Cargando…

A hypothetical astrocyte–microglia lactate shuttle derived from a (1)H NMR metabolomics analysis of cerebrospinal fluid from a cohort of South African children with tuberculous meningitis

Tuberculosis meningitis (TBM) is the most severe form of extra-pulmonary tuberculosis and is particularly intense in small children; there is no universally accepted algorithm for the diagnosis and substantiation of TB infection, which can lead to delayed intervention, a high risk factor for morbidi...

Descripción completa

Detalles Bibliográficos
Autores principales: Mason, Shayne, van Furth, A. Marceline, Mienie, Lodewyk J., Engelke, Udo F. H., Wevers, Ron A., Solomons, Regan, Reinecke, Carolus J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4475545/
https://www.ncbi.nlm.nih.gov/pubmed/26109926
http://dx.doi.org/10.1007/s11306-014-0741-z
_version_ 1782377469832069120
author Mason, Shayne
van Furth, A. Marceline
Mienie, Lodewyk J.
Engelke, Udo F. H.
Wevers, Ron A.
Solomons, Regan
Reinecke, Carolus J.
author_facet Mason, Shayne
van Furth, A. Marceline
Mienie, Lodewyk J.
Engelke, Udo F. H.
Wevers, Ron A.
Solomons, Regan
Reinecke, Carolus J.
author_sort Mason, Shayne
collection PubMed
description Tuberculosis meningitis (TBM) is the most severe form of extra-pulmonary tuberculosis and is particularly intense in small children; there is no universally accepted algorithm for the diagnosis and substantiation of TB infection, which can lead to delayed intervention, a high risk factor for morbidity and mortality. In this study a proton magnetic resonance ((1)H NMR)-based metabolomics analysis and several chemometric methods were applied to data generated from lumber cerebrospinal fluid (CSF) samples from three experimental groups: (1) South African infants and children with confirmed TBM, (2) non-meningitis South African infants and children as controls, and (3) neurological controls from the Netherlands. A total of 16 NMR-derived CSF metabolites were identified, which clearly differentiated between the controls and TBM cases under investigation. The defining metabolites were the combination of perturbed glucose and highly elevated lactate, common to some other neurological disorders. The remaining 14 metabolites of the host’s response to TBM were likewise mainly energy-associated indicators. We subsequently generated a hypothesis expressed as an “astrocyte–microglia lactate shuttle” (AMLS) based on the host’s response, which emerged from the NMR-metabolomics information. Activation of microglia, as implied by the AMLS hypothesis, does not, however, present a uniform process and involves intricate interactions and feedback loops between the microglia, astrocytes and neurons that hamper attempts to construct basic and linear cascades of cause and effect; TBM involves a complex integration of the responses from the various cell types present within the CNS, with microglia and the astrocytes as main players. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11306-014-0741-z) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4475545
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-44755452015-06-22 A hypothetical astrocyte–microglia lactate shuttle derived from a (1)H NMR metabolomics analysis of cerebrospinal fluid from a cohort of South African children with tuberculous meningitis Mason, Shayne van Furth, A. Marceline Mienie, Lodewyk J. Engelke, Udo F. H. Wevers, Ron A. Solomons, Regan Reinecke, Carolus J. Metabolomics Original Article Tuberculosis meningitis (TBM) is the most severe form of extra-pulmonary tuberculosis and is particularly intense in small children; there is no universally accepted algorithm for the diagnosis and substantiation of TB infection, which can lead to delayed intervention, a high risk factor for morbidity and mortality. In this study a proton magnetic resonance ((1)H NMR)-based metabolomics analysis and several chemometric methods were applied to data generated from lumber cerebrospinal fluid (CSF) samples from three experimental groups: (1) South African infants and children with confirmed TBM, (2) non-meningitis South African infants and children as controls, and (3) neurological controls from the Netherlands. A total of 16 NMR-derived CSF metabolites were identified, which clearly differentiated between the controls and TBM cases under investigation. The defining metabolites were the combination of perturbed glucose and highly elevated lactate, common to some other neurological disorders. The remaining 14 metabolites of the host’s response to TBM were likewise mainly energy-associated indicators. We subsequently generated a hypothesis expressed as an “astrocyte–microglia lactate shuttle” (AMLS) based on the host’s response, which emerged from the NMR-metabolomics information. Activation of microglia, as implied by the AMLS hypothesis, does not, however, present a uniform process and involves intricate interactions and feedback loops between the microglia, astrocytes and neurons that hamper attempts to construct basic and linear cascades of cause and effect; TBM involves a complex integration of the responses from the various cell types present within the CNS, with microglia and the astrocytes as main players. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11306-014-0741-z) contains supplementary material, which is available to authorized users. Springer US 2014-10-11 2015 /pmc/articles/PMC4475545/ /pubmed/26109926 http://dx.doi.org/10.1007/s11306-014-0741-z Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Mason, Shayne
van Furth, A. Marceline
Mienie, Lodewyk J.
Engelke, Udo F. H.
Wevers, Ron A.
Solomons, Regan
Reinecke, Carolus J.
A hypothetical astrocyte–microglia lactate shuttle derived from a (1)H NMR metabolomics analysis of cerebrospinal fluid from a cohort of South African children with tuberculous meningitis
title A hypothetical astrocyte–microglia lactate shuttle derived from a (1)H NMR metabolomics analysis of cerebrospinal fluid from a cohort of South African children with tuberculous meningitis
title_full A hypothetical astrocyte–microglia lactate shuttle derived from a (1)H NMR metabolomics analysis of cerebrospinal fluid from a cohort of South African children with tuberculous meningitis
title_fullStr A hypothetical astrocyte–microglia lactate shuttle derived from a (1)H NMR metabolomics analysis of cerebrospinal fluid from a cohort of South African children with tuberculous meningitis
title_full_unstemmed A hypothetical astrocyte–microglia lactate shuttle derived from a (1)H NMR metabolomics analysis of cerebrospinal fluid from a cohort of South African children with tuberculous meningitis
title_short A hypothetical astrocyte–microglia lactate shuttle derived from a (1)H NMR metabolomics analysis of cerebrospinal fluid from a cohort of South African children with tuberculous meningitis
title_sort hypothetical astrocyte–microglia lactate shuttle derived from a (1)h nmr metabolomics analysis of cerebrospinal fluid from a cohort of south african children with tuberculous meningitis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4475545/
https://www.ncbi.nlm.nih.gov/pubmed/26109926
http://dx.doi.org/10.1007/s11306-014-0741-z
work_keys_str_mv AT masonshayne ahypotheticalastrocytemicroglialactateshuttlederivedfroma1hnmrmetabolomicsanalysisofcerebrospinalfluidfromacohortofsouthafricanchildrenwithtuberculousmeningitis
AT vanfurthamarceline ahypotheticalastrocytemicroglialactateshuttlederivedfroma1hnmrmetabolomicsanalysisofcerebrospinalfluidfromacohortofsouthafricanchildrenwithtuberculousmeningitis
AT mienielodewykj ahypotheticalastrocytemicroglialactateshuttlederivedfroma1hnmrmetabolomicsanalysisofcerebrospinalfluidfromacohortofsouthafricanchildrenwithtuberculousmeningitis
AT engelkeudofh ahypotheticalastrocytemicroglialactateshuttlederivedfroma1hnmrmetabolomicsanalysisofcerebrospinalfluidfromacohortofsouthafricanchildrenwithtuberculousmeningitis
AT weversrona ahypotheticalastrocytemicroglialactateshuttlederivedfroma1hnmrmetabolomicsanalysisofcerebrospinalfluidfromacohortofsouthafricanchildrenwithtuberculousmeningitis
AT solomonsregan ahypotheticalastrocytemicroglialactateshuttlederivedfroma1hnmrmetabolomicsanalysisofcerebrospinalfluidfromacohortofsouthafricanchildrenwithtuberculousmeningitis
AT reineckecarolusj ahypotheticalastrocytemicroglialactateshuttlederivedfroma1hnmrmetabolomicsanalysisofcerebrospinalfluidfromacohortofsouthafricanchildrenwithtuberculousmeningitis
AT masonshayne hypotheticalastrocytemicroglialactateshuttlederivedfroma1hnmrmetabolomicsanalysisofcerebrospinalfluidfromacohortofsouthafricanchildrenwithtuberculousmeningitis
AT vanfurthamarceline hypotheticalastrocytemicroglialactateshuttlederivedfroma1hnmrmetabolomicsanalysisofcerebrospinalfluidfromacohortofsouthafricanchildrenwithtuberculousmeningitis
AT mienielodewykj hypotheticalastrocytemicroglialactateshuttlederivedfroma1hnmrmetabolomicsanalysisofcerebrospinalfluidfromacohortofsouthafricanchildrenwithtuberculousmeningitis
AT engelkeudofh hypotheticalastrocytemicroglialactateshuttlederivedfroma1hnmrmetabolomicsanalysisofcerebrospinalfluidfromacohortofsouthafricanchildrenwithtuberculousmeningitis
AT weversrona hypotheticalastrocytemicroglialactateshuttlederivedfroma1hnmrmetabolomicsanalysisofcerebrospinalfluidfromacohortofsouthafricanchildrenwithtuberculousmeningitis
AT solomonsregan hypotheticalastrocytemicroglialactateshuttlederivedfroma1hnmrmetabolomicsanalysisofcerebrospinalfluidfromacohortofsouthafricanchildrenwithtuberculousmeningitis
AT reineckecarolusj hypotheticalastrocytemicroglialactateshuttlederivedfroma1hnmrmetabolomicsanalysisofcerebrospinalfluidfromacohortofsouthafricanchildrenwithtuberculousmeningitis