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 language | English |
|---|---|
| Article number | 111086 |
| Number of pages | 14 |
| Journal | Journal of Biological Chemistry |
| Volume | 302 |
| Issue number | 2 |
| Online published | 22 Dec 2025 |
| DOIs | |
| Publication status | Published - 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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CRF-ExtU-Lead: Deciphering the Physiological Functions and Regulation of the Endogenous CRISPR-Cas System for Biotechnological
Yan, A. (Main Project Coordinator [External]) & DENG, X. (Principal Investigator / Project Coordinator)
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TBRS-ExtU-Lead: Assess Antibiotic Resistome Flows from Pollution Hotspots to Environments and Explore the Control Strategies
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