The primary goals of the proposed training program are first to recruit talented and highly motivated graduate students and postdoctoral fellows and second to provide them with first-rate training which will prepare them for careers in academic research as competitive, independent investigators. The program faculty's research interests span a wide range of questions regarding host-microbe interactions and related topics in pathogenesis, which allows the entering trainee a considerable breadth of choice of experimental systems, approaches, and research topics. Training options include animal and human systems, thus enhancing our ability to attract and train M.D.'s for research careers. Another strength of the proposed training grant is the quality of the research programs of the participating faculty. This proposal includes 13 well-funded program faculty members who have productive, timely, and energetic research efforts in numerous areas of current interest. Particular areas of strength are molecular genetics of bacterial, parasitic, and viral pathogenesis; cellular and immunobiology of parasites; B cell activation and interaction with T helper cells and lymphokines; mucosal immune responses; signaling events in host-pathogen interactions; involvement of various immune mechanisms in resistance to infectious diseases including those caused by parasites, bacteria, and retroviruses such as HIV and mouse AIDS (MAIDS) virus; immunotherapeutics and vaccine design. These areas are pursued using the full range of modem genetic, immunologic, biochemical, and molecular biologic techniques. We have excellent facilities, including new laboratories in the Borwell Research Building constructed in 1992. The proposal also benefits from the presence of strong existing graduate programs leading to the Ph.D. degree. Training in molecular pathogenesis spans six departments that encompass two graduate programs - Physiology, and Molecular and Cellular Biology - with the latter containing the majority of the participating faculty and students. Consistent with this organization, graduate training in molecular pathogenesis at Dartmouth is an interdisciplinary approach that is nurtured by a highly interactive environment in which the trainees are regularly exposed to diverse areas of faculty expertise, from clinical to basic science studies, in a variety of forums, including a number of advanced courses, weekly seminar series and journal clubs, and retreats. By these means our trainees benefit from a vigorous faculty involvement and scientific exchange that results in maximized communication of their work, the program faculty's work, and the progress of the various interdisciplinary fields on the international level.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Institutional National Research Service Award (T32)
Project #
5T32AI007519-09
Application #
7108586
Study Section
Microbiology and Infectious Diseases B Subcommittee (MID)
Program Officer
Mcsweegan, Edward
Project Start
1997-09-30
Project End
2008-08-31
Budget Start
2006-09-01
Budget End
2007-08-31
Support Year
9
Fiscal Year
2006
Total Cost
$255,836
Indirect Cost
Name
Dartmouth College
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
041027822
City
Hanover
State
NH
Country
United States
Zip Code
03755
Ries, Laure Nicolas Annick; Beattie, Sarah; Cramer, Robert A et al. (2018) Overview of carbon and nitrogen catabolite metabolism in the virulence of human pathogenic fungi. Mol Microbiol 107:277-297
Roymans, Dirk; Alnajjar, Sarhad S; Battles, Michael B et al. (2017) Therapeutic efficacy of a respiratory syncytial virus fusion inhibitor. Nat Commun 8:167
Beattie, Sarah R; Mark, Kenneth M K; Thammahong, Arsa et al. (2017) Filamentous fungal carbon catabolite repression supports metabolic plasticity and stress responses essential for disease progression. PLoS Pathog 13:e1006340
Orazi, Giulia; O'Toole, George A (2017) Pseudomonas aeruginosa Alters Staphylococcus aureus Sensitivity to Vancomycin in a Biofilm Model of Cystic Fibrosis Infection. MBio 8:
Battles, Michael B; Más, Vicente; Olmedillas, Eduardo et al. (2017) Structure and immunogenicity of pre-fusion-stabilized human metapneumovirus F glycoprotein. Nat Commun 8:1528
Jiang, Yike; Patel, Chaya D; Manivanh, Richard et al. (2017) Maternal Antiviral Immunoglobulin Accumulates in Neural Tissue of Neonates To Prevent HSV Neurological Disease. MBio 8:
Tian, Daiyin; Battles, Michael B; Moin, Syed M et al. (2017) Structural basis of respiratory syncytial virus subtype-dependent neutralization by an antibody targeting the fusion glycoprotein. Nat Commun 8:1877
Bahl, Christopher D; St Laurent, Jessica D; Karthikeyan, R Siva Ganesa et al. (2017) The cif Virulence Factor Gene Is Present in Isolates From Patients With Pseudomonas aeruginosa Keratitis. Cornea 36:358-362
Gao, Yang; Hauke, Caitlyn A; Marles, Jarrad M et al. (2016) Effects of tcpB Mutations on Biogenesis and Function of the Toxin-Coregulated Pilus, the Type IVb Pilus of Vibrio cholerae. J Bacteriol 198:2818-28
Battles, Michael B; Langedijk, Johannes P; Furmanova-Hollenstein, Polina et al. (2016) Molecular mechanism of respiratory syncytial virus fusion inhibitors. Nat Chem Biol 12:87-93

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