Genes Contributing to Staphylococcus aureus Fitness in Abscess- and Infection-Related Ecologies
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Genes Contributing to Staphylococcus aureus Fitness in Abscess- and Infection-Related Ecologies
| Title: | Genes Contributing to Staphylococcus aureus Fitness in Abscess- and Infection-Related Ecologies |
| Author: |
Valentino, Michael D.; Foulston, Lucy; Sadaka, Ama; Kos, Veronica N.; Villet, Regis A.; Santa Maria, John; Lazinski, David W.; Camilli, Andrew; Walker, Suzanne; Hooper, David C.; Gilmore, Michael S.
Note: Order does not necessarily reflect citation order of authors. |
| Citation: | Valentino, M. D., L. Foulston, A. Sadaka, V. N. Kos, R. A. Villet, J. Santa Maria, D. W. Lazinski, et al. 2014. “Genes Contributing to Staphylococcus aureus Fitness in Abscess- and Infection-Related Ecologies.” mBio 5 (5): e01729-14. doi:10.1128/mBio.01729-14. http://dx.doi.org/10.1128/mBio.01729-14. |
| Full Text & Related Files: |
4173792.pdf (1.737Mb; PDF) 
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| Abstract: | ABSTRACT Staphylococcus aureus is a leading cause of both community- and hospital-acquired infections that are increasingly antibiotic resistant. The emergence of S. aureus resistance to even last-line antibiotics heightens the need for the development of new drugs with novel targets. We generated a highly saturated transposon insertion mutant library in the genome of S. aureus and used Tn-seq analysis to probe the entire genome, with unprecedented resolution and sensitivity, for genes of importance in infection. We further identified genes contributing to fitness in various infected compartments (blood and ocular fluids) and compared them to genes required for growth in rich medium. This resulted in the identification of 426 genes that were important for S. aureus fitness during growth in infection models, including 71 genes that could be considered essential for survival specifically during infection. These findings highlight novel as well as previously known genes encoding virulence traits and metabolic pathways important for S. aureus proliferation at sites of infection, which may represent new therapeutic targets. |
| Published Version: | doi:10.1128/mBio.01729-14 |
| Other Sources: | http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173792/pdf/ |
| Terms of Use: | This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA |
| Citable link to this page: | http://nrs.harvard.edu/urn-3:HUL.InstRepos:13347407 |
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