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Emerging broad-spectrum resistance in Pseudomonas aeruginosa and Acinetobacter baumannii: Mechanisms and epidemiology
Anaïs Potron1, Laurent Poirel2, Patrice Nordmann3
1Laboratoire de Bactériologie, Faculté de Médecine-Pharmacie, Centre Hospitalier Régional Universitaire, Université de Franche-Comté, Besançon, France.
Abstract:
Multidrug resistance is quite common among non-fermenting Gram-negative rods, in particular among clinically relevant species including Pseudomonas aeruginosa and Acinetobacter baumannii. These bacterial species, which are mainly nosocomial pathogens, possess a diversity of resistance mechanisms that may lead to multidrug or even pandrug resistance. Extended-spectrum β-lactamases (ESBLs) conferring resistance to broad-spectrum cephalosporins, carbapenemases conferring resistance to carbapenems, and 16S rRNA methylases conferring resistance to all clinically relevant aminoglycosides are the most important causes of concern. Concomitant resistance to fluoroquinolones, polymyxins (colistin) and tigecycline may lead to pandrug resistance. The most important mechanisms of resistance in P. aeruginosa and A. baumannii and their most recent dissemination worldwide are detailed here.
Insights
Multidrug resistance is a significant challenge in Gram-negative bacteria like Pseudomonas aeruginosa and Acinetobacter baumannii. This review details their resistance mechanisms and global spread, impacting treatment options.
Area of Science:
- Microbiology
- Infectious Diseases
- Antimicrobial Resistance
Background:
- Non-fermenting Gram-negative rods, particularly Pseudomonas aeruginosa and Acinetobacter baumannii, are common nosocomial pathogens.
- These bacteria exhibit diverse resistance mechanisms, often leading to multidrug or pandrug resistance.
Purpose of the Study:
- To detail the primary resistance mechanisms in P. aeruginosa and A. baumannii.
- To review the global dissemination of these multidrug-resistant pathogens.
Main Methods:
- Literature review of resistance mechanisms.
- Analysis of global dissemination data for P. aeruginosa and A. baumannii.
Main Results:
- Key resistance mechanisms include extended-spectrum β-lactamases (ESBLs), carbapenemases, and 16S rRNA methylases.
- Co-resistance to fluoroquinolones, polymyxins, and tigecycline contributes to pandrug resistance.
- Recent worldwide dissemination patterns of these resistant strains are discussed.
Conclusions:
- Understanding resistance mechanisms and dissemination is crucial for combating P. aeruginosa and A. baumannii infections.
- Effective strategies are needed to manage the growing threat of multidrug and pandrug resistance in these critical pathogens.
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