2022
DOI: 10.1016/j.cub.2022.10.052
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Collective decision-making in Pseudomonas aeruginosa involves transient segregation of quorum-sensing activities across cells

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Cited by 7 publications
(3 citation statements)
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“…We conducted two follow-up experiments to validate our main observations that P. aeruginosa upregulates T6SS and pyoverdine genes under iron-rich conditions, and phenazine and hydrogen cyanide genes under iron-limited conditions (see Supplementary Information). First, we constructed four reporter strains, in which we cloned the promoter region of icmF1 (T6SS structure component gene), pvdA (pyoverdine synthesis gene), phzA1 (phenazine synthesis gene), and hcnA (hydrogen cyanide synthesis gene) in front of a gfp (green fluorescent protein) reporter gene 62 . We subjected these reporter strains to the same treatments used in the RNA-Seq experiment and followed GFP expression over time (Supplementary Fig.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…We conducted two follow-up experiments to validate our main observations that P. aeruginosa upregulates T6SS and pyoverdine genes under iron-rich conditions, and phenazine and hydrogen cyanide genes under iron-limited conditions (see Supplementary Information). First, we constructed four reporter strains, in which we cloned the promoter region of icmF1 (T6SS structure component gene), pvdA (pyoverdine synthesis gene), phzA1 (phenazine synthesis gene), and hcnA (hydrogen cyanide synthesis gene) in front of a gfp (green fluorescent protein) reporter gene 62 . We subjected these reporter strains to the same treatments used in the RNA-Seq experiment and followed GFP expression over time (Supplementary Fig.…”
Section: Resultsmentioning
confidence: 99%
“…To validate the RNA-Seq results, we looked at the expression of specific genes using fluorescent gene-expression reporter strains. These strains were constructed following the protocol from Jayakumar et al 62 . Briefly, we chromosomally integrated a transcriptional reporter fusion (in which the promoter of the gene of interest was fused to the fluorescent gene marker GFP) into the P. aeruginosa PAO1 wild type strain.…”
Section: Methodsmentioning
confidence: 99%
“…Understanding QS at the single-cell level offers critical insights into bacterial communication that bulk experiments cannot capture. QS heterogeneity or bimodality has been documented, indicating a mix of QS-activated and -inactivated states within bacterial populations 11,15,16 . However, these observations were typically derived indirectly using bulk cultures – either grown on agar or in liquid media – where QS signals could accumulate or establish spatial gradients, which can mask the dynamics of QS by allowing bacteria to experience different local conditions.…”
Section: Introductionmentioning
confidence: 99%