The function of YbeY in the cholera bacterium is examined in a new study published on June 5th in PLOS Pathogens.

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.
In addition, they find that YbeY targets virulence-associated small regulatory RNAs. Consistent with these functions, reducing the amount of YbeY makes V. cholerae less harmful (or virulent) in a mouse cholera model. The researchers also show that YbeY belongs to a set of conserved RNases that are essential in many different pathogens, including Streptococcus pneumoniae and Mycobacterium tuberculosis.
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."
Source-Eurekalert