Zoonotic and emerging infectious diseases represent an increasing and very real threat to global health, and it is essential that we expand our understanding of the pathogenesis and prevention of these diseases because of the increasing density of human populations, the increased exposure to domestic animal populations, and the crowding of wildlife into limited areas with frequent livestock and human contact. To address the growing need for infectious disease research, a COBRE Center of Excellence was established at Montana State University (MSU), with the goal of positioning Montana as a national leader in research on zoonotic infectious diseases. Over the past 9 years, the Center has been extremely successful, resulting in infrastructure development (facilities and equipment), recruitment and support of junior investigators (7 COBRE Projects, 6 new hires, and 20 Pilot Projects), and formation of a coiiesive Center of investigators. The synergism of these components has resulted in the establishment of a solid foundation for infectious disease research in the region. Importantly, these efforts have fostered faculty career development and have created a pipeline of new researchers with interest and expertise in infectious disease pathogenesis. The primary objectives in COBRE III will be to continue to expand the capabilities and use of the Animal Models Core, and position it for long-term sustainability.
Four specific Aims will be pursued to address these objectives:
Specific Aim 1 : To provide and maintain state-of-the-art facilities for research involving animal models in support of COBRE-funded Pilot Grants, as well as all other Center and MSU research programs, including access to the Animal Resources Center (ARC), small animal BSL-2 and BSL-3 facilities, and a large animal ABSL-2 facility;
Specific Aim 2 : To provide instruction, mentoring, and expertise that encourages, guides, and fosters advanced strategic use of animal models by Center investigators and other biomedical researchers at MSU;
Specific Aim 3 : To expand, improve, and encourage use of advanced small animal models or relevant large animal models for biomedical research to help investigators select more appropriate or more advanced models and by improving strategies for colony maintenance, husbandry, genetic analyses, and production;
and Specific Aim 4 : To use ongoing assessment to guide further improvement and evolution of the Animal Models Core to better meet users' needs and to help ensure sustainability beyond COBRE III. One of the linchpins for an active, vibrant research environment is interdisciplinary collaboration. Therefore, in evolving toward sustainability, the COBRE III Animal Models Core will offer its services to all interested animal users at MSU, thus building the interactions and collaborations that will lead to long-term research vitality.

Public Health Relevance

The Animal Models Core provides the infrastructure and organizational support necessary for effective efficient use of animals in biomedical research. Animal models are of central importance to research on zoonotic and emerging diseases, and the Animal Models Core will facilitate accomplishment of the goals of COBRE Phase III, thus leading to a sustainable Centerof Biomedical Research Excellence.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Center Core Grants (P30)
Project #
1P30GM110732-01
Application #
8751041
Study Section
Special Emphasis Panel (ZGM1)
Project Start
Project End
Budget Start
2014-07-01
Budget End
2015-06-30
Support Year
1
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Montana State University - Bozeman
Department
Type
DUNS #
City
Bozeman
State
MT
Country
United States
Zip Code
59717
Shepardson, Kelly M; Larson, Kyle; Johns, Laura L et al. (2018) IFNAR2 Is Required for Anti-influenza Immunity and Alters Susceptibility to Post-influenza Bacterial Superinfections. Front Immunol 9:2589
Sebrell, T Andrew; Sidar, Barkan; Bruns, Rachel et al. (2018) Live imaging analysis of human gastric epithelial spheroids reveals spontaneous rupture, rotation and fusion events. Cell Tissue Res 371:293-307
Schepetkin, Igor A; Kirpotina, Liliya N; Mitchell, Pete T et al. (2018) The natural sesquiterpene lactones arglabin, grosheimin, agracin, parthenolide, and estafiatin inhibit T cell receptor (TCR) activation. Phytochemistry 146:36-46
Rashid, Dana J; Surya, Kevin; Chiappe, Luis M et al. (2018) Avian tail ontogeny, pygostyle formation, and interpretation of juvenile Mesozoic specimens. Sci Rep 8:9014
Zykova, Maria V; Schepetkin, Igor A; Belousov, Michael V et al. (2018) Physicochemical Characterization and Antioxidant Activity of Humic Acids Isolated from Peat of Various Origins. Molecules 23:
Borges, Adair L; Zhang, Jenny Y; Rollins, MaryClare F et al. (2018) Bacteriophage Cooperation Suppresses CRISPR-Cas3 and Cas9 Immunity. Cell 174:917-925.e10
van Erp, Paul B G; Patterson, Angela; Kant, Ravi et al. (2018) Conformational Dynamics of DNA Binding and Cas3 Recruitment by the CRISPR RNA-Guided Cascade Complex. ACS Chem Biol 13:481-490
Giles, John R; Eby, Peggy; Parry, Hazel et al. (2018) Environmental drivers of spatiotemporal foraging intensity in fruit bats and implications for Hendra virus ecology. Sci Rep 8:9555
Andrews, Kimberly R; Adams, Jennifer R; Cassirer, E Frances et al. (2018) A bioinformatic pipeline for identifying informative SNP panels for parentage assignment from RADseq data. Mol Ecol Resour 18:1263-1281
Lei, Benfang; Minor, Dylan; Feng, Wenchao et al. (2018) Hypervirulent Group A Streptococcus of Genotype emm3 Invades the Vascular System in Pulmonary Infection of Mice. Infect Immun 86:

Showing the most recent 10 out of 106 publications