Cryptosporidiosis Modulates the Gut Microbiome and Metabolism in a Murine Infection Model

Bibliographic Details
Title: Cryptosporidiosis Modulates the Gut Microbiome and Metabolism in a Murine Infection Model
Authors: Avinash V. Karpe, Melanie L. Hutton, Steven J. Mileto, Meagan L. James, Chris Evans, Rohan M. Shah, Amol B. Ghodke, Katie E. Hillyer, Suzanne S. Metcalfe, Jian-Wei Liu, Tom Walsh, Dena Lyras, Enzo A. Palombo, David J. Beale
Source: Metabolites, Vol 11, Iss 6, p 380 (2021)
Publisher Information: MDPI AG, 2021.
Publication Year: 2021
Collection: LCC:Microbiology
Subject Terms: interactomics, host–parasite–microbiome relationships, extra-intestinal effects, D-amino acid/SCFA-induced modulation, yeast ubiquinone salvation, Microbiology, QR1-502
More Details: Cryptosporidiosis is a major human health concern globally. Despite well-established methods, misdiagnosis remains common. Our understanding of the cryptosporidiosis biochemical mechanism remains limited, compounding the difficulty of clinical diagnosis. Here, we used a systems biology approach to investigate the underlying biochemical interactions in C57BL/6J mice infected with Cryptosporidium parvum. Faecal samples were collected daily following infection. Blood, liver tissues and luminal contents were collected 10 days post infection. High-resolution liquid chromatography and low-resolution gas chromatography coupled with mass spectrometry were used to analyse the proteomes and metabolomes of these samples. Faeces and luminal contents were additionally subjected to 16S rRNA gene sequencing. Univariate and multivariate statistical analysis of the acquired data illustrated altered host and microbial energy pathways during infection. Glycolysis/citrate cycle metabolites were depleted, while short-chain fatty acids and D-amino acids accumulated. An increased abundance of bacteria associated with a stressed gut environment was seen. Host proteins involved in energy pathways and Lactobacillus glyceraldehyde-3-phosphate dehydrogenase were upregulated during cryptosporidiosis. Liver oxalate also increased during infection. Microbiome–parasite relationships were observed to be more influential than the host–parasite association in mediating major biochemical changes in the mouse gut during cryptosporidiosis. Defining this parasite–microbiome interaction is the first step towards building a comprehensive cryptosporidiosis model towards biomarker discovery, and rapid and accurate diagnostics.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2218-1989
Relation: https://www.mdpi.com/2218-1989/11/6/380; https://doaj.org/toc/2218-1989
DOI: 10.3390/metabo11060380
Access URL: https://doaj.org/article/d440e1d4863b4a40a4b7ac06b4d87df7
Accession Number: edsdoj.440e1d4863b4a40a4b7ac06b4d87df7
Database: Directory of Open Access Journals
More Details
ISSN:22181989
DOI:10.3390/metabo11060380
Published in:Metabolites
Language:English