1987
DOI: 10.1139/m87-025
|View full text |Cite
|
Sign up to set email alerts
|

Cell wall alterations in staphylococci growing in situ in experimental osteomyelitis

Abstract: When cells of both Staphylococcus aureus and Staphylococcus epidermidis are grown in batch culture in nutrient-rich media, their cell walls are regular in thickness, their cell size is within the normal range for each species, and their septation patterns are orderly. When cells of each of these species are examined directly in infected tissue in the rabbit tibia model infection, their cell wall thickness is often much increased and very irregular around the circumference of the cell, their cell size is often … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
6
0

Year Published

1988
1988
2015
2015

Publication Types

Select...
8
1

Relationship

0
9

Authors

Journals

citations
Cited by 13 publications
(6 citation statements)
references
References 19 publications
0
6
0
Order By: Relevance
“…Phagocytic mixtures containing neutrophils preincubated with UHMWE wear particles and/or S. aureus suspensions, prepared as described above, were centrifuged and each pellet was suspended in sodium cacodylate buffer (0.1 M, pH 7.2) supplemented with 2.5 mM CaCl 2 , 5 mM MgCl 2 and 0.1 M sucrose, and fixed with 2.5% glutaraldehyde for 1 h at room temperature or overnight at 4°C (Costerton et al , 1987). Then, the fixed material was washed twice in cacodylate buffer, postfixed for 1 h at room temperature in 2 mL 1% osmium tetroxide in the same buffer, then embedded in Epon and sectioned.…”
Section: Methodsmentioning
confidence: 99%
“…Phagocytic mixtures containing neutrophils preincubated with UHMWE wear particles and/or S. aureus suspensions, prepared as described above, were centrifuged and each pellet was suspended in sodium cacodylate buffer (0.1 M, pH 7.2) supplemented with 2.5 mM CaCl 2 , 5 mM MgCl 2 and 0.1 M sucrose, and fixed with 2.5% glutaraldehyde for 1 h at room temperature or overnight at 4°C (Costerton et al , 1987). Then, the fixed material was washed twice in cacodylate buffer, postfixed for 1 h at room temperature in 2 mL 1% osmium tetroxide in the same buffer, then embedded in Epon and sectioned.…”
Section: Methodsmentioning
confidence: 99%
“…aureus cells were grown overnight in TSB and the culture was washed two times with HBSS and prepared TEM. 28 For intracellular S. aureus, bacteria from three wells were released after time 0, 6, 12, and 24 h (as described above) and harvested by centrifugation. The resulting pellets were washed two times with HBSS and samples were prepared for TEM as described.…”
Section: Transmission Electron Microscopy (Tem)mentioning
confidence: 99%
“…Fibrin is a regular component of the inflammatory process which accompanies many infections. Ultrastructural alterations of organisms suggesting reduced metabolic activity have been described in chronic refractory infections, such as experimental osteomyelitis (16). Glycocalyx-enclosed biofilms of bacteria have also been identified in experimental or clinical infections that arise from osteomyelitis or contaminated prostheses (15).…”
Section: Pharmacokinetics Of Antibiotic Penetration Into Fibrin Vegetmentioning
confidence: 99%