R01TW012183
Project Grant
Overview
Grant Description
Source Attribution and Transmission Dynamics of Campylobacter and Shigella Using Culture-Independent Molecular Methods in an Urban Slum in Dhaka, Bangladesh
While the broad routes of exposure to enteric pathogens through fecal-oral contact are well-known, there are critical limitations to our understanding of pathogen-specific transmission, especially in young children in low-resource settings. A key reason for this evidence gap is the difficulty in detecting these pathogens due to the poor sensitivity of bacterial culture, which is particularly a problem for Shigella and Campylobacter. The development and application of quantitative, culture-independent molecular diagnostics for these pathogens has substantially revised our understanding of the human burden of disease and is poised to do the same for our understanding of the broader ecology of these pathogens.
Shigella and Campylobacter are model organisms to interrogate transmission ecology because they lie on opposite ends of the continuum of person-to-person (Shigella) versus environmental (Campylobacter) transmission. The inclusion of both in this project provides a range of likely transmission pathways from which we can advance our understanding of enteric pathogen transmission.
The objective of this proposal is therefore to understand the sources and routes of transmission of enteric pathogens in an urban low-resource setting in Dhaka, Bangladesh using culture-independent methods for detection. We will accomplish this by using a systems-dynamic modeling approach to analyze pathogen detection data generated in a household-level longitudinal study. The transmission cohort will include structured observations to quantify human contacts with the environment and broad sampling of household contacts, animal reservoirs, and the environment to identify and attribute sources for index infections.
Viability PCR will be used to differentiate nucleic acid from viable organisms, which will allow us to directly measure the duration of shedding of transmissible pathogen after illness and establish quantitative thresholds for inferring viable pathogen from a wide range of samples. These data will then be used to parameterize two complementary mathematical models, a household dynamics and endemic incidence model, to interrogate the interdependence and relative importance of person-to-person and environmental transmission pathways.
Pathogens will be characterized to the genome level using hybrid assembly from short- and long-read metagenomic sequencing of a subset of stool and environmental samples. This project will transform our understanding of enteric pathogen transmission by moving from a broad understanding of fecal-oral transmission routes to pathogen-specific household and environmental pathways of highest relevance.
In endemic and urban settings, the relative importance of direct household contact versus environmental contamination for transmission of both Shigella and Campylobacter is unknown, and our modeling approach will contextualize where these model pathogens lie on this continuum.
While the broad routes of exposure to enteric pathogens through fecal-oral contact are well-known, there are critical limitations to our understanding of pathogen-specific transmission, especially in young children in low-resource settings. A key reason for this evidence gap is the difficulty in detecting these pathogens due to the poor sensitivity of bacterial culture, which is particularly a problem for Shigella and Campylobacter. The development and application of quantitative, culture-independent molecular diagnostics for these pathogens has substantially revised our understanding of the human burden of disease and is poised to do the same for our understanding of the broader ecology of these pathogens.
Shigella and Campylobacter are model organisms to interrogate transmission ecology because they lie on opposite ends of the continuum of person-to-person (Shigella) versus environmental (Campylobacter) transmission. The inclusion of both in this project provides a range of likely transmission pathways from which we can advance our understanding of enteric pathogen transmission.
The objective of this proposal is therefore to understand the sources and routes of transmission of enteric pathogens in an urban low-resource setting in Dhaka, Bangladesh using culture-independent methods for detection. We will accomplish this by using a systems-dynamic modeling approach to analyze pathogen detection data generated in a household-level longitudinal study. The transmission cohort will include structured observations to quantify human contacts with the environment and broad sampling of household contacts, animal reservoirs, and the environment to identify and attribute sources for index infections.
Viability PCR will be used to differentiate nucleic acid from viable organisms, which will allow us to directly measure the duration of shedding of transmissible pathogen after illness and establish quantitative thresholds for inferring viable pathogen from a wide range of samples. These data will then be used to parameterize two complementary mathematical models, a household dynamics and endemic incidence model, to interrogate the interdependence and relative importance of person-to-person and environmental transmission pathways.
Pathogens will be characterized to the genome level using hybrid assembly from short- and long-read metagenomic sequencing of a subset of stool and environmental samples. This project will transform our understanding of enteric pathogen transmission by moving from a broad understanding of fecal-oral transmission routes to pathogen-specific household and environmental pathways of highest relevance.
In endemic and urban settings, the relative importance of direct household contact versus environmental contamination for transmission of both Shigella and Campylobacter is unknown, and our modeling approach will contextualize where these model pathogens lie on this continuum.
Funding Goals
THE JOHN E. FOGARTY INTERNATIONAL CENTER (FIC) SUPPORTS RESEARCH AND RESEARCH TRAINING TO REDUCE DISPARITIES IN GLOBAL HEALTH AND TO FOSTER PARTNERSHIPS BETWEEN U.S. SCIENTISTS AND THEIR COUNTERPARTS ABROAD. FIC SUPPORTS BASIC BIOLOGICAL, BEHAVIORAL, AND SOCIAL SCIENCE RESEARCH, AS WELL AS RELATED RESEARCH TRAINING AND CAREER DEVELOPMENT. THE RESEARCH PORTFOLIO IS DIVIDED INTO SEVERAL PROGRAMS THAT SUPPORT A WIDE VARIETY OF FUNDING MECHANISMS TO MEET PROGRAMMATIC OBJECTIVES.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Virginia
United States
Geographic Scope
State-Wide
Related Opportunity
PAR-21-003
Analysis Notes
Amendment Since initial award the total obligations have increased 401% from $496,735 to $2,490,041.
Rector & Visitors Of The University Of Virginia was awarded
Campylobacter & Shigella Transmission Dynamics in Urban Slum
Project Grant R01TW012183
worth $2,490,041
from Fogarty International Center in August 2021 with work to be completed primarily in Virginia United States.
The grant
has a duration of 4 years 9 months and
was awarded through assistance program 93.989 International Research and Research Training.
Status
(Ongoing)
Last Modified 9/24/25
Period of Performance
8/4/21
Start Date
5/31/26
End Date
Funding Split
$2.5M
Federal Obligation
$0.0
Non-Federal Obligation
$2.5M
Total Obligated
Activity Timeline
Transaction History
Modifications to R01TW012183
Additional Detail
Award ID FAIN
R01TW012183
SAI Number
R01TW012183-2221162794
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
75NF00 NIH Fogarty International Center
Funding Office
75NF00 NIH Fogarty International Center
Awardee UEI
JJG6HU8PA4S5
Awardee CAGE
9B982
Performance District
VA-90
Senators
Mark Warner
Timothy Kaine
Timothy Kaine
Budget Funding
Federal Account | Budget Subfunction | Object Class | Total | Percentage |
---|---|---|---|---|
John E. Fogarty International Center, National Institutes of Health, Health and Human Services (075-0819) | Health research and training | Grants, subsidies, and contributions (41.0) | $993,307 | 100% |
Modified: 9/24/25