- GVS Home
- Important Dates
- Prospective Scholars
- 2011 Scholars
- The Science of Veterinary Medicine - Research Day
- Past Scholars
- FAQ
- Photos
- Opportunities
- Resources
- Mentors
- 2010 National Veterinary Scholars Symposium
- Contacts for GVS
- Program Sponsors
- 2012 Merial-NIH Program
- Athens Area Information

Georgia Veterinary Scholars Program
GVSP Summer 2011 Scholars
Georgia Veterinary Scholar
|
Faculty Mentor
|
![]() |
|
| Kelly Cummings UGA College of Veterinary Medicine Class of 2014 |
Dr. Kaori Sakamoto Department of Pathology UGA College of Veterinary Medicine |
Development of a murine model for intestinal helminth and Mycobacterium bovis co-infection
Kelly Cummings, Brandon Bringuel, Lindsey Megow, Llewelyn Sellers, Vanessa Ezenwa, Sarah Budischak, Andrew Moorhead, Kaori Sakamoto
Mycobacterial and intestinal helminth co-infection is a problem in veterinary species and in humans in developing countries. Previous studies have focused on the opposing immune responses induced by Mycobacterium bovis and single helminth infections; however, wild hosts are typically infected with multiple parasites, which may further alter immune dynamics. Recent work by the Ezenwa laboratory has shown that anthelminthic treatment of African buffalos leads to a reduction in pulmonary lesions due to M. bovis infection and that immune suppression caused by nematode infection can facilitate the invasion of bovine TB in buffalo. We hypothesize that intestinal helminth infection causes a shift to a T-helper type 2 (Th2) over a type 1 (Th1) response, reducing the ability of the host to control M. bovis infection. To study this interaction, we worked on developing a mouse model by infecting mice with the intestinal nematodes Heligmosomoides polygyrus and Nippostrongylus brasiliensis. Mice in our initial infection group died within seven days due to septicemia. Work with the subsequent infection groups is ongoing. Once this intestinal helminth co-infection is optimized, mice will be intratracheally infected with M. bovis. Local and systemic immune responses will be analyzed by histopathology, immunohistochemistry, flow cytometry, lymphocyte proliferation assays, and serum cytokine analysis.


