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MAB_3551cencodes the primary triacylglycerol synthase involved in lipid accumulation inMycobacterium abscessus
- Source :
- Molecular Microbiology. 102:611-627
- Publication Year :
- 2016
- Publisher :
- Wiley, 2016.
-
Abstract
- Slow growing pathogenic mycobacteria utilize host-derived lipids and accumulate large amounts of triacylglycerol (TAG) in the form of intracytoplasmic lipid inclusions (ILI), serving as a source of carbon and energy during prolonged infection. Mycobacterium abscessus is an emerging and rapidly growing species capable to induce severe and chronic pulmonary infections. However, whether M. abscessus, like Mycobacterium tuberculosis, possesses the machinery to acquire and store host lipids, remains unaddressed. Herein, we aimed at deciphering the contribution of the seven putative M. abscessus TAG synthases (Tgs) in TAG synthesis/accumulation thanks to a combination of genetic and biochemical techniques and a well-defined foamy macrophage (FM) model along with electron microscopy. Targeted gene deletion and functional complementation studies identified the MAB_3551c product, Tgs1, as the major Tgs involved in TAG production. Tgs1 exhibits a preference for long acyl-CoA substrates and site-directed mutagenesis demonstrated that His144 and Gln145 are essential for enzymatic activity. Importantly, in the lipid-rich intracellular context of FM, M. abscessus formed large ILI in a Tgs1-dependent manner. This supports the ability of M. abscessus to assimilate host lipids and the crucial role of Tgs1 in intramycobacterial TAG production, which may represent important mechanisms for long-term storage of a rich energy supply. This article is protected by copyright. All rights reserved.
- Subjects :
- 0301 basic medicine
chemistry.chemical_classification
ATP synthase
biology
030106 microbiology
Mutagenesis (molecular biology technique)
Context (language use)
Mycobacterium abscessus
biology.organism_classification
Microbiology
3. Good health
Complementation
Mycobacterium tuberculosis
03 medical and health sciences
Enzyme
chemistry
Biochemistry
biology.protein
lipids (amino acids, peptides, and proteins)
Molecular Biology
Intracellular
Subjects
Details
- ISSN :
- 0950382X
- Volume :
- 102
- Database :
- OpenAIRE
- Journal :
- Molecular Microbiology
- Accession number :
- edsair.doi...........4e09f7e2e8347c33152f4c6bc621a2c6
- Full Text :
- https://doi.org/10.1111/mmi.13482