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Published on: November 21, 2011
Interactions of staphyloxanthin and enterobactin with myeloperoxidase and reactive chlorine species
Melanie S Coker1, Louisa V Forbes1, Matthew Plowman-Holmes1
1Centre for Free Radical Research, University of Otago Christchurch, P.O. Box 4345, Christchurch, New Zealand.
Abstract:
When neutrophils engulf bacteria, myeloperoxidase converts hydrogen peroxide to hypochlorous acid, which is toxic to all micro-organisms. It has been suggested that some pathogens have virulence factors that target myeloperoxidase to dampen the oxidative reactions of neutrophils. These virulence factors include staphyloxanthin, the golden pigment of Staphylococcus aureus, and enterobactin - a siderophore released by gram-negative bacteria. We investigated the potential of staphyloxanthin and enterobactin to shield bacteria from hypochlorous acid and related chloramines. Clinical strains of S. aureus with high levels of staphyloxanthin and related carotenoids were in general more resistant to low doses of hypochlorous acid than non-pigmented bacteria. But some non-pigmented strains were also resistant to the oxidant. Doses of reactive chlorine species that killed bacteria also bleached their carotenoids. Hypochlorous acid, NH2Cl, and NHCl2 bleached purified staphyloxanthin. When S. aureus were phagocytosed by neutrophils there was no discernible loss of staphyloxanthin. These data suggest that staphyloxanthin is capable of protecting bacteria from low doses of reactive chlorine species formed inside phagosomes. Enterobactin was not an inhibitor of myeloperoxidase. We conclude that staphyloxanthin may protect some bacterial strains against oxidative killing by neutrophils, but enterobactin will not inhibit the production of hypochlorous acid.
Insights
Staphyloxanthin, a pigment from Staphylococcus aureus, helps shield bacteria from neutrophil-generated hypochlorous acid. Enterobactin does not inhibit this oxidative defense mechanism.
Area of Science:
- Immunology
- Microbiology
- Biochemistry
Background:
- Neutrophils produce hypochlorous acid (HOCl) via myeloperoxidase to kill microbes.
- Bacterial virulence factors, like Staphylococcus aureus staphyloxanthin and enterobactin, may counteract neutrophil oxidative defenses.
- Understanding these interactions is crucial for combating bacterial infections.
Purpose of the Study:
- To investigate the protective role of staphyloxanthin and enterobactin against neutrophil-derived reactive chlorine species.
- To determine if these bacterial compounds can inhibit myeloperoxidase activity or neutralize hypochlorous acid.
Main Methods:
- Comparing the resistance of pigmented and non-pigmented Staphylococcus aureus strains to hypochlorous acid.
- Assessing the effect of reactive chlorine species on purified staphyloxanthin.
- Evaluating enterobactin's ability to inhibit myeloperoxidase activity.
Main Results:
- Pigmented S. aureus strains showed increased resistance to low doses of hypochlorous acid.
- Reactive chlorine species bleached staphyloxanthin and its associated carotenoids.
- Enterobactin did not inhibit myeloperoxidase activity.
- Staphyloxanthin remained intact within phagocytosed S. aureus.
Conclusions:
- Staphyloxanthin can protect bacteria from low levels of reactive chlorine species generated within phagosomes.
- Enterobactin does not inhibit hypochlorous acid production by neutrophils.
- Staphyloxanthin represents a potential bacterial defense mechanism against neutrophil oxidative killing.
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