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Journal of Clinical Microbiology, August 2005, p. 4046-4051, Vol. 43, No. 8
0095-1137/05/$08.00+0 doi:10.1128/JCM.43.8.4046-4051.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology,1 Department of Obstetrics and Gynecology,2 Division of Infectious Diseases, Department of Internal Medicine, Mayo Clinic and Mayo Clinic College of Medicine, Rochester, Minnesota,3 Department of Laboratory Medicine and Pathology and Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota,4 Institute of Medical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany5
Received 29 October 2004/ Returned for modification 6 December 2004/ Accepted 10 May 2005
The results for a real-time PCR assay, using the LightCycler Strep B analyte-specific reagents (Roche Diagnostics Corporation, Indianapolis, Ind.), were compared to a direct plate method combined with a broth enrichment culture method for detection of group B streptococcus colonization in pregnant women. Two separate evaluations were conducted using two different automated nucleic extraction instruments, the MagNA Pure LC instrument (Roche Diagnostics Corporation) and the lower-capacity MagNA Pure Compact instrument (Roche Diagnostics Corporation). The sensitivities, specificities, and positive and negative predictive values for the different evaluation methods were as follow: for the LightCycler Strep B assay with MagNA Pure LC, 100, 97, 90, and 100%, respectively; for the LightCycler Strep B assay with MagNA Pure Compact, 92.5, 99, 97, and 97.5%, respectively. The LightCycler Strep B assay combined with either MagNA Pure LC or MagNA Pure Compact extraction is a suitable method for detecting group B streptococcus colonization in pregnant women. An advantage of the LightCycler assay over culture is the considerably reduced turnaround time for results.
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