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SCREENING OF TOMATO ACCESSIONS FOR RESISTANCE TO ...

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Due to the growth of the fungus within the plant's vascular tissue, the plant's water supply is greatly<br />

affected. This lack of water induces the leaves' stomata to close, the leaves wilt, and the plant<br />

eventually dies. It is at this point that the fungus invades the plant's parenchymatous<br />

tissue, until it<br />

finally reaches the surface of the dead tissue, where it sporulates abundantly (Agrios, 1988). The<br />

resulting spores can then be used as new inoculums for further spread of the fungus<br />

Due to prolonged survival in soil as a saprophyte and as resistant structures, F<br />

oxysporum is difficult to control (Mujeebur and Shahana, 2002; Borrero et al., 2004). Among control<br />

strategies available for Fusarium wilt management, soil fumigation and use of resistant cultivars are<br />

the most used. Biological control of plant pathogens using antagonistic<br />

fungal and bacterial strains is<br />

gaining increasing importance. Soil has untapped potential and contains several potential biocontrol<br />

agents (BCAs) such as Pseudomonas spp., Trichoderma spp. and non-pathogenic Fusarium spp. that<br />

have shown high antagonistic activity against several soil-borne pathogens (Fuchs et al., 1999;<br />

Ramamoorthy et aI., 2001). So far, several bacterial and fungal antagonistic strains have been shown<br />

to reduce the damage caused by different pathogens, including F oxysporum f. sp. Iycopersici<br />

(Postma and Rattink, 1992; Alabouvette, 200 I; Moretti et al., 2008).<br />

The best recommended<br />

way to control the disease is selecting resistant varieties of tomato (Silva and<br />

Bettiol, 2005). Recently there have been many reports about using bioactive compounds from<br />

biological control agents which were extracted from different fungi that inhibit many plant<br />

pathogenic fungi, including Fusarium wilt of tomato (Soytong, 1992). These bioactive compounds<br />

are Tricotoxin A50 extracted from Trichoderma harzianum PCO1; and Chaetoglobosin C extracted

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