Abstract

Pseudomonas aeruginosa, a Gram-negative opportunistic pathogenic bacterium, causes acute and chronic infections. Upon entering the host, P. aeruginosa alters global gene expression to adapt to host environment and avoid clearance by the host immune system. Proline utilization A (PutA) is a bifunctional enzyme, which converts proline to glutamate. Here we report that PutA was required for the virulence of P. aeruginosa in a murine acute pneumonia model. A putA mutant was more susceptible to oxidative stress compared to the wild type strain. An AraC/XylS family protein, PruR, directly bound to the upstream of −35 box in the putA promoter and activated putA expression. High concentration of proline in bacteria up-regulated pruR expression, which led to the activation of putA expression. As a feedback regulation, glutamate produced by PutA released PruR from the putA promoter and turned off the putA expression. PruR affected bacterial virulence through the regulation of the putA expression. Altogether, these data are the first to reveal that PutA plays an important role in the pathogenesis of P. aeruginosa, as well as to describe the genetic regulation of PutA in P. aeruginosa.

Highlights

  • Pseudomonas aeruginosa is a wide-spread Gram-negative opportunistic human pathogen, which causes acute and chronic infections, such as pneumonia, severe burn infections, sepsis, and urinary tract infections (Williams et al, 2010; Gellatly and Hancock, 2013)

  • Given that little information is currently available about the role of the proline utilization system in P. aeruginosa infection, we sought to define the function of Proline utilization A (PutA) by assessing the requirement of PutA for P. aeruginosa virulence

  • These results indicated that PruR is required for the virulence of P. aeruginosa in the murine acute pneumonia model

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Summary

Introduction

Pseudomonas aeruginosa is a wide-spread Gram-negative opportunistic human pathogen, which causes acute and chronic infections, such as pneumonia, severe burn infections, sepsis, and urinary tract infections (Williams et al, 2010; Gellatly and Hancock, 2013). In a mouse acute pneumonia model, neutrophils are rapidly recruited to the infection site in response to the invading bacteria (Shaver and Hauser, 2004). Neutrophils are the major phagocytes that generate reactive oxygen species (ROS) to kill bacteria (Ziltener et al, 2016). In P. aeruginosa, the H2O2-responsive regulator OxyR senses oxidative stress and activates the expression of defensive genes, such as katA (catalase A), katB (catalase B), ahpB (alkyl hydroperoxide reductases B), and ahpCF (alkyl hydroperoxide reductases CF), to breakdown the ROS (Ochsner et al, 2000; Heo et al, 2010).

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