The administrative core of this PPG, led by Dr. Kenneth Bayles, will provide the organizational structure for the entire program project and will give leadership, oversight, and direction for the individual projects and cores. The first specific aim of this core, to set and implement the programmatic goals for the PPG, will be achieved through regular interactions with each of the participants in this PPG to monitor the progress and reinforce the specific aims of each project.
The second aim will be to assure that the participants of this PPG are communicating effectively by organizing regular meetings to promote the exchange of ideas and to ensure that off-campus participants are fully integrated into this project. Developing the scientific program will be the third aim focusing primarily on pursuing additional funding opportunities that will complement and foster the continued growth of our program.
The fourth aim will be to maintain a system for fiscal accountability and resource allocation, ensuring that all budgetary issues related to this PPG are handled appropriately by trained personnel who are experienced with NIH and UNMC policies related to grants administration. The fifth and final aim will be to offer statistical support for all projects in the planning of experiments and interpretation of results. This support will be coordinated by Dr. Fang Yu in the Department of Biostatistics at the University of Nebraska Medical Center, who will participate in regular meetings with the members of this PPG. The successful implementation of these specific aims will form a solid foundation of administrative support needed by each of the scientific projects in this PPG and will help to assure the continued success of our program.
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|Hanamsagar, Richa; Aldrich, Amy; Kielian, Tammy (2014) Critical role for the AIM2 inflammasome during acute CNS bacterial infection. J Neurochem 129:704-11|
|Scherr, Tyler D; Lindgren, Kevin E; Schaeffer, Carolyn R et al. (2014) Mouse model of post-arthroplasty Staphylococcus epidermidis joint infection. Methods Mol Biol 1106:173-81|
|Heim, Cortney E; Vidlak, Debbie; Scherr, Tyler D et al. (2014) Myeloid-derived suppressor cells contribute to Staphylococcus aureus orthopedic biofilm infection. J Immunol 192:3778-92|
|Hernandez, Frank J; Huang, Lingyan; Olson, Michael E et al. (2014) Noninvasive imaging of Staphylococcus aureus infections with a nuclease-activated probe. Nat Med 20:301-6|
|Zurek, Oliwia W; Nygaard, Tyler K; Watkins, Robert L et al. (2014) The role of innate immunity in promoting SaeR/S-mediated virulence in Staphylococcus aureus. J Innate Immun 6:21-30|
|Kiedrowski, Megan R; Crosby, Heidi A; Hernandez, Frank J et al. (2014) Staphylococcus aureus Nuc2 is a functional, surface-attached extracellular nuclease. PLoS One 9:e95574|
|Sapp, April M; Mogen, Austin B; Almand, Erin A et al. (2014) Contribution of the nos-pdt operon to virulence phenotypes in methicillin-sensitive Staphylococcus aureus. PLoS One 9:e108868|
|Olson, Michael E; Todd, Daniel A; Schaeffer, Carolyn R et al. (2014) Staphylococcus epidermidis agr quorum-sensing system: signal identification, cross talk, and importance in colonization. J Bacteriol 196:3482-93|
|Lindgren, J K; Thomas, V C; Olson, M E et al. (2014) Arginine deiminase in Staphylococcus epidermidis functions to augment biofilm maturation through pH homeostasis. J Bacteriol 196:2277-89|
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