| Literature DB >> 29483118 |
Nacim Bouheraoua1, Laurent Poirel2,3,4, Baptiste Bourreau5,6,7, Rémy Bonnin5,6,7, Laurent Laroche1, Thierry Naas5,6,7, Patrice Nordmann8,3,4,9.
Abstract
Integrons are genetic elements that can acquire and rearrange gene cassettes. The blaBEL-1 gene encodes an extended-spectrum β-lactamase, BEL-1, that is present at the second position of the variable region of class 1 integrons identified in Pseudomonas aeruginosa The mobility of the bel-1 gene cassette was analyzed under physiological conditions and with the integrase gene being overexpressed. Cassette mobility in Escherichia coli was detected by excision/integration into the recipient integron In3 on the conjugative plasmid R388 with the overproduced integrase. Despite several antibiotic pressures, the bel-1 cassette remained at the second position in the integron, highlighting its stability in P. aeruginosa Overexpression of the integrase gene in E. coli induced bel-1 cassette recombination. However, cassettes containing two genes (blaBEL-1 and smr2 or blaBEL-1 and aacA4) were excised, suggesting that the bel-1 cassette attC site was defective. We show that bel-1 is a stable gene cassette under physiological growth conditions, irrespective of the selective antibiotic pressure, that may be mobilized upon overexpression of the integrase gene.Entities:
Keywords: BEL-1; ESBL; Pseudomonas aeruginosa; integron; site-specific recombination
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Year: 2018 PMID: 29483118 PMCID: PMC5923138 DOI: 10.1128/AAC.00030-18
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191