Skip header information|
Wadsworth Center Home - Science in the Pursuit of Health|
NY.gov Portal State Agency Listing
Main Body

Investigators and Program Directors

April D. Burch

April D. Burch

Research Scientist, Wadsworth Center, Microbial Genetics
Assistant Professor, School of Public Health, Biomedical Sciences

Ph.D., University of Arizona, Tucson (2000)
Postdoctoral Training at the University of Connecticut Health Center, Farmington, CT

E-mail: aburch@wadsworth.org

Research Interests

Subcellular localization of the host chaperones Hsc70 and Hsp90 during HSV-1 infectionVirus Assembly and the Host-Pathogen Interface

Many viruses have evolved mechanisms to not only counter, but also exploit the cellular reaction to infection. For example, during infection, several stress pathways are activated in response to incoming nucleic acids, changes in the amount of unfolded proteins, or the oxidation state of the cell. It has recently been shown that Herpes Simplex Virus Type-1 (HSV-1) has evolved a mechanism to sequester various stress-activated chaperone molecules within discrete compartments in the infected cell (Figure 1).

We are interested in:

  • whether these chaperone molecules are required for virus-specific mechanisms, such as virus assembly or DNA encapsidation, and
  • whether the redistribution of these stress factors results in a temporary anti-apoptotic state that is beneficial for virus production.

Our research will provide information about chaperone-dependent viral processes and may reveal connections between viral infection and the activation of cancer-related anti-apoptotic pathways. Moreover, unique interactions made between viral proteins and cellular chaperone molecules may represent a new frontier of targets for antiviral therapies directly aimed at the host-pathogen interface.

>> Select Publications

Contact Information

Phone: 518-402-2233
Fax: 518-402-4773
E-mail: aburch@wadsworth.org