Dry eye is a multifactorial disease of the ocular surface. With the prevalence of dry eye continuing to increase and only two FDA approved drugs available that are effective in only a subset of patients, there is an unmet need for the development of new therapies. Here I propose that butyrate, a short-chain fatty acid (SCFA) and a byproduct of the fermentation of dietary fiber by anaerobic commensal bacteria, is essential in maintaining ocular surface homeostasis. We will test the hypothesis that in homeostasis, normal gut microbial communities have an abundance of different butyrate-producing bacteria, that can ferment dietary fiber and produce SCFA, including butyrate. We will address this hypothesis with 3 aims.
Aim #1 : to investigate the protective mechanism of action of butyrate on the ocular surface epithelium. I will determine if butyrate signals through its receptors or through its transporter to exert anti-inflammatory actions.
Aim #2 : to investigate the role of butyrate in the development of ocular surface inflammation and Sjgren Syndrome-like disease in-vivo. I will determine if butyrate signaling through its transporter essential for maintaining ocular homeostasis under stress conditions. To accomplish this, I will modulate the microbiome and expose mice to well-known stressors.
Aim #3 : to investigate butyrate as a novel therapy for ocular surface diseases. In this aim, I will test if modulation of gut microbiome through diet or supplementation can have a beneficial effect on the ocular surface by promoting SCFA production by commensal bacteria. Overall, these studies aim to explore a novel byproduct of the microbiome that is involved in maintaining ocular surface homeostasis. These data will be invaluable to the field of dry eye and could provide new therapeutic targets.

Public Health Relevance

Dry eye is one of the leading ocular morbidities around the world and current therapeutics are only effective in only a subset of patients. Recent evidence suggests that the gut microbiome can modulate ocular surface homeostasis, leading to dry eye. The goal of this proposal is to understand how butyrate, a microbial byproduct, protects the ocular surface from dry eye insults.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32EY030342-01
Application #
9760960
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Agarwal, Neeraj
Project Start
2020-01-16
Project End
Budget Start
2020-01-16
Budget End
Support Year
1
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030