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Introduction to Fungi, Third Edition

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HYPOCREALES<br />

347<br />

Fig12.22 Fusarium culmorum. (a) Part of a sporodochium with clusters of phialides producing macroconidia. (b) Mature<br />

macroconidium from a two-week-old culture.The foot cell is indicated by an arrowhead. (c) Older macroconidia (eight-week-old)<br />

in which some cells have collapsed and the others have turned in<strong>to</strong> chlamydospores. (d) Chlamydospores formed by a hypha<br />

submerged in agar. (b d) <strong>to</strong> same scale.<br />

F. oxysporum, and this has been summarized by Di<br />

Pietro et al. (2003).<br />

The control of diseases caused by Fusarium is<br />

mainly through the use of resistant host plant<br />

cultivars (Beckman, 1987). The disastrous economic<br />

consequences of the outbreak and spread<br />

of Panama wilt of banana caused by F. oxysporum<br />

f. sp. cubense which attacked the popular banana<br />

variety ‘Gros Michel’ were overcome by switching<br />

production <strong>to</strong> clones of the resistant variety<br />

‘Cavendish’ which could be planted in<strong>to</strong> soils<br />

heavily contaminated with F. oxysporum f. sp.<br />

cubense (Moore et al., 2001). Another wellcharacterized<br />

example is <strong>to</strong>ma<strong>to</strong> wilt caused by<br />

F. oxysporum f. sp. lycopersici. Resistance seems <strong>to</strong><br />

be based mainly on major-gene resistance, and<br />

numerous resistance genes have been crossed<br />

in<strong>to</strong> the cultivated <strong>to</strong>ma<strong>to</strong> plant from wild<br />

relatives. These occur in several discrete gene<br />

clusters (Sela-Buurlage et al., 2001). A range of<br />

<strong>to</strong>ma<strong>to</strong> cultivars with resistance against one or<br />

more of the three races of F. oxysporum f. sp.<br />

lycopersici is available for planting.<br />

Another approach actively pursued at present<br />

is the biological control of F. oxysporum. An<br />

interesting strategy is the use of apathogenic<br />

strains of F. oxysporum which colonize the root<br />

cortex but not the vascular system, and therefore<br />

have an endophytic lifestyle. They inhibit infections<br />

by pathogenic strains. Various explanations<br />

have been offered, including competition for<br />

nutrients, the induction of systemic acquired<br />

resistance in plants pre-infected with the apathogenic<br />

strains, and direct competition between<br />

apathogenic and pathogenic strains in the root<br />

cortex (Larkin & Fravel, 1999; Bao & Lasarovits,<br />

2001). Other soil micro-organisms such as<br />

Pseudomonas spp. are also being developed as<br />

biocontrol agents.<br />

Myco<strong>to</strong>xins<br />

Some species of Fusarium (e.g. F. graminearum and<br />

F. moniliforme) are seed-borne, with mycelium<br />

being present inside the grain and often producing<br />

macroconidia on the surface. Infected seed<br />

not only ensures carry-over of the disease <strong>to</strong><br />

following seasons but can be a source of<br />

myco<strong>to</strong>xins if fed <strong>to</strong> lives<strong>to</strong>ck or consumed by<br />

humans. Myco<strong>to</strong>xins such as zearalenone, fumonisin,<br />

trichothecenes and vomi<strong>to</strong>xin (Fig. 12.23)

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