CcpA Affects Infectivity of Staphylococcus aureus in a Hyperglycemic Environment
Many bacteria regulate the expression of virulence factors via carbon catabolite responsive elements. In Gram-positive bacteria, the predominant mediator of carbon catabolite repression is the catabolite control protein A (CcpA). Hyperglycemia is a widespread disorder that predisposes individuals to...
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Published in | Frontiers in cellular and infection microbiology Vol. 7; p. 172 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers
09.05.2017
Frontiers Media S.A |
Subjects | |
Online Access | Get full text |
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Summary: | Many bacteria regulate the expression of virulence factors via carbon catabolite responsive elements. In Gram-positive bacteria, the predominant mediator of carbon catabolite repression is the catabolite control protein A (CcpA). Hyperglycemia is a widespread disorder that predisposes individuals to an array of symptoms and an increased risk of infections. In hyperglycemic individuals, the bacterium
causes serious, life-threatening infections. The importance of CcpA in regulating carbon catabolite repression in
suggests it may be important for infections in hyperglycemic individuals. To test this suggestion, hyperglycemic non-obese diabetic (NOD; blood glucose level ≥20 mM) mice were challenged with the mouse pathogenic
strain Newman and the isogenic
deletion mutant (MST14), and the effects on infectivity were determined. Diabetic NOD mice challenged with the
deletion mutant enhanced the symptoms of infection in an acute murine pneumonia model relative to the parental strain. Interestingly, when diabetic NOD mice were used in footpad or catheter infection models, infectivity of the
mutant decreased relative to the parental strain. These differences greatly diminished when normoglycemic NOD mice (blood glucose level ≤ 10 mM) were used. These data suggest that CcpA is important for infectivity of
in hyperglycemic individuals. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 PMCID: PMC5422431 Edited by: Yinduo Ji, University of Minnesota, USA Reviewed by: Lefu Lan, Shanghai Institute of Materia Medica (CAS), China; William Schwan, University of Wisconsin–La Crosse, USA |
ISSN: | 2235-2988 2235-2988 |
DOI: | 10.3389/fcimb.2017.00172 |