This application proposes the establishment of the New England Regional Center of Excellence (NERCE) for Biodefense and Emerging Infectious Diseases Research. The NERCE will support the timely development of preventive and therapeutic interventions against microbes that can be used as weapons of bioterrorism. In performing its mission, the NERCE will leverage the region's tremendous biomedical research strength which resides not only in our nation's finest academic institutions and teaching hospitals, but also in dynamic industrial research facilities of many of the world's leading pharmaceutical and biotechnology companies. The Center will strive to become the focal point for New England's research and development in biodefense, catalyzing collaborative work, creative thinking, and innovative solutions to the myriad challenges posed by biological threats. The NERCE will consist of a series of collaborative projects of various scales supported by core laboratories providing critical services important to biodefense research. These services will include biosafety level-3 animal model support, genomic-scale proteomics, high-throughput screening for chemical inhibitors, large-scale biological molecule production, and clinical investigation of vaccines, therapeutics, and diagnostics. The flexible administrative structure governing NERCE assures that outstanding projects in biodefense will have access to the Center's core services and appropriate levels of internal support. The immediate goal in establishing NERCE will be to translate existing scientific information into deployable technology. This goal will encompass the development of vaccines for some of the major biodefense CDC/NIH Category A threats, vectors for delivery of vaccine antigens, inhibitors of toxin action, and small molecules that block the penetration of viruses through cell membranes. Thus, the NERCE will seek to apply recent dramatic advances in genomics, proteomics, structural biology, immunology, vaccinology, chemistry, drug screening, and material sciences to problems of biodefense importance. NERCE's faculty members will also be involved in basic microbiological training specific to the study of organisms that represent threats as biological weapons and in clinical training in the management of biological casualties. Thus, the NERCE will greatly improve the preparedness of the United States to resist and respond to attacks by infectious agents, whether their source is bioterrorism or nature. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
5U54AI057159-04
Application #
7028907
Study Section
Special Emphasis Panel (ZAI1-NBS-M (M2))
Program Officer
Hirschberg, Rona L
Project Start
2003-09-04
Project End
2008-02-29
Budget Start
2006-03-01
Budget End
2007-02-28
Support Year
4
Fiscal Year
2006
Total Cost
$10,436,968
Indirect Cost
Name
Harvard University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
047006379
City
Boston
State
MA
Country
United States
Zip Code
02115
de Wispelaere, Melissanne; Lian, Wenlong; Potisopon, Supanee et al. (2018) Inhibition of Flaviviruses by Targeting a Conserved Pocket on the Viral Envelope Protein. Cell Chem Biol 25:1006-1016.e8
Huang, Nai-Jia; Pishesha, Novalia; Mukherjee, Jean et al. (2017) Genetically engineered red cells expressing single domain camelid antibodies confer long-term protection against botulinum neurotoxin. Nat Commun 8:423
Mertins, Philipp; Przybylski, Dariusz; Yosef, Nir et al. (2017) An Integrative Framework Reveals Signaling-to-Transcription Events in Toll-like Receptor Signaling. Cell Rep 19:2853-2866
Nair, Dhanalakshmi R; Chen, Ji; Monteiro, João M et al. (2017) A quinolinol-based small molecule with anti-MRSA activity that targets bacterial membrane and promotes fermentative metabolism. J Antibiot (Tokyo) 70:1009-1019
Choo, Min-Kyung; Sano, Yasuyo; Kim, Changhoon et al. (2017) TLR sensing of bacterial spore-associated RNA triggers host immune responses with detrimental effects. J Exp Med 214:1297-1311
de Wispelaere, Mélissanne; Carocci, Margot; Liang, Yanke et al. (2017) Discovery of host-targeted covalent inhibitors of dengue virus. Antiviral Res 139:171-179
Umetsu, Dale T (2017) Mechanisms by which obesity impacts upon asthma. Thorax 72:174-177
Zheng, Huiqing; Colvin, Christopher J; Johnson, Benjamin K et al. (2017) Inhibitors of Mycobacterium tuberculosis DosRST signaling and persistence. Nat Chem Biol 13:218-225
Coulson, Garry B; Johnson, Benjamin K; Zheng, Huiqing et al. (2017) Targeting Mycobacterium tuberculosis Sensitivity to Thiol Stress at Acidic pH Kills the Bacterium and Potentiates Antibiotics. Cell Chem Biol 24:993-1004.e4
Carocci, Margot; Yang, Priscilla L (2016) Lactimidomycin is a broad-spectrum inhibitor of dengue and other RNA viruses. Antiviral Res 128:57-62

Showing the most recent 10 out of 417 publications