Current issues in research on fumonisins, mycotoxins which may cause nephropathy

W. Thomas Shier, Hamed K. Abbas

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

The fumonsins are a series of mycotoxins produced by the ubiquitous corn (maize) contaminant, Fusarium moniliforme, and several other Fusarium species. Fumonisin B1 (FB1), the major component of the fumonisins, causes leukoencephalomalacia in horses, pulmonary edema in swine and hepatocellular carcinoma, cirrhosis and chronic interstitial nephritis in rats. Also, consumption of corn-derived food products contaminated with F. moniliforme has been correlated with increased risk of human esophageal cancer in epidemiological studies in South Africa and China. In the kidneys of rodents, dietary exposure to FB1 produces a dose-related non-inflammatory nephrosis with regeneration at low doses. Individual cells die by induction of apoptosis. The fumonisins have chemical structures analogous to sphingosine, a putative intracellular regulatory molecule, and a component of sphingolipids. The alkylamine structure of FB1 makes possible sensitive high performance liquid chromatography (HPLC) assays based on pre-column derivatization of the amino group with fluorogenic reagents. These assays have been used to demonstrate that FB1 contaminates most corn and corn- derived processed food products intended for human consumption. Conventional thermal food processing techniques reduce FB1 levels, but do not completely eliminate it. Structure-activity relationship studies carried out in our laboratories on natural and synthetic fumonisins indicate that extensive alterations in structure are possible without loss of biological activity. This observation raises the concern that the FB1 eliminated during food processing may actually be converted to other biologically active forms. The full extent of the threat to food safety posed by fumonisins will not be known until it is determined what substances the toxin is converted to during food processing, the bioavailability of those substances, the extent they retain biological activity and the additivity of their toxic effects with other nephrotoxic mycotoxins such as ochratoxins A and B.

Original languageEnglish (US)
Pages (from-to)323-335
Number of pages13
JournalJournal of Toxicology - Toxin Reviews
Volume18
Issue number3-4
DOIs
StatePublished - 1999

Bibliographical note

Funding Information:
Acknowledgmenrs -- Some of the research descnbed in this review was supported in part by NRICGP research grants 93-37201-9561 and 96-35201-3271 from the United States Department of Agnculture.

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