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Mycotoxins, toxic secondary metabolites of fungi are now recognised as major cause of food intoxications in Sub Saharan Africa (SSA). Aflatoxins, the most important of the group have been implicated in acute aflatoxicoses, carcinogenicity, growth retardation, neonatal jaundice and immunological suppression in SSA. The hot and humid tropical climate provides ideal condition for growth of toxigenicAspergillus spp, making food contamination to be widespread in SSA, with maize and groundnuts being the most contaminated. The available data suggests that cassava products (the most important African food) are not prone to aflatoxin contamination. Recent data on ochratoxin A produced by species ofAspergillus on grains have indicated the necessity for it to be monitored in SSA. Fumonisins represent the most importantFusarium mycotoxins in SSA, and surveillance data indicate very high contamination rates of almost 100% in maize samples from West Africa. Limited information exists on the occurrence of trichothecenes, while the data currently available suggest that zearalenone contamination seems not to be a problem in SSA. The strategies under investigation to mitigate the mycotoxin problem in SSA include education of the people on the danger of consuming mouldy foods, pre and post harvest management strategies with emphasis on biological control, use of plant products to arrest fungal growth during storage, enterosorbent clay technology, and the search for traditional techniques that could reduce/detoxify mycotoxins during food processing.

A survey was conducted on the incidence of fungi, and the natural occurrence of aflatoxins and fumonisins in preharvest maize from fields in south-western Nigeria. Mycological examinations revealed the predominance of F. verticillioides (Zea mays) (syn. F. moniliforme), occurring in 89.3% of samples with a mean kernel infection of 49.4%, while Aspergillus flavus was isolated from 65% of samples having a mean kernel infection of 6.8%. Aflatoxin B1 was detected in 18.4% of samples with a mean of 22 micrograms kg-1, while aflatoxins B2, G1 and G2 were present in 7.8, 2.9 and 1% of the samples with mean levels of 10, 8 and 7 micrograms kg-1, respectively, in contaminated samples. Total aflatoxins ranged from 3 to 138 micrograms kg-1 in positive samples, with a mean of 28 micrograms kg-1. Fumonsin B1 was the predominant toxin detected in terms of frequency (78.6% of samples) and quantity (concentration range 70-1780 micrograms kg-1, mean = 495 micrograms kg-1). Fumonisin B2 was detected in 68 samples (66%) with a mean of 114 micrograms kg-1. Fifteen samples were contaminated with both aflatoxins and fumonisins.

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