| Autor: |
Schneider, William P., Ho, Sun K., Christine, Jillian, Yao, Monique, Marra, Andrea, Hromockyj, Alexander E. |
| Zdroj: |
Infection and Immunity; March 2002, Vol. 70 Issue: 3 p1326-1333, 8p |
| Abstrakt: |
ABSTRACTWe have employed a strategy utilizing differential fluorescence induction (DFI) in an effort to identify Staphylococcus aureusgenes whose products can be targeted for antimicrobial drug development. DFI allows identification of promoters preferentially active under given growth conditions on the basis of their ability to drive expression of a promoterless green fluorescent protein gene (gfp). A plasmid-based promoter trap library was constructed of 200- to 1,000-bp fragments of S. aureusgenomic DNA fused to gfp, and clones with active promoters were isolated under seven different in vitro growth conditions simulating infection. Six thousand two hundred sixty-seven clones with active promoters were screened to identify those that exhibited differential promoter activity. Bioinformatic analysis allowed the identification of 42 unique operons, containing a total of 61 genes, immediately downstream of the differentially active putative promoters. Replacement mutations were generated for most of these operons, and the abilities of the resulting mutants to cause infection were assessed in two different murine infection models. Approximately 40% of the mutants were attenuated in at least one infection model. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
|
