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Monitor microbial communities cell by cell
In any biological community, gene expression is heterogeneous, which may be manifested in genetically identical individuals with different phenotypes
.
We must observe individuals in context and analyze patterns in space and time in order to see the complete picture
.
Microbial populations exhibit heterogeneous gene expression profiles, leading to phenotypic differences between individual bacteria
.
This diversity allows populations to survive under uncertain and fluctuating conditions, such as sudden exposure to antibiotics, dividing expensive functions between different subpopulations, and enabling interactions between different phenotypes
.
The micro-scale heterogeneity that defines microbial life can play an important role in areas such as antibiotic resistance and virulence
.
However, our understanding of these basic characteristics is limited by our ability to capture this heterogeneity on relevant temporal and spatial scales
.
This article developed par-seqFISH (Parallel Sequential Fluorescence In Situ Hybridization), which is a high-throughput method that can capture the gene expression profile of individual bacteria while preserving their physical environment in a spatial structure environment
.
We apply this method to the study of Pseudomonas aeruginosa, which is a typical biofilm-forming bacteria and an opportunistic human pathogen
.
In terms of P.
aeruginosa (P.
aeruginosa) physiology and virulence, we have studied the transcription profiles of more than 600,000 bacteria under dozens of growth conditions
Transcriptional composition using par-seqFISH captures micro-scale phenotypic changes in free-living and sessile bacterial populations
.
This article reports the population of P.
aeruginosa in growth, and proves that a single multicellular biofilm can contain coexisting but separate subpopulations with different physiological activities
.
Science, abi4882, this issue p.