ABSTRACT
Infection-induced vascular pathologies are a side effect of the immune response to contact with a range of pathogens. Mycobacteria, including Mycobacterium tuberculosis, are particularly adept at co-opting vascular leakiness as a survival mechanism to shape the host immune response and impede the delivery of antibiotics to sites of infection. Here using the zebrafish-Mycobacterium marinum infection model, we confirm a critical role for Signal transducer and activator of transcription 3 (STAT3) in mediating infection-induced vascular permeability, and demonstrate the ability of FDA-approved drugs atovaquone and pyrimethamine to restore vascular barrier function without compromising immune control of mycobacterial infection. Additionally, we find an antibiotic effect of pyrimethamine against Mycobacterium marinum via inhibition of bacterial dihydrofolate reductase. Together our findings suggest pyrimethamine could be used as adjunctive therapy against mycobacterial infection.
Competing Interest Statement
The authors have declared no competing interest.
