The discovery of antibiotics nearly 80 years ago was a major milestone in the battle against infectious disease, yet bacterial infections continue to be a significant cause of death worldwide. In fact, management of many bacterial infections is becoming progressively more difficult due to the emergence of new and rapidly evolving pathogens with increased virulence, resistance to antibiotics, a greater ability to evade host responses, and heightened transmissibility. To reverse this trend, a systematic understanding of the complex dynamics between the pathogen and host is needed at every level of interaction, including those between cells, individuals, microbial communities, and populations. We will develop and implement an integrated experimental framework that provides systematic and complementary insights into bacterial infections encompassing single cells, animal models, and human patients, to investigate cellular genomics, transcriptional networks, and host microecologies. Three of the most deadly and costly bacterial pathogens will be used as examples to develop this framework and probe the host-pathogen interaction. Specifically, we will dissect the interaction between Mycobacterium tuberculosis and its host at the single cell level to gain a deep and highly resolved characterization of the host cellular states that contribute to susceptibility to infection. We will follow the dynamics of uropathogenic Escherichia coli (UPEC) infection in animals and humans to gain insights into the role of UPEC, the host and the host microbiome in the persistence of recurrent urinary tract infections. We will track the movement and evolution of carbapenem resistant Enterobacteriaceae (CRE) as they emerge in patient populations contributing critical details about how CRE and the resistance elements that they carry are transmitted among patients and patient populations. There are two goals of this work. One is to develop an adaptable framework of multi-omic approaches to be applied to a wide-range of pathogens for the dissection of bacterial infection at the single cell, infected individual and clinical population levels. The second is to capitalize on the output from this framework to identify points

Public Health Relevance

Bacterial infections remain a major global threat to human health despite a century of concerted effort to combat them. We will develop an integrated and universal framework of genomic approaches to identify specific host and pathogen factors linked to disease susceptibility, transmission and virulence as a consequence of the interaction of bacterial pathogens and their hosts. Data resulting from these investigations will highlight much-needed targets for novel therapeutic and intervention strategies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program--Cooperative Agreements (U19)
Project #
1U19AI110818-01
Application #
8710820
Study Section
Special Emphasis Panel ()
Project Start
2014-04-10
Project End
2019-03-31
Budget Start
2014-04-10
Budget End
2015-03-31
Support Year
1
Fiscal Year
2014
Total Cost
$778,440
Indirect Cost
$283,322
Name
Broad Institute, Inc.
Department
Type
DUNS #
623544785
City
Cambridge
State
MA
Country
United States
Zip Code
02142
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