Aggressiveness of green mould on cultivated mushroom (Agaricus bisporus) in Turkey

2020 ◽  
Vol 127 (5) ◽  
pp. 695-708 ◽  
Author(s):  
Mehmet Aydoğdu ◽  
İlker Kurbetli ◽  
Aytül Kitapçı ◽  
Görkem Sülü
2019 ◽  
Vol 126 ◽  
pp. 104944
Author(s):  
Olja Stanojević ◽  
Tanja Berić ◽  
Ivana Potočnik ◽  
Emil Rekanović ◽  
Slaviša Stanković ◽  
...  

2021 ◽  
Vol 36 (2) ◽  
pp. 83-90
Author(s):  
Ivana Potocnik ◽  
Biljana Todorovic ◽  
Svetlana Milijasevic-Marcic ◽  
Jelena Lukovic ◽  
Gabriella Kanizai-Saric ◽  
...  

The aim of this study was to test a biofungicide based on Bacillus subtilis Ch-13 and its effectiveness in the control of green mould disease of cultivated mushroom in comparison with the fungicide prochloraz. Biofungicide effectiveness in disease control and impact on yield were evaluated on Agaricus bisporus after its natural infection with Trichoderma aggressivum in a commercial mushroom growing facility. An assay for testing the microbial efficacy of the biofungicide was conducted in two different procedures involving either three or two split doses. The highest statistically significant effectiveness in green mould control was shown by the fungicide prochloraz (71.43%), followed by the biofungicide applied in tree split doses (53.57%), and finally its two doses (45.46%). The biofungicide significantly improved yield in comparison with an untreated control and the fungicide prochloraz. Three split applications of B. subtilis strain Ch-13 enhanced mushroom yield to a larger extent than its two split doses, although the same final amount was used in both procedures. Biofungicide application in three split doses increased the total mass of harvested mushrooms 8.41% compared to the untreated control, and 10.53% compared to the fungicide prochloraz. These results implied that the biofungicide should be applied in three split applications: 30 ml (second day after casing) + 15 ml (two weeks after casing) + 15 ml (after first flush, 20-25 days after casing). The biofungicide B. subtilis Ch-13 should be further investigated regarding its joint usage with chemical fungicides in different application procedures, as it showed remarkable characteristics both in terms of promoting mushroom yield and inhibiting the spread of mycopathogenic T. aggressivum.


Chemosphere ◽  
1998 ◽  
Vol 36 (8) ◽  
pp. 1787-1798 ◽  
Author(s):  
Johannes T. van Elteren ◽  
Urszula D. Woroniecka ◽  
Koos J. Kroon

2018 ◽  
Vol 278 ◽  
pp. 10-19 ◽  
Author(s):  
Caroline Pandin ◽  
Dominique Le Coq ◽  
Julien Deschamps ◽  
Régis Védie ◽  
Thierry Rousseau ◽  
...  

1982 ◽  
Vol 52 (1) ◽  
pp. 43-48 ◽  
Author(s):  
W.C. Wong ◽  
J.T. Fletcher ◽  
B.A. Unsworth ◽  
T.F. Preece

1993 ◽  
Vol 139 (6) ◽  
pp. 1209-1218 ◽  
Author(s):  
C. R. Perry ◽  
M. Smith ◽  
C. H. Britnell ◽  
D. A. Wood ◽  
C. F. Thurston

Plant Disease ◽  
2003 ◽  
Vol 87 (12) ◽  
pp. 1457-1461 ◽  
Author(s):  
X. Chen ◽  
M. D. Ospina-Giraldo ◽  
V. Wilkinson ◽  
D. J. Royse ◽  
C. P. Romaine

Since the early 1990s, the epidemic of green mold on the cultivated mushroom Agaricus bisporus in North America has been caused by Trichoderma aggressivum f. aggressivum. The findings of earlier research suggested that the microevolutionary emergence of T. aggressivum f. aggressivum coincided with the onset of the epidemic. This hypothesis was tested further by determining the disease susceptibility of mushroom strains grown widely before the epidemic manifested. The results of complementary methods of analysis, which entailed a grain protection assay and cropping trials, established that two pre-epidemic strains were more susceptible to green mold than three post-epidemic strains being cultivated at the time of the epidemic. Thus, if T. aggressivum f. aggressivum had been present within cultivated mushrooms prior to the epidemic, it should have been detected. It still appears to be true that T. aggressivum f. aggressivum emerged during the 1990s in a manner that remains unclear.


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