MtrR Regulates a Major Lytic Transglycosylase (ltgA) Responsible for Peptidoglycan-Derived Cytotoxin Release and Autolysis in Neisseria gonorrhoeae

The multiple-transferable resistance protein (MtrR) is a transcriptional repressor of the <i>mtrCDE</i>-encoded drug efflux pump and Type IV pilus biosynthesis (<i>pilM</i>), and an activator of penicillin-binding protein 1 (<i>ponA</i>) expression in <i>Neisseria gonorrhoeae</i>. Previously published microarray data suggested that MtrR is also an activator of <i>ltgA</i> expression in the gonococcus. LtgA is a lytic transglycosylase responsible for approximately half of recycled peptidoglycan fragments and released peptidoglycan-derived cytotoxins, which cause ciliary damage and induce specific inflammatory responses. The fragments generated by LtgA during peptidoglycan remodeling can either be recognized by the permease AmpG for uptake into the bacterial cytoplasm and recycled for new cell wall growth and general metabolism or released into the external milieu. Therefore, we sought to define the capacity of MtrR to regulate LtgA expression in gonococci. We show that MtrR binds to the <i>ltgA</i> promoter region in a concentration-dependent manner, and that this binding results both in increased <i>ltgA</i> mRNA transcription and LtgA protein levels during exponential growth. Deletion of <i>mtrR</i> in <i>N. gonorrhoeae</i> decreased peptidoglycan monomer release from growing cells and increased autolysis. These results suggest that MtrR regulation of <i>ltgA</i> impacts peptidoglycan-derived cytotoxin release and autolysis in the gonococcus. This study suggests a central role of MtrR in coordinating aspects of the cellular envelope that may contribute to gonococcal pathogenesis.