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Untargeted Multimodal Metabolomics Investigation of the Haemonchus contortus Exsheathment Secretome
In nematodes that invade the gastro-intestinal tract of the ruminant, the process of larval exsheathment marks the transition from the free-living to the parasitic stages of these parasites. To investigate the secretome associated with larval exsheathment, a closed in vitro system that effectively r...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406637/ https://www.ncbi.nlm.nih.gov/pubmed/36010603 http://dx.doi.org/10.3390/cells11162525 |
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author | Palevich, Nikola Maclean, Paul H. Candy, Paul M. Taylor, Wendy Mladineo, Ivona Cao, Mingshu |
author_facet | Palevich, Nikola Maclean, Paul H. Candy, Paul M. Taylor, Wendy Mladineo, Ivona Cao, Mingshu |
author_sort | Palevich, Nikola |
collection | PubMed |
description | In nematodes that invade the gastro-intestinal tract of the ruminant, the process of larval exsheathment marks the transition from the free-living to the parasitic stages of these parasites. To investigate the secretome associated with larval exsheathment, a closed in vitro system that effectively reproduces the two basic components of an anaerobic rumen environment (CO(2) and 39 °C) was developed to trigger exsheathment in one of the most pathogenic and model gastrointestinal parasitic nematodes, Haemonchus contortus (barber‘s pole worm). This study reports the use of multimodal untargeted metabolomics and lipidomics methodologies to identify the metabolic signatures and compounds secreted during in vitro larval exsheathment in the H. contortus infective third-stage larva (iL3). A combination of statistical and chemoinformatic analyses using three analytical platforms revealed a panel of metabolites detected post exsheathment and associated with amino acids, purines, as well as select organic compounds. The major lipid classes identified by the non-targeted lipidomics method applied were lysophosphatidylglycerols, diglycerides, fatty acyls, glycerophospholipids, and a triglyceride. The identified metabolites may serve as metabolic signatures to improve tractability of parasitic nematodes for characterizing small molecule host–parasite interactions related to pathogenesis, vaccine and drug design, as well as the discovery of metabolic biomarkers. |
format | Online Article Text |
id | pubmed-9406637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94066372022-08-26 Untargeted Multimodal Metabolomics Investigation of the Haemonchus contortus Exsheathment Secretome Palevich, Nikola Maclean, Paul H. Candy, Paul M. Taylor, Wendy Mladineo, Ivona Cao, Mingshu Cells Communication In nematodes that invade the gastro-intestinal tract of the ruminant, the process of larval exsheathment marks the transition from the free-living to the parasitic stages of these parasites. To investigate the secretome associated with larval exsheathment, a closed in vitro system that effectively reproduces the two basic components of an anaerobic rumen environment (CO(2) and 39 °C) was developed to trigger exsheathment in one of the most pathogenic and model gastrointestinal parasitic nematodes, Haemonchus contortus (barber‘s pole worm). This study reports the use of multimodal untargeted metabolomics and lipidomics methodologies to identify the metabolic signatures and compounds secreted during in vitro larval exsheathment in the H. contortus infective third-stage larva (iL3). A combination of statistical and chemoinformatic analyses using three analytical platforms revealed a panel of metabolites detected post exsheathment and associated with amino acids, purines, as well as select organic compounds. The major lipid classes identified by the non-targeted lipidomics method applied were lysophosphatidylglycerols, diglycerides, fatty acyls, glycerophospholipids, and a triglyceride. The identified metabolites may serve as metabolic signatures to improve tractability of parasitic nematodes for characterizing small molecule host–parasite interactions related to pathogenesis, vaccine and drug design, as well as the discovery of metabolic biomarkers. MDPI 2022-08-15 /pmc/articles/PMC9406637/ /pubmed/36010603 http://dx.doi.org/10.3390/cells11162525 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Palevich, Nikola Maclean, Paul H. Candy, Paul M. Taylor, Wendy Mladineo, Ivona Cao, Mingshu Untargeted Multimodal Metabolomics Investigation of the Haemonchus contortus Exsheathment Secretome |
title | Untargeted Multimodal Metabolomics Investigation of the Haemonchus contortus Exsheathment Secretome |
title_full | Untargeted Multimodal Metabolomics Investigation of the Haemonchus contortus Exsheathment Secretome |
title_fullStr | Untargeted Multimodal Metabolomics Investigation of the Haemonchus contortus Exsheathment Secretome |
title_full_unstemmed | Untargeted Multimodal Metabolomics Investigation of the Haemonchus contortus Exsheathment Secretome |
title_short | Untargeted Multimodal Metabolomics Investigation of the Haemonchus contortus Exsheathment Secretome |
title_sort | untargeted multimodal metabolomics investigation of the haemonchus contortus exsheathment secretome |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406637/ https://www.ncbi.nlm.nih.gov/pubmed/36010603 http://dx.doi.org/10.3390/cells11162525 |
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