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VeA is Required for Toxin and Sclerotial Production in Aspergillus Parasiticus

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Date 2004 Aug 6
PMID 15294809
Citations 127
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Abstract

It was long been noted that secondary metabolism is associated with fungal development. In Aspergillus nidulans, conidiation and mycotoxin production are linked by a G protein signaling pathway. Also in A. nidulans, cleistothecial development and mycotoxin production are controlled by a gene called veA. Here we report the characterization of a veA ortholog in the aflatoxin-producing fungus A. parasiticus. Cleistothecia are not produced by Aspergillus parasiticus; instead, this fungus produces spherical structures called sclerotia that allow for survival under adverse conditions. Deletion of veA from A. parasiticus resulted in the blockage of sclerotial formation as well as a blockage in the production of aflatoxin intermediates. Our results indicate that A. parasiticus veA is required for the expression of aflR and aflJ, which regulate the activation of the aflatoxin gene cluster. In addition to these findings, we observed that deletion of veA reduced conidiation both on the culture medium and on peanut seed. The fact that veA is necessary for conidiation, production of resistant structures, and aflatoxin biosynthesis makes veA a good candidate gene to control aflatoxin biosynthesis or fungal development and in this way to greatly decrease its devastating impact on health and the economy.

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References
1.
Adams T, Wieser J, Yu J . Asexual sporulation in Aspergillus nidulans. Microbiol Mol Biol Rev. 1998; 62(1):35-54. PMC: 98905. DOI: 10.1128/MMBR.62.1.35-54.1998. View

2.
Rosen S, Yu J, Adams T . The Aspergillus nidulans sfaD gene encodes a G protein beta subunit that is required for normal growth and repression of sporulation. EMBO J. 1999; 18(20):5592-600. PMC: 1171627. DOI: 10.1093/emboj/18.20.5592. View

3.
Calvo A, Hinze L, Gardner H, Keller N . Sporogenic effect of polyunsaturated fatty acids on development of Aspergillus spp. Appl Environ Microbiol. 1999; 65(8):3668-73. PMC: 91549. DOI: 10.1128/AEM.65.8.3668-3673.1999. View

4.
Chang P . The Aspergillus parasiticus protein AFLJ interacts with the aflatoxin pathway-specific regulator AFLR. Mol Genet Genomics. 2003; 268(6):711-9. DOI: 10.1007/s00438-003-0809-3. View

5.
CHANG P, Cary J, Bhatnagar D, Cleveland T, Bennett J, Linz J . Cloning of the Aspergillus parasiticus apa-2 gene associated with the regulation of aflatoxin biosynthesis. Appl Environ Microbiol. 1993; 59(10):3273-9. PMC: 182448. DOI: 10.1128/aem.59.10.3273-3279.1993. View