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Data · dataset · 2026

TsrF, a transcriptional regulator in clinical Pseudomonas aeruginosa, modulates H4-T6SS expression and bacterial virulence

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The Type VI secretion system (T6SS) is a key nanoweapon in Gram-negative bacteria that mediates microbial competition and pathogenesis via toxic effector delivery.

Description

Three functionally distinct T6SS clusters (H1-H3) are known in Pseudomonas aeruginosa, yet the broader evolutionary diversity and regulatory networks of T6SS in this pathogen remain poorly defined. Here, we identify TsrF, a transcriptional regulator linked to a novel fourth T6SS (H4-T6SS) in clinical isolate LYSZa7.

TsrF directly binds the amrZ and H4-T6SS cluster to activate their transcription. AmrZ, in turn, directly regulates all four T6SS clusters. TsrF also elevates intracellular c-di-GMP levels, which via FleQ coordinately enhance H4-T6SS activity, biofilm formation, and virulence in A549 alveolar epithelial cells and Galleria mellonella models.

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Phylogenetic analysis shows TsrF homologs are widespread in Gram-negative bacteria, implying conserved T6SS-regulatory functions. Collectively, our findings shed new light on T6SS diversity and regulatory cascades, and highlight the adaptive benefits of novel T6SS operons in bacterial pathogens.

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Provenance · 1 source records, 11 field assertions
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ScienceDB10.57760/sciencedb.297238 d agoJSON v1
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