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1.
Antimicrob Agents Chemother ; 40(3): 616-20, 1996 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-8851581

RESUMEN

Plasmidic extended-spectrum beta-lactamases of Ambler class A are mostly inactive against ceftibuten. Salmonella typhimurium JMC isolated in Argentina harbors a bla gene located on a plasmid (pMVP-5) which confers transferable resistance to oxyiminocephalosporins, aztreonam, and ceftibuten. The beta-lactamase PER-2 (formerly ceftibutenase-1; CTI-1) is highly susceptible to inhibition by clavulanate and is located at a pI of 5.4 after isoelectric focusing. The blaPER-2 gene was cloned and sequenced. The nucleotide sequence of a 2.2-kb insert in vector pBluescript includes an open reading frame of 927 bp. Comparison of the deduced amino acid sequence of PER-2 with those of other beta-lactamases indicates that PER-2 is not closely related to TEM or SHV enzymes (25 to 26% homology). PER-2 is most closely related to PER-1 (86.4% homology), an Ambler class A enzyme first detected in Pseudomonas aeruginosa. An enzyme with an amino acid sequence identical to that of PER-1, meanwhile, was found in various members of the family Enterobacteriaceae isolated from patients in Turkey. Our data indicate that PER-2 and PER-1 represent a new group of Ambler class A extended-spectrum beta-lactamases. PER-2 so far has been detected only in pathogens (S. typhimurium, Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis) isolated from patients in South America, while the incidence of PER-1-producing strains so far has been restricted to Turkey, where it occurs both in members of the family Enterobacteriaceae and in P. aeruginosa.


Asunto(s)
Genes Bacterianos/genética , beta-Lactamasas/genética , Secuencia de Aminoácidos , Antibacterianos/farmacología , Secuencia de Bases , Ceftibuteno , Cefalosporinas/metabolismo , Clonación Molecular , Conjugación Genética , ADN Bacteriano/metabolismo , Escherichia coli/enzimología , Escherichia coli/genética , Vectores Genéticos , Focalización Isoeléctrica , Pruebas de Sensibilidad Microbiana , Datos de Secuencia Molecular , Reacción en Cadena de la Polimerasa , Salmonella typhimurium/enzimología , Salmonella typhimurium/genética
2.
Infection ; 20(3): 158-63, 1992.
Artículo en Inglés | MEDLINE | ID: mdl-1644493

RESUMEN

Salmonella typhimurium strains resistant to most beta-lactams, co-trimoxazole, tobramycin and gentamicin were isolated from patients in two hospitals in Buenos Aires, Argentina, beginning in August 1990. The patients were suffering from meningitis, septicaemia or enteritis. Therapy including ampicillin, ceftriaxone and gentamicin failed. The strains produced a plasmidic (pMVP-4) extended broad-spectrum beta-lactamase which is more active against cefotaxime than against ceftazidime (Vmax for cefotaxime 350 times higher than for ceftazidime). This cefotaximase demonstrates similarity to the previously described CTX-ase-M-1 from Escherichia coli, but it is distinctly different from CTX-ase-M-1 by its isoelectric point (7.9 for CTX-ase-M-2 in comparison with 8.9 for CTX-ase-M-1) as well as in its lower susceptibility to the beta-lactamase inhibitors sulbactam, clavulanic acid, tazobactam and BRL 42715. Thus, the beta-lactamase produced by S. typhimurium strains from Argentina appears to represent a new member (CTX-ase-M-2) of a novel group of plasmidic extended broad-spectrum beta-lactamases designated as cefotaximases.


Asunto(s)
Cefotaxima/farmacología , Factores R/genética , Infecciones por Salmonella/microbiología , Salmonella typhimurium/enzimología , beta-Lactamasas/biosíntesis , Argentina/epidemiología , Farmacorresistencia Microbiana , Humanos , Lactante , Punto Isoeléctrico , Pruebas de Sensibilidad Microbiana , Peso Molecular , Fenotipo , Infecciones por Salmonella/tratamiento farmacológico , Infecciones por Salmonella/epidemiología , beta-Lactamasas/química , beta-Lactamasas/genética
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