4.7 Article

Opisthorchis viverrini Infection Induces Metabolic and Fecal Microbial Disturbances in Association with Liver and Kidney Pathologies in Hamsters

期刊

JOURNAL OF PROTEOME RESEARCH
卷 20, 期 8, 页码 3940-3951

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jproteome.1c00246

关键词

opisthorchiasis; H-1 NMR spectroscopy; host-microbial cometabolism; metabolic profiling; gut micro biota; kidney pathology; liver pathology

资金

  1. Thailand Research Fund's Royal Golden Jubilee Ph.D. Program [PHD/0037/2558]
  2. Invitation Research Grant from the Faculty of Medicine [IN61110]
  3. Chronic Kidney Disease Prevention in Northeast Thailand, Khon Kaen University
  4. Research Publication Scholarship, Graduate School, Khon Kaen University
  5. Newton Fund Ph.D. scholarship
  6. Research Affairs and Graduate School, Khon Kaen University, Thailand [60163]
  7. MRC [MR/P002536/1]
  8. ERC [715662]
  9. European Research Council (ERC) [715662] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Opisthorchis viverrini infection causes hepatobiliary diseases and is a major risk factor for cholangiocarcinoma. The infection leads to disturbances in host amino acid metabolism, TCA cycle, liver, and kidney pathologies, as well as changes in fecal microbial composition and urinary host-microbial cometabolism.
Opisthorchis viverrini (Ov) infection causes hepatobiliary diseases and is a major risk factor for cholangiocarcinoma. While several omics approaches have been employed to understand the pathogenesis of opisthorchiasis, effects of Ov infection on the host systemic metabolism and fecal microbiota have not been fully explored. Here, we used a H-1 NMR spectroscopy-based metabolic phenotyping approach to investigate Ov infection-induced metabolic disturbances at both the acute (1 month postinfection, 1 mpi) and chronic (4 mpi) stages in hamsters. A total of 22, 3, and 4 metabolites were found to be significantly different in the liver, serum, and urine, respectively, between Ov+ and Ov- groups. Elevated levels of hepatic amino acids and tricarboxylic acid (TCA)-cycle intermediates (fumarate and malate) were co-observed with liver injury in acute infection, whereas fibrosis-associated metabolites (e.g., glycine and glutamate) increased at the chronic infection stage. Lower levels of lipid signals ((CH2)(n) and CH2CH2CO) and higher levels of lysine and scyllo-inositol were observed in serum from Ov+ hamsters at 1 mpi compared to Ov- controls. Urinary levels of phenylacetylglycine (a host-bacterial cometabolite) and tauro-beta-muricholic acid were higher in the Ov+ group, which coexisted with hepatic and mild kidney fibrosis. Furthermore, Ov+ animals showed higher relative abundances of fecal Methanobrevibacter (Archaea), Akkermansia, and Burkholderia-Paraburkholderia compared to the noninfected controls. In conclusion, along with liver and kidney pathologies, O. viverrini infection resulted in hepatic and mild renal pathologies, disturbed hepatic amino acid metabolism and the TCA cycle, and induced changes in the fecal microbial composition and urinary host-microbial cometabolism. This study provides the initial step toward an understanding of local and systemic metabolic responses of the host to O. viverrini infection.

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