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Published on: May 2, 2018
Bacterial diversity in intestinal mucosa of antibiotic-associated diarrhea mice
Guozhen Xie1, Kai Tan2, Maijiao Peng1
11Hunan University of Chinese Medicine, Xueshi Road 300, Yuelu District, Changsha, 410208 Hunan Province China.
Abstract:
To probe into the mechanism of antibiotic-associated diarrhea (AAD), the bacterial diversity and composition in the intestinal mucosa of AAD mice were investigated. Twelve specific pathogen-free Kunming mice were divided into control group and model group. The mouse model of AAD was established by gavaging with antibiotics (mixture of gentamycin sulfate and cefradine) at a total dose of 23.33 ml kg-1 day-1 for 5 days continuously, twice a day. The mice in the control group were given with an equal amount of sterile water. Then, the intestinal mucosa DNA was extracted for 16S rRNA gene sequence analysis by high-throughput sequencing. The results showed that the alpha diversity of the two groups did not differ significantly from each other, while the composition of intestinal mucosa bacteria differed dramatically between the two groups. The model group showed a higher abundance of Proteobacteria and Actinobacteria. More importantly, Lactobacillus was significantly less abundant (p = 0.000), while Enterococcus was significantly more abundant (p = 0.019) in the model group than in the control group. Furthermore, antibiotic treatment increased the abundance of Citrobacter, Stenotrophomonas, and Glutamicibacter,whereas antibiotics decreased the abundance of Mycoplasma and Helicobacter. In addition, 6 and 11 unique genera were found in the control group and model group, respectively. The combination of gentamycin sulfate and cefradine changed the intestinal mucosa bacterial composition, reduced colonization resistance and damaged the intestinal mucosal barrier by reducing the abundance of Lactobacillus.
Insights
Antibiotic-associated diarrhea (AAD) in mice was studied by analyzing gut bacteria. Antibiotics significantly altered gut microbiota composition, reducing beneficial Lactobacillus and increasing harmful Enterococcus, leading to gut barrier damage.
Area of Science:
- Microbiology
- Gastroenterology
- Pharmacology
Background:
- Antibiotic-associated diarrhea (AAD) is a common complication of antibiotic therapy.
- The precise mechanisms underlying AAD, particularly alterations in intestinal mucosal bacteria, require further elucidation.
Purpose of the Study:
- To investigate the impact of a combined antibiotic treatment (gentamicin sulfate and cefradine) on the bacterial diversity and composition of the intestinal mucosa in a mouse model of AAD.
- To identify specific bacterial genera affected by antibiotic treatment and their potential role in AAD pathogenesis.
Main Methods:
- Establishment of an AAD mouse model using a combination of gentamicin sulfate and cefradine.
- Extraction of intestinal mucosa DNA for 16S rRNA gene sequencing via high-throughput sequencing.
- Comparative analysis of bacterial alpha diversity and composition between control and AAD groups.
Main Results:
- No significant difference in alpha diversity was observed between control and AAD groups.
- Significant differences in intestinal mucosa bacterial composition were found, with increased abundance of Proteobacteria and Actinobacteria in the AAD group.
- Antibiotic treatment led to a significant decrease in *Lactobacillus* and a significant increase in *Enterococcus* abundance.
- Specific genera such as *Citrobacter*, *Stenotrophomonas*, and *Glutamicibacter* increased, while *Mycoplasma* and *Helicobacter* decreased in the AAD group.
Conclusions:
- The combination of gentamicin sulfate and cefradine dramatically alters intestinal mucosa bacterial composition in AAD mice.
- Reduced abundance of *Lactobacillus* and increased abundance of *Enterococcus* are key changes associated with AAD.
- Antibiotic-induced alterations in gut microbiota composition compromise colonization resistance and damage the intestinal mucosal barrier.
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