Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, California, United States of America.
Division of Biological Sciences, University of California San Diego, La Jolla, California, United States of America.
PLoS Negl Trop Dis. 2018 Mar 12;12(3):e0006344. doi: 10.1371/journal.pntd.0006344. eCollection 2018 Mar.
Trypanosoma cruzi parasites are the causative agents of Chagas disease. These parasites infect cardiac and gastrointestinal tissues, leading to local inflammation and tissue damage. Digestive Chagas disease is associated with perturbations in food absorption, intestinal traffic and defecation. However, the impact of T. cruzi infection on the gut microbiota and metabolome have yet to be characterized. In this study, we applied mass spectrometry-based metabolomics and 16S rRNA sequencing to profile infection-associated alterations in fecal bacterial composition and fecal metabolome through the acute-stage and into the chronic stage of infection, in a murine model of Chagas disease. We observed joint microbial and chemical perturbations associated with T. cruzi infection. These included alterations in conjugated linoleic acid (CLA) derivatives and in specific members of families Ruminococcaceae and Lachnospiraceae, as well as alterations in secondary bile acids and members of order Clostridiales. These results highlight the importance of multi-'omics' and poly-microbial studies in understanding parasitic diseases in general, and Chagas disease in particular.
克氏锥虫寄生虫是恰加斯病的病原体。这些寄生虫感染心脏和胃肠道组织,导致局部炎症和组织损伤。消化道恰加斯病与食物吸收、肠道运输和排便的改变有关。然而,克氏锥虫感染对肠道微生物群和代谢组的影响尚未得到描述。在这项研究中,我们应用基于质谱的代谢组学和 16S rRNA 测序技术,通过急性和慢性阶段的感染,在恰加斯病的小鼠模型中,对粪便细菌组成和粪便代谢组的感染相关变化进行了分析。我们观察到与克氏锥虫感染相关的微生物和化学变化。这些变化包括共轭亚油酸(CLA)衍生物以及瘤胃球菌科和lachnospiraceae 家族的特定成员的改变,以及次级胆汁酸和梭状芽胞杆菌目成员的改变。这些结果强调了多组学和多微生物研究在理解寄生虫病,特别是恰加斯病的重要性。