Power analysis for real-time PCR quantification of genes in activated sludge and analysis of the variability introduced by DNA extraction

HEBE M. DIONISI; GERDA HARMS; ALICE C. LAYTON; IGRID GREGORY; JACK J. PARKER; SHAWN HAWKINS; KEVIN ROBINSON; GARY S. SAYLER

APPLIED AND ENVIRONMENTAL MICROBIOLOGY

ASM Press

Año: 2003 vol. 69 p. 6597 - 6604

0099-2240

The aims of this study were to determine the power of discrimination of the real-time PCR assay for monitoring fluctuations in microbial populations within activated sludge and to identify sample processing points where methodological changes are needed to minimize the variability in target quantification.  DNA was extracted using a commercially available kit from  mixed liquor samples taken from the aeration tank of four bench-scale activated-sludge reactors operating at 2-, 5-, 10- and 20-day solids retention times, with mixed-liquor volatile suspended solid (MLVSS) values ranging from 260 to 2,610 mg/L. Real-time PCR assays for bacterial and Nitrospira 16S rRNA genes were chosen because they represent, respectively, a highly abundant and a lower abundant bacterial target subject to clustering within the activated sludge matrix. The mean coefficient of variation in DNA yields (measured as µg DNA per mg MLVSS) in triplicate extractions of twelve different samples was 12.2%.  Based on power analyses, the variability associated with DNA extraction had a small impact on the overall variability of the real-time PCR assay.   Instead, a larger variability was associated with the PCR assay.   The less abundant target (Nitrospira 16S rRNA gene) had more variability than the highly abundant target (bacterial 16S rRNA gene) and samples from the lower biomass reactors had more variability than samples from the higher biomass reactors.   Power analysis of real-time PCR assays indicated that 3 to 5 samples were necessary to detect a 2-fold increase in bacterial 16S rRNA genes, whereas 3 to 5 samples were required to detect a 5-fold increase in Nitrospira 16S rRNA genes.