bioRxivMicrobiologyPreprint
Single-cell quantification of the microbiota by flow cytometry: MicFLY
Christine M. TiniD, Bianca Cordazzo Vargas, Darryl Adelaide AbbottiD, Aditi R. Lohar, Tiffany C. TayloriD, Ivan A. Valishev, Sarah N. Weinshel, Vung Lian, Kacey J. Sullinger, Matthew Butoryak, Michael A. SilvermaniD, Liat ShenhaviD, William H. DePasiD, Timothy Wesley HandiD
Abstract
The intestinal microbiota regulates multiple host functions, including digestion and immune development. Our knowledge of the microbiota has been shaped by available technology that primarily measures relative abundance. However, understanding the basis of shifts in microbiota composition requires single cell, absolute abundance measurements. In response to this problem, we developed Microbiota Flow Cytometry (MicFLY), a single cell technology that directly quantifies and characterizes total bacterial abundances with species-level resolution in the microbiota. Using MicFLY, we can identify all major intestinal taxa, discriminate live from dead bacteria, perform single cell measurements of heterogeneous bacterial mRNA expression and concurrently quantify Immunoglobulin (Ig) A and G binding to intestinal bacteria. Using longitudinal species-resolved, quantitative analysis of the preterm infant microbiota, we identify that E. coli unbound by IgG and IgA associates with the development of necrotizing enterocolitis. The application of MicFLY single cell technology permits measurement of the microbiota at a finer scale and with deeper mechanistic understanding of compositional changes.
- organism: human
- assay: flow cytometry
- research focus: host-pathogen & immune response
- approach: experimental assay
- Citations
- 0
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