Age of Antibiotic Resistance in MDR/XDR Clinical Pathogen of Pseudomonas aeruginosa

Author:

Kothari Ashish1ORCID,Kherdekar Radhika2,Mago Vishal3ORCID,Uniyal Madhur4,Mamgain Garima5,Kalia Roop Bhushan6,Kumar Sandeep7,Jain Neeraj89ORCID,Pandey Atul10ORCID,Omar Balram Ji1ORCID

Affiliation:

1. Department of Microbiology, All India Institute of Medical Sciences, Rishikesh 249203, India

2. Department of Dentistry, All India Institute of Medical Sciences, Rishikesh 249203, India

3. Department of Burn and Plastic Surgery, All India Institute of Medical Sciences, Rishikesh 249203, India

4. Department of Trauma Surgery, All India Institute of Medical Sciences, Rishikesh 249203, India

5. Department of Biochemistry, All India Institute of Medical Sciences, Rishikesh 249203, India

6. Department of Orthopaedics, All India Institute of Medical Sciences, Rishikesh 249203, India

7. Department of Cellular Biology and Anatomy, Augusta University, Augusta, GA 30912, USA

8. Department of Medical Oncology, All India Institute of Medical Sciences, Rishikesh 249203, India

9. Division of Cancer Biology, Central Drug Research Institute, Lucknow 226031, India

10. Department of Entomology, University of Kentucky, Lexington, KY 40503, USA

Abstract

Antibiotic resistance in Pseudomonas aeruginosa remains one of the most challenging phenomena of everyday medical science. The universal spread of high-risk clones of multidrug-resistant/extensively drug-resistant (MDR/XDR) clinical P. aeruginosa has become a public health threat. The P. aeruginosa bacteria exhibits remarkable genome plasticity that utilizes highly acquired and intrinsic resistance mechanisms to counter most antibiotic challenges. In addition, the adaptive antibiotic resistance of P. aeruginosa, including biofilm-mediated resistance and the formation of multidrug-tolerant persisted cells, are accountable for recalcitrance and relapse of infections. We highlighted the AMR mechanism considering the most common pathogen P. aeruginosa, its clinical impact, epidemiology, and save our souls (SOS)-mediated resistance. We further discussed the current therapeutic options against MDR/XDR P. aeruginosa infections, and described those treatment options in clinical practice. Finally, other therapeutic strategies, such as bacteriophage-based therapy and antimicrobial peptides, were described with clinical relevance.

Funder

SERB-DST core research

ICMR SRF/RA fellowship

Publisher

MDPI AG

Subject

Drug Discovery,Pharmaceutical Science,Molecular Medicine

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