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Journal of Clinical Microbiology, February 2000, p. 643-650, Vol. 38, No. 2
Department of Microbiology, University of
Otago, Dunedin, New Zealand
Received 20 May 1999/Returned for modification 10 September
1999/Accepted 14 October 1999
A new selective medium (CNA-P) that reduces or eliminates the
inhibitory activity of bacteriocin-producing Streptococcus
salivarius against
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
A New Alkaline pH-Adjusted Medium Enhances
Detection of
-Hemolytic Streptococci by Minimizing Bacterial
Interference Due to Streptococcus salivarius
-hemolytic streptococci has been developed
and compared with sheep blood agar (SBA) for the sensitive detection of
small numbers of
-hemolytic streptococci in clinical specimens.
CNA-P has as its basis a commercial medium (Difco Columbia CNA agar) supplemented with 5% (vol/vol) sheep blood, and the CNA is further modified by addition of 100 mM PIPES buffer
[piperazine-N,N'-bis(2-ethanesulfonic acid)]
(pH 7.5) to maintain cultures at an alkaline pH during incubation.
CNA-P was shown to inhibit the production and/or release of four
different types of S. salivarius bacteriocins or
bacteriocin-like inhibitory molecules. The efficacies of CNA-P and SBA
for detection of
-hemolytic streptococci in 1,352 pharyngeal samples
from 376 children were compared. The
-hemolytic streptococcal
isolates recovered from the samples included 314 group A (S. pyogenes), 61 group G, 33 group B, and 5 group C streptococci. Of
314 samples that yielded S. pyogenes, 300 were positive on
CNA-P (96%) and 264 (86%) were positive on SBA. A significantly
greater number of S. pyogenes isolates from these samples
were recovered only on CNA-P (50 of 314) compared with the number of
isolates recovered only on SBA (14 of 314). In addition, the degree of
positivity, a measure of the total numbers of S. pyogenes
isolates on the plate, was significantly higher on CNA-P than on SBA
(2.40 versus 2.07; P < 0.001). Interestingly, CNA-P
was also found to enhance the hemolytic activity of streptolysin O,
allowing detection of streptolysin S-deficient S. pyogenes
strains which might otherwise go undetected on SBA and other isolation media.
*
Corresponding author. Mailing address: Department of
Microbiology, University of Otago, P.O. Box 56, Dunedin, New Zealand. Phone: 643 479 7714. Fax: 643 479 8540. E-mail:
john.tagg{at}stonebow.otago.ac.nz.
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