Year: 2026
Type: preprint
Abstract: The ocular surface is one of the body's most environmentally exposed mucosal barriers, yet it is considered low biomass and harbors orders of magnitude fewer bacteria than microbe-rich sites like the gut. This has cast doubt on whether a functional core ocular microbiome exists at all. Having previously defined a protective gd T cell and IL-17 axis engaged by the murine commensal Corynebacterium mastitidis, we asked whether human-derived bacteria could do the same. Pairing sequencing and culturomics of healthy human conjunctiva from two geographically distinct cohorts, we define a stable core microbiome and identify Corynebacterium bovis as a consistent eye-resident commensal rather than a transient contaminant. In humans, C. bovis elicits a non-pathogenic response marked by IL-17 secretion by γδ T cells and circulating C. bovis-specific IgG, which suggests commensalism rather than pathology. Colonizing mice with human C. bovis strains from Pittsburgh or Miami reproduced this program and conferred protection against ocular infection with Staphylococcus aureus. Together, these findings identify C. bovis as a human-derived ocular commensal that can drive protective γδ T cell immunity, translating a mechanism previously defined only in mice into human relevance and a rational target against sight-threatening infection.
Authors: Jaishree Gandhi, Brinna Desai, Simran Mangwani-Mordani, Jackie Shane, Julia Bierker, Alysha Wessell, Daphne M. Rodriguez J., Simran Kaur Randhawa, Sinning Ma, Catherine M. Phelps, Marlies Meisel, Asha Patel, Kelvin Li, Adam Fitch, Methe Barbara, Vishal Jhanji, Anat Galor, Anthony J. St. Leger
Institution: University of Pittsburgh
Language: English
Subfield: Ophthalmology
Field: Medicine
Domain: Health Sciences
Open Access status: green
Awards: G1970662503, G8199950076, G9000020868
OpenAlex ID: W7225082917
