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KSA-1, a naturally occurring Ambler class A extended spectrum ß-lactamase from the enterobacterial species Kosakonia sacchari.
Fournier, Claudine; Nordmann, Patrice; de la Rosa, Jose-Manuel Ortìz; Kusaksizoglu, Ayda; Poirel, Laurent.
Afiliação
  • Fournier C; Medical and Molecular Microbiology Unit, University of Fribourg, Fribourg, Switzerland; Laboratory of Clinical Microbiology, Hôpital Cantonal Fribourgeois, Fribourg, Switzerland; Swiss National Center for Emerging Antibiotic Resistance, University of Fribourg, Fribourg, Switzerland.
  • Nordmann P; Medical and Molecular Microbiology Unit, University of Fribourg, Fribourg, Switzerland; Swiss National Center for Emerging Antibiotic Resistance, University of Fribourg, Fribourg, Switzerland; University of Lausanne and University Hospital Centre, Lausanne, Switzerland.
  • de la Rosa JO; Medical and Molecular Microbiology Unit, University of Fribourg, Fribourg, Switzerland.
  • Kusaksizoglu A; Medical and Molecular Microbiology Unit, University of Fribourg, Fribourg, Switzerland.
  • Poirel L; Medical and Molecular Microbiology Unit, University of Fribourg, Fribourg, Switzerland; Swiss National Center for Emerging Antibiotic Resistance, University of Fribourg, Fribourg, Switzerland. Electronic address: laurent.poirel@unifr.ch.
J Glob Antimicrob Resist ; 39: 6-11, 2024 Aug 13.
Article em En | MEDLINE | ID: mdl-39147026
ABSTRACT

BACKGROUND:

Several bacterial species belonging to the Gammaproteobacteria possess intrinsic class A ß-lactamase genes that may represent a source of further dissemination and acquisition to other Gram-negative species. Here we characterised KSA-1 class A ß-lactamase, the gene of which was identified within the chromosome of an environmental Enterobacterales species, namely Kosakonia sacchari, which was also recently identified as the progenitor of an MCR-like colistin-resistance determinant.

METHODS:

In silico analysis using the GenBank database identified a class A ß-lactamase gene within the chromosome of K. sacchari SP1 (GenBank accession no. WP_017456759). The corresponding protein KSA-1 shared 63% amino acid identity with the intrinsic CKO-1 from Citrobacter koseri and 53% with TEM-1. Using the K. sacchari DSM 100203 reference strain as a template, blaKSA-1 was amplified, cloned into the plasmid pUCp24 and expressed in Escherchia coli TOP10. Minimal inhibitory concentrations and kinetic parameters were obtained from the purified enzyme.

RESULTS:

K. sacchari strain SP1 conferred resistance to amino-, carboxy- and ureido-penicillins only. Once produced within E. coli, KSA-1 showed a typical clavulanic acid-inhibited extended spectrum ß-lactamase associated with a peculiar temocillin resistance profile. Kinetic assays were performed using a purified extract of KSA-1 and demonstrated a high hydrolysis rate for benzylpenicillin and piperacillin, as well as weakly extended spectrum cephalosporins. Determination of inhibitory constants showed 50% inhibitory concentration values of 2.2, 3 and 1.8 nM for clavulanic acid, tazobactam and avibactam, respectively. Analysis of sequences surrounding the blaKSA-1 gene did not reveal any mobile element that could have been involved in the acquisition of this ß-lactamase gene in that species.

CONCLUSION:

KSA-1 is a class A extended spectrum ß-lactamase distantly related to known extended spectrum or broad-spectrum Ambler class A ß-lactamases, which is highly resistant to temocillin. The blaKSA-1 gene could be considered as intrinsic within the species.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Glob Antimicrob Resist Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Glob Antimicrob Resist Ano de publicação: 2024 Tipo de documento: Article