Skip to Search Skip to Global Navigation Skip to Local Navigation Skip to Content
Show/Hide University Links
Dr. Anand K. Ramasubramanian, Ph.D.

Anand K. Ramasubramanian, Ph.D.

Associate Professor

Department of Biomedical Engineering
South Texas Center for Emerging Infectious Diseases

Educational Background:

  • B.S., Ch.E. (Annamalai University, India)
  • M.S., Ch.E. (IISc, India)
  • Ph.D., BioE (Rice University, Houston, TX)

Areas of Teaching Interest:

  • Applied Mathematics
  • Transport Phenomena
  • Cellular Engineering

Areas of Research Interest:

  • Microbial Bioengineering
  • Vascular Mechanobiology

Description of Research:

In the recent years, we have pursued three lines of investigation.

    1. High-throughput antimicrobial drug discovery and diagnostics. Infectious diseases are still the leading cause of death in the world as new organisms and drug resistance strains emerge. There is an urgent need for early detection and targeted treatment of the pathogens. To fill this technology gap, we have developed a miniaturized microbial culture platform that has cut down the time, cost, and reagent use. Our platform consists of several thousand spots of 3-dimensional, 30 nL cultures of single or multiple bacterial (Staphylococcus aureus, Pseudomonas aeruginosa) and fungal (Candida albicans) species grown on glass or paper substrates. We have shown that despite more than 3000-fold reduction in volume, our nano-scale cultures on the chip are comparable to current industry standards. We have used this screen to identify novel drugs and their combinations with effective antimicrobial activity. We have also modified this platform for a rapid and inexpensive point-of-care for testing drug efficacy.
    2. Role of fluid shear stresses and transport on cellular response. The focus of medicine has been on chemical factors as the chief determinant of disease development and treatment. Recently, we have come to recognize that physical factors such as mechanical forces can be just as important. We have investigated the role of fluid shear stresses and transport due to blood flow on infection and inflammation. Using in vitro microscale models of the blood vessels, we have shown that physiological levels of fluid shear stress can significantly upregulate pro-inflammatory responses from monocytes infected with Chlamydia pneumoniae, a pathogen implicated in atherosclerosis. In another study, we have shown that blood flow can monocytes assist in the adhesion of the otherwise non-adherent metastatic breast tumor cells to the microvascular endothelium under flow thus increasing the chances of hematogenous metastasis.
    3. Platelet storage for transfusion. Platelets are transfused to prevent bleeding and induce hemostasis, and can thus be critical in saving lives following trauma. Currently, platelets isolated from volunteers are stored at room temperature (RT) with gentle agitation for up to 5 days, before transfusion. This short shelf-life severely compromises platelet inventories and creates chronic shortages with the major issue being bacterial contamination. To address this issue, we are pursuing refrigerated platelets as a viable product for transfusion. We have shown that refrigerated platelets are superior to platelets stored at RT under standard blood-banking conditions by several metrics: metabolic and hemostatic functions, response to physiologic inhibitors, and clot mechanical properties.  Our work, in collaboration with the U.S. Army, has recently prompted the FDA to clarify that cold-stored platelets may be used as a therapeutic product for active hemorrhage.

Selected Publications

  • Nair, P.M., H.F. Pidcoke, A.P. Cap, A.K. Ramasubramanian (2014), “Effect of cold storage on shear-induced platelet aggregation and clot strength”, J. Trauma Acute Care Surg., 77: S88-93. PMID: 25159368
  • Reddoch, K.M., H.F. Pidcoke, R.K. Montgomery, C.G. Fedyk, A.K. Ramasubramanian*, A.P. Cap* (2014), “Hemostatic capacity of apheresis platelets is better preserved by storage at 4 °C than 22 °C”, Shock, 41: 54-61 (*Co-corresponding authors). PMID: 24169210
  • Cheeniyil, A., S.J. Evani, S.F. Dallo, A.K. Ramasubramanian (2014), “Shear stress upregulates IL-1β secretion by Chlamydia pneumoniae-infected monocytes”, Biotechnology & Bioengineering, 112(4): 838-42. PMID:25336058.
  • Evani, S.J., R.G. Prabhu, V. Gnanaruban, E. Finol, A.K. Ramasubramanian (2013), “Monocytes mediate metastatic breast tumor cell adhesion to endothelium under flow”, FASEB J., 27(8):3017-29. PMID: 23616566.
  • Srinivasan, A., P. Uppuluri, J.L. Lopez-Ribot, A.K. Ramasubramanian (2011), “Development of a high-throughput fungal biofilm chip”, PLoS ONE, 6(4), e19036, PMID: 21544190.
  • M.-Y. Lee*, Kumar, R. A.*, M. Hogg, S. Sukumaran, J.S. Dordick, D.S. Clark (2008), “Three-dimensional cellular microarray for high-throughput toxicology assays”, Proc. Natl. Acad. Sci. (USA), 105, 59-63 (* equal contribution). PMID: 18160535
  • Evani, S.J., R.K. Montgomery, A.K. Murthy, B.P. Arulanandam, and A.K. Ramasubramanian (2010), “Hydrodynamic regulation of monocyte inflammatory response to an obligate intracellular pathogen”, Submitted.

  • Uppuluri, P., A.K. Chaturvedi, A. Srinivasan, M. Banerjee, A.K. Ramasubramanian, J.R. Kohler, D. Kadosh, and J.L. Lopez-Ribot (2010), “Dispersion as an Important Step in the Candida albicans Biofilm Developmental Cycle”, PLoS Pathogen, 6: e1000828

  • R.A. Kumar, N. Prasteyojo, S. Hyunh, and D.S. Clark (2009), “Differential in vitro cytotoxicity of doxorubicin and 5-fluorouracil to cancer and normal human mammary epithelial cells”, Submitted

  • Kumar, R.A., N. Papaiconomou, J. Salminen, J.M. Lee, D.S. Clark and J.M. Prausnitz (2009), “In vitro cytotoxicities of ionic liquids: Effect of cation rings, anions and functional groups”, 24:388-395.

  • Lee, M.-Y.*, Kumar, R. A.*, M. Hogg, S. Sukumaran, J.S. Dordick, D.S. Clark (2008), “Three-dimensional cellular microarray for high-throughput toxicology assays”, PNAS, 105, 59-63 (* equal contribution)

  • J. Salminen, N. Papaiconomou, R.A. Kumar, J.-M. Lee, and J.M. Prausnitz (2007), “Physicochemical properties and toxicities of hydrophobic piperidinium and pyrrolidinium ionic liquids”, Fluid Phase Equilibria, 261, 421-426.

  • Kumar, R.A., D.S. Clark (2006) “High-throughput assays for biocatalysis: applications in drug discovery”, Curr. Opin. Chem. Biol. 10, 162-168.

  • Arora, P., R.A. Kumar and K.V. Venkatesh (1999), “Analysis of the Optimal model for substrate substitutability in continuous microbial cultures”, Chem. Engng. Sci., 54, 987-997.

  • Kumar, R.A., J.-f. Dong, J. Thaggard, M.A. Cruz, J.A. Lopez and L.V. McIntire (2003), “Kinetics of GPIba - VWf-A1 tether bond under flow: Effect of GPIba mutations on the association and dissociation rates”, Biophys. J., 85, 4099-4109.

  • Arora, P., R.A. Kumar and K.V. Venkatesh (1999), “Analysis of the Optimal model for substrate substitutability in continuous microbial cultures”, Chem. Engng. Sci., 54, 987-997.

  • Venkatesh, K.V., P.J. Bhat, R.A. Kumar and P. Doshi (1999), “Quantitative model for Gal4p-mediated expression of the Gal/Mel regulon in S. cerevisiae”, Biotech. Prog. , 15, 51-57.

  • Kumar, R.A. and J.M. Modak (1997), “Transient Analysis of mammalian cell growth in hollow fiber bioreactor”, Chem. Engng. Sci., 52(12), pp. 1845-1860.

 

Back to top