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Cold Atmospheric Plasma Promotes Killing of Staphylococcus aureus by Macrophages
Constance Duchesne1,2, Nadira Frescaline1,2, Océane Blaise1,2
1Institut de Recherche Biomédicale des Armées, INSERM UMRS-MD 1197, Centre de Transfusion Sanguine des Armées, Clamart, France.
Abstract:
Macrophages are important immune cells that are involved in the elimination of microbial pathogens. Following host invasion, macrophages are recruited to the site of infection, where they launch antimicrobial defense mechanisms. Effective microbial clearance by macrophages depends on phagocytosis and phagolysosomal killing mediated by oxidative burst, acidification, and degradative enzymes. However, some pathogenic microorganisms, including some drug-resistant bacteria, have evolved sophisticated mechanisms to prevent phagocytosis or escape intracellular degradation. Cold atmospheric plasma (CAP) is an emerging technology with promising bactericidal effects. Here, we investigated the effect of CAP on Staphylococcus aureus phagocytosis by RAW 264.7 macrophage-like cells. We demonstrate that CAP treatment increases intracellular concentrations of reactive oxygen species (ROS) and nitric oxide and promotes the elimination of both antibiotic-sensitive and antibiotic-resistant S. aureus by RAW 264.7 cells. This effect was inhibited by antioxidants indicating that the bactericidal effect of CAP was mediated by oxidative killing of intracellular bacteria. Furthermore, we show that CAP promotes the association of S. aureus to lysosomal-associated membrane protein 1 (LAMP-1)-positive phagosomes, in which bacteria are exposed to low pH and cathepsin D hydrolase. Taken together, our results provide the first evidence that CAP activates defense mechanisms of macrophages, ultimately leading to bacterial elimination. IMPORTANCE Staphylococcus aureus is the most frequent cause of skin and soft tissue infections. Treatment failures are increasingly common due to antibiotic resistance and the emergence of resistant strains. Macrophages participate in the first line of immune defense and are critical for coordinated defense against pathogenic bacteria. However, S. aureus has evolved sophisticated mechanisms to escape macrophage killing. In the quest to identify novel antimicrobial therapeutic approaches, we investigated the activity of cold atmospheric plasma (CAP) on macrophages infected with S. aureus. Here, we show that CAP treatment promotes macrophage ability to eliminate internalized bacteria. Importantly, CAP could trigger killing of both antibiotic-sensitive and antibiotic-resistant strains of S. aureus. While CAP did not affect the internalization capacity of macrophages, it increased oxidative-dependent bactericidal activity and promoted the formation of degradative phagosomes. Our study shows that CAP has beneficial effects on macrophage defense mechanisms and may potentially be useful in adjuvant antimicrobial therapies.
Insights
Cold atmospheric plasma (CAP) enhances macrophage immune responses to eliminate both antibiotic-sensitive and resistant Staphylococcus aureus. CAP treatment boosts reactive oxygen species and promotes bacterial degradation within phagosomes, offering a novel therapeutic approach.
Area of Science:
- Immunology and Microbiology
- Plasma Medicine
- Bacteriology
Background:
- Macrophages are crucial immune cells for clearing microbial pathogens, employing mechanisms like phagocytosis and oxidative burst.
- Pathogenic bacteria, including antibiotic-resistant Staphylococcus aureus, have evolved strategies to evade macrophage-mediated killing.
- Cold atmospheric plasma (CAP) is an emerging technology demonstrating potent bactericidal effects.
Purpose of the Study:
- To investigate the impact of CAP on the phagocytosis and intracellular elimination of Staphylococcus aureus by macrophage-like cells.
- To elucidate the mechanisms by which CAP enhances macrophage antimicrobial activity against S. aureus.
Main Methods:
- RAW 264.7 macrophage-like cells were treated with CAP in the presence of Staphylococcus aureus (both antibiotic-sensitive and resistant strains).
- Intracellular reactive oxygen species (ROS) and nitric oxide levels were measured.
- Bacterial survival, phagosome-bacteria association with LAMP-1, and phagosomal pH were assessed; antioxidant inhibition was evaluated.
Main Results:
- CAP treatment significantly enhanced the elimination of both antibiotic-sensitive and resistant S. aureus by RAW 264.7 cells.
- CAP increased intracellular ROS and nitric oxide, and this effect was abrogated by antioxidants, indicating oxidative killing.
- CAP promoted the maturation of phagosomes containing S. aureus, leading to increased association with LAMP-1 and acidification.
Conclusions:
- Cold atmospheric plasma activates macrophage defense mechanisms, enhancing their ability to eliminate intracellular Staphylococcus aureus.
- The bactericidal effect of CAP is mediated by oxidative stress and the promotion of degradative phagosome formation.
- CAP shows potential as an adjuvant therapy to combat infections caused by both antibiotic-sensitive and resistant strains of S. aureus.
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