This application represents the first competitive renewal for our Training in Bacteriology T32 program that currently supports 3 predoctoral and 1 Ph.D. postdoctoral trainees per year. Our program, which is based at the University of Pennsylvania and Children's Hospital of Philadelphia, includes 10 laboratories directed by well established principle investigators located on a single contiguous campus. This program has allowed us to recruit some of the best and brightest trainees from among a talented pool at Penn where students and post-docs have a very large number of microbiology labs to choose among. The organized training mission of this program has helped our efforts to collaborate and interact more effectively as a group: unlike our first application, our trainers now have several joint NIH grants, a growing number of joint publications, and a network of collaborations that involve our trainees. Compared to four years ago, our program has five new trainers with more likely to be added in the near future as several new assistant professors establish their research programs. Our research in progress meetings and seminars within the microbiology program have helped spur the rapid growth of exciting, collaborative work in bacterial pathogenesis, microbial immunopathogenesis, and bacterial metagenomics, with institutional support for deep-sequencing facilities, bioinformatics, and a germ-free mouse core playing important roles in these efforts. Because of our increasing emphasis on genomic approaches and technologies, we have updated the title of our program to Training in Microbial Pathogenesis and Genomics to more accurately reflect its breadth by including microbial genomic studies. This rapidly evolving area has been the focus of the projects chosen by three of our best recent predoctoral trainees as well as one of our predoctoral graduates who is now a postdoctoral fellow with Jeff Gordon at Washington University. In light of this, we have modified our training program to accommodate trainees who are interested in microbial genomics, adding new mentors, courses, and training activities. To date, a total of 12 trainees from 7 different laboratories have been supported by this T32, including 5 Ph.D. students, 4 M.D./Ph.D. students and 3 Ph.D. postdoctoral fellows. Of our trainees, 7/12 are been women and 3/12 are under-represented minorities. The research opportunities provided by the trainers coupled with strong institutional commitment and an extensive and well-organized training program will continue to provide excellent training in microbial pathogenesis and genomics to both students and postdoctoral fellows.

Public Health Relevance

The enclosed application is for renewal for our Training Program in Microbial Pathogenesis and Genomics. Our program, which is based at the University of Pennsylvania, will support the research of 3 predoctoral and 1 Ph.D. postdoctoral trainees per year in one of 10 laboratories directed by well established principle investigators. The training experience will enable a talented group of trainees to further our understanding of and address the increasing public health problem of infectious diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Institutional National Research Service Award (T32)
Project #
5T32AI060516-10
Application #
8852043
Study Section
Microbiology and Infectious Diseases B Subcommittee (MID)
Program Officer
Coomes, Stephanie
Project Start
2006-07-01
Project End
2017-05-31
Budget Start
2015-06-01
Budget End
2017-05-31
Support Year
10
Fiscal Year
2015
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Mo, Charlie Y; Culyba, Matthew J; Selwood, Trevor et al. (2018) Inhibitors of LexA Autoproteolysis and the Bacterial SOS Response Discovered by an Academic-Industry Partnership. ACS Infect Dis 4:349-359
Carey, Jeffrey N; Mettert, Erin L; Roggiani, Manuela et al. (2018) Regulated Stochasticity in a Bacterial Signaling Network Permits Tolerance to a Rapid Environmental Change. Cell 173:196-207.e14
Kubiak, Jeffrey M; Culyba, Matthew J; Liu, Monica Yun et al. (2017) A Small-Molecule Inducible Synthetic Circuit for Control of the SOS Gene Network without DNA Damage. ACS Synth Biol 6:2067-2076
Zwack, Erin E; Feeley, Eric M; Burton, Amanda R et al. (2017) Guanylate Binding Proteins Regulate Inflammasome Activation in Response to Hyperinjected Yersinia Translocon Components. Infect Immun 85:
Hergott, Christopher B; Roche, Aoife M; Tamashiro, Edwin et al. (2016) Peptidoglycan from the gut microbiota governs the lifespan of circulating phagocytes at homeostasis. Blood 127:2460-71
Yadavalli, Srujana S; Carey, Jeffrey N; Leibman, Rachel S et al. (2016) Antimicrobial peptides trigger a division block in Escherichia coli through stimulation of a signalling system. Nat Commun 7:12340
Hunt, Vicky L; Tsai, Isheng J; Coghlan, Avril et al. (2016) The genomic basis of parasitism in the Strongyloides clade of nematodes. Nat Genet 48:299-307
Alex, Aneesh; Tait Wojno, Elia D; Artis, David et al. (2016) Label-Free Imaging of Eosinophilic Esophagitis Mouse Models Using Optical Coherence Tomography. Methods Mol Biol 1422:127-36
Hergott, Christopher B; Roche, Aoife M; Naidu, Nikhil A et al. (2015) Bacterial exploitation of phosphorylcholine mimicry suppresses inflammation to promote airway infection. J Clin Invest 125:3878-90
Zwack, Erin E; Snyder, Annelise G; Wynosky-Dolfi, Meghan A et al. (2015) Inflammasome activation in response to the Yersinia type III secretion system requires hyperinjection of translocon proteins YopB and YopD. MBio 6:e02095-14

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