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CTX-M-1, CTX-M-3, and CTX-M-14 beta-lactamases from Enterobacteriaceae isolated in France
C Dutour1, R Bonnet, H Marchandin
1Laboratoire de Bactériologie, Faculté de Médecine, 63001 Clermont-Ferrand Cedex, France.
Abstract:
Six clinical CTX-M-producing isolates of the family Enterobacteriaceae were detected between 1999 and 2000 in different French hospitals. Two strains produced CTX-M-1 and CTX-M-3 and four strains produced CTX-M-14, a mutant Ala-231-->Val of CTX-M-9. A putative transposable element, ISEcp-1, was located 43 bp upstream of all the bla(CTX-M) genes. Two CTX-M-14-encoding plasmids exhibited similar restriction patterns. The CTX-M-1- and CTX-M-3-encoding plasmids were related to the CTX-M-1- and CTX-M-3-encoding plasmids previously reported in 1990 in France and in 1998 in Poland, respectively.
Insights
CTX-M-producing Enterobacteriaceae strains were identified in French hospitals. These isolates carried CTX-M-1, CTX-M-3, or CTX-M-14 enzymes, with the latter linked to the ISEcp-1 element.
Area of Science:
- Microbiology
- Molecular Biology
- Genetics
Background:
- CTX-M enzymes are a growing cause of antimicrobial resistance in Enterobacteriaceae.
- Understanding the genetic basis and spread of CTX-M enzymes is crucial for infection control.
Purpose of the Study:
- To characterize CTX-M-producing Enterobacteriaceae isolates from French hospitals.
- To investigate the genetic elements associated with CTX-M gene expression and dissemination.
Main Methods:
- Clinical isolates of Enterobacteriaceae were collected and screened for CTX-M production.
- Molecular techniques were used to identify specific CTX-M variants (CTX-M-1, CTX-M-3, CTX-M-14).
- Plasmid analysis and sequencing were performed to identify associated genetic elements like ISEcp-1.
Main Results:
- Six clinical CTX-M-producing Enterobacteriaceae isolates were detected between 1999-2000.
- Four isolates produced CTX-M-14, a CTX-M-9 mutant, while two produced CTX-M-1 and CTX-M-3.
- The transposable element ISEcp-1 was found upstream of all bla(CTX-M) genes.
- CTX-M-14-encoding plasmids showed similar restriction patterns, and CTX-M-1/3 plasmids were related to previously reported ones.
Conclusions:
- The emergence of CTX-M-14, a CTX-M-9 mutant, was observed in French clinical isolates.
- The ISEcp-1 element appears to play a role in the mobilization and expression of CTX-M genes.
- Plasmid-mediated dissemination of CTX-M genes, including relatedness to older strains, continues to be a concern.
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