Affiliation:
1. Departments of Medical Microbiology and Infection Control
2. Internal Medicine
3. Intensive Care, VU University Medical Center, Amsterdam, The Netherlands
Abstract
ABSTRACT
Direct detection of bacterial DNA in blood offers a fast alternative to blood culture and is presumably unaffected by the prior use of antibiotics. We evaluated the performance of two real-time PCR assays for the quantitative detection of
Staphylococcus aureus
bacteremia and for
Enterococcus faecalis
bacteremia directly in blood samples, without prior cultivation. Whole-blood samples for PCR were obtained simultaneously with blood cultures from patients admitted to the intensive care unit of our hospital. After the extraction of DNA from 200 μl of blood, real-time PCR was performed for the specific detection and quantification of
S. aureus
and
E. faecalis
DNA. The sensitivity for bacteremia of the
S. aureus
PCR was 75% and that of the
E. faecalis
PCR was 73%, and both tests had high specificity values (93 and 96%, respectively). PCR amplification reactions were positive for
S. aureus
for 10 (7%) blood samples with negative blood cultures, and 7 (4%) PCR reactions were positive for
E. faecalis
. The majority of these PCR results were likely (50%) or possibly (42%) related to infection with the specific microorganism, based on clinical data and radiological and microbiological investigations. PCR results were concordant for 95% of paired whole-blood samples, and blood culture results were concordant for 97% of the paired samples. We conclude that the detection of
S. aureus
and
E. faecalis
DNA in blood by real-time PCR enables a rapid diagnosis of bacteremia and that a positive DNAemia is related to proven or possible infection with the specific microorganism in the majority of patients with negative blood cultures.
Publisher
American Society for Microbiology
Cited by
70 articles.
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