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Biological Control of Wilt Disease Complex on Tomato Crop Caused by Meloidogyne Javanica and Fusarium Oxysporum F.sp. Lycopersici by Verticillium Leptobactrum

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Publisher Springer
Date 2017 Sep 24
PMID 28939938
Citations 8
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Abstract

The efficacy of Verticillium leptobactrum isolate (HR1) was evaluated in the control of root-knot nematode and Fusarium wilt fungus under laboratory and greenhouse conditions. Five concentrations of V. leptobactrum (HR1) isolate were tested for their nematicidal and fungicidal activities against Meloidogyne javanica and Fusarium oxysporum f.sp. lycopersici in vitro. Laboratory trials showed that mycelium growth inhibition of Fusarium wilt fungus was correlated to the increase of the concentration of culture filtrate. All dilutions showed efficiency in reducing the growth of Fusarium oxysporum f.sp. lycopersici. The greatest nematicidal activity was observed at 50, 75, and 100% filtrate dilutions. The egg hatching percentage reached 42%, and the juvenile's corrected mortality registered 90% for the above treatments. In greenhouse experiment, the biocontrol agent fungus enhanced significantly tomato growth components (height and weight of plant and root). The multiplication rate of root-knot nematode and the Fusarium wilt disease incidence declined significantly with soil application of V. leptobactrum as with chemical treatments. The isolate HR1 was efficient to control wilt disease complex caused by M. javanica and Fusarium oxysporum f.sp. lycopersici.

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References
1.
El-Sherif A, Elwakil M . Interaction between Meloidogyne incognita and Agrobacterium tumefaciens or Fusarium oxysporum f. sp. lycopersici on Tomato. J Nematol. 2009; 23(2):239-42. PMC: 2619142. View

2.
Park J, Seo Y, Kim Y . Biological Control of Meloidogyne hapla Using an Antagonistic Bacterium. Plant Pathol J. 2014; 30(3):288-98. PMC: 4181115. DOI: 10.5423/PPJ.OA.02.2014.0013. View

3.
Janssen A, Scheffer J, BAERHEIM SVENDSEN A . Antimicrobial activity of essential oils: a 1976-1986 literature review. Aspects of the test methods. Planta Med. 1987; 53(5):395-8. DOI: 10.1055/s-2006-962755. View

4.
ABBOTT W . A method of computing the effectiveness of an insecticide. 1925. J Am Mosq Control Assoc. 1987; 3(2):302-3. View