生物
代谢组
毛螺菌科
隐孢子虫
微生物学
肠道菌群
代谢途径
脂肪酸
代谢组学
微生物群
生物化学
新陈代谢
粪便
代谢物
厚壁菌
生物信息学
基因
16S核糖体RNA
作者
Luyang Wang,Letian Cao,Yankai Chang,Yin Fu,Yuexin Wang,Kaihui Zhang,Sumei Zhang,Longxian Zhang
出处
期刊:Microbiology spectrum
[American Society for Microbiology]
日期:2022-12-19
卷期号:11 (1): e0217522-e0217522
被引量:23
标识
DOI:10.1128/spectrum.02175-22
摘要
Cryptosporidiosis is a gastrointestinal disease in humans and animals caused by the protozoan parasite Cryptosporidium. Control and treatment of the disease is challenging due to the lack of sensitive diagnostic tools and effective chemotherapy. The dynamics of gut microbiota and metabolites during Cryptosporidium infection may be the key to finding drugs and targets for parasite infection control. Our results indicate that C. muris infection can disrupt gut microbiota and metabolites, resulting in decreased bacterial abundance at the parasitic site. Unsaturated fatty acid pathway biosynthesis-related metabolites are significantly elevated at the patent period. Interestingly, the metabolite pathway that significantly elevated during peak parasite growth was bile acid, the metabolites of which may be important for the circulation of infection of Cryptosporidium oocysts in the host. The enhancing effects of short-chain fatty acid and bile acid metabolism on the growth and development of Cryptosporidium proposed in this study may provide a theoretical basis for future research on novel drugs and vaccines against this intestinal parasite.
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