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Metabolic Homeostasis in Chronic Helminth Infection Is Sustained by Organ-Specific Metabolic Rewiring
[Image: see text] Opisthorchiasis, is a hepatobiliary disease caused by flukes of the trematode family Opisthorchiidae. A chronic form of the disease implies a prolonged coexistence of a host and the parasite. The pathological changes inflicted by the worm to the host’s hepatobiliary system are well...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8154418/ https://www.ncbi.nlm.nih.gov/pubmed/33764039 http://dx.doi.org/10.1021/acsinfecdis.1c00026 |
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author | Kokova, Daria Verhoeven, Aswin Perina, Ekaterina A. Ivanov, Vladimir V. Heijink, Marieke Yazdanbakhsh, Maria Mayboroda, Oleg A. |
author_facet | Kokova, Daria Verhoeven, Aswin Perina, Ekaterina A. Ivanov, Vladimir V. Heijink, Marieke Yazdanbakhsh, Maria Mayboroda, Oleg A. |
author_sort | Kokova, Daria |
collection | PubMed |
description | [Image: see text] Opisthorchiasis, is a hepatobiliary disease caused by flukes of the trematode family Opisthorchiidae. A chronic form of the disease implies a prolonged coexistence of a host and the parasite. The pathological changes inflicted by the worm to the host’s hepatobiliary system are well documented. Yet, the response to the infection also triggers a deep remodeling of the host systemic metabolism reaching a new homeostasis and affecting the organs beyond the worm location. Understanding the metabolic alternation in chronic opisthorchiasis, could help us to pinpoint pathways that underlie infection opening possibilities for the development of more selective treatment strategies. Here, with this report we apply an integrative, multicompartment metabolomics analysis, using multiple biofluids, stool samples and tissue extracts to describe metabolic changes in Opisthorchis felineus infected animals at the chronic stage. We show that the shift in lipid metabolism in the serum, a depletion of the amino acids pool, an alteration of the ketogenic pathways in the jejunum and a suppressed metabolic activity of the spleen are the key features of the metabolic host adaptation at the chronic stage of O. felineus infection. We describe this combination of the metabolic changes as a “metabolically mediated immunosuppressive status of organism” which develops during a chronic infection. This status in combination with other factors (e.g., parasite-derived immunomodulators) might increase risk of infection-related malignancy. |
format | Online Article Text |
id | pubmed-8154418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-81544182021-05-27 Metabolic Homeostasis in Chronic Helminth Infection Is Sustained by Organ-Specific Metabolic Rewiring Kokova, Daria Verhoeven, Aswin Perina, Ekaterina A. Ivanov, Vladimir V. Heijink, Marieke Yazdanbakhsh, Maria Mayboroda, Oleg A. ACS Infect Dis [Image: see text] Opisthorchiasis, is a hepatobiliary disease caused by flukes of the trematode family Opisthorchiidae. A chronic form of the disease implies a prolonged coexistence of a host and the parasite. The pathological changes inflicted by the worm to the host’s hepatobiliary system are well documented. Yet, the response to the infection also triggers a deep remodeling of the host systemic metabolism reaching a new homeostasis and affecting the organs beyond the worm location. Understanding the metabolic alternation in chronic opisthorchiasis, could help us to pinpoint pathways that underlie infection opening possibilities for the development of more selective treatment strategies. Here, with this report we apply an integrative, multicompartment metabolomics analysis, using multiple biofluids, stool samples and tissue extracts to describe metabolic changes in Opisthorchis felineus infected animals at the chronic stage. We show that the shift in lipid metabolism in the serum, a depletion of the amino acids pool, an alteration of the ketogenic pathways in the jejunum and a suppressed metabolic activity of the spleen are the key features of the metabolic host adaptation at the chronic stage of O. felineus infection. We describe this combination of the metabolic changes as a “metabolically mediated immunosuppressive status of organism” which develops during a chronic infection. This status in combination with other factors (e.g., parasite-derived immunomodulators) might increase risk of infection-related malignancy. American Chemical Society 2021-03-25 2021-04-09 /pmc/articles/PMC8154418/ /pubmed/33764039 http://dx.doi.org/10.1021/acsinfecdis.1c00026 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Kokova, Daria Verhoeven, Aswin Perina, Ekaterina A. Ivanov, Vladimir V. Heijink, Marieke Yazdanbakhsh, Maria Mayboroda, Oleg A. Metabolic Homeostasis in Chronic Helminth Infection Is Sustained by Organ-Specific Metabolic Rewiring |
title | Metabolic Homeostasis in Chronic Helminth Infection
Is Sustained by Organ-Specific Metabolic Rewiring |
title_full | Metabolic Homeostasis in Chronic Helminth Infection
Is Sustained by Organ-Specific Metabolic Rewiring |
title_fullStr | Metabolic Homeostasis in Chronic Helminth Infection
Is Sustained by Organ-Specific Metabolic Rewiring |
title_full_unstemmed | Metabolic Homeostasis in Chronic Helminth Infection
Is Sustained by Organ-Specific Metabolic Rewiring |
title_short | Metabolic Homeostasis in Chronic Helminth Infection
Is Sustained by Organ-Specific Metabolic Rewiring |
title_sort | metabolic homeostasis in chronic helminth infection
is sustained by organ-specific metabolic rewiring |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8154418/ https://www.ncbi.nlm.nih.gov/pubmed/33764039 http://dx.doi.org/10.1021/acsinfecdis.1c00026 |
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