Abstract |
Septic arthritis and sepsis are common and feared complications of staphylococcal infections, and the increasing antibiotic resistance among staphylococci urge the extended research for virulence factors involved in these diseases. Staphylcoccus aureus produces a number of virulence factors controlled by several global regulatory genes including agr and sarA. MgrA is a recently identified global regulator, belonging to the SarA subfamily, which upregulates expression of several virulence factors including capsule and sortase. In addition, MgrA has been shown to regulate antibiotic resistance and decrease bacterial autolysis. In this study we have assessed the role of mgrA gene expression on induction and progression of septic arthritis and sepsis. Mice inoculated with the mgrA mutant displayed significantly less severe arthritis and showed a significantly better weight development, than wild-type inoculated mice. Importantly, all 10 mice inoculated with the mgrA mutant survived as compared to 70% mortality in the wild-type inoculated mice (p=0.003). In addition, the mgrA mutant showed significantly less bacterial persistence in kidneys as compared to the wild-type strain. We conclude that mgrA regulates virulence factors important for establishment and progression of septic arthritis and sepsis.
|
Authors | Ing-Marie Jonsson, Catharina Lindholm, Thanh T Luong, Chia Y Lee, Andrej Tarkowski |
Journal | Microbes and infection
(Microbes Infect)
Vol. 10
Issue 12-13
Pg. 1229-35
(Oct 2008)
ISSN: 1286-4579 [Print] France |
PMID | 18692591
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Bacterial Proteins
- Trans-Activators
- Virulence Factors
|
Topics |
- Animals
- Arthritis, Infectious
(microbiology, pathology)
- Bacterial Proteins
(genetics, metabolism)
- Disease Models, Animal
- Female
- Gene Expression Regulation, Bacterial
- Humans
- Mice
- Sepsis
(microbiology, pathology)
- Staphylococcal Infections
(microbiology, pathology)
- Staphylococcus aureus
(genetics, metabolism, pathogenicity)
- Trans-Activators
(genetics, metabolism)
- Virulence Factors
(genetics, metabolism)
|