Structural and Cellular Insights into the l,d-Transpeptidase YcbB as a Therapeutic Target in Citrobacter rodentium, Salmonella Typhimurium, and Salmonella Typhi Infections.
Nathanael A CaveneyAntonio Serapio-PalaciosS E WoodwardT BozorgmehrG CaballeroM VuckovicW DengBarton Brett FinlayNatalie C J StrynadkaPublished in: Antimicrobial agents and chemotherapy (2021)
The bacterial cell wall plays a key role in viability and is an important drug target. The cell wall is made of elongated polymers that are cross-linked to one another to form a load-bearing mesh. An alternative cell wall cross-linking mechanism used by the l,d-transpeptidase YcbB has been implicated in the stress-regulated roles of β-lactam resistance, outer membrane defect rescue, and typhoid toxin release. The role for this stress-linked cross-linking in the context of a host infection was unclear. Here, we resolve the crystallographic structures of both Salmonella Typhi YcbB and Citrobacter rodentium YcbB acylated with ertapenem that delineate the conserved structural characteristics of YcbB. In parallel, we show that the general involvement of YcbB in peptidoglycan reinforcement under conditions of bacterial outer envelope stress does not play a significant role in acute infections of mice by C. rodentium and S Typhimurium. Cumulatively, in this work we provide a foundation for the development of novel YcbB-specific antibacterial therapeutics to assist in treatment of increasingly drug-resistant S Typhi infections.
Keyphrases
- cell wall
- drug resistant
- listeria monocytogenes
- escherichia coli
- multidrug resistant
- acinetobacter baumannii
- liver failure
- stress induced
- emergency department
- small molecule
- pseudomonas aeruginosa
- gram negative
- cystic fibrosis
- intensive care unit
- high fat diet induced
- combination therapy
- anti inflammatory
- soft tissue
- wild type