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Temperature downshifts induce biofilm formation in Pseudomonas aeruginosa through the SiaABCD signal and functional module

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

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Abstract

Pseudomonas aeruginosa is a highly adaptable Gram-negative pathogen known for its remarkable ability of forming biofilms. Understanding the environmental cues and regulatory mechanisms that drive biofilm formation is essential for developing effective control strategies. In this study, we screened 57 clinical and environmental P. aeruginosa isolates and discovered that a universal environmental cue, temperature downshift from host-associated 37 °C to room temperature (21 °C), significantly promotes biofilm formation in 63% of the strains. Using the ATCC 27853 strain as a model, we demonstrate that this enhancement results from increased production of the Psl exopolysaccharides at lower temperature. LC-MS/MS analysis revealed elevated levels of the secondary messenger c-di-GMP, a key regulator of the motile-to-sessile transition, at room temperature. Through screening a mutant library targeting 18 c-di-GMP metabolic enzymes, we identified the diguanylate cyclase SiaD within the SiaABCD signaling and functional module as a principal driver of c-di-GMP elevation and biofilm promotion. Further investigation showed that the entire SiaABCD module, especially the signal-sensing domain of SiaA, mediates the temperature-dependent response. Integrating lipidomics with genetics and physiological assays, we show that a temperature downshift triggers rapid membrane perturbations that activate the SiaABCD signaling module, thereby increasing Psl production to strengthen surface adhesion and drive robust biofilm formation. These findings establish temperature downshift as a previously unrecognized physiological cue that promotes biofilm formation in P. aeruginosa and define an adaptive regulatory pathway linking specific environmental stresses of membrane perturbation to dedicated c-di-GMP signaling module, paving the way for new strategies to disrupt biofilm-associated infections and transmission. © 2025 The Authors
Original languageEnglish
Article number111086
Number of pages14
JournalJournal of Biological Chemistry
Volume302
Issue number2
Online published22 Dec 2025
DOIs
Publication statusPublished - Feb 2026

Funding

This study was supported by the General Research Fund (17124719), the Collaborative Research Fund (C7033-20G), and Theme-based Research Scheme (T21-705/20-N).

Research Keywords

  • biofilm
  • c-di-GMP metabolic enzymes
  • cyclic di-GMP (c-di-GMP)
  • Pseudomonas aeruginosa (P. aeruginosa)
  • temperature response

Publisher's Copyright Statement

  • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

RGC Funding Information

  • RGC-funded

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