Seasonal and epidemic conjunctivitis (pink eye) infections are highly contagious and impose significant economic burden in the United States and worldwide. Long-term visual impairment can occur. In children, conjunctivitis may herald more serious systemic complications leading to hospitalizations and even deaths. Current challenges to effective mechanisms to curtail outbreaks are the lack of tracking and reporting, poor access to sample collection for analysis, limited diagnostic testing capabilities, and an incomplete understanding of the pathogens involved. The overall goal of this project is to combine international collaboration efforts and advances in genomic technologies to identify pathogens, global trends, pathogen evolution, and the immune responses involved in the epidemiology of conjunctivitis. We propose to enhance the understanding of the pathogenesis of conjunctivitis with the following aims.
The first aim will determine how adenovirus genome types vary within a region and across regions.
The second aim will identify emerging causes of seasonal and epidemic conjunctivitis. Finally, we will identify the local immune response signatures of children and adults with infectious conjunctivitis. We expect that conjunctival gene expression profiles will accurately predict disease associated complications. This project has the potential to improve public health surveillance, guide targeted interventions, improve vaccine development, and elevate existing diagnostic paradigms for conjunctivitis, to reduce both the financial and ocular health burden worldwide.

Public Health Relevance

(RELEVENCE) Conjunctivitis results in significant economic burden worldwide and can result in long-term vision impairment and severe systemic complications in children. This project takes advantage of international collaborations and recent advances in genomic technologies to enhance our understanding of conjunctivitis epidemics globally by identifying the pathogens involved, characterizing the evolution of pathogen genomes across time and space, and defining the immune responses to these infections. The results of this study will improve prevention methods and help to curtail spread, thus reducing the burden on cost and human ocular health.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
1R01EY032041-01
Application #
10092776
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Mckie, George Ann
Project Start
2021-03-01
Project End
2026-02-28
Budget Start
2021-03-01
Budget End
2022-02-28
Support Year
1
Fiscal Year
2021
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143