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Standardization of laboratory practices for the study of the human gut microbiome

Jolanda Kool, Liza Tymchenko, Sudarshan Shetty, View ORCID ProfileSusana Fuentes
doi: https://doi.org/10.1101/2022.11.10.515556
Jolanda Kool
1Centre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), the Netherlands
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Liza Tymchenko
1Centre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), the Netherlands
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Sudarshan Shetty
1Centre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), the Netherlands
2Department of Medical Microbiology and Infection prevention, Virology and Immunology research Group, University Medical Center Groningen, the Netherlands
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Susana Fuentes
1Centre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), the Netherlands
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  • ORCID record for Susana Fuentes
  • For correspondence: susana.fuentes@rivm.nl
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Abstract

Technical advances in next-generation sequencing (NGS) have made it more accessible to study the human microbiome, resulting in more available data and knowledge. As a result of this expansion of data, the need to obtain comparable and reproducible data has become one of the most important challenges facing microbiome research nowadays. In this study, we aim to contribute to existing knowledge to promote high quality microbiome data and minimize bias introduced by technical variation throughout studies, from sample collection, storage, to sequencing strategies. While immediate freezing upon sampling has been the “golden standard” in the field, this method is often logistically difficult and expensive, becoming a limiting factor when conducting large scale studies or in regions where maintenance of the cold-chain presents difficulties. Therefore, we compared the immediately frozen method to storage at room temperature for 3 – 5 days in two commercially available stabilization solutions (Omnigene gut and Zymo Research) as well as without buffer. Other important aspects were tested, such as DNA extraction, bacterial DNA input or number of PCR cycles. Method choice for cell disruption resulted in the biggest difference in compositional profiles. The changes observed in microbiome profiles in samples stored at RT without stabilization solution was prevented by the use of these. For library preparation and sequencing, we found the highest heterogeneity in the DNA extraction step, followed by the use of different Illumina barcodes, indicating that both of these steps have an impact during library preparation. We did not observe a batch effect between the different sequencing runs. Standardized methods are important to allow comparison of results between different research groups worldwide and reliably expand microbiome data to a broad range of diseases, ethnical backgrounds and geographic locations. A more global perspective will increase our understanding of the human microbiome around the world.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted November 10, 2022.
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Standardization of laboratory practices for the study of the human gut microbiome
Jolanda Kool, Liza Tymchenko, Sudarshan Shetty, Susana Fuentes
bioRxiv 2022.11.10.515556; doi: https://doi.org/10.1101/2022.11.10.515556
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Standardization of laboratory practices for the study of the human gut microbiome
Jolanda Kool, Liza Tymchenko, Sudarshan Shetty, Susana Fuentes
bioRxiv 2022.11.10.515556; doi: https://doi.org/10.1101/2022.11.10.515556

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