The primary role of the Administrative Core is to coordinate research activities among the four individual research projects, the Technology Core, and the Data Management and Resource Dissemination Core. High-quality functional annotation requires experimental effort on multiple scales, from the biochemical/biophysical to the cellular levels. We will combine experimental microbiological studies, in which we examine gene function in the pathogen, with in vitro biochemical analyses on purified gene products. To maximize our collective output the proper leadership and administrative structure must be in place. We recognize a need to set in place an effective environment to foster the full engagement of each investigator and their staffs, and to provide the scope of resources that not only facilitates, but also enhances individual research. The goal of the proposed administrative structure is """"""""efficient integration"""""""". This integration will be key to our major goal of providing the research community with the highest quality functional assignment of as many uncharacterized genes as possible.

Public Health Relevance

Our multi-scale approach to the determination of gene function is beyond the scope of an individual laboratory and must therefore occur within the auspices of a larger program. Appropriate administration of the research program will ensure that we attain our goal of the highest quality functional annotation of uncharacterized genes in NIAID category A and B priority pathogens.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program--Cooperative Agreements (U19)
Project #
1U19AI107792-01
Application #
8597752
Study Section
Special Emphasis Panel (ZAI1-FDS-M (M1))
Project Start
Project End
Budget Start
2013-08-13
Budget End
2014-07-31
Support Year
1
Fiscal Year
2013
Total Cost
$77,798
Indirect Cost
$21,673
Name
University of Chicago
Department
Type
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Herrou, Julien; Willett, Jonathan W; Fiebig, Aretha et al. (2018) Periplasmic protein EipA determines envelope stress resistance and virulence in Brucella abortus. Mol Microbiol :
Tien, Matthew; Fiebig, Aretha; Crosson, Sean (2018) Gene network analysis identifies a central post-transcriptional regulator of cellular stress survival. Elife 7:
Herrou, Julien; Czy?, Daniel M; Fiebig, Aretha et al. (2018) Molecular control of gene expression by Brucella BaaR, an IclR-type transcriptional repressor. J Biol Chem 293:7437-7456
Czy?, Daniel M; Willett, Jonathan W; Crosson, Sean (2017) Brucella abortus Induces a Warburg Shift in Host Metabolism That Is Linked to Enhanced Intracellular Survival of the Pathogen. J Bacteriol 199:
Mitchell, Anthony; Tam, Christina; Elli, Derek et al. (2017) Glutathionylation of Yersinia pestis LcrV and Its Effects on Plague Pathogenesis. MBio 8:
Herrou, Julien; Willett, Jonathan W; Czy?, Daniel M et al. (2017) Conserved ABC Transport System Regulated by the General Stress Response Pathways of Alpha- and Gammaproteobacteria. J Bacteriol 199:
Baric, Ralph S; Crosson, Sean; Damania, Blossom et al. (2016) Next-Generation High-Throughput Functional Annotation of Microbial Genomes. MBio 7:
Czy?, Daniel M; Jain-Gupta, Neeta; Shuman, Howard A et al. (2016) A dual-targeting approach to inhibit Brucella abortus replication in human cells. Sci Rep 6:35835
Willett, Jonathan W; Herrou, Julien; Czyz, Daniel M et al. (2016) Brucella abortus ?rpoE1 confers protective immunity against wild type challenge in a mouse model of brucellosis. Vaccine 34:5073-5081
Herrou, Julien; Czy?, Daniel M; Willett, Jonathan W et al. (2016) WrpA Is an Atypical Flavodoxin Family Protein under Regulatory Control of the Brucella abortus General Stress Response System. J Bacteriol 198:1281-93

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