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Finally, the toxicity of ENP for microbiological cells was quantified with EC50 values.
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Adhesion of wild type B. cenocepacia strain K56-2 and Δlxa mutant strain to CFBE41o− cells was determined by microbiological plating (A) and confirmed by confocal microscopy (B,C).
Using microbiological cultures, bacterial cells were isolated from 35% of closed fractures with delayed healing and also in 14% of uneventfully healing fractures [ 7].
Conventional markers of infection (C-reactive proteine, fibrinogen, white blood cell count and body temperature) as well as microbiological screening was performed simultaneously.
All MSU specimen were centrifuged extensively to eradicate contamination with any urothelial or microbiological cell material.
Microbiological confirmation was scarce.
Microbiological documentation was achieved in 38.6%.
Specificity of all microbiological techniques was 100%.
Microbiological monitoring was performed according to FELASA recommendations [23].
Microbiological status was monitored according to the FELASA recommendations [23].
Microbiological culture was negative.
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