Valery Z. Grdzelishvili, Ph.D.
Professor, Molecular Virology and Cancer Therapy
RESEARCH INTERESTS: molecular virology, cancer biology, anticancer therapy based on replication-competent viruses (“oncolytic virotherapy”), virus-host interactions in normal and cancer cells, host factors of virus replication in normal and cancer cells, innate immunity in normal and cancer cells, virus-based gene therapy and vaccine vectors
|Grdzelishvili Lab Twitter: https://twitter.com/Virology_Lab|
|Dr. Grdzelishvili’s publications at PubMed|
|Dr. Grdzelishvili’s Google Scholar Profile|
- Ph.D. in Virology: Lomonosov Moscow State University, Department of Virology, Russia (1998)
- M.S./B.S. in Biochemistry: Lomonosov Moscow State University, Department of Virology, Russia (1995)
- Professor (July 2018-present): University of North Carolina at Charlotte, Department of Biological Sciences
- Associate Professor (July 2012-June 2018): University of North Carolina at Charlotte, Department of Biological Sciences
- Assistant Professor (July 2006-June2012): University of North Carolina at Charlotte, Department of Biological Sciences
- Research Assistant Professor (2004-2006): University of Florida College of Medicine, Dept. of Molecular Genetics and Microbiology [Mentor: Dr. Sue Moyer]
- Postdoctoral Research Associate (2001 – 2004): University of Wisconsin-Madison, Institute for Molecular Virology and Howard Hughes Medical Institute (HHMI) [Mentor: Dr. Paul Ahlquist]
- Postdoctoral Research Associate (1999 – 2000): University of Florida, Institute of Food and Agricultural Sciences, CREC [Mentor: Dr. William Dawson]
Dr. Grdzelishvili’s laboratory is focused on molecular biology and applications of nonsegmented negative-strand (NNS) RNA viruses (order Mononegavirales). The major focus is the exploitation of existing and engineering new NNS RNA viruses [vesicular stomatitis virus (VSV) in particular] as clinically important anticancer (“oncolytic”) agents. We are particularly interested in the identification and characterization of cellular and viral determinants of susceptibility or resistance of pancreatic cancer cells to VSV and other oncolytic viruses. Other projects are focused on mechanistic understanding of viral replication cycle of NNS RNA viruses, which is fundamental to developing reagents to prevent and combat viral diseases. The order Mononegavirales includes many important human and animal pathogens, such as rabies, measles, Ebola, Marburg, Nipah, Hendra, and other viruses.
Grdzelishvili’s Lab (October 2019, left to right): Valery Grdzelishvili, Abdul Hajjar, Isha Wilson, Sara Seegers, Dakota Goad, Britanie Blackhurst, Molly Penton
CLICK ON PICTURE
Grdzelishvili’s Lab (October 2019, left to right): Abdul Hajjar, Sara Seegers, Dakota Goad, Molly Penton, Isha Wilson, Britanie Blackhurst, Valery Grdzelishvili
CLICK ON PICTURE
ONCOLYTIC VIROTHERAPY OVERVIEW
(the illustration was created by Dr. Eric Hastie and is from Hastie and Grdzelishvili 2012 “Vesicular stomatitis virus as a flexible platform for oncolytic virotherapy against cancer” Journal of General Virology, 93:2529-45)
Scheme of VSV-based OV therapy. (a) Reverse genetics allows generation of a recombinant VSV encoding a foreign gene of interest between the VSV G and L genes. The asterisk above M indicates M protein mutation(s) resulting in VSV attenuation in normal cells. Plasmids encoding VSV replication machinery and the modified genome are co-transfected into a cell line, and complete virions are produced and amplified using good manufacturing practices. (b) For evaluation of oncolytic efficacy, VSV can be administered directly, via cell-based delivery, or in combination with other treatments (chemotherapy, radiotherapy or other OVs). (c) In infected cells, VSV recombinants may express a foreign gene that facilitates killing of the adjacent uninfected cancer cells (e.g. suicide-gene approach or immunostimulation). Innate antiviral responses and other mechanisms prevent cell death in normal cells. Ideally, stimulation of innate and adaptive immune cells by VSV and/or the foreign gene product should lead to tumour-specific immune responses, including memory responses that prevent cancer recurrence.