Beta-lactamases in Enterobacteriaceae infections in children.

Abstract

Multi-drug resistance in Gram negative bacteria, particularly in Enterobacteriaceae, is a major clinical and public health challenge. The main mechanism of resistance in Enterobacteriaceae is linked to the production of beta-lactamase hydrolysing enzymes such as extended spectrum beta-lactamases (ESBL), AmpC beta-lactamases and carbapenemases (Carbapenemase Producing Enterobacteriaceae (CPE)). ESBL and CPE resistance genes are located on plasmids, which can be transmitted between Enterobacteriaceae, facilitating their spread in hospitals and communities. These plasmids usually harbour multiple additional co-resistance genes, including to trimethoprim-sulfamethoxazole, aminoglycosides, and fluoroquinolones, making these infections challenging to treat. Asymptomatic carriage in healthy children as well as community acquired infections are increasingly reported, particularly with ESBL. Therapeutic options are limited and previously little used antimicrobials such as fosfomycin and colistin have been re-introduced in clinical practice. Paediatric experience with these agents is limited hence there is a need to further examine their clinical efficacy, dosage and toxicity in children. Antimicrobial stewardship along with strict infection prevention and control practices need to be adopted widely in order to preserve currently available antimicrobials. The future development of novel agents effective against beta-lactamases producers and their applicability in children is urgently needed to address the challenge of multi-resistant Gram negative infections.

• Authors: Christopher Alan Moxon, Stéphane Paulus
• Journal: The Journal of infection (J Infect) Vol. 72 Suppl Pg. S41-9 (07 05 2016) ISSN: 1532-2742 [Electronic] England
• PMID: 27180312 (Publication Type: Journal Article, Review)
• Copyright: Copyright © 2016 The British Infection Association. Published by Elsevier Ltd. All rights reserved.

Chemical References

• Anti-Bacterial Agents
• Bacterial Proteins
• Fosfomycin
• AmpC beta-lactamases
• beta-Lactamases
• carbapenemase
• Colistin

Topics

• Anti-Bacterial Agents (therapeutic use)
• Bacterial Proteins (biosynthesis)
• Child
• Colistin (administration & dosage, therapeutic use)
• Community-Acquired Infections (drug therapy, microbiology)
• Drug Resistance, Multiple, Bacterial
• Enterobacteriaceae (drug effects, enzymology, genetics)
• Enterobacteriaceae Infections (drug therapy, epidemiology, microbiology)
• Fosfomycin (administration & dosage, therapeutic use)
• Humans
• Microbial Sensitivity Tests
• Plasmids (genetics)
• beta-Lactam Resistance
• beta-Lactamases (biosynthesis, metabolism)