A primary goal of this application is the development of new vaccines, diagnostics, and therapeuticsfor category A-C priority agents. Animal models will be needed to improve our understanding of the hostpathogenrelationship and to test newly developed products. Since many of the pathogens require BSL-3containment, state-of-the-art BSL-3 vivaria will be critical in reaching our research goals. Thus, we haveestablished an Animal Core in order to the meet the current and expanding needs of NBC scientists. Theobjectives of the Animal Core are: 1) to provide high quality BSL-3 animal facilities; 2) to advise and traininvestigators in animal models for category A-C priority agents; and 3) to encourage collaborations betweenNBC members.The NBC Animal Core consists of BSL-3 vivaria at four sites within region 2 and provides facilities fora wide variety of animal species. Small animal studies involving rodents, rabbits, and birds will be performedat one of two BSL-3 vivaria at PHRI, Newark, NJ or Wadsworth Center, Albany, NY. Studies in livestock onzoonotic pathogens will be located at the Plum Island Animal Disease Center, Plum Island, NY. Non-humanprimate studies will be conducted at the Caribbean Primate Research Center, Puerto Rico. The diversity ofanimal species available at these four facilities is essential in order to address the diversity of the categoryA-C priority agents. In addition, the diverse scientific expertise at these facilities will provide excellent trainingand collaborative opportunities for the NBC research community.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
3U54AI057158-05S1
Application #
7706294
Study Section
Special Emphasis Panel (ZAI1-NBS-M (M2))
Project Start
2008-03-01
Project End
2009-02-28
Budget Start
2008-03-01
Budget End
2009-02-28
Support Year
5
Fiscal Year
2008
Total Cost
$920,836
Indirect Cost
Name
Wadsworth Center
Department
Type
DUNS #
153695478
City
Menands
State
NY
Country
United States
Zip Code
12204
Li, Xiao-Ping; Kahn, Jennifer N; Tumer, Nilgun E (2018) Peptide Mimics of the Ribosomal P Stalk Inhibit the Activity of Ricin A Chain by Preventing Ribosome Binding. Toxins (Basel) 10:
Goldman, David L; Nieves, Edward; Nakouzi, Antonio et al. (2018) Serum-Mediated Cleavage of Bacillus anthracis Protective Antigen Is a Two-Step Process That Involves a Serum Carboxypeptidase. mSphere 3:
Marié, Isabelle J; Chang, Hao-Ming; Levy, David E (2018) HDAC stimulates gene expression through BRD4 availability in response to IFN and in interferonopathies. J Exp Med 215:3194-3212
Aguilar, Jorge L; Varshney, Avanish K; Pechuan, Ximo et al. (2017) Monoclonal antibodies protect from Staphylococcal Enterotoxin K (SEK) induced toxic shock and sepsis by USA300 Staphylococcus aureus. Virulence 8:741-750
Zhou, Yijun; Li, Xiao-Ping; Chen, Brian Y et al. (2017) Ricin uses arginine 235 as an anchor residue to bind to P-proteins of the ribosomal stalk. Sci Rep 7:42912
Uhde, Melanie; Ajamian, Mary; Wormser, Gary P et al. (2017) Reply to Naktin. Clin Infect Dis 64:1145-1146
Chen, Han; Coseno, Molly; Ficarro, Scott B et al. (2017) A Small Covalent Allosteric Inhibitor of Human Cytomegalovirus DNA Polymerase Subunit Interactions. ACS Infect Dis 3:112-118
Lauretti, Flavio; Chattopadhyay, Anasuya; de Oliveira França, Rafael Freitas et al. (2016) Recombinant vesicular stomatitis virus-based dengue-2 vaccine candidate induces humoral response and protects mice against lethal infection. Hum Vaccin Immunother 12:2327-33
Tadin, Ante; Tokarz, Rafal; Markoti?, Alemka et al. (2016) Molecular Survey of Zoonotic Agents in Rodents and Other Small Mammals in Croatia. Am J Trop Med Hyg 94:466-73
Basu, Debaleena; Li, Xiao-Ping; Kahn, Jennifer N et al. (2016) The A1 Subunit of Shiga Toxin 2 Has Higher Affinity for Ribosomes and Higher Catalytic Activity than the A1 Subunit of Shiga Toxin 1. Infect Immun 84:149-61

Showing the most recent 10 out of 655 publications