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Cited 14 time in webofscience Cited 12 time in scopus
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Growth Dynamics of Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa as a Function of Time to Detection in BacT/Alert 3D Blood Culture Bottles with Various Preincubation Conditionsopen access

Authors
Lee, Dong-HyunKoh, Eun-HaChoi, Sae-RomKim, Sunjoo
Issue Date
Nov-2013
Publisher
KOREAN SOC LABORATORY MEDICINE
Keywords
Blood culture; Detection; Storage; Preincubation
Citation
ANNALS OF LABORATORY MEDICINE, v.33, no.6, pp 406 - 409
Pages
4
Indexed
SCIE
SCOPUS
KCI
Journal Title
ANNALS OF LABORATORY MEDICINE
Volume
33
Number
6
Start Page
406
End Page
409
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/20408
DOI
10.3343/alm.2013.33.6.406
ISSN
2234-3806
2234-3814
Abstract
Background: Delayed entry of blood culture bottles is inevitable when microbiological laboratories do not operate for 24 hr. There are few studies reported for prestorage of these bottles. The growth dynamics of Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa were investigated with respect to various preincubation conditions. Methods: Fifteen or 150 colony-forming units (CFU) of bacteria were inoculated into standard aerobic or anaerobic blood culture bottles. Bottles were preincubated at 25 degrees C or 37 degrees C for 0, 2, 4, 8, 12, 24, or 48 hr. The time to detection (TTD) then was monitored using the BacT/Alert 3D system (bioMerieux Inc., USA). Results: Significant difference in TTD was observed following preincubation for 8 hr at 25 degrees C vs. 4 hr at 37 degrees C for S. aureus, 4 hr at 25 degrees C vs. 4 hr at 37 degrees C for E. coli, 12 hr at 25 degrees C vs. 4 hr at 37 degrees C for P aeruginosa, compared to no preincubation (P<0.005). TTD values did not vary significantly with bacterial CFU or with aerobic or anaerobic bottle type. The BacT/Alert 3D system returned false negatives following preincubation of P. aeruginosa for 48 hr at 25 degrees C or 24 hr at 37 degrees C. Conclusions: TTD was mainly affected by preincubation temperature and duration rather than by input CFU quantity or bottle type for the 3 experimental bacteria.
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