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Journal of Clinical Microbiology, Nov 1997, 2773-2777, Vol 35, No. 11
KA Hengstler, R Hammann and AM Fahr
The microbiological performance of BBL CHROMagar Orientation medium and CPS
ID2 agar was compared to that of Columbia agar with 5% sheep blood and
MacConkey agar without crystal violet for the enumeration and presumptive
identification of bacteria responsible for urinary tract infections. Of a
total of 658 clinical urine specimens, 118 specimens yielded no growth, 402
specimens yielded growth with cell counts of > or = 10(5) CFU/ml, and
138 specimens yielded growth with cell counts of < 10(5) CFU/ml. Of the
specimens with cell counts of > or = 10(5) CFU/ml, 163 were pure
cultures and 239 were mixed cultures. A total of 266 Escherichia coli
organisms were isolated on both chromogenic media, 260 were isolated on
blood agar, and 248 were isolated on MacConkey agar. One strain (0.4%)
failed to develop the expected pink color on CHROMagar Orientation medium,
and 23 strains (8.7%) failed to develop the expected pink color on CPS ID2
agar. Enterococci (CHROMagar Orientation medium, n = 266; CPS ID2 agar, n =
265) produced small blue- green colonies on both chromogenic media. Fifty
of the mixed cultures contained enterococci that were detected only on the
chromogenic media. The Klebsiella-Enterobacter-Serratia (KES) and the
Proteus-Morganella- Providencia (PMP) groups could be identified on both
chromogenic media. Of 66 isolates of the KES group, 63 grew with the
expected color on CHROMagar Orientation medium and 58 of 64 isolates grew
with the expected color on CPS ID2 agar. Other microorganisms required
further identification. The use of chromogenic medium formulations offers a
time-saving method for the reliable detection, enumeration, and presumptive
identification of urinary tract pathogens. One of the greatest advantages
of these media is the easy recognition of mixed cultures.
Copyright © 1997 by the American Society for Microbiology. All rights reserved.
Evaluation of BBL CHROMagar orientation medium for detection and presumptive identification of urinary tract pathogens [In Process Citation]
Laboratory Group, Department of Microbiology, Heidelberg, Germany.
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