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Published on: July 22, 2019
Vibrio campbellii encodes a distinct set of type III secretion system effectors that mediate cytotoxicity in
Abstract:
Type III secretion systems (T3SS) are common virulence factors that facilitate the injection of anti-eukaryotic effector toxins that damage and kill target host cells. The sequence and function of the structural and regulatory proteins of these systems are conserved across Gram-negative pathogens, including Pseudomonas , Yersinia, and Salmonella. However, the identity and function of effector proteins are not conserved and are unknown in several relevant human and animal pathogens. Here, we used comparative genomics to identify and characterize the effectors encoded by Vibrio campbellii BB120, a crustacean and fish pathogen. We showed that most sequenced Vibrio strains belonging to the Harveyi clade, including V. campbellii , encode a full set of structural and regulatory genes corresponding to the T3SS1 of V. parahaemolyticus ; the exception is V. natriegens . Transcriptomic and proteomic analyses identified four V. campbellii effectors that are secreted by the T3SS. Among these, two effectors are encoded outside the T3SS island, and all effector genes were co-regulated by both the master T3SS regulator ExsA and by the master quorum sensing regulator LuxR. Three effectors - VopS, CopA, and VIBHAR_06684 - exhibited toxic activity in yeast cells or bone marrow-derived macrophages, and the toxicity phenotypes were dependent on a functional T3SS. VopS and CopA are conserved among the queried species of the Harveyi clade. VIBHAR_06684 or VIBHAR_05674 did not show conservation among the queried species. These findings demonstrate that T3SSs in bacteria from the same clade have conserved structural secretion apparatuses but exhibit variance in effector repertoires. We postulate that the functions of effectors differ between species to impart roles in host specificity.
Author Summary:
Pathogenic Vibrio bacteria employ many virulence factors to cause disease in marine animals, including biofilms, proteases, and the secretion of toxins. Here, we identify four secreted toxins encoded by V. campbellii that are toxic to eukaryotic cells. These toxins are secreted by the type III secretion system, a needle-like apparatus used by many bacteria to inject toxins into host cells. The toxins identified in this study are regulated by quorum sensing, a method bacteria use to communicate and control virulence genes required for pathogenesis. The results of this study indicate that different Vibrio species employ distinct sets of toxins that possibly facilitate their interaction with a host.
Insights
Type III secretion systems (T3SS) in Vibrio campbellii inject toxins to cause disease. Researchers identified four novel T3SS toxins, revealing conserved systems but diverse effectors across Vibrio species, impacting host specificity.
Area of Science:
- Microbiology
- Genomics
- Pathogenesis
Background:
- Type III secretion systems (T3SS) are crucial virulence factors in Gram-negative pathogens, injecting effector proteins into eukaryotic host cells.
- While T3SS structural components are conserved, effector proteins vary significantly among bacterial species, with many remaining uncharacterized in important pathogens.
Purpose of the Study:
- To identify and characterize the effector proteins secreted by the T3SS of *Vibrio campbellii*, a significant pathogen of crustaceans and fish.
- To investigate the genetic regulation and functional roles of these identified effectors.
Main Methods:
- Comparative genomics was employed to identify potential effector genes in *V. campbellii*.
- Transcriptomics and proteomics analyses were performed to identify secreted effectors.
- Functional assays in yeast and macrophages were used to assess effector toxicity.
- Gene regulation was studied by analyzing the roles of the T3SS regulator ExsA and quorum sensing regulator LuxR.
Main Results:
- Four *V. campbellii* effectors were identified as being secreted via T3SS, with two encoded outside the T3SS island.
- All identified effector genes were co-regulated by ExsA and LuxR.
- Three effectors (VopS, CopA, VIBHAR_06684) demonstrated toxicity in eukaryotic cells, dependent on a functional T3SS.
- Effector conservation varied, with VopS conserved in the Harveyi clade and CopA only in *V. campbellii*.
Conclusions:
- *Vibrio* species within the same clade share conserved T3SS structural components but possess distinct effector repertoires.
- The identified effectors play roles in virulence and contribute to host specificity.
- T3SS effectors in *V. campbellii* are regulated by both T3SS-specific and quorum sensing systems.
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