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Benchmarking DNA isolation kits used in analyses of the urinary microbiome

Lisa Karstens, Nazema Y. Siddiqui, Tamara Zaza, Alecsander Barstad, Cindy L. Amundsen, View ORCID ProfileTatyana A. Sysoeva
doi: https://doi.org/10.1101/2020.11.10.375279
Lisa Karstens
1Department of Obstetrics & Gynecology, Division of Urogynecology, Oregon Health & Science University, Portland, OR, 97239
2Department of Medical Informatics and Clinical Epidemiology, Division of Bioinformatics and Computational Biomedicine, Oregon Health & Science University, Portland, OR, 97239
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Nazema Y. Siddiqui
3Department of Obstetrics & Gynecology, Division of Urogynecology and Reconstructive Pelvic Surgery, Duke University Medical Center, Durham, NC 27710
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Tamara Zaza
4Department of Biological Sciences, University of Alabama in Huntsville, Huntsville, AL 35899
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Alecsander Barstad
2Department of Medical Informatics and Clinical Epidemiology, Division of Bioinformatics and Computational Biomedicine, Oregon Health & Science University, Portland, OR, 97239
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Cindy L. Amundsen
3Department of Obstetrics & Gynecology, Division of Urogynecology and Reconstructive Pelvic Surgery, Duke University Medical Center, Durham, NC 27710
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Tatyana A. Sysoeva
4Department of Biological Sciences, University of Alabama in Huntsville, Huntsville, AL 35899
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  • ORCID record for Tatyana A. Sysoeva
  • For correspondence: tatyana.sysoeva@uah.edu
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Abstract

The urinary microbiome has been increasingly characterized using next-generation sequencing. However, many of the technical methods have not yet been specifically optimized for urine. We sought to compare the performance of several DNA isolation kits used in urinary microbiome studies. A total of 11 voided urine samples and one buffer control were divided into 5 equal aliquots and processed in parallel using five commercial DNA isolation kits. DNA was quantified and the V4 segment of the 16S rRNA gene was sequenced. Data were processed to identify the microbial composition and to assess alpha and beta diversity of the samples. Tested DNA isolation kits result in significantly different DNA yields from urine samples but non-significant differences in the number of reads recovered, alpha, or beta diversity. DNA extracted with the Qiagen Biostic Bacteremia and DNeasy Blood & Tissue kits showed the fewest technical issues in downstream analyses, with the DNeasy Blood & Tissue kit also demonstrating the highest DNA yield. The Promega kit recovered fewer Gram positive bacteria compared to other kits. The Promega and DNeasy PowerSoil kits also appear to have some important biases towards over-representing certain Gram negative bacteria of biologic relevance within the urinary microbiome.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • https://www.ncbi.nlm.nih.gov/bioproject/PRJNA662669

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, 2020.
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Benchmarking DNA isolation kits used in analyses of the urinary microbiome
Lisa Karstens, Nazema Y. Siddiqui, Tamara Zaza, Alecsander Barstad, Cindy L. Amundsen, Tatyana A. Sysoeva
bioRxiv 2020.11.10.375279; doi: https://doi.org/10.1101/2020.11.10.375279
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Benchmarking DNA isolation kits used in analyses of the urinary microbiome
Lisa Karstens, Nazema Y. Siddiqui, Tamara Zaza, Alecsander Barstad, Cindy L. Amundsen, Tatyana A. Sysoeva
bioRxiv 2020.11.10.375279; doi: https://doi.org/10.1101/2020.11.10.375279

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