Rapid detection of simulated bacteremia by centrifugation and filtration
Author(s) -
M B Herlich,
Ronald F. Schell,
Moisés Francisco,
Jack L. Le Frock
Publication year - 1982
Publication title -
journal of clinical microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.349
H-Index - 255
eISSN - 1070-633X
pISSN - 0095-1137
DOI - 10.1128/jcm.16.1.99-102.1982
Subject(s) - filtration (mathematics) , ficoll , centrifugation , microorganism , chromatography , membrane filter , agar , microbiology and biotechnology , agar plate , differential centrifugation , biology , bacteremia , chemistry , bacteria , membrane , biochemistry , antibiotics , in vitro , genetics , mathematics , statistics , peripheral blood mononuclear cell
A centrifugation-filtration procedure was developed to expedite the recovery of microorganisms from blood. Fresh whole human blood was inoculated with various aerobic and facultatively anaerobic microorganisms (3 to 18 per ml). The seeded blood was carefully overlaid on a Ficoll-Hypaque gradient (density, 1.114 g/ml) and centrifuged (400 x g) for 45 min at ambient temperature. The entire gradient (plasma, leukocytes, and Ficoll-Hypaque) was removed and filtered through a 0.22-micrometer membrane filter. The filters were then placed on chocolate agar and incubated at 35 degrees C in humidified air containing 5% CO2. No statistically significant differences were detected between the numbers of microorganisms recovered by filtration and by direct culture of the original inoculum. Most microorganisms were detected within 18 h after filtration. This system has excellent sensitivity and negligible toxicity.
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