PUBLICATION
Mycobacterial fatty acid catabolism is repressed by FdmR to sustain lipogenesis and virulence
- Authors
- Dong, W., Nie, X., Zhu, H., Liu, Q., Shi, K., You, L., Zhang, Y., Fan, H., Yan, B., Niu, C., Lyu, L.D., Zhao, G.P., Yang, C.
- ID
- ZDB-PUB-210416-2
- Date
- 2021
- Source
- Proceedings of the National Academy of Sciences of the United States of America 118(16): (Journal)
- Registered Authors
- Keywords
- Mycobacterium, fatty acid, lipid homeostasis, metabolic regulation
- MeSH Terms
-
- Animals
- Bacterial Proteins/metabolism
- Fatty Acids/metabolism*
- Lipogenesis/physiology*
- Lipolysis
- Metabolism/physiology
- Models, Animal
- Mycobacterium/metabolism
- Mycobacterium Infections, Nontuberculous/metabolism
- Mycobacterium Infections, Nontuberculous/physiopathology
- Mycobacterium marinum/metabolism*
- Oxidation-Reduction
- Transcription Factors/metabolism
- Virulence/physiology
- Zebrafish/metabolism
- Zebrafish/microbiology
- PubMed
- 33853942 Full text @ Proc. Natl. Acad. Sci. USA
Citation
Dong, W., Nie, X., Zhu, H., Liu, Q., Shi, K., You, L., Zhang, Y., Fan, H., Yan, B., Niu, C., Lyu, L.D., Zhao, G.P., Yang, C. (2021) Mycobacterial fatty acid catabolism is repressed by FdmR to sustain lipogenesis and virulence. Proceedings of the National Academy of Sciences of the United States of America. 118(16):.
Abstract
Host-derived fatty acids are an important carbon source for pathogenic mycobacteria during infection. How mycobacterial cells regulate the catabolism of fatty acids to serve the pathogenicity, however, remains unknown. Here, we identified a TetR-family transcriptional factor, FdmR, as the key regulator of fatty acid catabolism in the pathogen Mycobacterium marinum by combining use of transcriptomics, chromatin immunoprecipitation followed by sequencing, dynamic 13C-based flux analysis, metabolomics, and lipidomics. An M. marinum mutant deficient in FdmR was severely attenuated in zebrafish larvae and adult zebrafish. The mutant showed defective growth but high substrate consumption on fatty acids. FdmR was identified as a long-chain acyl-coenzyme A (acyl-CoA)-responsive repressor of genes involved in fatty acid degradation and modification. We demonstrated that FdmR functions as a valve to direct the flux of exogenously derived fatty acids away from β-oxidation toward lipid biosynthesis, thereby avoiding the overactive catabolism and accumulation of biologically toxic intermediates. Moreover, we found that FdmR suppresses degradation of long-chain acyl-CoAs endogenously synthesized through the type I fatty acid synthase. By modulating the supply of long-chain acyl-CoAs for lipogenesis, FdmR controls the abundance and chain length of virulence-associated lipids and mycolates and plays an important role in the impermeability of the cell envelope. These results reveal that despite the fact that host-derived fatty acids are used as an important carbon source, overactive catabolism of fatty acids is detrimental to mycobacterial cell growth and pathogenicity. This study thus presents FdmR as a potentially attractive target for chemotherapy.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping