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BMC Infect Dis. 2016 May 31;16:235. doi: 10.1186/s12879-016-1568-1.

Enrichment of bacterial DNA for the diagnosis of blood stream infections.

Author information

1
Department of Molecular Biology, 108 Military Central Hospital, Hanoi, Vietnam.
2
Vietnamese - German Centre for Medical Research (VG-CARE), Hanoi, Vietnam.
3
Institute of Clinical Infectious Diseases, 108 Military Central Hospital, Hanoi, Vietnam.
4
Department of Clinical Microbiology, 108 Military Central Hospital, Hanoi, Vietnam.
5
Faculty of Infectious Diseases, Hai Phong Medical University, Hai Phong, Vietnam.
6
Department of Gastroenterology, 108 Military Central Hospital, Hanoi, Vietnam.
7
Institute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
8
Institute of Tropical Medicine, University of Tübingen, Tübingen, Germany. velavan@medizin.uni-tuebingen.de.
9
Vietnamese - German Centre for Medical Research (VG-CARE), Hanoi, Vietnam. velavan@medizin.uni-tuebingen.de.
10
Department of Molecular Biology, 108 Military Central Hospital, Hanoi, Vietnam. lehuusong@108-icid.com.
11
Institute of Clinical Infectious Diseases, 108 Military Central Hospital, Hanoi, Vietnam. lehuusong@108-icid.com.
12
Vietnamese - German Centre for Medical Research (VG-CARE), Hanoi, Vietnam. lehuusong@108-icid.com.

Abstract

BACKGROUND:

Blood cultures are commonly employed to identify bacterial pathogens causing sepsis. PCR assays to diagnose septicemia require extraction of bacterial DNA from blood samples and thus, delay the initiation of appropriate antimicrobial treatment. The presence of abundant human DNA may hamper the sensitivity of PCR in the detection of bacteria.

METHODS:

We used serial dilutions of E. Coli spiked pseudo-blood-sepsis samples to develop a simple method that combines the use of a polar detergent solvent and adjustment of the basic pH to remove human DNA. A 16S rRNA gene-based screening algorithm was established to differentiate Gram-positive and Gram-negative groups of bacteria and the family of Enterobacteriaceae. A stringent validation with appropriate controls was implemented. The method of human DNA removal was then applied on 194 sepsis blood samples and 44 cerebrospinal fluid (CSF) samples by real-time PCR.

RESULTS:

This uncomplicated and straightforward approach allows to remove up to 98 % of human DNA from peripheral blood of septic patients. The inhibitory effect of human DNA is efficiently prevented and the detection limit of real-time PCR is increased to 10 E. Coli CFUs/ml. This sensitivity is 10 times higher compared to conventional real-time PCR assays. The classical blood culture detected 58/194 (30 %) of sepsis and 9/44 (21 %) of CSF samples. Out of the 194 blood samples tested, the conventional real-time PCR targeting 13 common sepsis causing pathogens correctly detected the bacterial DNA in 16/194 (8 %) only and 14/44 (32 %) in cerebrospinal fluid samples. Our newly established approach was able to provide correct diagnoses in 78 (40 %) of the 194 blood samples and in 14 (32 %) of the CSF samples. The combination of both blood cultures and our technique raised the rate of sepsis diagnoses to 112/194 (58 %). Of the total group tested positive, 46 (24 %) cases showed overlap with the classical methodology.

CONCLUSION:

We report a simple optimized in-house protocol for removal of human DNA from blood sepsis samples as a pre-analytical tool to prepare DNA for subsequent PCR assays. With the detection increase of our in-house DNA removal approach, subsequent PCR assays can reach detection limits of 10 E. coli CFUs/ml and significantly improve the diagnostic rate in blood sepsis cases.

KEYWORDS:

Blood culture; Bloodstream infection; Human DNA removal; Molecular diagnosis; Sepsis

PMID:
27246723
PMCID:
PMC4888298
DOI:
10.1186/s12879-016-1568-1
[Indexed for MEDLINE]
Free PMC Article

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