PENICILLIUM CLAVIFORME: SUGAR BEET PATHOGEN AND ANTAGONIST OF BOTRYTIS CINEREA

1976 ◽  
Vol 56 (3) ◽  
pp. 647-649 ◽  
Author(s):  
W. M. BUGBEE

Sugar beet storage rot caused by Botrytis cinerea was completely inhibited by a storage rot isolate of Penicillium claviforme in sugar beet tissue. Storage rot caused by Phoma betae was not inhibited. Growth of B. cinerea was inhibited 50–100% in liquid cultures containing diluted filtrates of P. claviforme. Differing reports as to the prevalence of B. cinerea as a storage rot pathogen may be due to this antagonism.

2012 ◽  
Vol 65 ◽  
pp. 1-4 ◽  
Author(s):  
Karen Klotz Fugate ◽  
Jocleita Peruzzo Ferrareze ◽  
Melvin D. Bolton ◽  
Edward L. Deckard ◽  
Larry G. Campbell

1972 ◽  
Vol 50 (8) ◽  
pp. 1705-1709 ◽  
Author(s):  
William M. Bugbee

Phoma betae from decayed sugar beet storage root tissue grew most rapidly in culture at 15C but produced more polygalacturonase (PG) at 20C. When the fungus was supplied with six different nitrogen sources, it produced the most PG on (NH4)2SO4.Assays of dialyzed culture filtrates using sodium polypectate and pectin or cell wall material from storage roots as the carbon sources showed the production of exopolygalacturonase (exo-PG) and endopolygalacturonate trans-eliminase (endo-PGTE). No pectin methyl esterase was detected. Exo-PG and endo-PGTE also were present in decayed sugar beet tissue. Only endo-PGTE was detected within 3 mm of tissue surrounding the rotted area.In culture, cell wall material from the susceptible variety A58 induced more endo-PGTE formation than the resistant 2B. But 2B induced more exo-PG formation than A58. It is suggested that endo-PGTE plays a major role in cell wall degradation because pH 7.5 was optimum for tissue maceration and pH 8.5 for enzyme activity and the advancing margins of rotted tissue contained only endo-PGTE.


2010 ◽  
Vol 40 (No. 4) ◽  
pp. 128-134 ◽  
Author(s):  
H. Bryk ◽  
B. Dyki ◽  
P. Sobiczewski

The influence of antagonistic Pseudomonas spp. on the development of Botrytis cinerea and Penicillium expansum was studied in liquid cultures. Two strains of Pseudomonas spp. (B194 and B224), originally isolated from apple leaves and fruits, respectively, inhibited spore germination and germ tube elongation of B. cinerea or P. expansum. The inhibitory effect depended on the concentration of bacteria in the cultures. After a prolonged time of incubation (48–76 h) lysis and fragmentation of hyphae of both fungi was observed. In some cases the hyphae of B. cinerea developed abnormally if the bacterial strains were present – the hyphal tips were swollen and ball-shaped spore-like structures aggregated in chains were formed.


1982 ◽  
Vol 54 (4) ◽  
pp. 225-244
Author(s):  
Mauritz Vestberg ◽  
Risto Tahvonen ◽  
Kyösti Raininko

The fungus Pythium debaryanum auct. non Hesse is the main cause of damping-off on sugar beet in Finland. The fungus is found especially in diseased seedlings during the first two weeks after emergence. Later on, when the plants have one or two pairs of true leaves, Fusarium spp. can be isolated to a rather great extent. However, pathogenicity tests with three different Fusarium species have shown that this fungus is unble cause damping-off on sugar beet when inoculated into peat substrate. Among the fungi tried in this respect, only Pythium debaryanum and Phoma betae Frank showed clear pathogenicity. Sugar beet seedlings that outlive the disease grow slower, and their quality at harvest in the autumn is poorer than that of healthy beets.


1998 ◽  
Vol 11 (10) ◽  
pp. 1009-1016 ◽  
Author(s):  
Arjen ten Have ◽  
Wietse Mulder ◽  
Jaap Visser ◽  
Jan A. L. van Kan

Botrytis cinerea, a fungus that causes diseases in over 200 plant species, secretes a number of endopolygalacturonases that have been suggested to be involved in pathogenesis. However, so far the corresponding genes have not been isolated from this fungus. We cloned Bcpg1, encoding endopolygalacturonase, with the pgaII gene from Aspergillus niger as a heterologous probe. The Bcpg1gene is expressed to similar levels in liquid cultures of B. cinerea containing either 1% polygalacturonic acid or 1% sucrose, and is expressed during infection of tomato leaves. The Bcpg1 gene was eliminated by partial gene replacement, and the resulting mutants were tested for virulence on tomato leaves and fruits, as well as on apple fruits. Although the mutants were still pathogenic and displayed similar primary infections when compared with control strains, a significant decrease in secondary infection, i.e., growth of the lesion beyond the inoculation spot, was observed on all three host tissues. These results indicate that the Bcpg1 gene is required for full virulence.


Plant Disease ◽  
2015 ◽  
Vol 99 (10) ◽  
pp. 1296-1309 ◽  
Author(s):  
Carl A. Strausbaugh ◽  
Oliver Neher ◽  
Eugene Rearick ◽  
Imad A. Eujayl

Root rots in sugar beet storage can lead to multimillion dollar losses because of reduced sucrose recovery. Thus, studies were conducted to establish additional fungicide treatments for sugar beet storage and a greater understanding of the fungi involved in the sugar beet storage rot complex in Idaho. A water control treatment and three fungicides (Mertect [product at 0.065 ml/kg of roots; 42.3% thiabendazole {vol/vol}], Propulse [product at 0.049 ml/kg of roots; 17.4% fluopyram and 17.4% prothioconazole {vol/vol}], and Stadium [product at 0.13 ml/kg of roots; 12.51% azoxystrobin, 12.51% fludioxonil, and 9.76% difenoconozole {vol/vol}]) were investigated for the ability to control fungal rots of sugar beet roots held up to 148 days in storage during the 2012 and 2013 storage seasons. At the end of September into October, roots were harvested weekly for 5 weeks from each of two sugar beet fields in Idaho, treated with the appropriate fungicide, and placed on top of a commercial indoor sugar beet storage pile until early February. Differences (P < 0.0001 to 0.0150) among fungicide treatments were evident. Propulse- and Stadium-treated roots had 84 to 100% less fungal growth versus the control roots, whereas fungal growth on Mertect-treated roots was not different from the control roots in 7 of 12 comparisons for roots harvested each of the first 3 weeks in both years of this study. The Propulse- and Stadium-treated roots also reduced (P < 0.0001 to 0.0146; based on weeks 1, 3, and 4 in 2012 and weeks 1, 3, 4, and 5 in 2013) sucrose loss by 14 to 46% versus the control roots, whereas roots treated with Mertect did not change sucrose loss compared with the control roots in 7 of 10 evaluations. The predominant fungi isolated from symptomatic roots were an Athelia-like sp., Botrytis cinerea, Penicillium spp., and Phoma betae. If Propulse and Stadium are labeled for use on sugar beet in storage, these fungicides should be considered for root rot control in commercial sugar beet storage and on roots held for vernalization for seed production of this biennial plant species.


1999 ◽  
Vol 89 (4) ◽  
pp. 298-302 ◽  
Author(s):  
Anne-Céline Breuil ◽  
Philippe Jeandet ◽  
Marielle Adrian ◽  
Florence Chopin ◽  
Nadine Pirio ◽  
...  

In the interaction between grapevines and Botrytis cinerea, one of the main aspects of pathogenicity is fungal ability to degrade phytoalexins synthesized by the plant in response to infection. Laccase-like stilbene oxidase activity in liquid cultures of B. cinerea has been shown to be related to the decrease of phytoalexin concentrations. Recent research and results presented in this paper determined the chemical structure of a pterostilbene metabolite produced by B. cinerea. Study of degradation of pterostilbene that has just one free hydroxy phenyl group function allowed us to determine the oxidative dimerization process undergone by grapevine phytoalexins after B. cinerea infection. The phytopathological significance of this degradation process in the B. cinerea interaction has also been discussed.


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