Spatial transcriptomics of planktonic and sessile bacterial populations at single-cell resolution

Author:

Dar Daniel12ORCID,Dar Nina1,Cai Long1ORCID,Newman Dianne K.12ORCID

Affiliation:

1. Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.

2. Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, CA, USA.

Abstract

Spying on microbial communities, cell by cell Within any community of organisms, gene expression is heterogeneous, which can manifest in genetically identical individuals having a different phenotype. One has to look at individuals in context and analyze patterns in both space and time to see the full picture. Aiming to fill a gap in current methods, Dar et al . developed a transcriptome-imaging method named parallel sequential fluorescence in situ hybridization (par-seqFISH). They applied this technique to the opportunistic pathogen Pseudomonas aeruginosa , focusing on biofilms where growth conditions can change at microscopic scale. Development of these communities, as revealed by mRNA composition, were followed in space and time. The results revealed a heterogeneous phenotypic landscape, with oxygen availability shaping the metabolism at a spatial scale of microns within a single contiguous biofilm segment. This tool should be applicable to complex microbial communities in the environment and the human microbiome. —MAF

Funder

National Institutes of Health

Army Research Office

European Molecular Biology Organization

California Institute of Technology

Alzheimer Nadační Fond

Lorentz Center

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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