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Data Acceptance Criteria for Standardized Human-Associated Fecal Source Identification Quantitative Real-Time PCR Methods.
Shanks, Orin C; Kelty, Catherine A; Oshiro, Robin; Haugland, Richard A; Madi, Tania; Brooks, Lauren; Field, Katharine G; Sivaganesan, Mano.
Afiliación
  • Shanks OC; U.S. Environmental Protection Agency, Office of Research and Development, Cincinnati, Ohio, USA shanks.orin@epa.gov.
  • Kelty CA; U.S. Environmental Protection Agency, Office of Research and Development, Cincinnati, Ohio, USA.
  • Oshiro R; U.S. Environmental Protection Agency, Office of Water, Washington DC, USA.
  • Haugland RA; U.S. Environmental Protection Agency, Office of Research and Development, Cincinnati, Ohio, USA.
  • Madi T; Source Molecular Corporation, Miami, Florida, USA.
  • Brooks L; Department of Microbiology, Oregon State University, Corvallis, Oregon, USA.
  • Field KG; Department of Microbiology, Oregon State University, Corvallis, Oregon, USA.
  • Sivaganesan M; U.S. Environmental Protection Agency, Office of Research and Development, Cincinnati, Ohio, USA.
Appl Environ Microbiol ; 82(9): 2773-2782, 2016 May.
Article en En | MEDLINE | ID: mdl-26921430
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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Microbiología del Agua / Contaminación del Agua / Calidad del Agua / Heces / Reacción en Cadena en Tiempo Real de la Polimerasa Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Microbiología del Agua / Contaminación del Agua / Calidad del Agua / Heces / Reacción en Cadena en Tiempo Real de la Polimerasa Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2016 Tipo del documento: Article