首页> 外文期刊>Gut Pathogens >Bacillus coagulans GBI-30, 6086 limits the recurrence of Clostridium difficile-Induced colitis following vancomycin withdrawal in mice
【24h】

Bacillus coagulans GBI-30, 6086 limits the recurrence of Clostridium difficile-Induced colitis following vancomycin withdrawal in mice

机译:凝结芽孢杆菌GBI-30、6086限制了万古霉素停用后艰难梭状芽胞杆菌诱导的结肠炎的复发

获取原文
           

摘要

Background Recently, we found that the probiotic strain Bacillus coagulans GBI-30, 6086 (GanedenBC30) improved indices of Clostridium difficile (C. difficile)-induced colitis in mice (Fitzpatrick et al., Gut Pathogens, 2011). Our goal was to determine if BC30 could also prevent the recurrence of C. difficile-induced colitis in mice, following initial treatment with vancomycin. During study days 0 through 5, mice were treated with antibiotics. On day 6, the C. difficile strain VPI 10463 was given by oro-gastric gavage at ≈ 5x104 CFU to induce colitis. Mice were treated on study days 6 to 10 with vancomycin (50 mg/kg) (vanco) or vehicle (saline) by gavage. On days 10 to16, mice were dosed by gavage with saline vehicle or BC30 (2 x 109 CFU per day). Mice were monitored for mortality, weight loss and diarrhea. On study days 14, 16 and 17, stools and colons were collected for analyzing other parameters of colitis. Results The mean stool consistency score in Vehicle/C.difficile/Vanco mice increased from 0.4 (day 10) to a range of 1.1 to 1.4 (days 14 to 17), indicating the recurrence of colitis. On days 13 through 17, the stool consistency scores for the vancomycin/BC30 mice were significantly lower (p< 0.05) than for the vancomycin/vehicle cohort of animals. On day 17, 88.9% of mice treated with BC30 had normal stools, while this value was 0% with vehicle treatment (p value = 0.0004). Colonic myeloperoxidase (Units/2 cm colon) was significantly (p < 0.05) reduced from 4.3 ± 0.7 (Vehicle/C.difficile/Vanco) to 2.6 ± 0.2 (BC30/C. Difficle/Vanco). The colonic histology score and Keratinocyte derived-chemokine level in the colon were also lower in BC30 treated mice. Summary In BC30-treated mice, there was evidence of better stool consistency, as well as improved biochemical and histological indices of colitis, following initial treatment of animals with vancomycin. Conclusion BC30 limited the recurrence of CD-induced colitis following vancomycin withdrawal in mice.
机译:背景技术最近,我们发现益生菌菌株凝结芽孢杆菌GBI-30,6086(GanedenBC30)改善了艰难梭菌(C. difficile)诱导的小鼠结肠炎的指标(Fitzpatrick等,Gut Pathogens,2011)。我们的目标是确定在用万古霉素进行初始治疗后,BC30是否还可以预防艰难梭菌诱导的结肠炎在小鼠中的复发。在研究的第0至5天,对小鼠进行了抗生素治疗。在第6天,通过在约5x104 CFU处经口胃管灌胃给予艰难梭菌菌株VPI 10463,以诱发结肠炎。在研究的第6-10天,用万古霉素(50 mg / kg)(vanco)或溶媒(盐水)通过管饲法治疗小鼠。在第10至16天,用食盐水或BC30(每天2 x 109 CFU)管饲法给小鼠给药。监测小鼠的死亡率,体重减轻和腹泻。在研究的第14、16和17天,收集粪便和结肠用于分析结肠炎的其他参数。结果赋形剂/艰难梭菌/ Vanco小鼠的平均粪便稠度评分从0.4(第10天)增加到1.1至1.4(第14至17天),表明结肠炎已复发。在第13天到第17天,万古霉素/ BC30小鼠的粪便稠度评分显着低于动物万古霉素/车辆组(p <0.05)。在第17天,用BC30治疗的小鼠中有88.9%的粪便正常,而用赋形剂治疗时该值为0%(p值= 0.0004)。结肠髓过氧化物酶(单位/ 2 cm结肠)显着(p <0.05)从4.3±0.7(车辆/艰难梭菌/ Vanco)降至2.6±0.2(BC30 / C。Difficle / Vanco)。在BC30治疗的小鼠中,结肠的结肠组织学评分和角质形成细胞衍生的趋化因子水平也较低。小结在用万古霉素对动物进行初次治疗后,有证据表明,在用BC30处理的小鼠中,粪便稠度更好,并且结肠炎的生化和组织学指标得到改善。结论BC30限制了万古霉素停药后CD诱发的结肠炎的复发。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号