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Bioprospecting
the fungicides compatible Trichoderma asperellum isolate effective
against multiple plant pathogens in vitro
M.
Manjunath1*, A. Singh1, A. N. Tripathi1, R.
Prasanna2, A.B. Rai1 and B. Singh1
1Division of Crop
Protection, ICAR- Indian Institute of Vegetable Research, Varanasi-221 305,
India
2Division of
Microbiology, ICAR-Indian Agricultural Research Institute, New Delhi-110 012,
India
*Corresponding
Author E-mail: manjumbl@gmail.com
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Key
words
Biocontrol agent,
Fungicides,
ITS Primers,
Phytopathogenic fungi ,
Trichoderma
Publication Data
Paper
received : 27.04.2016
Revised
received : 16.08.2016
Re-revised
received : 15.11.2016
Accepted : 01.12.2016
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Abstract
Aim: It is essential to
develop an efficient ecofriendly disease management programme which helps in
gradual reduction in use of harmful chemicals. The objective of the study was
to isolate, purify and identify Trichoderma isolate from diseased
plant tissues and to identify its compatibility with commonly used fungicides
for the eco-friendly management of vegetable diseases.
Methodology:
Trichoderma
asperellum
was isolated from Sclerotinia sclerotiorum infected stem tissues of pea on potato
dextrose agar. The morphological, cultural characteristics and molecular
identification of Trichoderma asperellum was carried out using ITS primers. In
vitro antagonistic efficiency of Trichoderma asperellum was studied
against phytopathogenic fungi viz., Pythium aphanidermatum, Pythium
debaryanum, Sclerotium rolfsii Sr1, Sclerotium rolfsii Sr3, Fusarium
oxysporum f.sp. lycopersici? and Alternaria solani.
Results:
The
nucleotide sequence of amplified ITS region was deposited at Genbank (NCBI)
with accession no. KT824429. The highest mycelial inhibition values of 43.57,
38.16, 42.56 and 54.87% were obtained for Pythium aphanidermatum, P.
debaryanum, Sclerotium rolfsii Sr1 and Sclerotium rolfsii Sr3,
respectively, after 6 days of T. asperellum inoculation. T. asperellum
exhibited 100% compatibility with Mancozeb, Azoxystrobin, Cymoxinil+Mancozeb,
Metalxyl+Mancozeb at 100, 200 and 300 ppm.? The per cent compatibility of
98.15, 74.82 and 50.38 with Carbendazim at 100, 200 and 300 ppm was also
recorded.
Interpretation:
These
studies established the aggressive nature of the isolate and its suitability
in integrated disease management practices
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