Gut Microbiota Contributes to Host Defense Against Klebsiella pneumoniae-Induced Liver Abscess

被引:21
作者
Zheng, Yahong [1 ]
Ding, Yuting [1 ]
Xu, Mengran [1 ]
Chen, Haoran [1 ]
Zhang, Hui [1 ]
Liu, Yanyan [1 ,2 ,3 ]
Shen, Weihua [4 ]
Li, Jiabin [1 ,2 ,3 ,5 ]
机构
[1] Anhui Med Univ, Dept Infect Dis, Affiliated Hosp 1, Jixi Rd 218, Hefei 230022, Anhui, Peoples R China
[2] Anhui Ctr Surveillance Bacterial Resistance, Hefei, Anhui, Peoples R China
[3] Anhui Med Univ, Inst Bacterial Resistance, Hefei, Anhui, Peoples R China
[4] Anhui Med Univ, Affiliated Hosp 1, Dept Special Clin, Jixi Rd 218, Hefei 230022, Anhui, Peoples R China
[5] Anhui Med Univ, Chaohu Affiliated Hosp, Dept Infect Dis, Jixi Rd 218, Hefei 230022, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Klebsiella pneumoniae; liver abscess; gut microbiome; fecal microbiota transplantation; inflammation; INTESTINAL MICROBIOTA; OBESITY; DISEASE;
D O I
10.2147/JIR.S334581
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose: Klebsiella pneumoniae-induced liver abscess (KLA) is a type of pyogenic liver abscess (PLA), which is a distinct invasive syndrome that has been increasingly reported worldwide over the past two decades. The intestinal microbiota is increasingly recognized as an important modulator that can promote and maintain host immune homeostasis. However, its precise role in liver abscess is unknown. We aimed to investigate the function of the gut microbiota in the host defense against K. pneumoniae infection. Methods: We constructed C57BL/6J mice with KLA and analyzed the diversity and richness of the intestinal microflora by 16S rRNA sequencing. Next, to create a microbiota-depleted (MD) mouse model, we administered multiple broad-spectrum anti-biotics and validated the model using 16S rRNA sequencing. At 48 h after K. pneumoniae infection, we assessed the general health condition, liver injury, bacterial loads, and inflam-matory factor levels in MD+KLA mice. Additionally, fecal microbiota transplantation (FMT) was conducted in another group of MD+KLA mice prior to K. pneumoniae infection, and we assessed whether the transplantation changed the outcomes. Results: The diversity of the intestinal flora was significantly changed in KLA mice compared to control mice, with a decrease in beneficial bacteria and an increase in harmful bacteria. The MD+KLA mice exhibited impaired antimicrobial capacity, reduced survival, increased inflammation and liver damage at 48 h after K. pneumoniae infection compared to the KLA mice. However, FMT normalized the inflammatory cytokine levels, reduced liver damage, and increased survival. Conclusion: This study identified the gut microbiota as a protective factor against K. pneumoniae infection. The role of FMT in KLA should be investigated in future clinical studies.
引用
收藏
页码:5215 / 5225
页数:11
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