Serum metabolic profiling of oocyst-induced Toxoplasma gondii acute and chronic infections in mice using mass-spectrometry

Toxoplasma gondii is an obligate intracellular parasite causing severe diseases in immunocompromised individuals and congenitally infected neonates, such as toxoplasmosis encephalitis and toxoplasmic chorioretinitis. This study aimed to determine whether serum metabolic profiling can (i) identify me...

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Main Authors: Zhou, Chun-Xue, Cong, Wei, Chen, Xiao-Qing, He, Shen-Yi, Elsheikha, Hany M., Zhu, Xing-Quan
Format: Article
Published: Frontiers Media 2018
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Online Access:https://eprints.nottingham.ac.uk/48831/
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author Zhou, Chun-Xue
Cong, Wei
Chen, Xiao-Qing
He, Shen-Yi
Elsheikha, Hany M.
Zhu, Xing-Quan
author_facet Zhou, Chun-Xue
Cong, Wei
Chen, Xiao-Qing
He, Shen-Yi
Elsheikha, Hany M.
Zhu, Xing-Quan
author_sort Zhou, Chun-Xue
building Nottingham Research Data Repository
collection Online Access
description Toxoplasma gondii is an obligate intracellular parasite causing severe diseases in immunocompromised individuals and congenitally infected neonates, such as toxoplasmosis encephalitis and toxoplasmic chorioretinitis. This study aimed to determine whether serum metabolic profiling can (i) identify metabolites associated with oocyst-induced T. gondii infection and (ii) detect systemic metabolic differences between T. gondii -infected mice patients and controls. We performed the first global metabolomics analysis of mice serum challenged with 100 sporulated T. gondii Pru oocysts (Genotype II). Sera from acutely infected mice (11 days post-infection, dpi), chronically infected mice (33 dpi) and control mice were collected and analysed using LC-MS/MS platform. Following False Discovery Rate filtering, we identified 3871 and 2825 ions in ESI + or ESI − mode, respectively. Principal Component Analysis (PCA) and Partial Least Squares Discriminant Analysis (PLS -DA) identified metabolomics profiles that clearly differentiated T. gondii -infected and -uninfected serum samples. Acute infection significantly influenced the serum metabolonme. Our results identified common and uniquely perturbed metabolites and pathways. Acutely infected mice showed perturbations in metabolites associated with glycerophospholipid metabolism, biosynthesis of amino acid, and tyrosine metabolism. These findings demonstrated that acute T. gondii oocyst induces a global perturbation of mice serum metabolonme, providing new insights into the mechanisms underlying systemic metabolic changes during early stage of T. gondii oocyst infection.
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spelling nottingham-488312020-05-04T19:25:55Z https://eprints.nottingham.ac.uk/48831/ Serum metabolic profiling of oocyst-induced Toxoplasma gondii acute and chronic infections in mice using mass-spectrometry Zhou, Chun-Xue Cong, Wei Chen, Xiao-Qing He, Shen-Yi Elsheikha, Hany M. Zhu, Xing-Quan Toxoplasma gondii is an obligate intracellular parasite causing severe diseases in immunocompromised individuals and congenitally infected neonates, such as toxoplasmosis encephalitis and toxoplasmic chorioretinitis. This study aimed to determine whether serum metabolic profiling can (i) identify metabolites associated with oocyst-induced T. gondii infection and (ii) detect systemic metabolic differences between T. gondii -infected mice patients and controls. We performed the first global metabolomics analysis of mice serum challenged with 100 sporulated T. gondii Pru oocysts (Genotype II). Sera from acutely infected mice (11 days post-infection, dpi), chronically infected mice (33 dpi) and control mice were collected and analysed using LC-MS/MS platform. Following False Discovery Rate filtering, we identified 3871 and 2825 ions in ESI + or ESI − mode, respectively. Principal Component Analysis (PCA) and Partial Least Squares Discriminant Analysis (PLS -DA) identified metabolomics profiles that clearly differentiated T. gondii -infected and -uninfected serum samples. Acute infection significantly influenced the serum metabolonme. Our results identified common and uniquely perturbed metabolites and pathways. Acutely infected mice showed perturbations in metabolites associated with glycerophospholipid metabolism, biosynthesis of amino acid, and tyrosine metabolism. These findings demonstrated that acute T. gondii oocyst induces a global perturbation of mice serum metabolonme, providing new insights into the mechanisms underlying systemic metabolic changes during early stage of T. gondii oocyst infection. Frontiers Media 2018-01-04 Article PeerReviewed Zhou, Chun-Xue, Cong, Wei, Chen, Xiao-Qing, He, Shen-Yi, Elsheikha, Hany M. and Zhu, Xing-Quan (2018) Serum metabolic profiling of oocyst-induced Toxoplasma gondii acute and chronic infections in mice using mass-spectrometry. Frontiers in Microbiology . ISSN 1664-302X Toxoplasma gondii oocyst LC-MS/MS metabolomics mouse model https://www.frontiersin.org/articles/10.3389/fmicb.2017.02612/full doi:10.3389/fmicb.2017.02612 doi:10.3389/fmicb.2017.02612
spellingShingle Toxoplasma gondii
oocyst
LC-MS/MS
metabolomics
mouse model
Zhou, Chun-Xue
Cong, Wei
Chen, Xiao-Qing
He, Shen-Yi
Elsheikha, Hany M.
Zhu, Xing-Quan
Serum metabolic profiling of oocyst-induced Toxoplasma gondii acute and chronic infections in mice using mass-spectrometry
title Serum metabolic profiling of oocyst-induced Toxoplasma gondii acute and chronic infections in mice using mass-spectrometry
title_full Serum metabolic profiling of oocyst-induced Toxoplasma gondii acute and chronic infections in mice using mass-spectrometry
title_fullStr Serum metabolic profiling of oocyst-induced Toxoplasma gondii acute and chronic infections in mice using mass-spectrometry
title_full_unstemmed Serum metabolic profiling of oocyst-induced Toxoplasma gondii acute and chronic infections in mice using mass-spectrometry
title_short Serum metabolic profiling of oocyst-induced Toxoplasma gondii acute and chronic infections in mice using mass-spectrometry
title_sort serum metabolic profiling of oocyst-induced toxoplasma gondii acute and chronic infections in mice using mass-spectrometry
topic Toxoplasma gondii
oocyst
LC-MS/MS
metabolomics
mouse model
url https://eprints.nottingham.ac.uk/48831/
https://eprints.nottingham.ac.uk/48831/
https://eprints.nottingham.ac.uk/48831/