They can also directly attack invading microorganisms via phagocytosis, neutrophil extracellular traps, cytokine secretion and degranulation.[28, 29] Studies of interaction of neutrophils and zygomycetes go back to 1978, where Diamond et al. [29] showed

that neutrophils could kill R. oryzae (the most common agent of mucormycosis) hyphae in vitro. Three years later, Chinn and Diamond [30], found that R. oryzae hyphae can generate various chemotactic factors and how the interaction between the host and hyphae could result in different outcome depending on the certain Sunitinib datasheet condition of the patients such as severe hyperglycaemia and ketoacidosis. A study was done to show how the oxygen-independent mechanism of neutrophils is important selleck screening library in terms of damaging the hyphae in both R. oryzae and A. fumigatus.[31] One of the studies demonstrated that swollen spores activate neutrophils’ migration in both R. oryzae and A. fumigatus in more efficient manner than that of resting spores in a mouse model.[32] Neutrophils activity against the fungi with administration of granulocyte colony-stimulating factor was also studied by Liles et al. [33], they showed that R. oryzae was more resistant to neutrophil killing than A. fumigatus, a more common causative agent of opportunistic fungal infection. One study measured the functionality of PMN against three clinically significant

Zygomycetes and found that combination of interferon-γ and/or granulocyte-macrophage colony-stimulating factor increased hyphal damage of all three species with higher amount of the release of Tumour necrosis factor-α (TNF-α).[34] Compared to non-opsonised hyphae of A. fumigatus, clinical isolates of zygomycetes exhibited reduced capacity of oxidative damage of PMN and these Interleukin-3 receptor exposure of fungi to polymorphonuclear leucocytes led to the increased gene expression of Toll-like-receptor (TLR)-2.[35] A study led by Simitsopoulou et al. [36], compared hyphae damage done by PMN against two Rhizopus species and Cunninghamella bertholletiae with and without antifungal agents via modified assay applying 2,3-Bis-(2-Methoxy-4-Nitro-5-Sulfophenyl)-2H-Tetrazolium-5-Carboxanilide

(XTT), which used to assess the metabolic activity of the cells as a function of redox potential giving rise to the staus of cellular viability. Actively respiring cells convert the water-soluble XTT to a water-soluble, orange coloured formazan product. The revealed results was interesting in that Cunninghamella bertholletiae was the most resistant to the antifungal activity of PMN with different cytokine responses compared to that of Rhizopus species.[36] Another study showed weakened hyphal damage after exposure to R. oryzae compared to that of A. fumigatus. R. oryzae activated proinflammatory response via TLR-2 in PMN[35] while A. fumigatus utilise both TLR-2 and TLR-4 to activate the innate immune response.[37] A study led by Chamilos et al.