Kumpunya Sarinya, Kawang Kornthara, Pollapong Kraiwit, Nilaratanakul Voraphoj
Division of Infectious Diseases, Department of Medicine, Faculty of Medicine, Chulalongkorn University and King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok, 10330, Thailand.
Excellence Center for Infectious Diseases, King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok, 10330, Thailand.
Sci Rep. 2025 Apr 22;15(1):13908. doi: 10.1038/s41598-025-96701-4.
Antibiotic treatment contributes to gut microbiota dysbiosis. Previous studies have shown that fecal microbiota transplantation (FMT), fecal filtrate (FF), and activated charcoal (AC) treatments can prevent gut microbiota disturbances caused by antibiotics or Clostridioides difficile infection. However, these treatments have typically been limited to restoring gut microbiota after dysbiosis, and antibiotics must be discontinued beforehand. Here, we investigated the protective effects of these treatments on gut microbiota to prevent dysbiosis during concurrent systemic ceftriaxone administration.
C57BL/6 mice that received intraperitoneal ceftriaxone for seven consecutive days were concomitantly treated with AC, FMT, FMT + AC, FF, or FF + AC via oral gavage. Gut microbiomes were analyzed using 16 S rRNA gene sequencing, and intestinal mucosal pathology was evaluated through H&E staining.
Systemic ceftriaxone administration significantly altered gut microbiota diversity and composition but did not affect intestinal mucosal histology. Alpha and beta diversity analyses showed that microbiota diversity decreased in all ceftriaxone-treated groups, with the ceftriaxone + FF + AC group retaining the highest diversity. The ceftriaxone + AC group had higher Enterococcus but lower Muribaculaceae relative abundances than the control (no ceftriaxone), ceftriaxone only, and ceftriaxone + FF + AC groups.
These results show that fecal filtrate transplantation combined with activated charcoal treatment may help balance gut microbiota diversity and reduce the presence of resistant bacteria during ceftriaxone exposure.
抗生素治疗会导致肠道微生物群失调。先前的研究表明,粪便微生物群移植(FMT)、粪便滤液(FF)和活性炭(AC)治疗可以预防由抗生素或艰难梭菌感染引起的肠道微生物群紊乱。然而,这些治疗通常仅限于在失调后恢复肠道微生物群,并且必须事先停用抗生素。在此,我们研究了这些治疗对肠道微生物群的保护作用,以预防在全身使用头孢曲松期间出现失调。
连续7天接受腹腔注射头孢曲松的C57BL/6小鼠,通过口服灌胃同时接受AC、FMT、FMT + AC、FF或FF + AC治疗。使用16S rRNA基因测序分析肠道微生物组,并通过苏木精和伊红染色评估肠道黏膜病理学。
全身使用头孢曲松显著改变了肠道微生物群的多样性和组成,但未影响肠道黏膜组织学。α和β多样性分析表明,所有头孢曲松治疗组的微生物群多样性均降低,其中头孢曲松 + FF + AC组的多样性最高。与对照组(未使用头孢曲松)、仅使用头孢曲松组和头孢曲松 + FF + AC组相比,头孢曲松 + AC组的肠球菌相对丰度较高,但毛螺菌科相对丰度较低。
这些结果表明,粪便滤液移植联合活性炭治疗可能有助于平衡肠道微生物群多样性,并减少头孢曲松暴露期间耐药菌的存在。