Improving Equivalency in Metagenomics: A Harmonized Process to Extract Fecal DNA.
The authors tested 21 DNA extraction protocols on the same fecal samples and quantified the differences observed in the microbial community compositions. Procedural variables of library preparation and sample storage were contrasted with biological variations observed within the same specimen or within an individual over time. Extraction protocols were then ranked by the resulting DNA quantity and quality, estimates of recovered community diversity, and the ratio between gram-positive and gram-negative bacteria. Procedure reproducibility was tested within and across laboratories, and the accuracy of the topper-forming DNA extraction methods was assessed using a mock community of bacterial species whose exact relative abundance was known.
If only the ranks of the bacterial species of interest are required, most of the available protocols tested gave highly comparable results. However, for many applications, species-specific abundance information is required, and this information needs to be commensurable between methods. Using this metric, many of the protocols tested were not equivalent and instead introduced large batch effects. Of the species particularly affected by the extraction protocol, the majority were gram-positive, an unsurprising finding given the higher mechanical strength of gram-positive bacterial cell walls. In the selection of the final protocol, reproducibility, recovery of bacterial diversity, and automation were factors. In addition, the selected winning protocol accurately extracted DNA from the spiked bacteria in the test stool samples.
As the literature regarding the harmonization of molecular methods in research or clinical laboratories expands, this article makes an important contribution. Variations in DNA extraction protocols can have large effects on the observed microbial composition of stool samples, and a harmonized method will improve the comparability of human gut microbiome studies and facilitate metaanalysis. Furthermore, because of its performance characteristics, the selected protocol should serve as a benchmark for new methods.
Author Contributions: All authors confirmed they have contributed to the intellectual content of this paper and have met the following 4 requirements: (a) significant contributions to the conception and design, acquisition of data, or analysis and interpretation of data; (b) drafting or revising the article for intellectual content; (c) final approval of the published article; and (d) agreement to be accountable for all aspects of the article thus ensuring that questions related to the accuracy or integrity of any part of the article are appropriately investigated and resolved.
Authors' Disclosures or Potential Conflicts of Interest: No authors declared any potential conflicts of interest.
(1.) Costea PI, Zeller G, Sunagawa S, Pelletier E, Alberti A, Levenez F, et al. Towards standards for human fecal sample processing in metagenomic studies. Nat Biotechnol 2017;35:1069-76.
Jessica L. Gifford * [dagger]
Calgary Laboratory Services and the Department of Pathology and Laboratory Medicine, University of Calgary, Calgary, Alberta, Canada.
* Address correspondence to the author at: Calgary Laboratory Services, Diagnostic and Scientific Research Centre, C-158 9,3535 Research Way NW, Calgary, AB, T2L 2K8 Canada. Fax 403-770-3543; e-mail firstname.lastname@example.org.
([dagger]) Member of the Society for Young Clinical Laboratorians (SYCL) (http://www.aacc.org/ community/sycl).
Received March 19, 2018; accepted March 26, 2018.
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|Title Annotation:||the Clinical Chemist: News & Views|
|Author:||Gifford, Jessica L.|
|Date:||Jun 1, 2018|
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