An Overview on Phenotypic and Genotypic Characterisation of Carbapenem-Resistant Enterobacterales

Medicina (Kaunas). 2022 Nov 19;58(11):1675. doi: 10.3390/medicina58111675.

Abstract

Improper use of antimicrobials has resulted in the emergence of antimicrobial resistance (AMR), including multi-drug resistance (MDR) among bacteria. Recently, a sudden increase in Carbapenem-resistant Enterobacterales (CRE) has been observed. This presents a substantial challenge in the treatment of CRE-infected individuals. Bacterial plasmids include the genes for carbapenem resistance, which can also spread to other bacteria to make them resistant. The incidence of CRE is rising significantly despite the efforts of health authorities, clinicians, and scientists. Many genotypic and phenotypic techniques are available to identify CRE. However, effective identification requires the integration of two or more methods. Whole genome sequencing (WGS), an advanced molecular approach, helps identify new strains of CRE and screening of the patient population; however, WGS is challenging to apply in clinical settings due to the complexity and high expense involved with this technique. The current review highlights the molecular mechanism of development of Carbapenem resistance, the epidemiology of CRE infections, spread of CRE, treatment options, and the phenotypic/genotypic characterisation of CRE. The potential of microorganisms to acquire resistance against Carbapenems remains high, which can lead to even more susceptible drugs such as colistin and polymyxins. Hence, the current study recommends running the antibiotic stewardship programs at an institutional level to control the use of antibiotics and to reduce the spread of CRE worldwide.

Keywords: Carbapenem; Enterobacterales; Enterobacteriaceae; MDR; antibiotic resistance; carbapenemase; multi-drug resistance; β-lactamase.

Publication types

  • Review

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • Anti-Bacterial Agents / therapeutic use
  • Antimicrobial Stewardship*
  • Carbapenems* / pharmacology
  • Carbapenems* / therapeutic use
  • Colistin
  • Genotype
  • Humans

Substances

  • Carbapenems
  • Colistin
  • Anti-Bacterial Agents

Grants and funding

This research received no external funding.