Abstract

Klebsiella pneumoniae is a rod-shaped, encapsulated, Gram-negative bacteria associated with multiple nosocomial infections. Multidrug-resistant (MDR) K. pneumoniae strains have been increasing and the therapeutic options are increasingly limited. Colistin is a long-used, polycationic, heptapeptide that has regained attention due to its activity against Gram-negative bacteria, including the MDR K. pneumoniae strains. However, this antibiotic has a complex mode of action that is still under research along with numerous side-effects. The acquisition of colistin resistance is mainly associated with alteration of lipid A net charge through the addition of cationic groups synthesized by the gene products of a multi-genic regulatory network. Besides mutations in these chromosomal genes, colistin resistance can also be achieved through the acquisition of plasmid-encoded genes. Nevertheless, the diversity of molecular markers for colistin resistance along with some adverse colistin properties compromises the reliability of colistin-resistance monitorization methods. The present review is focused on the colistin action and molecular resistance mechanisms, along with specific limitations on drug susceptibility testing for K. pneumoniae.

Highlights

  • Under antibiotic pressure, bacteria can rapidly evolve and develop resistance, mainly through genetic alterations in the antibiotic target genes that decrease or inhibit antimicrobial activity [1]

  • Bacteria can acquire genes encoded in genetic elements that can be mobilized via horizontal gene transfer (HGT), which eases the spread of resistance genes between different strains or species and drives the emergence of multidrug-resistant (MDR) bacteria [2,3]

  • The most frequent agents associated with life-threatening nosocomial infections and high levels of resistance reported are known as the “ESKAPE” pathogens, where ESKAPE is an acronym for Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter species [5]

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Summary

A Molecular Perspective on Colistin and Klebsiella pneumoniae

Centro de Investigação Interdisciplinar Egas Moniz, Instituto Universitário Egas Moniz, Monte da Caparica, 2829-511 Almada, Portugal

Introduction
Colistin’s Structure and Mechanism of Action
Chromosomal Mutations Leading to LPS Modification
Capsule
Efflux Pumps
Plasmid-Mediated Resistance
(Supplementary
Findings
Conclusions
Full Text
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