Despite the devastating global human toll of infectious diseases, we lack fundamental knowledge about the viruses, bacteria, fungi, parasites and insect vectors that cause and spread disease. This ignorance leaves us with very few opportunities to intervene in the cycle of infection and transmission, especially in the face of the emergence of new infectious diseases and the rapid rise in drug resistance. Our Genomic Center for Infectious Disease (GCID) develops and applies cutting-edge genomic technologies to address fundamental gaps in our knowledge of the basic biology that underlies the interactions between hosts, pathogens, and vectors. Our GCID is comprised of highly experienced managers with a history of working together effectively to develop and apply innovative genomic approaches. Our GCID employs industrial practices and management systems in directing the world-leading facilities of our Technology, Data and Administrative Cores. Outstanding scientists lead our four Research Projects, devoted to viral, bacterial, fungal, and parasitic diseases and vectors that transmit them. Our collective work will target high priority pathogens and pathogen-host-vector systems that have a major impact on the global burden of disease. Each Research Project leverages our expertise in genomics, technology development, bioinformatics and computational biology, and with collaborating researchers and clinicians applies them to thoughtfully acquired samples and proven model systems. Moreover, the laboratory and analytical methods we develop will have broad applicability to other pathogen-host systems. Our Research Projects benefit from synergies arising from their shared space, approaches and tools, and together they will pursue three long-range, cross-cutting objectives: 1) Explore the genomic epidemiology of pathogens and vectors at individual and population scales; 2) Understand interactions among vertebrate hosts, pathogens, and arthropod vectors using genomic and transcriptomic approaches; and, 3) Define the functional basis of virulence, immunity, and the functional consequences of metagenomic diversity. By applying powerful new genomic technologies to probe host and pathogen contributions to infection processes we will obtain crucial knowledge, and open new avenues for tracking, preventing and managing infectious diseases. We will produce and disseminate data, methodologies, and expertise, broaden participation in genomic research into infectious disease, and generate data and knowledge that will enable a wide community to benefit from our expertise, and, ultimately improve global public health.

Public Health Relevance

Our limited knowledge of the individual organisms responsible for infectious diseases, and the way they interact with the hosts they infect, and the insects that transmit them, prevents us from better managing the staggering global burden of these diseases. We will focus on defining the genes and genomes of these organisms, and how these genes influence disease and drug resistance. We will use collaborative approaches and powerful new laboratory and analytical techniques to study diseases caused by viruses, bacteria, fungi and parasites to develop new ways to diagnose, prevent and treat them.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program--Cooperative Agreements (U19)
Project #
5U19AI110818-07
Application #
9919476
Study Section
Special Emphasis Panel (ZAI1)
Program Officer
Lee, Eun MI
Project Start
2014-04-10
Project End
2024-03-31
Budget Start
2020-04-01
Budget End
2021-03-31
Support Year
7
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Broad Institute, Inc.
Department
Type
DUNS #
623544785
City
Cambridge
State
MA
Country
United States
Zip Code
02142
Donaldson, G P; Ladinsky, M S; Yu, K B et al. (2018) Gut microbiota utilize immunoglobulin A for mucosal colonization. Science 360:795-800
Fernandes, Kenya E; Brockway, Adam; Haverkamp, Miriam et al. (2018) Phenotypic Variability Correlates with Clinical Outcome in Cryptococcus Isolates Obtained from Botswanan HIV/AIDS Patients. MBio 9:
Muñoz, José F; Gade, Lalitha; Chow, Nancy A et al. (2018) Genomic insights into multidrug-resistance, mating and virulence in Candida auris and related emerging species. Nat Commun 9:5346
Lebreton, François; Valentino, Michael D; Schaufler, Katharina et al. (2018) Transferable vancomycin resistance in clade B commensal-type Enterococcus faecium. J Antimicrob Chemother 73:1479-1486
Yadav, Vikas; Sun, Sheng; Billmyre, R Blake et al. (2018) RNAi is a critical determinant of centromere evolution in closely related fungi. Proc Natl Acad Sci U S A 115:3108-3113
Hommel, Benjamin; Mukaremera, Liliane; Cordero, Radames J B et al. (2018) Titan cells formation in Cryptococcus neoformans is finely tuned by environmental conditions and modulated by positive and negative genetic regulators. PLoS Pathog 14:e1006982
Muñoz, José F; McEwen, Juan G; Clay, Oliver K et al. (2018) Genome analysis reveals evolutionary mechanisms of adaptation in systemic dimorphic fungi. Sci Rep 8:4473
Zhang, Wei; Lun, Shichun; Wang, Shu-Huan et al. (2018) Identification of Novel Coumestan Derivatives as Polyketide Synthase 13 Inhibitors Against Mycobacterium Tuberculosis. J Med Chem :
Rhodes, Johanna; Abdolrasouli, Alireza; Farrer, Rhys A et al. (2018) Genomic epidemiology of the UK outbreak of the emerging human fungal pathogen Candida auris. Emerg Microbes Infect 7:43
Sephton-Clark, Poppy C S; Muñoz, Jose F; Ballou, Elizabeth R et al. (2018) Pathways of Pathogenicity: Transcriptional Stages of Germination in the Fatal Fungal Pathogen Rhizopus delemar. mSphere 3:

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