Abstract

Treatment with antibiotics leads to the selection of isolates with increased resistance. We investigated if evolution towards resistance was associated with virulence changes, in the context of P. aeruginosa ventilator-associated pneumonia (VAP). Four patients were selected because they had multiple VAP episodes during short periods (12 days to 5 weeks), with emergence of resistance. We performed whole-genome sequencing of 12 P. aeruginosa from bronchoalveolar lavages or blood culture (3 isolates per patient). Production of quorum sensing-dependent virulence factors, serum resistance, cytotoxicity against A549 cells, biofilm production, and twitching motility were studied. Each patient was infected with a unique strain. For all patients, resistance development was explained by genetic events in ampD, mexR or oprD. Additional variations were detected in virulence- and/or fitness-associated genes (algB, gacA, groEL, lasR, mpl, pilE, pilM, rhlR) depending on the strain. We noticed a convergence towards quorum sensing deficiency, correlated with a decrease of pyocyanin and protease production, survival in serum, twitching motility and cytotoxicity. In one patient, changes in pilM and pilE were related to enhanced twitching. We show that the emergence of resistance in P. aeruginosa is associated with virulence modification, even in acute infections. The consequences of this short-term pathoadaptation need to be explored.

Highlights

  • Pseudomonas aeruginosa is an opportunistic pathogen and one of the main agents of ventilator-associated pneumonia (VAP)[1,2]

  • Three studies in rabbit or mouse models showed that multidrug-resistant P. aeruginosa isolates were less virulent, but these studies included a small number of genetically unrelated isolates[7,8,9]

  • The 12 P. aeruginosa isolates studied here were collected at Nantes Universitary Hospital in 4 VAP patients hospitalised in intensive care units

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Summary

Introduction

Pseudomonas aeruginosa is an opportunistic pathogen and one of the main agents of ventilator-associated pneumonia (VAP)[1,2]. P. aeruginosa has a broad arsenal of virulence factors Their production is finely regulated, in particular by the quorum sensing. Quorum sensing regulates 10% of P. aeruginosa genome based on bacterial density and probably on environmental stress cues[4]. Antibiotic resistance is another key factor in the evolution of P. aeruginosa infections. Multidrug-resistant P. aeruginosa clones have caused outbreaks of healthcare-associated infections worldwide[5]. This leads to wonder about the intrinsic virulence of these multidrug-resistant strains[6]. Like loss of OprD or AmpC overexpression, could be associated with modification of virulence

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