Priming of innate antimycobacterial immunity by heat-killed Listeria monocytogenes induces sterilizing response in the adult zebrafish tuberculosis model
Author(s) -
Hanna Luukinen,
Milka Marjut Hammarén,
Leena-Maija Vanha-aho,
Aleksandra Svorjova,
Laura Kantanen,
Sampsa Järvinen,
Bruno Luukinen,
Éric Dufour,
Mika Rämet,
Vesa P. Hytönen,
Mataleena Parikka
Publication year - 2018
Publication title -
disease models and mechanisms
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.327
H-Index - 83
eISSN - 1754-8411
pISSN - 1754-8403
DOI - 10.1242/dmm.031658
Subject(s) - innate immune system , biology , immunity , immune system , immunology , mycobacterium tuberculosis , microbiology and biotechnology , mycobacterium marinum , priming (agriculture) , listeria monocytogenes , acquired immune system , tuberculosis , medicine , bacteria , botany , germination , genetics , pathology
Mycobacterium tuberculosis remains one of the most problematic infectious agents, owing to its highly developed mechanisms to evade host immune responses combined with the increasing emergence of antibiotic resistance. Host-directed therapies aiming to optimize immune responses to improve bacterial eradication or to limit excessive inflammation are a new strategy for the treatment of tuberculosis. In this study, we have established a zebrafish- Mycobacterium marinum natural host-pathogen model system to study induced protective immune responses in mycobacterial infection. We show that priming adult zebrafish with heat-killed Listeria monocytogenes (HKLm) at 1 day prior to M. marinum infection leads to significantly decreased mycobacterial loads in the infected zebrafish. Using rag1 -/- fish, we show that the protective immunity conferred by HKLm priming can be induced through innate immunity alone. At 24 h post-infection, HKLm priming leads to a significant increase in the expression levels of macrophage-expressed gene 1 ( mpeg1 ), tumor necrosis factor α ( tnfa ) and nitric oxide synthase 2b ( nos2b ), whereas superoxide dismutase 2 ( sod2 ) expression is downregulated, implying that HKLm priming increases the number of macrophages and boosts intracellular killing mechanisms. The protective effects of HKLm are abolished when the injected material is pretreated with nucleases or proteinase K. Importantly, HKLm priming significantly increases the frequency of clearance of M. marinum infection by evoking sterilizing immunity (25 vs 3.7%, P =0.0021). In this study, immune priming is successfully used to induce sterilizing immunity against mycobacterial infection. This model provides a promising new platform for elucidating the mechanisms underlying sterilizing immunity and to develop host-directed treatment or prevention strategies against tuberculosis.This article has an associated First Person interview with the first author of the paper.
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