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Dietary Manganese Promotes Staphylococcal Infection of the Heart.
- Source :
-
Cell host & microbe [Cell Host Microbe] 2017 Oct 11; Vol. 22 (4), pp. 531-542.e8. Date of Electronic Publication: 2017 Sep 21. - Publication Year :
- 2017
-
Abstract
- Diet, and specifically dietary metals, can modify the risk of infection. However, the mechanisms by which manganese (Mn), a common dietary supplement, alters infection remain unexplored. We report that dietary Mn levels dictate the outcome of systemic infections caused by Staphylococcus aureus, a leading cause of bacterial endocarditis. Mice fed a high Mn diet display alterations in Mn levels and localization within infected tissues, and S. aureus virulence and infection of the heart are enhanced. Although the canonical mammalian Mn-sequestering protein calprotectin surrounds staphylococcal heart abscesses, calprotectin is not released into the abscess nidus and does not limit Mn in this organ. Consequently, excess Mn is bioavailable to S. aureus in the heart. Bioavailable Mn is utilized by S. aureus to detoxify reactive oxygen species and protect against neutrophil killing, enhancing fitness within the heart. Therefore, a single dietary modification overwhelms vital host antimicrobial strategies, leading to fatal staphylococcal infection.<br /> (Copyright © 2017 Elsevier Inc. All rights reserved.)
- Subjects :
- Abscess
Animals
Diet
Disease Models, Animal
Heart physiopathology
Humans
Leukocyte L1 Antigen Complex metabolism
Liver microbiology
Liver physiopathology
Manganese analysis
Mice
Mice, Congenic
Mice, Inbred C57BL
Neutrophils metabolism
Reactive Oxygen Species metabolism
Staphylococcus aureus pathogenicity
Endocarditis, Bacterial microbiology
Heart microbiology
Manganese metabolism
Staphylococcal Infections microbiology
Staphylococcus aureus metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1934-6069
- Volume :
- 22
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Cell host & microbe
- Publication Type :
- Academic Journal
- Accession number :
- 28943329
- Full Text :
- https://doi.org/10.1016/j.chom.2017.08.009