Measuring gene expression in single bacterial cells: recent advances in methods and micro-devices

Abstract

Populations of bacterial cells that grow under the same conditions and/or environments are often considered to be uniform and thus can be described by ensemble average values of their physiologic, phenotypic, genotypic or other parameters. However, recent evidence suggests that cell-to-cell differences at the gene expression level could be an order of magnitude greater than previously thought even for isogenic bacterial populations. Such gene expression or transcriptional-level heterogeneity determines not only the fate of individual bacterial cells in a population but could also affect the ultimate fate of the population itself. Although techniques for single-cell gene expression measurement in eukaryotic cells have been successfully implemented for a decade or so, they have only recently become available for single bacterial cells. This is due to the difficulty of efficient lysis of most bacterial cells, as well as short half-life time (low stability) of bacterial mRNA. In this article, we review the recent progress and challenges associated with analyzing gene expression levels in single bacterial cells using various semi-quantitative and quantitative methods. In addition, a review of the recent progress in applying microfluidic devices to isolate single bacterial cells for gene expression analysis is also included.

• Bacteria
• gene expression
• microfluidics
• single cells
• transcriptome

Acknowledgements

We thank ASU’s NEPTUNE fund to Prof. Deirdre Meldrum for the support of this research and Dr. Laimonas Kelbauskas of ASU for editing.

Declaration of interest

The authors declare no conflict of interest. Dr. Weiwen Zhang is currently funded by a grant from the National Natural Science Foundation of China (project no. 31170043).