Stuti K DESAI
Alumni, Mechanobiology Institute, National University of Singapore
What is Myosin?
What is Myosin? An Introduction to the Myosin Superfamily of Proteins Myosin I has unique tail domain(s) relative to other myosin members which allows myosin I to bind to membrane lipids or to more [...]
Membrane Dynamics
What are cell membranes? What are the physiological functions of biological membranes? Eukaryotic cells and their organelles are enveloped by viscoelastic layers made of lipids and proteins. These layers are generally referred to as [...]
What steps are involved in the myosin powerstroke?
What steps are involved in the myosin powerstroke? Each myosin motor protein possesses ATPase activity and functions in a cyclical manner that couples ATP binding and hydrolysis to a conformational change in the protein. [...]
What is Myosin Light Chain Kinase?
What is Myosin Light Chain Kinase? Myosin light chain kinase (MLCK) is a calcium/calmodulin-dependent serine/threonine kinase, belonging to the immunoglobulin superfamily. It phosphorylates the regulatory myosin light chains of myosin II, in order to [...]
What are cytoskeletal cages?
What are cytoskeletal cages? Cytoskeletal components can assemble into cage-like structures within the cell. These cages serve to segregate intracellular regions or organelles, and can protect their contents from mechanical stress. At the level [...]
Why are membrane lipids asymmetrical?
Why are membrane lipids asymmetrical? The human red blood cell is functionally specialized for transporting oxygen. In order to maximize oxygen capacity, it has no nucleus or organelles, consisting primarily of plasma membrane and [...]
Stuti K Desai
Alumni 2020
Principal Investigator
Research Interests
Molecular Mechanisms of Mechanobiology
A fundamental trait shared amongst many mammalian pathogens is their ability to exist in different forms in order to survive and replicate in often fluctuating host and non-host environments. Two important gut pathogens, Salmonella Typhimurium and Salmonella Typhi, which cause gastroenteritis and typhoid fever, respectively, survive inside host cells by activation of a specific class of virulence genes. Salmonellae also develop to form hardy multi-cellular communities, called biofilms, on host tissues for successful survival and persistence in asymptomatic carriers. An active area of research focuses on understanding how the genetic program is regulated in coordination with environmental changes to evoke lifestyle changes. We recently discovered that SsrB, the transcriptional regulator of virulence genes, has the additional function of inducing biofilm formation by activating expression of the central biofilm regulator, CsgD. Generally, specific environmental changes activate a membrane-bound kinase, which in turn transfers the phosphoryl group to a transcriptional regulator in order to regulate virulence gene transcription. But, we discovered that even without phosphorylation, SsrB retains the ability to bind DNA and relieve the H-NS-mediated repressive effect on csgD transcription. SsrB is thus a molecular switch which drives the twin lifestyles of Salmonella Typhimurium; as SsrB~P, when phosphorylated by an actived SsrA kinase, it activates around 30 virulence genes required for survival within the host; and as SsrB, in the case when SsrA is inactive or absent, it counters transcriptional silencing at csgD to form biofilms.
For this study, we utilized the highly collaborative atmosphere at MBI and studied the behavior of the activator, SsrB, and the repressor, H-NS, at the csgD regulatory site using single molecule approaches with Prof. Yan Jie’s group. Going forward, I want to build on the diverse expertise at MBI and other groups in the region to extend these findings and study the specific mechanisms of lifestyle changes in more aggressive strains of Salmonella and validate the underlying signaling pathways in heterologous hosts as model systems.
Research Areas
Bacterial gene regulation, Biofilms, Host-pathogen interactions and Virulence strategies of Salmonellae
Biography
Dr. Stuti Desai joined the group of Prof. Linda Kenney at the Mechanobiology Institute, in 2012, after obtaining her doctorate from the Indian Institute of Science, Bangalore, India, under the guidance of Prof. Subramony Mahadevan. Her graduate studies involved deciphering the regulatory mechanisms that maintain the beta-glucoside utilization systems in a silent state in commensal as well as pathogenic gut bacteria. Prior to that, she studied Biochemistry for her Masters degree at the Maharaja Sayajirao University of Baroda, Baroda, India.
Recent Publications
- Desai SK, and Kenney LJ. Switching Lifestyles Is an in vivo Adaptive Strategy of Bacterial Pathogens. Front Cell Infect Microbiol 2019; 9:421. [PMID: 31921700]
- Desai SK, Padmanabhan A, Harshe S, Zaidel-Bar R, and Kenney LJ. Salmonella biofilms program innate immunity for persistence in Caenorhabditis elegans. Proc. Natl. Acad. Sci. U.S.A. 2019;. [PMID: 31160462]
- Dykas MM, Desai SK, Patra A, Motapothula MR, Poddar K, Kenney LJ, and Venkatesan T. Identification of Biofilm Inhibitors by Screening Combinatorial Libraries of Metal Oxide Thin Films. ACS Appl Mater Interfaces 2018;. [PMID: 29553712]
- Desai SK, and Kenney LJ. To ∼P or Not to ∼P? Non-canonical Activation by Two-Component Response Regulators. Mol. Microbiol. 2016;. [PMID: 27656860]
- Desai SK, Winardhi RS, Periasamy S, Dykas MM, Jie Y, and Kenney LJ. The horizontally-acquired response regulator SsrB drives a Salmonella lifestyle switch by relieving biofilm silencing. Elife 2016; 5. [PMID: 26880544]
