Data Acceptance Criteria for Standardized Human-Associated Fecal Source Identification Quantitative Real-Time PCR Methods

Author:

Shanks Orin C.1,Kelty Catherine A.1,Oshiro Robin2,Haugland Richard A.1,Madi Tania3,Brooks Lauren4,Field Katharine G.4,Sivaganesan Mano1

Affiliation:

1. U.S. Environmental Protection Agency, Office of Research and Development, Cincinnati, Ohio, USA

2. U.S. Environmental Protection Agency, Office of Water, Washington DC, USA

3. Source Molecular Corporation, Miami, Florida, USA

4. Department of Microbiology, Oregon State University, Corvallis, Oregon, USA

Abstract

ABSTRACT There is growing interest in the application of human-associated fecal source identification quantitative real-time PCR (qPCR) technologies for water quality management. The transition from a research tool to a standardized protocol requires a high degree of confidence in data quality across laboratories. Data quality is typically determined through a series of specifications that ensure good experimental practice and the absence of bias in the results due to DNA isolation and amplification interferences. However, there is currently a lack of consensus on how best to evaluate and interpret human fecal source identification qPCR experiments. This is, in part, due to the lack of standardized protocols and information on interlaboratory variability under conditions for data acceptance. The aim of this study is to provide users and reviewers with a complete series of conditions for data acceptance derived from a multiple laboratory data set using standardized procedures. To establish these benchmarks, data from HF183/BacR287 and HumM2 human-associated qPCR methods were generated across 14 laboratories. Each laboratory followed a standardized protocol utilizing the same lot of reference DNA materials, DNA isolation kits, amplification reagents, and test samples to generate comparable data. After removal of outliers, a nested analysis of variance (ANOVA) was used to establish proficiency metrics that include lab-to-lab, replicate testing within a lab, and random error for amplification inhibition and sample processing controls. Other data acceptance measurements included extraneous DNA contamination assessments (no-template and extraction blank controls) and calibration model performance (correlation coefficient, amplification efficiency, and lower limit of quantification). To demonstrate the implementation of the proposed standardized protocols and data acceptance criteria, comparable data from two additional laboratories were reviewed. The data acceptance criteria proposed in this study should help scientists, managers, reviewers, and the public evaluate the technical quality of future findings against an established benchmark.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference50 articles.

1. US Environmental Protection Agency. 2015. Assessment and total maximum daily load tracking and implementation system (ATTAINS). National Water Quality Inventory Report to Congress. www.epa.gov/waterdata/assessment-and-total-maximum-daily-load-tracking-and-implementation-system-attains.

2. A PCR Assay To Discriminate Human and Ruminant Feces on the Basis of Host Differences in Bacteroides-Prevotella Genes Encoding 16S rRNA

3. Development of Rapid Canine Fecal Source Identification PCR-Based Assays

4. Carbon source utilization profiles as a method to identify sources of faecal pollution in water

5. 16S rRNA-based assays for quantitative detection of universal, human-, cow-, and dog-specific fecal Bacteroidales: A Bayesian approach

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