Saprophytic microorganisms with potential for biological control of Botrytis cinerea on Geraldton waxflower flowers

被引:15
作者
Beasley, DR
Joyce, DC [1 ]
Coates, LM
Wearing, AH
机构
[1] Cranfield Univ, Postharvest Technol Lab, Silsoe MK45 4DT, Beds, England
[2] Univ Queensland, Sch Agr & Hort, Brisbane, Qld 4345, Australia
[3] Queensland Dept Primary Ind, Queensland Hort Inst, Indooroopilly, Qld 4068, Australia
来源
AUSTRALIAN JOURNAL OF EXPERIMENTAL AGRICULTURE | 2001年 / 41卷 / 05期
关键词
D O I
10.1071/EA00112
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Saprophytic bacteria, yeasts and filamentous fungi were isolated from Geraldton waxflower flowers and screened to identify potential antagonism towards Botrytis cinerea. Isolates from other sources (e.g. avocado) were also tested. Isolates were initially screened in vitro for inhibition of B. cinerea conidial germination, germ tube elongation and mycelial growth. The most antagonistic bacteria, yeasts and fungi were selected for further testing on detached waxflower flowers. Conidia of the pathogen were mixed with conidia or cells of the selected antagonists, co-inoculated onto waxflower flowers, and the flowers were sealed in glass jars and incubated at 20 degreesC. The number of days required for the pathogen to cause flower abscission was determined. The most antagonistic bacterial isolate, Pseudomonas sp. 677, significantly reduced conidial germination and retarded germ tube elongation of B. cinerea. None of the yeast or fungal isolates tested was found to significantly reduce conidial germination or retard germ tube elongation, but several significantly inhibited growth of B. cinerea. Fusarium sp., Epicoccum sp. and Trichoderma spp. were the most antagonistic of these isolates. Of the isolates tested on waxflower, Pseudomonas sp. 677 was highly antagonistic towards B. cinerea and delayed waxflower abscission by about 3 days. Trichoderma harzianum also significantly delayed flower abscission. However, as with most of the fungal antagonists used, inoculation of waxflower flowers with this isolate resulted in unsightly mycelial growth.
引用
收藏
页码:697 / 703
页数:7
相关论文
共 31 条
[1]  
BARNETT HL, 1960, ILLUSTRATED GENERA I
[2]  
Blakeman J.P., 1981, Microbial ecology of the phylloplane, P245
[3]   PATHOGENS IN THE FOLIAR ENVIRONMENT [J].
BLAKEMAN, JP .
PLANT PATHOLOGY, 1993, 42 (04) :479-493
[4]   COMPETITION FOR CARBON-COMPOUNDS BY A LEAF SURFACE BACTERIUM AND CONIDIA OF BOTRYTIS-CINEREA [J].
BRODIE, IDS ;
BLAKEMAN, JP .
PHYSIOLOGICAL PLANT PATHOLOGY, 1975, 6 (02) :125-135
[5]   POSTHARVEST DECAY OF CANTALOUPE CAUSED BY EPICOCCUM-NIGRUM [J].
BRUTON, BD ;
REDLIN, SC ;
COLLINS, JK ;
SAMS, CE .
PLANT DISEASE, 1993, 77 (10) :1060-1062
[6]   Biological control of Botrytis cinerea on chickpea seed with Trichoderma spp and Gliocladium roseum:: indigenous versus non-indigenous isolates [J].
Burgess, DR ;
Keane, PJ .
PLANT PATHOLOGY, 1997, 46 (06) :910-918
[7]   REASONS FOR THE DELAY IN DEVELOPMENT OF BIOLOGICAL-CONTROL OF FOLIAR PATHOGENS [J].
ELAD, Y .
PHYTOPARASITICA, 1990, 18 (02) :99-105
[8]   BIOLOGICAL-CONTROL OF GRAPE GRAY MOLD BY TRICHODERMA-HARZIANUM [J].
ELAD, Y .
CROP PROTECTION, 1994, 13 (01) :35-38
[9]   CONTROL OF INFECTION AND SPORULATION OF BOTRYTIS-CINEREA ON BEAN AND TOMATO BY SAPROPHYTIC YEASTS [J].
ELAD, Y ;
KOHL, J ;
FOKKEMA, NJ .
PHYTOPATHOLOGY, 1994, 84 (10) :1193-1200
[10]  
ELGHAOUTH A, 1992, PHYTOPATHOLOGY, V82, P398, DOI 10.1094/Phyto-82-398