scholarly journals Genetic Analysis of Fungicide-Resistant Sclerotinia homoeocarpa Isolates from Tennessee and Northern Mississippi

Plant Disease ◽  
2008 ◽  
Vol 92 (1) ◽  
pp. 83-90 ◽  
Author(s):  
R. E. DeVries ◽  
R. N. Trigiano ◽  
M. T. Windham ◽  
A. S. Windham ◽  
J. C. Sorochan ◽  
...  

Sclerotinia homoeocarpa is the causal agent of dollar spot disease that reduces the uniformity and aesthetic value of golf putting greens. Fungicide-resistant isolates of S. homoeocarpa were collected from putting greens at 10 locations across Tennessee and northern Mississippi. Genetic diversity among the 60 isolates was investigated using vegetative compatibility, conserved gene sequences, and amplified fragment length polymorphism (AFLP). Six tester strains were paired with Tennessee and northern Mississippi isolates on potato dextrose agar. Some of the 60 isolates were delineated into vegetative compatibility groups, but fungicide resistance could not be associated with a particular vegetative compatibility group. Genetic similarities of isolates at the vegetative compatibility level could be attributed to founder effects. Sequencing the regions of CAD, EF1-α, β-tubulin, and internal transcribed spacers revealed 100% homology among isolates. Capillary gel electrophoresis and analysis of AFLP fragments indicated 86 to 100% similarity between the isolates. Vegetative compatibility and molecular data indicate that the populations of the pathogen are clonal. Isolates did not cluster according to fungicide resistance during unweighted pair group with arithmetic means analysis, but did appear to cluster according to vegetative compatibility group and location. Although associations could not be made between molecular markers and fungicide resistance, links between vegetative compatibility and AFLP markers may provide a foundation from which other studies could be performed.

Plant Disease ◽  
2005 ◽  
Vol 89 (3) ◽  
pp. 237-240 ◽  
Author(s):  
Matias Pasquali ◽  
Flavia Dematheis ◽  
Giovanna Gilardi ◽  
Maria Lodovica Gullino ◽  
Angelo Garibaldi

Fusarium oxysporum f. sp. lactucae, the causal agent of Fusarium wilt of lettuce, has been reported in three continents in the last 10 years. Forty-seven isolates obtained from infected plants and seed in Italy, the United States, Japan, and Taiwan were evaluated for pathogenicity and vegetative compatibility. Chlorate-resistant, nitrate-nonutilizing mutants were used to determine genetic relatedness among isolates from different locations. Using the vegetative compatibility group (VCG) approach, all Italian and American isolates, type 2 Taiwanese isolates, and a Japanese race 1 were assigned to the major VCG 0300. Taiwanese isolates type 1 were assigned to VCG 0301. The hypothesis that propagules of Fusarium oxysporum f. sp. lactucae that caused epidemics on lettuce in 2001-02 in Italian fields might have spread via import and use of contaminated seeds is discussed.


1995 ◽  
Vol 73 (4) ◽  
pp. 680-682 ◽  
Author(s):  
Karol S. Elias ◽  
Peter J. Cotty

A rose bengal amended medium for selecting nitrate-metabolism mutants from fungi with reduced sensitivity to chlorate is described. Isolates of several species known to resist development of nitrate-metabolism mutants on chlorate medium formed such mutants when grown on the rose bengal – chlorate medium. These species include Aspergillus flavus (Link.), Fusarium lateritium (Nees ex Link.), Fusarium oxysporum (Schlecht.), Fusarium solani (Mart.) Sacc., Alternaria cassiae (Jurair and Khan), Alternaria macrospora (Zimmerman), and Alternaria tagetica (Shome and Mustafee). The medium allows selection of nitrate-metabolism mutants of certain fungal strains for which chlorate-based techniques have not been satisfactory. Resulting mutants, following phenotype determination and identification of complementary testers, can be paired to enable macroscopic observation of heterokaryon formation during vegetative compatibility analyses. Thus, this medium may facilitate development of information on delimitation of vegetative compatibility groups among strains within these taxa. Key words: chlorate resistance, population structure, vegetative compatibility group, VCG.


1990 ◽  
Vol 68 (6) ◽  
pp. 1245-1248 ◽  
Author(s):  
D. J. Jacobson ◽  
T. R. Gordon

One hundred and nineteen strains of Fusarium oxysporum f.sp. melonis were characterized by virulence and vegetative compatibility. One hundred and seven strains were placed in four previously reported vegetative compatibility groups: 0130, 0131, 0133, and 0134. Four strains were placed in three new vegetative compatibility groups, and the remaining eight strains were vegetatively self-incompatible. Two of the three new vegetative compatibility groups shared similar geographic origins and distribution with two previously reported vegetative compatibility groups; the third represented a more isolated infestation. All vegetatively self-incompatible isolates originated from culture collections; none have been recently isolated from nature. These newly characterized strains extend our knowledge of genetic diversity in F. oxysporum f.sp. melonis. All four F. oxysporum f.sp. melonis races exist in more than one vegetative compatibility group. European strains represent four vegetative compatibility groups, one of which is present in North America and another in the Middle East. The significance of this diversity is unknown, as are the phylogenetic relationships among strains in this forma specialis.


1991 ◽  
Vol 69 (8) ◽  
pp. 1756-1763 ◽  
Author(s):  
Katherine J. Lewis ◽  
Everett M. Hansen

The importance of spore infection in the spread of Inonotus tomentosus was assessed using vegetative compatibility and protein electrophoresis. Isolates were collected from diseased spruce (Picea glauca × engelmannii) trees from five sites. Each site had several small (two or three trees) discrete disease centres, or larger patchy centres, or both. Within each site, the vegetative compatibility group and protein profiles of isolates were examined in all combinations of paired isolates. Vegetatively compatible isolates had identical protein profiles in 74% of the comparisons. Vegetatively incompatible isolates had different protein profiles 97% of the time. Usually isolates differed by only one or two protein bands. Isolates from a discrete centre were usually vegetatively compatible with identical protein patterns. Larger patchy centres consisted of multiple vegetatively compatible groups. The number of unique vegetatively compatible groups found suggests that spores are an important course of infection. Key words: vegetative compatibility, disease centre, protein electrophoresis.


1990 ◽  
Vol 68 (6) ◽  
pp. 1357-1363 ◽  
Author(s):  
R. C. Ploetz

A worldwide collection of 96 isolates of Fusarium oxysporum f.sp. cubense (incitant of fusarial wilt of banana or Panama disease) from 12 countries was used to assess population structure in the pathogen; isolates were diverse for vegetative compatibility (11 vegetative compatibility groups) and race-specific virulence (races 1, 2, and 4). Rates of radial growth on potato dextrose agar differed at temperatures ranging from 8–36 °C for isolates in different VCGs and races (P < 0.05). On a KClO3-amended medium used to generate nitrate-nonutilizing (nit) mutants, variability in chlorate (a toxic analog of nitrate) sensitivity and the time required before nit mutants arose on the medium (mutability) was related primarily to vegetative compatibility group. In addition, cultural morphology on modified Komada's medium and potato dextrose agar was related primarily to vegetative compatibility group, whereas race was not as consistently related to these traits. In studies on the population biology and diversity in F. oxysporum f.sp. cubense, vegetative compatibility was a more useful character than race. On the basis of these results, it is suggested that F. oxysporum f.sp. cubense has had diverse origins.


1996 ◽  
Vol 74 (11) ◽  
pp. 1695-1700 ◽  
Author(s):  
Naoyuki Matsumoto ◽  
Selya Tsushima ◽  
Kazuko Uchiyama

Vegetative compatibility groups of Typhula ishikariensis biotype A include different isolates from various localities, and the most prevalent one (super vegetative compatibility group) was studied to reveal that this super group consisted of several genets existing throughout the habitat of T. ishikariensis biotype A in Hokkaido, Japan. Random amplified polymorphic DNA and mating incompatibility alleles were studied for 10 isolates belonging to the super vegetative compatibility group from two localities 250 km distant from each other and for five isolates belonging to different groups. Seven primers, which distinguished vegetative compatibility groups, were screened out of 60 and produced a total of 55 bands. The 10 super group isolates were divided into 5 subgroups, and the five unique isolates did not cluster with each other. Protoplasts were produced from each isolate to obtain monokaryons. They were then mated with tester monokaryons derived from basidiospores of two parental isolates, one of which belonged to the super vegetative compatibility group. Mating patterns suggested that the 10 super group isolates shared common mating incompatibility alleles but this was not the case with those belonging to unique groups. The super vegetative compatibility group was found to consist of several genets with many ramets distributed throughout the habitat of T. ishikariensis biotype A in Hokkaido. These genets were regarded as sib-related dikaryons derived from basidiospores. Keywords: Typhula ishikariensis, snow mold, genet, RAPD, mating incompatibility.


1992 ◽  
Vol 70 (6) ◽  
pp. 1211-1217 ◽  
Author(s):  
T. R. Gordon ◽  
D. Okamoto

Two hundred isolates of Fusarium oxysporum, 100 from each of two different locations, were collected from agricultural field soils in the San Joaquin Valley of California. These isolates comprised 39 different vegetative compatibility groups. Based on the frequency distribution of vegetative compatibility groups, populations of F. oxysporum at the two collection sites were different. At least one isolate from each vegetative compatibility group was examined for polymorphisms in mitochondrial DNA. A total of 41 differences in mitochondrial DNA were identified, each of which was treated as a character and scored as present or absent in each strain. There were 11 unique combinations (haplotypes) of the 41 characters. Three mitochondrial DNA haplotypes were common to both sites and the remaining eight occurred at only one of the two sites. Isolates in the same vegetative compatibility group were always associated with the same mitochondrial DNA haplotype. Many isolates in different vegetative compatibility groups also shared a common mitochondrial DNA haplotype. Fusarium oxysporum f.sp. melonis, cause of Fusarium wilt of muskmelon, was associated with the same mitochondrial DNA haplotype as eight vegetative compatibility groups of F. oxysporum that were not pathogenic to muskmelon. This result may indicate that either the pathogen was a recent derivative of nonpathogenic strains at the same location or avirulent strains have been derived from the pathogen. Key words: anastomosis, fungi, heterokaryon, Fusarium wilt.


1992 ◽  
Vol 32 (5) ◽  
pp. 651 ◽  
Author(s):  
MD Ramsey ◽  
RG O'Brien ◽  
KG Pegg

Twenty-two isolates of Fusarium oxysporum, from Queensland's major tomato growing areas, were studied in glasshouse pathogenicity tests and assessed for vegetative compatibility. Isolates of Fusarium oxysporum f. sp. lycopersici were identified to race using pathogenicity tests with 4 differential tomato cultivars: Grosse Lisse, Scorpio, moradade and Delta Tristar. The occurrence of race 3 in the Bundaberg district in 1988 was established. In glasshouse experiments, Fusarium wilt severity was influenced by inoculum concentration (1 x 106 v. 5 x 106 conidia/ml). Pathogenic and non-pathogenic isolates were distinguished by vegetative compatibility group analysis. However, all races were in a single vegetative compatibility group and could not be differentiated using this technique. Isolates collected from discoloured vascular tissue in the lower stems of plants with severe root rot (Pythium spp. associated), were non-pathogenic to tomato, bean and pea, although some isolates caused slight damage to cucumber. These isolates were distinctly different from Fusarium oxysporum f. sp. radicis-lycopersici, the cause of root and crown rot.


Author(s):  
Pearl Dadd Daigle ◽  
Karen Kirkby ◽  
Damian Collins ◽  
Will Cuddy ◽  
Peter Lonergan ◽  
...  

Verticillium dahliae, the causal agent of Verticillium wilt, is a soil-borne ascomycete that infects numerous agriculturally important crops globally, including cotton. As a billion-dollar industry, cotton is economically important to Australia and the management of disease such as Verticillium wilt is key for the success of the industry. Internationally, defoliating V. dahliae isolates belonging to Vegetative Compatibility Group (VCG) 1A cause severe damage to cotton, while non-defoliating VCG2A isolates result in significantly less disease. However, in Australia, VCG2A is causing more severe damage to crops in the field than the defoliating VCG1A. This study aimed to replicate field observations in controlled greenhouse conditions. We examined and compared disease symptoms on a range of Australian commercial cotton varieties when inoculated with different V. dahliae VCGs. Seedlings were root dipped in conidial suspensions and assessed over seven weeks. The final disease score, disease over time and root length were analysed. Plant mortality resulted from both V. dahliae VCG1A and VCG2A isolates across all cotton varieties used, confirming that there are virulent VCG2A isolates present in Australia. To our knowledge, although virulent on other plant hosts, V. dahliae VCG2A has not previously been reported to be highly virulent in cotton. We infer that virulence cannot be defined solely by VCG in Australian V. dahliae isolates causing disease in cotton.


1991 ◽  
Vol 69 (8) ◽  
pp. 1707-1711 ◽  
Author(s):  
Paul Bayman ◽  
Peter J. Cotty

Aspergillus flavus was isolated from soil from a single Arizona cotton field in 1987, 1988, and 1989. Isolates from infected cotton bolls were collected from the same field in 1988. Isolates were assigned to vegetative compatibility groups via complementation tests between nitrate-nonutilizing mutants. Sixty-one of 105 isolates composed 13 vegetative compatibility groups; the remaining 44 isolates could not be assigned to groups. Forty-three isolates from other fields in Arizona composed 21 groups, 6 of which were also found in the test field. Distribution of vegetative compatibility groups in and outside the field was significantly different, based on a G-test. One vegetative compatibility group included 20% of all isolates from the test field, but was not found elsewhere. It was common in the test field in 1987 and 1988, but was not found in 1989. Boll and soil populations from 1988 were not significantly different. Single infected boll locules and 25-g soil samples often contained A. flavus individuals from more than one group. These results suggest that although many vegetative compatibility groups are widely distributed, a single field may have a unique population profile that changes significantly from year to year. Key words: Aspergillus flavus, vegetative compatibility, Nit−, imperfect fungi.


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