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Journal of Clinical Microbiology, October 2007, p. 3478-3479, Vol. 45, No. 10
0095-1137/07/$08.00+0 doi:10.1128/JCM.01477-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.
Thermostable DNase Is Superior to Tube Coagulase for Direct Detection of Staphylococcus aureus in Positive Blood Cultures

LETTER
In a recent edition of the
Journal of Clinical Microbiology,
Qian et al. described the sensitivity and specificity of the
direct tube coagulase (DTC) test for the presumptive identification
of
Staphylococcus aureus directly from positive blood culture
bottles from which Gram stains were consistent with staphylococci
(
7). The reported sensitivities of 34% at 2 h of incubation
and 65% at 4 h of incubation (
7) are considerably lower than
those previously described and suggest an unacceptably high
rate of false negatives (
1,
4,
5,
6,
8,
9,
11). The authors
draw the conclusion that despite its low sensitivity the DTC
test is clinically valuable, particularly in experienced hands,
because of its low cost and simplicity (
7).
However, Qian et al. neither evaluated nor commented on the use of the thermostable DNase test for the presumptive identification of S. aureus directly from positive blood culture bottles, as described by Madison and Baselski (4) and others (1, 6, 8, 9, 10). In these studies, the thermostable DNase test has been reported to be sensitive (85% to 100%) and specific (93 to 100%), to have a high degree of correlation with the DTC test (92.7 to 100%), to be relatively simple to perform, and to have low material cost (1, 4, 6, 8, 9, 10). In our laboratory, the material cost per test is 79¢, compared to 22 ¢ for the DTC test. Furthermore, the thermostable DNase test has the advantage of having a more rapid turn-around time than the DTC test, often being positive at 1 h (4, 8).
We recently compared the thermostable DNase test with the DTC test for the presumptive identification of S. aureus from BacT/Alert (bioMérieux, Marcy l'Étoile, France) blood culture bottles in two tertiary-care teaching hospitals over a period of 50 days. The DTC test was performed by mixing 50 µl of positive blood culture broth with 450 µl of rabbit plasma (Becton Dickinson, Oakville, Ontario, Canada) in a glass test tube and incubating at 37°C. The thermostable DNase test was performed using the agar diffusion method. A 2-ml aliquot of blood culture broth was boiled for 15 min and then cooled to room temperature. Six-millimeter holes were cut in toluidine blue DNase agar plates produced in-house according to the method described by Lachica et al. (3), and 100 µl of the boiled blood culture broth was placed into the well and then incubated at 37°C. Positive and negative controls were used in all tests. Tests were read at 2 and 4 h. Sensitivities, specificities, positive predictive values (PPV), and negative predictive values (NPV) were calculated according to the method of Elder (2). Of 81 positive blood culture bottles from unique patients with initial Gram stains showing gram-positive cocci in clusters, the DTC test demonstrated a sensitivity of 56.7% at 2 h and 93.3% at 4 h while the thermostable DNase test had a sensitivity of 96.7% at 2 h and 100% at 4 h (Table 1). The specificity for both methods was 100% at both 2 and 4 h.
Based on our findings, we propose that although the DTC test
used with BacT/Alert blood culture bottles has an acceptable
sensitivity at 4 h (93.3%), the thermostable DNase test is more
rapid, has greater sensitivity, and is nearly as simple and
affordable as the DTC test and should be the test of choice
for the rapid diagnosis of
S. aureus from positive blood culture
bottles with initial Gram stains showing gram-positive cocci
in clusters. Although our study is small, it does underscore
two important points: first, that the DTC test may have variable
sensitivities depending on the operator and the culture system
used, which Qian et al. have suggested, and second, that simple
rapid tests such as the thermostable DNase test are reliable,
easily interpreted, accurate, and potentially more useful than
the DTC test.

ACKNOWLEDGMENTS
The technical expertise of the technologists who performed the
testing at Saint Boniface General Hospital and the Health Sciences
Centre is gratefully acknowledged.

FOOTNOTES

Published ahead of print on 8 August 2007.


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Philippe R. S. Lagacé-Wiens*
Department of Medical Microbiology and Infectious Diseases 543-730 William Avenue Winnipeg, Manitoba R3E 0W3, Canada
Michelle J. Alfa
Kanchana Manickam
Department of Clinical Microbiology Saint Boniface General Hospital Winnipeg, Manitoba, Canada
James A. Karlowsky
Department of Clinical Microbiology Health Sciences Centre Winnipeg, Manitoba, Canada
|
| | | | | |
* Phone: (204) 237-2053, Fax: (204) 789-3926, E-mail: plagacewiens{at}hotmail.com |
Journal of Clinical Microbiology, October 2007, p. 3478-3479, Vol. 45, No. 10
0095-1137/07/$08.00+0 doi:10.1128/JCM.01477-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.
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