DocumentCode
386530
Title
Fluid shear influences binding magnitude of S. aureus suspended in blood to collagen
Author
Mascari, Lisa ; Ross, Julia M.
Author_Institution
Dept. of Chem. & Biochem., Maryland Univ., Baltimore, MD, USA
Volume
1
fYear
2002
fDate
2002
Firstpage
709
Abstract
S. aureus is responsible for many blood-born infections and has demonstrated increasing antibiotic resistance. S. aureus-collagen binding interactions have been shown important in infections such as osteomyelitis and septic arthritis. However, their role in blood-born infections has not been determined. In infective endocarditis, bacteria and platelets combine forming thrombi on the traumatized vasculature surface. In this process collagen serves as a potential binding surface for S. aureus. Platelets and S. aureus both bind collagen under shear conditions, with platelets being much more reactive. We examined the ability of S. aureus cells suspended in whole blood to bind a collagen surface under physiologically low (100 s-1) and high (1000 s-1) fluid shear conditions. A parallel plate flow chamber was used to create a defined shear environment. The location (at the collagen surface or in the platelet aggregate above the collagen surface) and number of bacteria cells were quantified under fluorescence using confocal laser microscopy. Despite the highly reactive platelet/collagen interactions, results demonstrate that under both shear conditions the S. aureus cells bind the collagen surface in significant number. However, there are more S. aureus-collagen interactions under low shear conditions than high, where the S. aureus-platelet interactions are more abundant.
Keywords
adhesion; cellular transport; fluorescence; haemorheology; microorganisms; optical microscopy; proteins; shear flow; 1 h; 20 min; 37 C; S. aureus; bacteria; binding interactions; binding magnitude; blood-born infections; collagen; confocal laser microscopy; fluid shear; fluorescence; infective endocarditis; osteomyelitis; parallel plate flow chamber; platelets; septic arthritis; thrombi; whole blood; Aggregates; Antibiotics; Arthritis; Blood; Cells (biology); Fluorescence; Immune system; Microorganisms; Surface emitting lasers; Surface resistance;
fLanguage
English
Publisher
ieee
Conference_Titel
Engineering in Medicine and Biology, 2002. 24th Annual Conference and the Annual Fall Meeting of the Biomedical Engineering Society EMBS/BMES Conference, 2002. Proceedings of the Second Joint
ISSN
1094-687X
Print_ISBN
0-7803-7612-9
Type
conf
DOI
10.1109/IEMBS.2002.1137029
Filename
1137029
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