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1.
The Korean Journal of Gastroenterology ; : 215-221, 2015.
Artículo en Inglés | WPRIM | ID: wpr-194208

RESUMEN

BACKGROUND/AIMS: Several clinical trials have revealed various advantages for probiotics in inflammatory bowel disease (IBD). The aim of this study was to further investigate the effects of probiotic yogurt consumption on gut microbiota in patients with this disease. METHODS: A total of 305 participants were divided into three groups; group A (IBD patients receiving probiotic yogurt; n=105), group B (IBD patients receiving placebo; n=105), and control group (healthy individuals receiving probiotic yogurt; n=95). Stool samples were collected both before and after 8 weeks of intervention; and population of Lactobacillus, Bifidobacterium and Bacteroides in the stool specimens was measured by Taqman real-time PCR method. ': By the end of the intervention, no significant variations in the mean weight and body mass index were observed between three groups (p>0.05). However, the mean numbers of Lactobacillus, Bifidobacterium, and Bacteroides in group A were significantly increased compared to group B (p<0.001, p<0.001, and p<0.01, respectively). There were also significant differences in the mean numbers of either of three bacteria between group A and the healthy control group; however, these differences between two groups were observed both at baseline and the end of the intervention. CONCLUSIONS: Consumption of probiotic yogurt by patients with IBD may help to improve intestinal function by increasing the number of probiotic bacteria in the intestine and colon. However, many more studies are required in order to prove the concept.


Asunto(s)
Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Bacteroides/genética , Bifidobacterium/genética , ADN Bacteriano/análisis , Método Doble Ciego , Heces/microbiología , Microbioma Gastrointestinal , Enfermedades Inflamatorias del Intestino/tratamiento farmacológico , Intestinos/microbiología , Lactobacillus/genética , Efecto Placebo , Probióticos/uso terapéutico , Reacción en Cadena en Tiempo Real de la Polimerasa
2.
Clinics ; 66(4): 543-547, 2011. tab
Artículo en Inglés | LILACS | ID: lil-588901

RESUMEN

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.


Asunto(s)
Niño , Humanos , Antibacterianos/farmacología , Bacteroides/efectos de los fármacos , Farmacorresistencia Bacteriana/genética , Intestinos/microbiología , Análisis de Varianza , Bacteroides/genética , Bacteroides/aislamiento & purificación , Farmacorresistencia Bacteriana/efectos de los fármacos , Genes Bacterianos/efectos de los fármacos , Genes Bacterianos/genética , Imipenem/farmacología , Pruebas de Sensibilidad Microbiana , Metronidazol/farmacología
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