The function of YbeY in the cholera bacterium is examined in a new study published on June 5th in PLOS Pathogens. The study reveals critical role of YbeY in RNA metabolism in this and other pathogenic bacteria.
Graham Walker, from the Massachusetts Institute of Technology, USA, and colleagues previously studied E. coli YbeY and found that it acts as an "RNase"—a protein that deliberately and specifically cuts RNA molecules and thereby regulates their availability and activity. Turning to Vibrio cholerae to examine the role of YbeY in disease-causing pathogens, they now report that YbeY is essential in this pathogen, critical for cell fitness and general stress tolerance, and involved in the regulation of different classes of RNA targets.
Like in higher organisms, genetic information contained in the DNA of bacteria gets "transcribed" into RNA molecules. Some of these RNAs serve as templates for proteins, others form part of the bacterial protein factories (so-called ribosomes), and yet another group consists of small regulatory RNAs that modulate cellular functions of the bacteria and their hosts. The researchers demonstrate that YbeY is needed in generating the components for functional ribosomes, for their assembly, and for ribosome quality control—eliminating defective protein factories before they turn out faulty products.
They conclude that "although functionally associated with a well-established antibiotic target, the ribosome, YbeY is so far unexploited as a drug target and its use . . . might lead to the discovery of completely novel antibiotic scaffolds" and suggest that "considering YbeY's high level of conservation, its essential nature in many pathogens, and its ability to sensitize pathogens by disrupting stress tolerance and virulence, a YbeY-specific antibiotic could have broad-spectrum antimicrobial activity."