| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 Department of Clinical Biochemistry, Ben-Gurion University of the Negev;
2 Department of Nephrology, Soroka Medical University Center, Beer-Sheva, Israel
Corresponding author: Amos Douvdevani, Nephrology Laboratory, Soroka Medical Center, Sderot Rager, P.O. Box 151, Beer-Sheva 84101, Israel. Email: amosd{at}bgu.ac.il
Background: Circulating cell-free DNA (CFD) levels may be elevated in trauma, stroke, sepsis, pre-eclampsia and cancer. Owing to the complex and expensive methodology, detection of CFD has hitherto been confined to research laboratories. This study presents a simple, inexpensive and accurate test for CFD.
Methods: Using the commercial fluorescent SYBR® Gold stain, biological fluids were directly assayed for CFD without prior DNA extraction and amplification. Stain was added to the sample in 96-well plates (final stain dilution: 1:10,000) and fluorescence was read by a fluorometer (excitation wavelength 488 nm, emission wavelength 535 nm).
Results: The assay was validated with serum, whole blood, urine and supernatant of cell cultures. Specificity and linearity were demonstrated over a wide range of concentrations; the results correlated with the conventional quantitative polymerase chain reaction assay of β-globin (R2 = 0.9987, P < 0.001). The assay was not affected by exposure of whole blood or serum to room temperature for four or 24 h, respectively. Intra and day-to-day coefficients of variation (16–4.8% and 31–8%, respectively; depending on DNA level) compared well with published data describing more work-intensive tests. The limit of quantitation (170 ng/mL) was below the mean DNA level in a cohort of normal individuals (471 [203] ng/mL). Finally, free DNA in supernatant of cell cultures after cell lysis accurately reflected cell number (R2 = 0.974, P < 0.0001).
Conclusions: The direct SYBR® Gold assay proved to be an accurate and simple technique for measuring CFD in biological fluids.
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?