Understanding the pathogenesis of leprosy granulomas has been hindered by a paucity of tractable experimental animal models. Mycobacterium leprae, which causes leprosy, grows optimally at approximately 30°C, so we sought to model granulomatous disease in the ectothermic zebrafish. We found that noncaseating granulomas develop rapidly and eventually eradicate infection. rag1 mutant zebrafish, which lack lymphocytes, also form noncaseating granulomas with similar kinetics, but these control infection more slowly. Our findings establish the zebrafish as a facile, genetically tractable model for leprosy and reveal the interplay between innate and adaptive immune determinants mediating leprosy granuloma formation and function.
BT - The Journal of infectious diseases C1 -http://www.ncbi.nlm.nih.gov/pubmed/28934421?dopt=Abstract
DO - 10.1093/infdis/jix329 IS - 6 J2 - J. Infect. Dis. LA - eng N2 -Understanding the pathogenesis of leprosy granulomas has been hindered by a paucity of tractable experimental animal models. Mycobacterium leprae, which causes leprosy, grows optimally at approximately 30°C, so we sought to model granulomatous disease in the ectothermic zebrafish. We found that noncaseating granulomas develop rapidly and eventually eradicate infection. rag1 mutant zebrafish, which lack lymphocytes, also form noncaseating granulomas with similar kinetics, but these control infection more slowly. Our findings establish the zebrafish as a facile, genetically tractable model for leprosy and reveal the interplay between innate and adaptive immune determinants mediating leprosy granuloma formation and function.
PY - 2017 SP - 776 EP - 779 T2 - The Journal of infectious diseases TI - A Zebrafish Model of Mycobacterium leprae Granulomatous Infection. UR - https://academic.oup.com/jid/article/216/6/776/3978667/A-Zebrafish-Model-of-Mycobacterium-leprae VL - 216 SN - 1537-6613 ER -