This new proposal, Biodefense Training in Host-Pathogen Interactions, is intended as a seed project for rigorous scientific education of graduate students in the study of pathogenic microbes, their mechanisms of establishing human or animal infections, as well as the discovery of novel therapies or countermeasures that prevent human disease. The proposal draws on scientific strengths of University of Chicago faculty in the Committees on Microbiology and Immunology as well as on infrastructure provided through the recently established Great Lakes Regional Center of Excellence in Biodefense &Emerging Infectious Diseases, with resources in core structures that permit the study of pathogens via state of the art microscopy, mass spectrometry, immunology, animal infection and genomics facilities. Infrastructural commitments at the University of Chicago permit work on host-pathogen interactions in BSL-2 and BSL-3 laboratories, specifically designed for CDC select agents of categories A-C as well as on the Ricketts Regional Biocontainment Laboratory at Argonne National Laboratory, a federal laboratory that is constructed and operated by the University of Chicago for the National Institute of Allergy and Infectious Diseases. The commitment of University of Chicago faculty towards research and training excellence in biodefense and host-pathogen research is reflected in the recent establishment of the Department of Microbiology. Expansive growth with the appointment of seven new faculty over the next five years is accompanied by the recent expansion of graduate training in Microbiology and by the already excellent achievements of faculty and graduate students in this area. Sixteen training faculty study bacterial pathogenesis, animal viruses, viral physiology and pathogenesis, plant pathogenesis, drug resistant microbes, microbial toxins and the immune response to infections. Trainees are selected from a pool of 150 applicants with Bachelor's degree and average GRE and GPA scores of 1375+5 (81%) and 3.3 respectively. The ultimate goals of our training program are ambitious and aim at establishing a premier research program in biodefense and host-pathogen interactions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Institutional National Research Service Award (T32)
Project #
5T32AI065382-05
Application #
7623156
Study Section
Microbiology and Infectious Diseases B Subcommittee (MID)
Program Officer
Peters, Kent
Project Start
2005-09-01
Project End
2010-08-31
Budget Start
2009-08-01
Budget End
2010-08-31
Support Year
5
Fiscal Year
2009
Total Cost
$159,856
Indirect Cost
Name
University of Chicago
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Ohr, Ryan Jay; Anderson, Mark; Shi, Miaomiao et al. (2017) EssD, a Nuclease Effector of the Staphylococcus aureus ESS Pathway. J Bacteriol 199:
Aly, Khaled A; Anderson, Mark; Ohr, Ryan Jay et al. (2017) Isolation of a Membrane Protein Complex for Type VII Secretion in Staphylococcus aureus. J Bacteriol 199:
Anderson, Mark; Ohr, Ryan Jay; Aly, Khaled A et al. (2017) EssE Promotes Staphylococcus aureus ESS-Dependent Protein Secretion To Modify Host Immune Responses during Infection. J Bacteriol 199:
Pickard, Joseph M; Maurice, Corinne F; Kinnebrew, Melissa A et al. (2014) Rapid fucosylation of intestinal epithelium sustains host-commensal symbiosis in sickness. Nature 514:638-41
Anderson, Mark; Aly, Khaled A; Chen, Yi-Hsing et al. (2013) Secretion of atypical protein substrates by the ESAT-6 secretion system of Staphylococcus aureus. Mol Microbiol 90:734-43
Dolan, Patrick T; Zhang, Chaoying; Khadka, Sudip et al. (2013) Identification and comparative analysis of hepatitis C virus-host cell protein interactions. Mol Biosyst 9:3199-209
Chen, Yi-Hsing; Anderson, Mark; Hendrickx, Antoni P A et al. (2012) Characterization of EssB, a protein required for secretion of ESAT-6 like proteins in Staphylococcus aureus. BMC Microbiol 12:219
Chukkapalli, Vineela; Heaton, Nicholas S; Randall, Glenn (2012) Lipids at the interface of virus-host interactions. Curr Opin Microbiol 15:512-8
Coller, Kelly E; Heaton, Nicholas S; Berger, Kristi L et al. (2012) Molecular determinants and dynamics of hepatitis C virus secretion. PLoS Pathog 8:e1002466
Nguyen-Mau, Sao-Mai; Oh, So-Young; Kern, Valerie J et al. (2012) Secretion genes as determinants of Bacillus anthracis chain length. J Bacteriol 194:3841-50

Showing the most recent 10 out of 23 publications