EC Accepts, published online ahead of print on 1 May 2009
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Amaike, S.
Right arrow Articles by Keller, N. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Amaike, S.
Right arrow Articles by Keller, N. P.

 Previous Article  |  Next Article 

Eukaryotic Cell doi:10.1128/EC.00088-09
Copyright (c) 2009, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.

Distinct roles for VeA and LaeA in development and pathogenesis of Aspergillus flavus

Saori Amaike and Nancy P. Keller*

Department of Plant Pathology, Department of Medical Microbiology and Immunology, and Department of Bacteriology, University of Wisconsin - Madison, 1550 Linden Dr., Madison, WI 53706-1598

* To whom correspondence should be addressed. Email: npkeller{at}wisc.edu.


arrow
Abstract

Aspergillus flavus, a mycotoxigenic filamentous fungus, colonizes several important agricultural crops, such as maize and peanuts. Two proteins, VeA and LaeA known to form a nuclear complex in A. nidulans, have been found to positively regulate developmental processes in several Aspergillus species. Here an examination of near-isogenic A. flavus mutants differing in copy number of veA and laeA alleles (0, 1 or 2+ each) revealed critical roles for VeA and LaeA in A. flavus development and seed colonization. In contrast to wildtype, both null mutants were unable to metabolize host cell lipid reserves and were inhibited by oleic acid in growth assays. Copy number of LaeA but not VeA appeared critical for a density dependent sclerotial-to-conidial shift as the MClaeA strain produced relatively constant sclerotial numbers with increasing population size rather than the decrease in sclerotia seen in both wildtype and MCveA strains. The MCveA/laeA strain yielded an intermediate phenotype. This study revealed unique roles of VeA and LaeA in seed pathogenesis and fungal biology, distinct from their cooperative regulatory functions in aflatoxin and sclerotial development.