Identification of the Staphylococcus aureus vfrAB Operon, a Novel Virulence Factor Regulatory Locus
Staphylococcus aureus
0303 health sciences
Virulence
Virulence Factors
Gene Expression Regulation, Bacterial
3. Good health
Mice
03 medical and health sciences
Bacterial Proteins
Mutation
Animals
Female
Staphylococcal Skin Infections
Genome, Bacterial
DOI:
10.1128/iai.01655-13
Publication Date:
2014-02-19T01:47:10Z
AUTHORS (4)
ABSTRACT
ABSTRACT
During a screen of the Nebraska Transposon Mutant Library, we identified 71 mutations in the
Staphylococcus aureus
genome that altered hemolysis on blood agar medium. Although many of these mutations disrupted genes known to affect the production of alpha-hemolysin, two of them were associated with an apparent operon, designated
vfrAB
, that had not been characterized previously. Interestingly, a Δ
vfrB
mutant exhibited only minor effects on the transcription of the
hla
gene, encoding alpha-hemolysin, when grown in broth, as well as on RNAIII, a posttranscriptional regulatory RNA important for alpha-hemolysin translation, suggesting that VfrB may function at the posttranscriptional level. Indeed, a Δ
vfrB
mutant had increased
aur
and
sspAB
protease expression under these conditions. However, disruption of the known secreted proteases in the Δ
vfrB
mutant did not restore hemolytic activity in the Δ
vfrB
mutant on blood agar. Further analysis revealed that, in contrast to the minor effects of VfrB on
hla
transcription when strains were cultured in liquid media, the level of
hla
transcription was decreased 50-fold in the absence of VfrB on solid media. These results demonstrate that while VfrB represses protease expression when strains are grown in broth,
hla
regulation is highly responsive to factors associated with growth on solid media. Intriguingly, the Δ
vfrB
mutant displayed increased pathogenesis in a model of
S. aureus
dermonecrosis, further highlighting the complexity of VfrB-dependent virulence regulation. The results of this study describe a phenotype associated with a class of highly conserved yet uncharacterized proteins found in Gram-positive bacteria, and they shed new light on the regulation of virulence factors necessary for
S. aureus
pathogenesis.
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