Journal
INFECTION AND IMMUNITY
Volume 75, Issue 9, Pages 4534-4540Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/IAI.00679-07
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Funding
- NIAID NIH HHS [R01-AI30138, R01 AI030138] Funding Source: Medline
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TraP is a triply phosphorylated staphylococcal protein that has been hypothesized to be the mediator of a second StaphylOCOCCUN aureus quorum-sensing system, SQS1, that controls expression of the agr system and therefore is essential for the organism's virulence. This hypothesis was based on the loss of agr expression and virulence by a traP mutant of strain 8325-4 and was supported by full complementation of both phenotypic defects by the cloned traP gene in strain NB8 (Y. Gov, 1. Borovok, M. Korem, V. K. Singh, R. K. Jayaswall, B. J. Wilkinson, S. M. Rich, and N. Balaban, J. Biol. Chem. 279:14665-14672, 2004), in which the wild-type traP gene was expressed in trans in the 8325-4 traP mutant. We initiated a study of the mechanism by which TraP activates agr and found that the traP mutant strain used for this and other recently published studies has a second mutation, an adventitious stop codon in the middle of agrA, the agr response regulator. The traP mutation, once separated from the agrA defect by outcrossing, had no effect on agr expression or virulence, indicating that the agrA defect accounts fully for the lack of agr expression and for the loss of virulence attributed to the traP mutation. In addition, DNA sequencing showed that the agrA gene in strain NB8 (Gov et a]., J. Biol. Chem., 2004), in contrast to that in the agr-defective 8325-4 traP mutant strain, had the wild-type sequence; further, the traP mutation in that strain, when outcrossed, also had no effect. on agr expression.
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