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Clinics ; 66(4): 543-547, 2011. tab
Article Dans Anglais | LILACS | ID: lil-588901

Résumé

OBJECTIVE: This study examined the antimicrobial resistance profile and the prevalence of resistance genes in Bacteroides spp. and Parabacteroides distasonis strains isolated from children's intestinal microbiota. METHODS: The susceptibility of these bacteria to 10 antimicrobials was determined using an agar dilution method. β-lactamase activity was assessed by hydrolysis of the chromogenic cephalosporin of 114 Bacteriodales strains isolated from the fecal samples of 39 children, and the presence of resistance genes was tested using a PCR assay. RESULTS: All strains were susceptible to imipenem and metronidazole. The following resistance rates were observed: amoxicillin (93 percent), amoxicillin/clavulanic acid (47.3 percent), ampicillin (96.4 percent), cephalexin (99 percent), cefoxitin (23 percent), penicillin (99 percent), clindamycin (34.2 percent) and tetracycline (53.5 percent). P-lactamase production was verified in 92 percent of the evaluated strains. The presence of the cfiA, cepA, ermF, tetQ and nim genes was observed in 62.3 percent, 76.3 percent, 27 percent, 79.8 percent and 7.8 percent of the strains, respectively. CONCLUSIONS: Our results indicate an increase in the resistance to several antibiotics in intestinal Bacteroides spp. and Parabacteroides distasonis and demonstrate that these microorganisms harbor antimicrobial resistance genes that may be transferred to other susceptible intestinal strains.


Sujets)
Enfant , Humains , Antibactériens/pharmacologie , Bacteroides/effets des médicaments et des substances chimiques , Résistance bactérienne aux médicaments/génétique , Intestins/microbiologie , Analyse de variance , Bacteroides/génétique , Bacteroides/isolement et purification , Résistance bactérienne aux médicaments/effets des médicaments et des substances chimiques , Gènes bactériens/effets des médicaments et des substances chimiques , Gènes bactériens/génétique , Imipénem/pharmacologie , Tests de sensibilité microbienne , Métronidazole/pharmacologie
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