Complementing 16S rRNA Gene Amplicon Sequencing with Total Bacterial Load To Infer Absolute Species Concentrations in the Vaginal Microbiome

Author:

Tettamanti Boshier Florencia A.1,Srinivasan Sujatha1,Lopez Anthony1,Hoffman Noah G.2,Proll Sean3,Fredricks David N.1456,Schiffer Joshua T.145

Affiliation:

1. Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA

2. Department of Laboratory Medicine, University of Washington, Seattle, Washington, USA

3. Department of Biostatistics, University of Washington, Seattle, Washington, USA

4. Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA

5. Department of Medicine, University of Washington, Seattle, Washington, USA

6. Department of Microbiology, University of Washington, Seattle, Washington, USA

Abstract

Microbiome studies primarily use 16S rRNA gene amplicon sequencing to assess the relative abundance of bacterial taxa in a community. However, these measurements do not accurately reflect absolute taxon concentrations. We sought to determine whether the product of species’ relative abundance and total bacterial load measured by broad-range qPCR is an accurate proxy for individual species’ concentrations, as measured by taxon-specific qPCR assays. Overall, the inferred bacterial concentrations were a reasonable proxy of species-specific qPCR values, particularly when bacteria are present at a higher relative abundance. This approach offers an opportunity to assess the concentrations of bacterial species and how they change in a community over time without developing individual qPCR assays for each taxon.

Funder

HHS | National Institutes of Health

Publisher

American Society for Microbiology

Subject

Computer Science Applications,Genetics,Molecular Biology,Modeling and Simulation,Ecology, Evolution, Behavior and Systematics,Biochemistry,Physiology,Microbiology

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