Santasabuj Das
Scientist E
Clinical Medicine
National Institute of Cholera and Enteric Diseases
India
Biography
Dr. Santasabuj Das is currently appointed as Scientist D at National Institute of Cholera and Enteric Diseases (NICED), Kolkata. He is also in-charge of the Biomedical Informatics Center of ICMR at NICED and the Biosafety Officer of the institute. Dr Das graduated in medical sciences (MBBS) in 1989 from the University of Calcutta and completed post-graduation (MD, General medicine) in 1996 from the same university. His post-doctoral training includes senior residency (clinical) at the Department of Clinical Immunology, Sanjay Gandhi Post-graduate Institute of Medical Sciences, Lucknow (1998) and post-doctoral fellowships at National Center for Biological Sciences, Tata Institute of Fundamental Research, Bangalore, India (1998-2000); Kimmel Cancer Centre, Thomas Jefferson University, Philadelphia, PA, USA and Molecular Oncology Research Institute, Tufts-New England Medical Center, Boston, MA, USA. During the early part of his research career, Dr Das worked on the role of Notch signaling in cervical carcinogenesis and transcriptional regulation of MHC Class II molecules. Susequently, he studied the role of Tpl2, an upstream MAPKinase, in the pro-inflammatory cytokine (TNF-a and IL-1b)-induced signal transduction pathways. Dr Das joined NICED in January, 2005 and initiated research on several aspects of the mucosal innate immune responses. His group is studying the regulation of cationic antimicrobial peptide release from the intestinal epithelial cells by enteric pathogens and host gene expression by bacterial motility protein flagellin. Studies to identify new virulence factors of Salmonella typhi and to explore the role of microRNAs in the pathogenesis of hepatitis B and HIV-1 infection are also underway. Dr. Das has 2 PhD students at present and he is the principal investigator of 4 extramural projects, 2 each from the Indian and international funding agencies. He has 5 publications in reputed international journals.
Research Interest
Small Cationic Antimicrobial peptides (AMPs): Regulation and Function Small cationic endogenous peptides with antimicrobial properties form a critical component of the host innate immune system and protect the body from pathogens that invade through the mucosal surfaces. In addition to direct microbicidal activities against a broad range of organisms, AMPs possess pleotrophicimmunomodulatory functions, which protect the host from pathogenic infections as well as a number of autoimmune, inflammatory and neoplastic diseases. While newer functions have been described recently, published reports suggest that downregulation of the AMPs may serve as an efficient mode of immune evasion by the mucosal pathogens and perhaps tumours. Both natural and synthetic AMPs have been proposed as exciting novel therapeutic agents for infectious and non-infectious diseases. A particularly useful approach may be to induce the production of endogenous peptides. We are studying the regulatory mechanisms behind AMP production and their modulation by intestinal pathogens. Synthetic peptides targeting microbial virulence factors are also under investigation. Salmonella Typhi: Virulence Mechanisms and Vaccine Development Salmonella Typhi poses significant threat to public health worldwide and the infection is endemic in parts of India. While pathogenesis of the disease (typhoid or enteric fever) is incompletely understood, treatment failures are not uncommon due to drug resistance. This is further complicated by the limited effectiveness of the currently available vaccines, particularly in very young children where prevalence of the disease is increasing. This necessitates further understanding of pathogenesis and identification of new drug / vaccine targets. More than half of all S. Typhi genes are currently un-annotated.We employed computational approaches coupled with experimental validation to functionally characterize genes with potential role in the pathogenesis of S. Typhi.Our experiments involved the use of mutant and complemented bacteria and the purified recombinant proteins in vitro (cell line based experiments) and in vivo (iron overload mouse model of S. Typhi developed in the lab). We have also identified novel candidates for the development of subunit vaccines. Indigenous Probiotics: Role in regulatory immune responses Probiotics are live microorganisms which, when administered in adequate amounts, confer a health benefit on the host. Protection is observed against various infectious and non-infectious diseases, and mainly achieved through modulation of the host immune responses. We screened indigenous probiotic strains on the basis of their ability to generate regulatory responses in the intestine, which would help to develop an improved therapeutic strategy against autoimmune and inflammatory disorders. Several strains induced significant numbers of CD103+tolerogenic dendritic cells (DCs) and CD4+CD25+FoxP3+ T-regulatory cells, in addition to regulatory cytokines/chemokines (IL-10 and TGF- ß) in the mouse intestine and protected the animals against colitis induced by trinitrobenzene sulfonic acid (TNBS) (a model for inflammatory bowel disease) and SalmonellaTyphimurium-induced enterocolitis. We are also investigating the probiotics-derived molecules and the underlying mechanisms responsible for intestinal tolerogenic responses. Bioinformatics: Computational prediction and network analysis of host-pathogen interactions, molecular modeling and drug designing, comparative genomics, development of cholera portal.
Publications
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Thakur B. K., P. Saha, G. Banik, D. R. Saha, S. Grover, V. K. Batish, and S. Das. 2016. Live and heat-killed probiotic Lactobacillus casei Lbs2 protects from experimental colitis through Toll-like receptor 2-dependent induction of T-regulatory response. Int Immunopharmacol. 36:39-50
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Thakur B. K., N. Dasgupta, A. Ta, and S. Das. 2016. Physiological TLR5 expression in the intestine is regulated by differential DNA binding of Sp1/Sp3 through simultaneous Sp1 dephosphorylation and Sp3 phosphorylation by two different PKC isoforms. Nucleic Acids Res. 2016 Jul 8;44(12):5658-72
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Dasgupta N., B. K. Thakur, A. Ta, P. Dutta, and S. Das. 2017. Suppression of Spleen Tyrosine Kinase (Syk) by Histone Deacetylation Promotes, Whereas BAY61-3606, a Synthetic Syk Inhibitor Abrogates Colonocyte Apoptosis by ERK Activation. J Cell Biochem. 118(1):191-203.