Experimental Chagas disease-induced perturbations of the fecal microbiome and metabolome.

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. Howev...

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Main Authors: Laura-Isobel McCall (Author), Anupriya Tripathi (Author), Fernando Vargas (Author), Rob Knight (Author), Pieter C Dorrestein (Author), Jair L Siqueira-Neto (Author)
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Published: Public Library of Science (PLoS), 2018-03-01T00:00:00Z.
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100 1 0 |a Laura-Isobel McCall  |e author 
700 1 0 |a Anupriya Tripathi  |e author 
700 1 0 |a Fernando Vargas  |e author 
700 1 0 |a Rob Knight  |e author 
700 1 0 |a Pieter C Dorrestein  |e author 
700 1 0 |a Jair L Siqueira-Neto  |e author 
245 0 0 |a Experimental Chagas disease-induced perturbations of the fecal microbiome and metabolome. 
260 |b Public Library of Science (PLoS),   |c 2018-03-01T00:00:00Z. 
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500 |a 10.1371/journal.pntd.0006344 
520 |a 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. 
546 |a EN 
690 |a Arctic medicine. Tropical medicine 
690 |a RC955-962 
690 |a Public aspects of medicine 
690 |a RA1-1270 
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786 0 |n PLoS Neglected Tropical Diseases, Vol 12, Iss 3, p e0006344 (2018) 
787 0 |n http://europepmc.org/articles/PMC5864088?pdf=render 
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787 0 |n https://doaj.org/toc/1935-2735 
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