This is a revised renewal application for a training program in Molecular and Cellular Bacterial Pathogenesis (MCBP). Progress in molecular and cellular biology over the last 20 years now permits major gains in our understanding of bacterial pathogenesis. These advances will lead to the development of better medical treatments, drugs, and vaccines for the control of human and animal infections. The study of pathogenesis requires that the researcher have expertise in the cellular and molecular biology of both the host and the pathogen. The researcher also requires training in the types of problems encountered during the study of pathogenic mechanisms and in the types of experimental approaches that can be used to solve these problems. For efficient progress to be made in pathogenesis research, it is also important that the researcher be fully aware of what is known about the natural history and pathology of the infections being studied. Knowledge of infection mechanisms of other pathogens is also important. To facilitate the progress of research on bacterial pathogenesis, we have developed this training program for two pre- and two postdoctoral positions. The preceptors include 14 faculty members with strong programs in basic bacterial pathogenesis and bacterial epidemiology, who have mutually interactive research and training programs in their laboratories. The foundation of the predoctoral program is a multi-departmental graduate training program in Cellular and Molecular Biology. This program recruits students from all over the country and the world for Ph.D. training in the biomedical sciences at The University of Alabama at Birmingham (UAB). During their first year at UAB, these students take a rigorous program of core courses in biochemistry, prokaryotic and eukaryotic genetics, cell biology, and immunology. After lab rotations in the first year, the students select a preceptor in one of the participating basic science departments or medical divisions. Their subsequent training in bacterial pathogenesis is under the auspices of the graduate programs of the Departments of Microbiology or Biochemistry. To be appointed to the MCBP program, students must complete their core courses, pass their preliminary exams, and select an appropriate project in bacterial pathogenesis with a MCMP preceptor. Subsequent training involves research supervision from the MCMP advisory committee, advanced courses in bacterial pathogenesis, a bacterial pathogenesis journal club, and laboratory and departmental seminar series. PhD. and M.D. postdoctoral trainees are also required to take the bacterial pathogenesis course and join the journal club. They may also take some of the CMB core courses if they have deficiencies in basic science that need to be remedied. The MCBP advisory committee will advise the trainees in their research and training programs and in their search for a job or postdoctoral position at the completion of their MCBP training. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Institutional National Research Service Award (T32)
Project #
5T32AI007041-25
Application #
7475669
Study Section
Microbiology and Infectious Diseases B Subcommittee (MID)
Program Officer
Mcsweegan, Edward
Project Start
1976-07-01
Project End
2010-06-30
Budget Start
2008-07-01
Budget End
2010-06-30
Support Year
25
Fiscal Year
2008
Total Cost
$238,383
Indirect Cost
Name
University of Alabama Birmingham
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
063690705
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Larson, Thomas R; Yother, Janet (2017) Streptococcus pneumoniae capsular polysaccharide is linked to peptidoglycan via a direct glycosidic bond to ?-D-N-acetylglucosamine. Proc Natl Acad Sci U S A 114:5695-5700
Barbee, Lindley A; Dhanireddy, Shireesha; Tat, Susana A et al. (2015) Barriers to Bacterial Sexually Transmitted Infection Testing of HIV-Infected Men Who Have Sex With Men Engaged in HIV Primary Care. Sex Transm Dis 42:590-4
Jones, Christopher M; Wells, Ryan M; Madduri, Ashoka V R et al. (2014) Self-poisoning of Mycobacterium tuberculosis by interrupting siderophore recycling. Proc Natl Acad Sci U S A 111:1945-50
Barbee, Lindley A (2014) Preparing for an era of untreatable gonorrhea. Curr Opin Infect Dis 27:282-7
Wells, Ryan M; Jones, Christopher M; Xi, Zhaoyong et al. (2013) Discovery of a siderophore export system essential for virulence of Mycobacterium tuberculosis. PLoS Pathog 9:e1003120
Ren, Bing; Li, Jie; Genschmer, Kristopher et al. (2012) The absence of PspA or presence of antibody to PspA facilitates the complement-dependent phagocytosis of pneumococci in vitro. Clin Vaccine Immunol 19:1574-82
Bolland, Jeffrey R; Simmons, Warren L; Daubenspeck, James M et al. (2012) Mycoplasma polysaccharide protects against complement. Microbiology 158:1867-73
Coats, Mamie T; Murphy, Trudy; Paton, James C et al. (2011) Exposure of Thomsen-Friedenreich antigen in Streptococcus pneumoniae infection is dependent on pneumococcal neuraminidase A. Microb Pathog 50:343-9
Wang, Lan; Clark, Mark E; Crossman, David K et al. (2010) Abundant lipid and protein components of drusen. PLoS One 5:e10329
Callahan, Brian; Nguyen, Kiet; Collins, Alissa et al. (2010) Conservation of structure and protein-protein interactions mediated by the secreted mycobacterial proteins EsxA, EsxB, and EspA. J Bacteriol 192:326-35

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