Cracking the Challenge of Antimicrobial Drug Resistance with CRISPR/Cas9, Nanotechnology and Other Strategies in ESKAPE Pathogens.
Tanzeel ZohraMuhammad NumanAamer IkramMuhammad SalmanTariq KhanMisbahud DinMuhammad SalmanAyesha FarooqAfreenish AmirMuhammad AliPublished in: Microorganisms (2021)
Antimicrobial resistance is mushrooming as a silent pandemic. It is considered among the most common priority areas identified by both national and international agencies. The global development of multidrug-resistant strains now threatens public health care improvement by introducing antibiotics against infectious agents. These strains are the product of both continuous evolution and unchecked antimicrobial usage (AMU). The ESKAPE pathogens (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter species) are the leading cause of nosocomial infections throughout the world. Most of them are now multidrug-resistant, which pose significant challenges in clinical practice. Understanding these bacteria's resistance mechanisms is crucial for developing novel antimicrobial agents or other alternative tools to fight against these pathogens. A mechanistic understanding of resistance in these pathogens would also help predict underlying or even unknown mechanisms of resistance of other emerging multidrug-resistant pathogens. Research and development to find better antibacterial drugs and research on tools like CRISPER-Cas9, vaccines, and nanoparticles for treatment of infections that can be further explored in the clinical practice health sector have recognized these alternatives as essential and highly effective tools to mitigate antimicrobial resistance. This review summarizes the known antimicrobial resistance mechanisms of ESKAPE pathogens and strategies for overcoming this resistance with an extensive overview of efforts made in this research area.
Keyphrases
- antimicrobial resistance
- multidrug resistant
- acinetobacter baumannii
- klebsiella pneumoniae
- gram negative
- drug resistant
- staphylococcus aureus
- healthcare
- crispr cas
- pseudomonas aeruginosa
- clinical practice
- escherichia coli
- genome editing
- biofilm formation
- sars cov
- mental health
- cystic fibrosis
- public health
- emergency department
- coronavirus disease
- quality improvement
- risk assessment
- silver nanoparticles
- health insurance
- human health