4.5 Article

Metabolic alterations in the hamster co-infected with Schistosoma japonicum and Necator americanus

期刊

INTERNATIONAL JOURNAL FOR PARASITOLOGY
卷 40, 期 6, 页码 695-703

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.ijpara.2009.11.003

关键词

Co-infection; Hamster; Metabonomics; Necator americanus; NMR spectroscopy; Schistosoma japonicum

资金

  1. Chinese Academy of Sciences [KJXC2-YVV-W11]
  2. NSFC
  3. Swiss National Science Foundation [PPOOB-102883, PPOOB-119129]

向作者/读者索取更多资源

Co-infection with hookworm and schistosomes is a common phenomenon in sub-Saharan Africa, as well as in parts of South America and southeast Asia. As a first step towards understanding the metabolic response of a hookworm-schistosome co-infection in humans, we investigated the metabolic consequences of co-infection in an animal model, using a nuclear magnetic resonance (NMR)-based metabolic profiling technique, combined with multivariate statistical analysis. Urine and serum samples were obtained from hamsters experimentally infected with 250 Necator americanus infective L-3 and 100 Schistosoma japonicum cercariae simultaneously. In the co-infection model, similar worm burdens were observed as reported for single infection models, whereas metabolic profiles of co-infection represented a combination of the altered metabolite profiles induced by single infections with these two parasites. Consistent differences in metabolic profiles between the co-infected and non-infected control hamsters were observed from 4 weeks p.i. onwards. The predominant metabolic alterations in co-infected hamsters consisted of depletion of amino acids, tricarboxylic acid cycle intermediates (e.g. citrate and succinate) and glucose. Moreover, alterations of a series of gut microbial-related metabolites, such as decreased levels of hippurate, 3-hydroxyphenylpropionic acid, 4-hydroxyphenylpropionic acid and tri-methylamine-N-oxide, and increased concentrations of 4-cresol glucuronide and phenylacetylglycine were associated with co-infection. Our results provide a first step towards understanding the metabolic response of an animal host to multiple parasitic infections. (C) 2009 Australian Society for Parasitology Inc. Published by Elsevier Ltd. All rights reserved.

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