Tuning the Mycobacterium tuberculosis Alternative Sigma Factor SigF through the Multidomain Regulator Rv1364c and Osmosensory Kinase Protein Kinase D

Author:

Misra Richa1,Menon Dilip23,Arora Gunjan1,Virmani Richa1,Gaur Mohita4,Naz Saba45,Jaisinghani Neetika23,Bhaduri Asani1,Bothra Ankur23,Maji Abhijit1,Singhal Anshika1,Karwal Preeti1,Hentschker Christian6,Becher Dörte6,Rao Vivek23,Nandicoori Vinay K.5,Gandotra Sheetal23,Singh Yogendra14

Affiliation:

1. Allergy and Infectious Disease Unit, CSIR-Institute of Genomics and Integrative Biology, Delhi, India

2. Respiratory Disease Biology, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India

3. Academy of Scientific and Innovative Research (AcSIR), New Delhi, India

4. Department of Zoology, University of Delhi, Delhi, India

5. National Institute of Immunology, Delhi, India

6. Institute of Microbiology, Ernst-Moritz-Arndt University Greifswald, Greifswald, Germany

Abstract

Mycobacterium tuberculosis , capable of latently infecting the host and causing aggressive tissue damage during active tuberculosis, is endowed with a complex regulatory capacity built of several sigma factors, protein kinases, and phosphatases. These proteins regulate expression of genes that allow the bacteria to adapt to various host-derived stresses, like nutrient starvation, acidic pH, and hypoxia. The cross talk between these systems is not well understood. SigF is one such regulator of gene expression that helps M. tuberculosis to adapt to stresses and imparts virulence. This work provides evidence for its inhibition by the multidomain regulator Rv1364c and activation by the kinase PknD. The coexistence of negative and positive regulators of SigF in pathogenic bacteria reveals an underlying requirement for tight control of virulence factor expression.

Funder

CSIR Task Force

DST Purse Grant

DST-SERB

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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