent isolate and also the relationship between virulence and mycelial compatibility groups (MCGs). Seventy eight isolates of this fungus from 10 host plants and six known MCGs were used in the experiment. The experiment was done in greenhouse conditions (25±5°C) using a complete randomized block design with three replications. Pots containing sterile soil (pH=6.7) were inoculated with barley seeds colonized by each isolate separately before being seeded with the peanut germplasm. Disease severity was assessed by scoring the wilting, yellowing or death of plants, mycelia or sclerotia production on the soil surface or on plant stem, stem area affected (%) and stem lesion length, at the stage of plant maturity. Also, shoot wet weight and plant height were recorded at this stage. According to the results of the pathogenicity tests, all of the isolates were virulent on the susceptible peanut germplasm and the virulence diff ered signifi cantly between the isolates (P≤0.01). There was no relationship between the virulence of the five groups of isolates identified in the present study and the MCGs. The peanut genotype 140, which was better than the others based on seed size, plant height and the canopy size, was also the most resistant one

Mycelial Compatibility and Pathogenic Diversity Among Sclerotium rolfsii Isolates in the Southern United States.

Sclerotium rolfsii is a soilborne fungus that causes southern blight on a wide range of plants in tropical and subtropical regions of the world. Eighty-four isolates collected from Florida, Georgia, Louisiana, South Carolina, Texas, and Virginia were paired and assigned to 23 mycelial compatibility groups (MCGs), of which 11 MCGs consisted of a single isolate. Isolates within an MCG typically originated from different hosts and different geographical areas, with the exception of MCG 11. In all, 13 of the 15 isolates in MCG 11 originated from peanut in Georgia and Florida, while the other 2 isolates originated from potato in Virginia and from the ornamental Barlaeria cristata in Florida. Significant differences in the size and number of sclerotia produced in vitro existed between isolates from peanut and other hosts. Nineteen isolates representative of the most common MCGs (1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 13, 14, 15, 16, 17, and 18) were tested for pathogenicity on tomato, pepper, and peanut. All isolates were pathogenic on all hosts but virulence differed significantly among isolates. Isolates collected from peanut were the most virulent on all three hosts compared with isolates collected from tomato and pepper. 'Georgia Green' peanut was more susceptible to peanut isolates from Georgia than to the other tested isolates. Of the two tomato entries, the commercial tomato 'Tygress' was less susceptible than the previously reported resistant breeding line 5635M to many of the S. rolfsii isolates tested, with the exception of the peanut isolates collected from Georgia. These initial findings suggest that considerable variation exists among S. rolfsii isolates throughout the southern United States, with some indications of specialization for the isolates collected from peanut.

Mycelial Compatibility Groups and Microsatellite Markers Reveal Genetic Diversity Within and Among Populations of Sunflower Sclerotinia Sclerotiorum in China

The genetic variability and differentiation among 101 sunflower Sclerotinia sclerotiorum isolates collected from four different geographic regions of China were analyzed using mycelial compatibility groupings (MCGs) and microsatellite markers. Twenty three MCGs were identified among all tested isolates. The majority of isolates collected from the same region were grouped in to the same MCGs, indicating less genetic variation of S. sclerotiorum within the same region. But there still have exceptions for some isolates. Also microsatellite marker data revealed that all tested isolates from four geographic populations could be divided into three distinct clusters, isolates from Inner Mongolia and Ninxia regions formed cluster I, isolates from Heilongjiang and Xinjiang formed separate clusters II and III . The percentage of variance within and among different geographic populations was 84.54% and 15.46% respectively and both variances were significantly different from each other (p0.01). Meanwhile, association between the microsatellite haplotype and MCGs was observed but not so significant; majority isolates from the same MCG showed the same haplotype, but certain samples showed different haplotypes, although they belonged to the same MCG. Based on the virulence test results, we also found that MCGs not only represent the genetic variation of tested isolates, but also reflect their pathogenic ability to a certain extent.

Mycelial compatibility and aggressiveness of Sclerotinia sclerotiorum isolates from Brazil and the United States

The objective of this work was to evaluate the genetic diversity among Sclerotinia sclerotiorum isolates from Brazil and the USA, assess their aggressiveness variability, and verify the existence of an isolate-cultivar interaction. Isolate variability was determined by mycelial compatibility grouping (MCG), and isolate aggressiveness by cut-stem inoculations of soybean cultivars. Two experiments for MCGs and two for aggressiveness were conducted with two sets of isolates. The first set included nine isolates from the same soybean field in Brazil and nine from the Midwest region of the USA. The second set included 16 isolates from several regions of Brazil and one from the USA. In the first set, 18 isolates formed 12 different MCGs. In the second set, 81% of the isolates from Brazil grouped into a single MCG. No common MCGs were observed among isolates from Brazil and the USA. The isolates showed aggressiveness differences in the first set, but not in the second. Although aggressiveness differed in the first set, soybean cultivars and isolates did not interact significantly. Cultivar rank remained the same, regardless of the genetic diversity, aggressiveness difference, and region or country of origin of the isolate. Results from screening of soybean cultivars, performed by the cut-stem method in the USA, can be used as reference for researchers in Brazil.