Medical Molecular Biology Laboratory, School of Medicine, Jinhua Polytechnic, No. 1188 Wuzhou Street, Wucheng District, Jinhua, Zhejiang Province, P.R. China.
Animal Center, Jinhua Food and Drug Inspection and Testing Research Institute, Jinhua, Zhejiang Province, P.R. China.
BMC Microbiol. 2024 May 9;24(1):156. doi: 10.1186/s12866-024-03313-5.
To establish a method to induce Campylobacter jejuni colonization in the intestines of C57BL/6 mice through antibiotic-induced microbiome depletion.
Fifty-four female C57BL/6 mice were divided into the normal, control, and experimental groups. The experimental group was administered intragastric cefoperazone sodium and sulbactam sodium (50 mg/mL) for 2 days; then, the experimental and control mice were intragastrically administered 200 µL C. jejuni, which was repeated once more after 2 days. Animal feces were collected, and the HipO gene of C. jejuni was detected using TaqMan qPCR from day 1 to day 14 after modeling completion. Immunofluorescence was used to detect intestinal C. jejuni colonization on day 14, and pathological changes were observed using hematoxylin and eosin staining. Additionally, 16S rDNA analyses of the intestinal contents were conducted on day 14. In the experimental group, C. jejuni was detected in the feces from days 1 to 14 on TaqMan qPCR, and immunofluorescence-labeled C. jejuni were visibly discernable in the intestinal lumen. The intestinal mucosa was generally intact and showed no significant inflammatory-cell infiltration. Diversity analysis of the colonic microbiota showed significant inter-group differences. In the experimental group, the composition of the colonic microbiota differed from that in the other 2 groups at the phylum level, and was characterized by a higher proportion of Bacteroidetes and a lower proportion of Firmicutes.
Microbiome depletion induced by cefoperazone sodium and sulbactam sodium could promote long-term colonization of C. jejuni in the intestines of mice.
通过抗生素诱导微生物组耗竭,在 C57BL/6 小鼠的肠道中建立空肠弯曲杆菌定植的方法。
将 54 只雌性 C57BL/6 小鼠分为正常组、对照组和实验组。实验组给予头孢哌酮钠和舒巴坦钠(50mg/mL)灌胃 2 天;然后实验组和对照组小鼠灌胃 200µL 空肠弯曲杆菌,2 天后重复一次。收集动物粪便,采用 TaqMan qPCR 法从建模完成后第 1 天至第 14 天检测空肠弯曲杆菌的 HipO 基因。第 14 天采用免疫荧光法检测肠道空肠弯曲杆菌定植情况,采用苏木精-伊红染色观察肠组织病理变化,同时采用 16S rDNA 分析肠道内容物。实验组小鼠在 TaqMan qPCR 中检测到粪便中从第 1 天到第 14 天的空肠弯曲杆菌,免疫荧光标记的空肠弯曲杆菌在肠腔中清晰可见。肠黏膜基本完整,无明显炎性细胞浸润。结肠菌群多样性分析显示组间差异有统计学意义。实验组小鼠的结肠菌群组成在门水平与其他两组不同,其特征是拟杆菌门的比例较高,厚壁菌门的比例较低。
头孢哌酮钠和舒巴坦钠诱导的微生物组耗竭可促进空肠弯曲杆菌在小鼠肠道中的长期定植。