Open AccessIron and iron chelating agents modulate Mycobacterium tuberculosis growth and monocyte‐macrophage viability and effector functions
Author(s) -
Cronjé Leandra,
Edmondson Nicole,
Eisenach Kathleen D.,
Bornman Liza
Publication year - 2005
Publication title -
fems immunology & medical microbiology
Language(s) - English
Resource type - Journals
eISSN - 1574-695X
pISSN - 0928-8244
DOI - 10.1016/j.femsim.2005.02.007
Subject(s) - viability assay , monocyte , biology , microbiology and biotechnology , mycobacterium tuberculosis , macrophage , deferoxamine , intracellular , immunology , tuberculosis , biochemistry , apoptosis , medicine , in vitro , pathology
Excess of iron promotes Mycobacterium tuberculosis infection, its replication and progression to clinical disease and death from tuberculosis. Chelation of iron may reduce M. tuberculosis replication, restore host defence mechanisms and it could constitute an application in the prevention and treatment strategies where both iron overload and tuberculosis are prevalent. We investigated the effect of iron and iron chelating agents, like desferrioxamine and silybin, individually and in combination with iron on mycobacterial number, viability in culture and after recovery from monocyte‐macrophages, together with monocyte‐macrophages viability and oxidative defence. Mycobacterial number and viability in culture were assessed using real‐time quantitative PCR of H37Rv IS 6110 DNA, 16S rRNA and 85B mRNA, whereas the microplate AlamarBlue TM assay was used to detect viability in culture post‐infection. Mitochondrial membrane potential and phosphatidyl serine exposure of monocyte‐macrophages, detected using Mitotracker Red fluorescence and Annexin V binding, respectively, served as indicators of host cell viability. Superoxide generation served as marker of monocyte‐macrophage effector functions. Extracellular H37Rv showed a significant increase in number and viability in presence of excess iron and, by large, a significant decrease in number and viability in presence of the iron chelating agents, silybin and desferrioxamine, compared to cultivation without supplementation. Intracellularly, excess iron increased H37Rv viability significantly but reduced monocyte‐macrophages mitochondrial membrane potential and compromised superoxide production. Desferrioxamine had little influence on intracellular parameters, but consistently prevented effects of excess iron, while silybin significantly altered most intracellular parameters and mostly failed to prevent effects of excess iron. These findings suggest that chelation therapy should be considered in conditions of iron overload and that effective chelating agents like desferrioxamine, with limited intracellular access might need to be used in combination with lypophilic chelating agents.