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|Title:||Interplay between manganese and iron in pneumococcal pathogenesis: Role of the orphan response regulator ritR|
|Citation:||Infection and Immunity, 2013; 81(2):421-429|
|Publisher:||Amer Soc Microbiology|
|Cheryl-Lynn Y. Ong, Adam J. Potter, Claudia Trappetti, Mark J. Walker, Michael P. Jennings, James C. Paton, Alastair G. McEwan|
|Abstract:||Streptococcus pneumoniae (the pneumococcus) is a major human pathogen that is carried asymptomatically in the nasopharynx by up to 70% of the human population. Translocation of the bacteria into internal sites can cause a range of diseases, such as pneumonia, otitis media, meningitis, and bacteremia. This transition from nasopharynx to growth at systemic sites means that the pneumococcus needs to adjust to a variety of environmental conditions, including transition metal ion availability. Although it is an important nutrient, iron potentiates oxidative stress, and it is established that in S. pneumoniae, expression of iron transport systems and proteins that protect against oxidative stress are regulated by an orphan response regulator, RitR. In this study, we investigated the effect of iron and manganese ion availability on the growth of a ritR mutant. Deletion of ritR led to impaired growth of bacteria in high-iron medium, but this phenotype could be suppressed with the addition of manganese. Measurement of metal ion accumulation indicated that manganese prevents iron accumulation. Furthermore, the addition of manganese also led to a reduction in the amount of hydrogen peroxide produced by bacterial cells. Studies of virulence in a murine model of infection indicated that RitR was not essential for pneumococcal survival and suggested that derepression of iron uptake systems may enhance the survival of pneumococci in some niches.|
Cation Transport Proteins
Gene Expression Regulation, Bacterial
|Rights:||Copyright © 2013, American Society for Microbiology. All Rights Reserved.|
|Appears in Collections:||Aurora harvest|
Molecular and Biomedical Science publications
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