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IARC MONOGRAPHS ON THE EVALUATION OF CARCINOGENIC ...

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282<br />

<strong>IARC</strong> <strong>M<strong>ON</strong>OGRAPHS</strong> VOLUME 82<br />

aflatoxin formation in peanuts (Pettit et al., 1971; Cole et al., 1982). However, peanuts<br />

throughout the world are recognized as a drought-resistant crop and are mostly grown<br />

under dry culture, with irrigation reserved for more moisture-sensitive crops such as rice<br />

or vegetables. In many areas where peanuts are grown, irrigation is not an option. Under<br />

these circumstances, reduction in drought stress by good agricultural practices can be a<br />

beneficial approach. For example, weed control and wider spacing between peanut rows<br />

can both assist in reducing drought stress (Rachaputi, 1999). Rapid drying of peanuts<br />

using mechanical dryers as soon as possible after pulling has a major effect in reducing<br />

the levels of aflatoxins in peanuts.<br />

For maize also, irrigation and improved farm management practices have a beneficial<br />

effect on aflatoxin formation (Payne et al., 1986). Resistant breeding stocks have been<br />

identified (Widstrom et al., 1987; Campbell & White, 1995) and resistant maize genotypes,<br />

dependent on kernel pericarp wax (Guo et al., 1995; Brown et al., 1999) or kernel<br />

proteins (Huang et al., 1997) have been developed recently. As maize is usually dried in<br />

the field, rapid drying techniques are not commonly practised, but should be in tropical<br />

countries.<br />

Cottonseed is a by-product of cotton production, so field drying is normal. Breeding<br />

of cotton without nectaries has been proposed as one means of limiting A. flavus access<br />

to cotton bolls (Klich & Chmielewski, 1985).<br />

Genetic engineering may offer novel ways of limiting pre-harvest contamination by<br />

mycotoxins, provided attention is paid to questions of importance specifically to developing<br />

countries (Wambugu, 1999). Genetic approaches to aflatoxin control include engineering<br />

of genes in Aspergillus species to influence the ability of the fungus to colonize<br />

the host plant. An alternative approach is to select or engineer varieties of cereal grains<br />

and oilseeds resistant to fungal infection or aflatoxin biosynthesis by the fungus once<br />

infection occurs.<br />

(b) Control of aflatoxin formation in other crops before and after<br />

harvest<br />

Entry of A. flavus into pistachio nuts depends on the time of splitting of hulls. Nuts<br />

in which hull splitting occurs early are much more susceptible to A. flavus invasion on<br />

the tree (Doster & Michailides, 1995). It is known that some cultivars are more prone to<br />

early splitting than others, and this is especially important where nuts are harvested from<br />

the ground, after contact with the soil.<br />

In tree nut crops, various techniques, including timing of harvesting, are used to keep<br />

aflatoxin formation to a minimum.<br />

Figs are sometimes infected by A. flavus, both because of their unique structure developed<br />

for insect fertilization and also because figs are harvested from the ground in some<br />

countries. Immature figs are not colonized by A. flavus, but once they are ripe infection<br />

occurs readily and fungal growth continues during drying (Buchanan et al., 1975; Le<br />

Bars, 1990). The proportion of figs infected is only about 1% (Steiner et al., 1988).

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