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Updated: Jul 8, 2026

Testing the Role of Multicopy Plasmids in the Evolution of Antibiotic Resistance
Published on: May 2, 2018
Genetic support of extended-spectrum beta-lactamases
1Service de Bactériologie-Virologie, Hôpital de Bicêtre, South-Paris Medical School, University Paris XI, Le Kremlin-Bicêtre, France. laurent.poirel@bct.aphp.fr
Extended-spectrum beta-lactamases (ESBLs) are found in Gram-negative bacteria, often spread by diverse genetic elements like insertion sequences and integrons. Understanding these mechanisms is key to combating ESBL resistance.
Area of Science:
- Microbiology
- Genetics
- Molecular Biology
Background:
- Extended-spectrum beta-lactamases (ESBLs) are enzymes conferring resistance to beta-lactam antibiotics.
- ESBL genes are prevalent in Gram-negative bacteria, particularly Enterobacteriaceae, Pseudomonas aeruginosa, and Acinetobacter baumannii.
- Common ESBL types include TEM, SHV, and CTX-M derivatives, with VEB, GES, and PER being less frequent.
Purpose of the Study:
- To investigate the genetic mechanisms underlying the acquisition and spread of ESBL genes in Gram-negative bacteria.
- To highlight the diversity of genetic elements involved in ESBL gene mobilization.
Main Methods:
- Review of scientific literature on ESBL gene dissemination.
- Analysis of genetic vehicles associated with ESBL acquisition.
Main Results:
- ESBL genes are acquired through various mechanisms, frequently involving mobile genetic elements.
- Key genetic vehicles include insertion sequences (ISs), transposons, and class 1 integrons.
- The presence of ISCR1 elements within sul1-type integrons also facilitates ESBL spread.
Conclusions:
- The diverse array of genetic vehicles significantly contributes to the widespread dissemination of ESBLs.
- Understanding these mobilization mechanisms is crucial for developing strategies to control antimicrobial resistance.
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