Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:3.4.21.69 (
APC
)
16,337
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Septic arthritis
and osteomyelitis in children is seldom accompanied by calf vein thrombosis and rarely by atrial thrombosis. We report the case of an 11-year, 5-month-old boy with
septic arthritis
and osteomyelitis of the sacroiliac region who developed deep venous thrombosis, in addition to life-threatening right atrial thrombosis. After an intensive hematologic investigation, a hereditary protein C deficiency was revealed. The association of venous thrombosis with
septic arthritis
or osteomyelitis should raise the possibility of the presence of
protein C
deficiency.
...
PMID:Atrial and venous thrombosis secondary to septic arthritis of the sacroiliac joint in a child with hereditary protein C deficiency. 1008 80
Biofilm formation is involved in numerous
Staphylococcus aureus
infections such as endocarditis,
septic arthritis
, osteomyelitis, and infections of indwelling medical devices. In these diseases,
S. aureus
forms biofilms as cell aggregates interspersed in host matrix material. Here, we have observed that the level of cell aggregation was significantly higher in the isogenic
spoVG
-deletion strain than in the wild-type strain. Reverse transcription-quantitative PCR data indicated that SpoVG could repress the expression of
sasC
, which codes for
S. aureus
surface
protein C
and is involved in cell aggregation and biofilm accumulation. Electromagnetic mobility shift assay demonstrated that SpoVG could specifically bind to the promoter region of
sasC
, indicating that SpoVG is a negative regulator and directly represses the expression of
sasC
In addition, deletion of the SasC aggregation domain in the
spoVG
-deletion strain indicated that high-level expression of
sasC
could be the underlying cause of significantly increased cell aggregation formation. Our previous study showed that SpoVG is involved in oxacillin resistance of methicillin-resistant
S. aureus
by regulating the expression of genes involved in cell wall synthesis and degradation. In this study, we also found that SpoVG was able to negatively modulate the
S. aureus
drug tolerance under conditions of a high concentration of oxacillin treatment. These findings can broaden our understanding of the regulation of biofilm formation and drug tolerance in
S. aureus
IMPORTANCE
This study revealed that SpoVG can modulate cell aggregation by repressing
sasC
expression and extracellular DNA (eDNA) release. Furthermore, we have demonstrated the potential linkage between cell aggregation and antibiotic resistance. Our findings provide novel insights into the regulatory mechanisms of SpoVG involved in cell aggregation and in biofilm development and formation in
Staphylococcus aureus
.
...
PMID:SpoVG Modulates Cell Aggregation in Staphylococcus aureus by Regulating
sasC
Expression and Extracellular DNA Release. 3244 67