Antibiotic resistance in Pseudomonas aeruginosa: mechanisms and alternative therapeutic strategies

Zheng Pang, Renee Raudonis, Bernard R. Glick, Tong Jun Lin, Zhenyu Cheng

Research output: Contribution to journalReview articlepeer-review

1509 Citations (Scopus)

Abstract

Pseudomonas aeruginosa is an opportunistic pathogen that is a leading cause of morbidity and mortality in cystic fibrosis patients and immunocompromised individuals. Eradication of P. aeruginosa has become increasingly difficult due to its remarkable capacity to resist antibiotics. Strains of Pseudomonas aeruginosa are known to utilize their high levels of intrinsic and acquired resistance mechanisms to counter most antibiotics. In addition, adaptive antibiotic resistance of P. aeruginosa is a recently characterized mechanism, which includes biofilm-mediated resistance and formation of multidrug-tolerant persister cells, and is responsible for recalcitrance and relapse of infections. The discovery and development of alternative therapeutic strategies that present novel avenues against P. aeruginosa infections are increasingly demanded and gaining more and more attention. Although mostly at the preclinical stages, many recent studies have reported several innovative therapeutic technologies that have demonstrated pronounced effectiveness in fighting against drug-resistant P. aeruginosa strains. This review highlights the mechanisms of antibiotic resistance in P. aeruginosa and discusses the current state of some novel therapeutic approaches for treatment of P. aeruginosa infections that can be further explored in clinical practice.

Original languageEnglish
Pages (from-to)177-192
Number of pages16
JournalBiotechnology Advances
Volume37
Issue number1
DOIs
Publication statusPublished - Jan 1 2019

Bibliographical note

Funding Information:
We thank Janie Zhang for assistance in making the figures. The work in Tong-Jun Lin's lab have been supported by the Discovery Grant from Natural Sciences and Engineering Research Council, Canada (NSERC) of Canada and Canadian Institute of Heath Research (CIHR). The research in Zhenyu Cheng's lab has been supported by Cystic Fibrosis Canada and a Discovery Grant from NSERC.

Funding Information:
We thank Janie Zhang for assistance in making the figures. The work in Tong-Jun Lin’s lab have been supported by the Discovery Grant from Natural Sciences and Engineering Research Council , Canada (NSERC) of Canada and Canadian Institute of Heath Research (CIHR). The research in Zhenyu Cheng’s lab has been supported by Cystic Fibrosis Canada and a Discovery Grant from NSERC.

Publisher Copyright:
© 2018 The Author(s)

ASJC Scopus Subject Areas

  • Biotechnology
  • Bioengineering
  • Applied Microbiology and Biotechnology

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