Key result
A cyclic peptide, RI20, identified via a novel cell-based reporter assay, successfully inhibited Hfq-mediated repression of gene expression by blocking its interactions with sRNAs.
The identification of RI20 provides a proof-of-concept for inhibiting the Hfq-sRNA regulatory pathway, a potential target for novel antibiotics against Gram-negative pathogens.
Supports Hfq-sRNA inhibition as antibiotic target; hypothesis-generating from animal data, clinical translation unproven.
Noncoding small RNAs (sRNAs) act in conjunction with the RNA chaperone Hfq to regulate gene expression in bacteria. Because Hfq is required for virulence in several bacterial pathogens, the Hfq-sRNA system is an attractive target for antibiotic development. A reporter strain in which the expression of yellow fluorescent protein (YFP) is controlled by Hfq-sRNA was engineered to identify inhibitors of this system. A reporter that is targeted by Hfq in conjunction with the RybB sRNA was used in a genetic screen to identify inhibitors from a library of cyclic peptides produced in Escherichia coli using split-intein circular ligation of peptides and proteins (SICLOPPS), an intein-based technology. One cyclic peptide identified in this screen, RI20, inhibited Hfq-mediated repression of gene expression in conjunction with both RybB and an unrelated sRNA, MicF. Gel mobility shift assays showed that RI20 inhibited binding of Hfq to RybB and MicF with similar Ki values. These data suggest that RI20 inhibits Hfq activity by blocking interactions with sRNAs and provide a paradigm for inhibiting virulence genes in Gram-negative pathogens.
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El-Mowafi et al. (2014) studied Bacterial pathogens. RI20 (cyclic peptide) was evaluated on Inhibition of Hfq-mediated repression of gene expression and binding of Hfq to sRNAs. A cyclic peptide, RI20, identified via a novel cell-based reporter assay, successfully inhibited Hfq-mediated repression of gene expression by blocking its interactions with sRNAs.
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