Absolute quantification of the living skin microbiome overcomes relic-DNA bias and reveals specific patterns across volunteers

Our results reveal the significant bias relic DNA has on the quantification of low biomass samples like the skin. The reduced intraindividual similarity across samples following relic-DNA depletion highlights the bias introduced by traditional (total DNA) sequencing in diversity comparisons across samples. The divergent levels of cell viability measured across different skin sites, along with the inconsistencies in taxa differential abundance determined by total vs live cell DNA sequencing, suggest an important hypothesis for certain sites being susceptible to pathogen infection. Overall, our study demonstrates a characterization of the skin microbiome that overcomes relic-DNA bias to provide a baseline for live microbiota that will further improve mechanistic studies of infection, disease progression, and the design of therapies for the skin. Video Abstract.

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Publication Details

Journal
Microbiome
Published
2025-03-04
DOI
https://doi.org/10.1186/s40168-025-02063-4
Citations
9
Primary Topic
Dermatology and Skin Diseases
Type
article
Field-Weighted Citation Impact
18.04

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article

Absolute quantification of the living skin microbiome overcomes relic-DNA bias and reveals specific patterns across volunteers

Lívia S. Zaramela, Clarisse Marotz, Perris Navarro, Oriane Moyne et al.
9 citations
Microbiome
Dermatology and Skin Diseases
18.04
article

Absolute quantification of the living skin microbiome overcomes relic-DNA bias and reveals specific patterns across volunteers

Lívia S. Zaramela, Clarisse Marotz, Perris Navarro, Oriane Moyne, Michael R. Williams, Deepan Thiruppathy, Karsten Zengler
article en
9 citations

Abstract

Our results reveal the significant bias relic DNA has on the quantification of low biomass samples like the skin. The reduced intraindividual similarity across samples following relic-DNA depletion highlights the bias introduced by traditional (total DNA) sequencing in diversity comparisons across samples. The divergent levels of cell viability measured across different skin sites, along with the inconsistencies in taxa differential abundance determined by total vs live cell DNA sequencing, suggest an important hypothesis for certain sites being susceptible to pathogen infection. Overall, our study demonstrates a characterization of the skin microbiome that overcomes relic-DNA bias to provide a baseline for live microbiota that will further improve mechanistic studies of infection, disease progression, and the design of therapies for the skin. Video Abstract.

MicrobiomeVol. 13(1)
University of California San Diego (US)
Evonik Industries, National Institutes of Health, University of California, San Diego
Openalex Percentile: Top 1%
Dermatology and Skin Diseases
18.04
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