Multiple metabolic pathways are predictive of ricin intoxication in a rat model
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Published version
Author(s)
Type
Journal Article
Abstract
Introduction
Exposure to ricin can be lethal and treatments that are under development have short windows of opportunity for administration after exposure. It is therefore essential to achieve early detection of ricin exposure to provide the best prognosis for exposed individuals. Ricin toxin can be detected in clinical samples via several antibody-based techniques, but the efficacy of these can be limited due to the rapid processing and cellular uptake of toxin in the body and subsequent low blood ricin concentrations. Other diagnostic tools that perform, in an orthogonal manner, are therefore desirable.
Objectives
To determine time-dependent metabolic changes in Sprague–Dawley rats following intravenous exposure to ricin.
Methods
Sprague–Dawley rats were intravenously exposed to ricin and multiple blood samples were collected from each animal for up to 48 h following exposure in two independent studies. Plasma samples were analysed applying HILIC and C18 reversed phase UHPLC–MS assays followed by univariate and multivariate analysis.
Results
In Sprague–Dawley rats we have demonstrated that metabolic changes measured in blood can distinguish between rats exposed intravenously to ricin and controls prior to the onset of behavioral signs of intoxication after 24 h. A total of 37 metabolites were significantly altered following exposure to ricin when compared to controls. The arginine/proline, bile acid and triacylglyceride metabolic pathways were highlighted as being important with two triacylglycerides at 8 h post exposure giving an AUROC score of 0.94. At 16 h and 24 h the AUROC score increased to 0.98 and 1.0 with the number of metabolites in the panel increasing to 5 and 7, respectively.
Conclusions
These data demonstrate that metabolites may be a useful tool to diagnose and detect ricin exposure, thus increasing the effectiveness of supportive therapy and future ricin-specific medical treatments.
Exposure to ricin can be lethal and treatments that are under development have short windows of opportunity for administration after exposure. It is therefore essential to achieve early detection of ricin exposure to provide the best prognosis for exposed individuals. Ricin toxin can be detected in clinical samples via several antibody-based techniques, but the efficacy of these can be limited due to the rapid processing and cellular uptake of toxin in the body and subsequent low blood ricin concentrations. Other diagnostic tools that perform, in an orthogonal manner, are therefore desirable.
Objectives
To determine time-dependent metabolic changes in Sprague–Dawley rats following intravenous exposure to ricin.
Methods
Sprague–Dawley rats were intravenously exposed to ricin and multiple blood samples were collected from each animal for up to 48 h following exposure in two independent studies. Plasma samples were analysed applying HILIC and C18 reversed phase UHPLC–MS assays followed by univariate and multivariate analysis.
Results
In Sprague–Dawley rats we have demonstrated that metabolic changes measured in blood can distinguish between rats exposed intravenously to ricin and controls prior to the onset of behavioral signs of intoxication after 24 h. A total of 37 metabolites were significantly altered following exposure to ricin when compared to controls. The arginine/proline, bile acid and triacylglyceride metabolic pathways were highlighted as being important with two triacylglycerides at 8 h post exposure giving an AUROC score of 0.94. At 16 h and 24 h the AUROC score increased to 0.98 and 1.0 with the number of metabolites in the panel increasing to 5 and 7, respectively.
Conclusions
These data demonstrate that metabolites may be a useful tool to diagnose and detect ricin exposure, thus increasing the effectiveness of supportive therapy and future ricin-specific medical treatments.
Date Issued
2019-07
Date Acceptance
2019-03-28
Citation
Metabolomics, 2019, 15 (7)
ISSN
1573-3882
Publisher
Springer Verlag
Journal / Book Title
Metabolomics
Volume
15
Issue
7
Copyright Statement
© Crown 2019. This article contains public sector information licensed under the Open Government Licence v3.0, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Open Government licence, and indicate if changes were made.
The images or other third party material in this article are included in the article’s Open Government licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Open Government licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.
To view a copy of this licence, visit http://www.nationalarchives.gov.uk/doc/open-governmentlicence/version/3/
The images or other third party material in this article are included in the article’s Open Government licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Open Government licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.
To view a copy of this licence, visit http://www.nationalarchives.gov.uk/doc/open-governmentlicence/version/3/
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000474401800001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Subjects
Science & Technology
Life Sciences & Biomedicine
Endocrinology & Metabolism
Ricin
Metabolomics
Arginine
proline metabolism
Bile acid metabolism
Triacylglyceride metabolism
BIOLOGICAL TERRORISM
ANIMAL-MODELS
TOXICITY
ARGININE
TOXIN
IDENTIFICATION
ANTIBODIES
TISSUES
ASSAY
MICE
Publication Status
Published
Article Number
ARTN 102
Date Publish Online
2019-07-03