Expression and action pattern of Botryotinia fuckeliana (Botrytis cinerea) rhamnogalacturonan hydrolase in Pichia pastoris

2001 ◽  
Vol 330 (1) ◽  
pp. 73-81 ◽  
Author(s):  
Jun Fu ◽  
Rolf Prade ◽  
Andrew Mort
1999 ◽  
Vol 64 (2) ◽  
pp. 85-100 ◽  
Author(s):  
Florence Chapeland ◽  
René Fritz ◽  
Catherine Lanen ◽  
Michel Gredt ◽  
Pierre Leroux

Plant Disease ◽  
2012 ◽  
Vol 96 (1) ◽  
pp. 147-147 ◽  
Author(s):  
G. W. Moorman ◽  
A.-S. Walker ◽  
S. May

Greenhouse-grown Heuchera plants, treated with fenhexamid (Decree, SePRO, Carmel, IN; FRAC group 17 hydroxyanilide), with active gray mold were submitted to the Penn State Plant Disease Clinic in December 2010 from a commercial operation in north-central Pennsylvania. Genetic and phenotypic analyses identified the isolate as Botrytis cinerea Pers. (teleomorph Botryotinia fuckeliana (de Bary) Whetzel), HydR3 phenotype (2) and not B. pseudocinerea (previously Botrytis group I) (4), naturally resistant to fenhexamid (phenotype HydR1) (1). While 0.2 μg of fenhexamid per ml or less is required to slow mycelial growth and germ tube elongation of sensitive isolates by 50% (EC50), the radial growth EC50 of the Heuchera isolate was approximately 2,000 μg of fenhexamid per ml in culture. Five cucumber seedlings receiving 25 μl of 0.1 M dextrose containing the label rate of Decree (1,800 μg/ml) on the growing tip were inoculated with colonized agar in the drop. Five check plants received 25 μl of 0.1 M dextrose. B. cinerea from silica gel storage since 1988 was also tested. This experiment was repeated three times. The 1988 isolate killed all fungicide-free but no fenhexamid-treated plants. The Heuchera isolate killed all fungicide-free and fenhexamid-treated plants within 4 days. To our knowledge, this is the first report of B. cinerea from a greenhouse in North America with fenhexamid resistance. Resistance occurs in U.S. fields (3). The Heuchera isolate's HydR3 resistance phenotype (2) has been detected in Germany, Japan, and France and has mutations affecting the 3-keto reductase protein, encoded by the erg27 gene, the specific target of fenhexamid and involved in Botrytis sterol biosynthesis. The Decree label states that it is to be used only twice on a crop before switching to a different mode of action. Greenhouses have resident Botrytis populations that are likely to be exposed to any fungicide applied in the structure. Growers should consider using fenhexamid only twice in a particular greenhouse, rather than on a particular crop, before switching to a different mode of action. References: (1) P. Leroux et al. Crop Prot. 18:687, 1999.(2) P. Leroux et al. Pest Manag. Sci. 58:876, 2002. (3) Z. Ma and T. J. Michailides. Plant Dis. 89:1083, 2005. (4) A.-S. Walker et al. Phytopathology 101:1433, 2011.


Mycologia ◽  
1953 ◽  
Vol 45 (3) ◽  
pp. 415-425 ◽  
Author(s):  
J. Walton Groves ◽  
Constance A. Loveland

2015 ◽  
Vol 31 (1–2) ◽  
pp. 205-220
Author(s):  
E. Arseniuk ◽  
H. Bryk

In the period 1975-1977 forms of the fungus <i>Botrytis cinerea</i> were found in Poland resistant to benzimidazole fungicides. The incidence of the resistant forms increases with the more intensive use of these fungicides. The resistance of <i>Botrytis cinerea</i> to benzimidazole compounds is a cross-resistance involving the whole group of these agents, nowithstanding wihich of them was applied. The resistance acquired by the fungus does not change its reaction to other prophylactic fungicides.


Microbiology ◽  
1988 ◽  
Vol 134 (9) ◽  
pp. 2543-2550 ◽  
Author(s):  
F. Faretra ◽  
E. Antonacci ◽  
S. Pollastro

2012 ◽  
Vol 68 (9) ◽  
pp. 1231-1240 ◽  
Author(s):  
Rita M De Miccolis Angelini ◽  
Caterina Rotolo ◽  
Mario Masiello ◽  
Stefania Pollastro ◽  
Hideo Ishii ◽  
...  

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