4.8 Article

Establishing reference material for the quest towards standardization in environmental microbial metagenomic studies

Journal

WATER RESEARCH
Volume 245, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2023.120641

Keywords

Metagenomics; Standardization; Accuracy; Reproducibility; Comparability; Environmental reference material; Technical variation

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Breakthroughs in DNA-based technologies have enhanced researchers' ability to explore environmental microbiome. However, the diversification and heterogeneity of metagenomic workflows pose challenges. This study quantified microbial profiling variations caused by technical variables and suggested the development of an environmental reference material to ensure reliable and reproducible sequencing outputs. The study also highlighted the importance of DNA isolation and sequencing library construction in minimizing variations, while DNA extraction kits and sequencing run batch were found to be major sources of variability.
Breakthroughs in DNA-based technologies, especially in metagenomic sequencing, have drastically enhanced researchers' ability to explore environmental microbiome and the associated interplays within. However, as new methodologies are being actively developed for improvements in different aspects, metagenomic workflows become diversified and heterogeneous. Through a single-variable control approach, we quantified the microbial profiling variations arising from 6 common technical variables associated with metagenomic workflows for both simple and complex samples. The incurred variations were constantly the lowest in replicates of DNA isolation and DNA sequencing library construction. Different DNA extraction kits often caused the highest variation among all the tested variables. Additionally, sequencing run batch was an important source of variability for targeted platforms. As such, the development of an environmental reference material for complex environmental samples could be beneficial in benchmarking accrued non-biological variability within and between protocols and insuring reliable and reproducible sequencing outputs immediately upstream of bioinformatic analysis. To develop an environment reference material, sequencing of a well-homogenized environmental sample composed of activated sludge was performed using different pre-analytical assays in replications. In parallel, a certified mock community was processed and sequenced. Assays were ranked based on the reconstruction of the theo-retical mock community profile. The reproducibility of the best-performing assay and the microbial profile of the reference material were further ascertained. We propose the adoption of our complex environmental reference material, which could reflect the degree of diversity in environmental microbiome studies, to facilitate accurate, reproducible, and comparable environmental metagenomics-based studies.

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