期刊
VIRULENCE
卷 10, 期 1, 页码 925-934出版社
TAYLOR & FRANCIS INC
DOI: 10.1080/21505594.2019.1682760
关键词
Aspergillus fumigatus; leucine; virulence; iron; amino acid biosynthesis
资金
- Austrian Science Fund (FWF) doctoral program host response in opportunistic infections (HOROS) [W1253]
- Medical University of Innsbruck (MUI) [19970]
- Israel Ministry of Health (Infect-ERA) [3-0000-11080]
In contrast to mammalia, fungi are able to synthesize the branched-chain amino acid leucine de novo. Recently, the transcription factor LeuB has been shown to cross-regulate leucine biosynthesis, nitrogen metabolism and iron homeostasis in Aspergillus fumigatus, the most common human mold pathogen. Moreover, the leucine biosynthetic pathway intermediate alpha-isopropylmalate (alpha-IPM) has previously been shown to posttranslationally activate LeuB homologs in S. cerevisiae and A. nidulans. Here, we demonstrate that in A. fumigatus inactivation of both leucine biosynthetic enzymes alpha-IPM synthase (LeuC), which disrupts alpha-IPM synthesis, and alpha-IPM isomerase (LeuA), which causes cellular alpha-IPM accumulation, results in leucine auxotrophy. However, compared to lack of LeuA, lack of LeuC resulted in increased leucine dependence, a growth defect during iron starvation and decreased expression of LeuB-regulated genes including genes involved in iron acquisition. Lack of either LeuA or LeuC decreased virulence in an insect infection model, and inactivation of LeuC rendered A. fumigatus avirulent in a pulmonary aspergillosis mouse model. Taken together, we demonstrate that the lack of two leucine biosynthetic enzymes, LeuA and LeuC, results in significant phenotypic consequences indicating that the regulator LeuB is activated by alpha-IPM in A. fumigatus and that the leucine biosynthetic pathway is an attractive target for the development of antifungal drugs.
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