Mycobacterium tuberculosis sensor kinase DosS modulates the autophagosome in a DosR-independent manner.

Abstract

Dormancy is a key characteristic of the intracellular life-cycle of Mtb. The importance of sensor kinase DosS in mycobacteria are attributed in part to our current findings that DosS is required for both persistence and full virulence of Mtb. Here we show that DosS is also required for optimal replication in macrophages and involved in the suppression of TNF-α and autophagy pathways. Silencing of these pathways during the infection process restored full virulence in MtbΔdosS mutant. Notably, a mutant of the response regulator DosR did not exhibit the attenuation in macrophages, suggesting that DosS can function independently of DosR. We identified four DosS targets in Mtb genome; Rv0440, Rv2859c, Rv0994, and Rv0260c. These genes encode functions related to hypoxia adaptation, which are not directly controlled by DosR, e.g., protein recycling and chaperoning, biosynthesis of molybdenum cofactor and nitrogen metabolism. Our results strongly suggest a DosR-independent role for DosS in Mtb.

• Authors: Uma S Gautam, Smriti Mehra, Priyanka Kumari, Xavier Alvarez, Tianhua Niu, Jaya S Tyagi, Deepak Kaushal
• Journal: Communications biology (Commun Biol) Vol. 2 Pg. 349 ( 2019) ISSN: 2399-3642 [Electronic] England
• PMID: 31552302 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)

Chemical References

• Bacterial Proteins
• DNA-Binding Proteins
• DosR protein, Mycobacterium tuberculosis
• Tumor Necrosis Factor-alpha
• Protein Kinases
• DevS protein, Mycobacterium tuberculosis
• Protamine Kinase

Topics

• Autophagosomes (immunology, metabolism, microbiology)
• Autophagy
• Bacterial Proteins (genetics, metabolism)
• DNA-Binding Proteins
• Gene Expression Profiling
• Gene Silencing
• Host-Pathogen Interactions (immunology)
• Humans
• Macrophages (immunology, metabolism, microbiology)
• Mutation
• Mycobacterium tuberculosis (enzymology, physiology)
• Phagocytes (immunology, metabolism, microbiology)
• Phosphorylation
• Protamine Kinase (genetics, metabolism)
• Protein Kinases (genetics, metabolism)
• Tuberculosis (immunology, metabolism, microbiology)
• Tumor Necrosis Factor-alpha (genetics, metabolism)
• Virulence