Priming of innate antimycobacterial immunity by heat-killed Listeria monocytogenes induces sterilizing response in the adult zebrafish tuberculosis model.
Hanna LuukinenMilka Marjut HammarénLeena-Maija Vanha-AhoAleksandra SvorjovaLaura KantanenSampsa JärvinenBruno Vincent LuukinenEric DufourMika RämetVesa Pekka HytönenMataleena ParikkaPublished in: Disease models & mechanisms (2018)
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.
Keyphrases
- mycobacterium tuberculosis
- immune response
- listeria monocytogenes
- nitric oxide synthase
- pulmonary tuberculosis
- poor prognosis
- emergency department
- high glucose
- hiv aids
- dendritic cells
- nitric oxide
- toll like receptor
- rheumatoid arthritis
- body mass index
- hiv infected
- copy number
- binding protein
- hepatitis c virus
- diabetic rats
- endothelial cells
- heat stress
- hydrogen peroxide
- weight gain
- human immunodeficiency virus
- young adults
- replacement therapy
- single cell