Mitochondria in human neutrophils mediate killing of Staphylococcus aureus

• Published in: Redox biology 2022-02, Vol.49, p.102225-102225, Article 102225
• Main Authors: Dunham-Snary, Kimberly J., Surewaard, Bas GJ, Mewburn, Jeffrey D., Bentley, Rachel ET, Martin, Ashley Y., Jones, Oliver, Al-Qazazi, Ruaa, Lima, Patricia AD, Kubes, Paul, Archer, Stephen L.
• Format: Article
• Language: English
• Subjects: Electron transport chain complex III; Female; Humans; Immunity; Male; Mitochondria - metabolism; NADPH Oxidases - metabolism; Neutrophil extracellular trap (NET); Neutrophils - metabolism; Nicotinamide adenine dinucleotide phosphate (NADPH) oxidases; Phagocytosis; Reactive Oxygen Species - metabolism; Research Paper; Staphylococcus aureus; Staphylococcus aureus - metabolism
• ISSN: 2213-2317; 2213-2317
• DOI: 10.1016/j.redox.2021.102225

Neutrophils play a role in innate immunity and are critical for clearance of Staphylococcus aureus. Current understanding of neutrophil bactericidal effects is that NADPH oxidase produces reactive oxygen species (ROS), mediating bacterial killing. Neutrophils also contain numerous mitochondria; since these organelles lack oxidative metabolism, their function is unclear. We hypothesize that mitochondria in human neutrophils contribute to the bactericidal capacity of S. aureus. and Findings: Using human neutrophils isolated from healthy volunteers (n = 13; 7 females, 6 males), we show that mitochondria are critical in the immune response to S. aureus. Using live-cell and fixed confocal, and transmission electron microscopy, we show mitochondrial tagging of bacteria prior to ingestion and surrounding of phagocytosed bacteria immediately upon engulfment. Further, we demonstrate that mitochondria are ejected from intact neutrophils and engage bacteria during vital NETosis. Inhibition of the mitochondrial electron transport chain at Complex III, but not Complex I, attenuates S. aureus killing by 50 ± 7%, comparable to the NADPH oxidase inhibitor apocynin. Similarly, mitochondrial ROS scavenging using MitoTEMPO attenuates bacterial killing 112 ± 60% versus vehicle control. Antimycin A treatment also reduces mitochondrial ROS production by 50 ± 12% and NETosis by 53 ± 5%. We identify a previously unrecognized role for mitochondria in human neutrophils in the killing of S. aureus. Inhibition of electron transport chain Complex III significantly impairs antimicrobial activity. This is the first demonstration that vital NETosis, an early event in the antimicrobial response, occurring within 5 min of bacterial exposure, depends on the function of mitochondrial Complex III. Mitochondria join NADPH oxidase as bactericidal ROS generators that mediate the bactericidal activities of human neutrophils. [Display omitted] •This study evaluates the role of neutrophil mitochondria in the immune response to Staphylococcus aureus.•Mitochondrial electron transport chain inhibition at Complex III significantly attenuates neutrophil bactericidal activity.