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Updated: Aug 23, 2025

A Visual Assay to Monitor T6SS-mediated Bacterial Competition
Published on: March 20, 2013
The P. aeruginosa effector Tse5 forms membrane pores disrupting the membrane potential of intoxicated bacteria
Amaia González-Magaña1, Jon Altuna1, María Queralt-Martín2
1Fundación Biofísica Bizkaia/Biofisika Bizkaia Fundazioa (FBB) and Departamento de Bioquímica y Biología Molecular, Instituto Biofisika (CSIC, UPV/EHU), University of the Basque Country, 48940, Leioa, Spain.
Abstract:
The type VI secretion system (T6SS) of Pseudomonas aeruginosa injects effector proteins into neighbouring competitors and host cells, providing a fitness advantage that allows this opportunistic nosocomial pathogen to persist and prevail during the onset of infections. However, despite the high clinical relevance of P. aeruginosa, the identity and mode of action of most P. aeruginosa T6SS-dependent effectors remain to be discovered. Here, we report the molecular mechanism of Tse5-CT, the toxic auto-proteolytic product of the P. aeruginosa T6SS exported effector Tse5. Our results demonstrate that Tse5-CT is a pore-forming toxin that can transport ions across the membrane, causing membrane depolarisation and bacterial death. The membrane potential regulates a wide range of essential cellular functions; therefore, membrane depolarisation is an efficient strategy to compete with other microorganisms in polymicrobial environments.
Insights
Pseudomonas aeruginosa uses its type VI secretion system (T6SS) to deliver Tse5-CT, a toxic protein that forms pores in membranes, causing bacterial death and aiding in competition. This discovery sheds light on T6SS effector mechanisms.
Area of Science:
- Microbiology
- Bacterial Pathogenesis
- Molecular Biology
Background:
- The Type VI Secretion System (T6SS) in Pseudomonas aeruginosa is crucial for its survival and virulence.
- Understanding T6SS effectors is vital for combating this opportunistic pathogen.
- Many T6SS effectors and their mechanisms remain uncharacterized.
Purpose of the Study:
- To elucidate the molecular mechanism of Tse5-CT, a P. aeruginosa T6SS effector.
- To investigate the function and cellular target of Tse5-CT.
Main Methods:
- Biochemical assays to characterize Tse5-CT.
- Membrane potential measurements.
- Bacterial viability assays.
Main Results:
- Tse5-CT is the toxic, auto-proteolytic product of the T6SS effector Tse5.
- Tse5-CT functions as a pore-forming toxin.
- It transports ions across bacterial membranes, leading to membrane depolarization and cell death.
Conclusions:
- Tse5-CT's pore-forming activity is a key mechanism for P. aeruginosa competition.
- Membrane depolarization is an effective strategy for P. aeruginosa in polymicrobial environments.
- This study reveals a novel T6SS effector mechanism contributing to bacterial fitness.
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