The challenge of drug-resistant microbes requires that a new generation of basic scientists be broadly trained and educated in anti-infective research so that a cadre of investigators will be available in the future to combat this global health problem. Coupled with the problem of resistance, this need is especially acute given the reduced number of new, effective antibiotics that have entered clinical practice in the past two decades. Thus, the objective of this new training grant at Emory University is to provide high quality training to a select group of highly motivated graduate students for careers as independent investigators in research on anti- infectives. The program will select three PhD candidates yearly from four graduate programs within the Graduate Division of Biological and Biomedical Sciences of Emory University for a two year period of training in the areas of antimicrobial resistance and therapeutic discovery. These graduate programs include faculty members from basic science and clinical departments of the School of Medicine, Emory College of Arts and Sciences and the Centers for Disease Control and Prevention (CDC). Educational training will consist of a course of study and programmatic events in sub-disciplines that emphasize research and education in anti-infective resistance and drug development; research training opportunities are provided in 25 laboratories with active research programs in these areas of research.
This new T32 grant will provide training in research on anti-infectives for graduate students. The training faculty work on a wide range of projects dealing with anti-infective resistance, drug discovery and development with respect to major microbial pathogens and their associated diseases that impact public health, including tuberculosis, malaria, HIV/AIDS, hepatitis, sexually transmitted infections, pneumonia, meningitis and skin/soft tissue infections. The over-arching goal of this training program is to prepare graduate students for careers as investigators to continue research on medically important pathogens and anti-infective discovery.
| Anderson, Sarah E; Sherman, Edgar X; Weiss, David S et al. (2018) Aminoglycoside Heteroresistance in Acinetobacter baumannii AB5075. mSphere 3: |
| Trost, Jessica F; LeMasters, Elizabeth H; Liu, Feng et al. (2018) Development of a high-throughput assay to detect antibody inhibition of low pH induced conformational changes of influenza virus hemagglutinin. PLoS One 13:e0199683 |
| Nawrocki, Kathryn L; Wetzel, Daniela; Jones, Joshua B et al. (2018) Ethanolamine is a valuable nutrient source that impacts Clostridium difficile pathogenesis. Environ Microbiol 20:1419-1435 |
| Phipps, Kara L; Marshall, Nicolle; Tao, Hui et al. (2017) Seasonal H3N2 and 2009 Pandemic H1N1 Influenza A Viruses Reassort Efficiently but Produce Attenuated Progeny. J Virol 91: |
| Prezioso, Samantha M; Brown, Nicole E; Goldberg, Joanna B (2017) Elfamycins: inhibitors of elongation factor-Tu. Mol Microbiol 106:22-34 |
| Hudson, Lauren E; Anderson, Sarah E; Corbett, Anita H et al. (2017) Gleaning Insights from Fecal Microbiota Transplantation and Probiotic Studies for the Rational Design of Combination Microbial Therapies. Clin Microbiol Rev 30:191-231 |
| Owings, Joshua P; Kuiper, Emily G; Prezioso, Samantha M et al. (2016) Pseudomonas aeruginosa EftM Is a Thermoregulated Methyltransferase. J Biol Chem 291:3280-90 |
| Nawrocki, Kathryn L; Edwards, Adrianne N; Daou, Nadine et al. (2016) CodY-Dependent Regulation of Sporulation in Clostridium difficile. J Bacteriol 198:2113-30 |
| Edwards, Adrianne N; Karim, Samiha T; Pascual, Ricardo A et al. (2016) Chemical and Stress Resistances of Clostridium difficile Spores and Vegetative Cells. Front Microbiol 7:1698 |
| Band, Victor I; Crispell, Emily K; Napier, Brooke A et al. (2016) Antibiotic failure mediated by a resistant subpopulation in Enterobacter cloacae. Nat Microbiol 1:16053 |
Showing the most recent 10 out of 15 publications
