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Following in Real Time the Impact of Pneumococcal Virulence Factors in an Acute Mouse Pneumonia Model Using Bioluminescent Bacteria
Published on: February 23, 2014
Pneumococcal surface protein C contributes to sepsis caused by Streptococcus pneumoniae in mice
Francesco Iannelli1, Damiana Chiavolini, Susanna Ricci
1Department of Molecular Biology, University of Siena, 53100 Siena, Italy. iannelli@unisi.it
Abstract:
The role of pneumococcal surface protein C (PspC; also called SpsA, CbpA, and Hic) in sepsis by Streptococcus pneumoniae was investigated in a murine infection model. The pspC gene was deleted in strains D39 (type 2) and A66 (type 3), and the mutants were tested by being injected intravenously into mice. The animals infected with the mutant strains showed a significant increase in survival, with the 50% lethal dose up to 250-fold higher than that for the wild type. Our findings indicate that PspC affords a decisive contribution to sepsis development.
Insights
Pneumococcal surface protein C (PspC) significantly contributes to Streptococcus pneumoniae sepsis development. Mice infected with PspC-deficient strains showed increased survival, indicating PspC
Area of Science:
- Microbiology
- Immunology
- Infectious Diseases
Background:
- Streptococcus pneumoniae causes sepsis.
- Pneumococcal surface protein C (PspC) is a virulence factor.
Purpose of the Study:
- Investigate the role of PspC in pneumococcal sepsis.
Main Methods:
- Generated pspC deletion mutants in S. pneumoniae strains D39 and A66.
- Infected mice intravenously with wild-type and mutant strains.
- Assessed survival rates and determined 50% lethal dose (LD50).
Main Results:
- Mice infected with pspC mutants showed significantly increased survival.
- LD50 for mutant strains was up to 250-fold higher than wild-type.
- PspC is crucial for sepsis development.
Conclusions:
- PspC plays a critical role in the pathogenesis of Streptococcus pneumoniae sepsis.
- Targeting PspC may be a therapeutic strategy against pneumococcal sepsis.
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