JAC Advance Access published online on June 27, 2006
Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dkl267
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1 Departamento de Biología Molecular, Facultad de Medicina, Universidad de Cantabria, Santander, Spain
* To whom correspondence should be addressed. Objectives: To study at the molecular level the heterogeneity of expression of the two chromosomal Methods: MIC determination by the agar dilution method and Results: The blaA allele from strain IP97 (blaA97) was found to carry a deletion of 51 bp which entirely abolished its Conclusions: The lack of activity observed in the
Received April 7, 2006
Revised May 8, 2006
Accepted June 1, 2006
Brief report
Characterization of defective
María Carmen de la Prieta 1,
María Victoria Francia 2,
Asunción Seoane 1,
and
Juan M. García Lobo 1 *
-lactamase genes in Yersinia enterocolitica
2 Servicio de Microbiología, Hospital Universitario Marqués de Valdecilla, Santander, Spain
Juan M. García Lobo, E-mail: jmglobo{at}unican.es
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Abstract
-lactamases, BlaA and BlaB, in Yersinia enterocolitica strains isolated from clinical samples.
-lactamase assays was performed to determine the resistance level conferred by these enzymes. DNA cloning, PCR and direct sequencing were used to detect the presence of mutations.
-lactamase activity. Both the ampR gene and the promoter region of strain Y56 were shown to be functional by a gene swapping experiment. The blaB allele from strain Y56 was found to carry two point mutations, only one of them resulting in a change in the amino acid sequence of the protein. This single amino acid change created a practically inactive BlaB or AmpC cephalosporinase in Y. enterocolitica Y56.
-lactamases of some Y. enterocolitica isolates was due to the presence of point mutations or small deletions in the corresponding genes.
-lactams; molecular characterization.
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