Arginine regulates the mucoid phenotype of hypervirulent Klebsiella pneumoniae
Brooke E. Ring, Caitlyn L. Holmes, Andrew J. Stark, Grace E. Shepard, Emma G. Mills, Saroj Khadka, Daria Van Tyne, Michael A. Bachman, Laura A. Mike
Abstract
Hypervirulent Klebsiella pneumoniae causes severe community-acquired infections, with its mucoid phenotype resulting from altered capsular polysaccharide chain length. While both environmental and genetic factors influence mucoidy, the cues regulating it remain unclear. Here, we show that casamino acids enhance mucoidy without affecting total capsular polysaccharide levels. We show that arginine is both necessary and sufficient in stimulating mucoid expression, activating the rmpADC promoter and increasing rmpADC transcript levels. The arginine regulator, ArgR, is crucial in this process; deleting argR reduces mucoidy and increases capsule chain length diversity. ArgR directly regulates the rmpADC promoter by binding to the ARG box. Loss of argR in vitro increases macrophage association and reduces competitive fitness in lungs, suggesting that ArgR influences adherence and fitness in the lung. Arginine-dependent regulation of mucoidy is conserved in hypervirulent K. pneumoniae isolates, suggesting that this regulatory mechanism broadly controls bacterial cell surface adaptations. Ryan et al. report a highly conserved mechanism by which arginine induces changes in hypervirulent Klebsiella pneumoniae bacterial cell surface capsule. K. pneumoniae arginine sensing is critical for full virulence potential.