Schistosoma haematobium infection is associated with alterations in energy and purine-related metabolism in preschool-aged children.


Journal

PLoS neglected tropical diseases
ISSN: 1935-2735
Titre abrégé: PLoS Negl Trop Dis
Pays: United States
ID NLM: 101291488

Informations de publication

Date de publication:
12 2020
Historique:
received: 26 05 2020
accepted: 08 10 2020
entrez: 14 12 2020
pubmed: 15 12 2020
medline: 23 2 2021
Statut: epublish

Résumé

Helminths are parasitic worms that infect over a billion people worldwide. The pathological consequences from infection are due in part, to parasite-induced changes in host metabolic pathways. Here, we analyse the changes in host metabolic profiles, in response to the first Schistosoma haematobium infection and treatment in Zimbabwean children. A cohort of 83 schistosome-negative children (2-5 years old) as determined by parasitological examination, guardian interviews and examination of medical records, was recruited at baseline. Children were followed up after three months for parasitological diagnosis of their first S. haematobium infection, by detection of parasite eggs excreted in urine. Children positive for infection were treated with the antihelminthic drug praziquantel, and treatment efficacy checked three months after treatment. Blood samples were taken at each time point, and capillary electrophoresis mass spectrometry in conjunction with multivariate analysis were used to compare the change in serum metabolite profiles in schistosome-infected versus uninfected children. Following baseline at the three-month follow up, 11 children had become infected with S. haematobium (incidence = 13.3%). Our results showed that infection with S. haematobium was associated with significant increases (>2-fold) in discriminatory metabolites, linked primarily with energy (G6P, 3-PG, AMP, ADP) and purine (AMP, ADP) metabolism. These observed changes were commensurate with schistosome infection intensity, and levels of the affected metabolites were reduced following treatment, albeit not significantly. This study demonstrates that early infection with S. haematobium is associated with alterations in host energy and purine metabolism. Taken together, these changes are consistent with parasite-related clinical manifestations of malnutrition, poor growth and poor physical and cognitive performance observed in schistosome-infected children.

Identifiants

pubmed: 33315875
doi: 10.1371/journal.pntd.0008866
pii: PNTD-D-20-00937
pmc: PMC7735607
doi:

Substances chimiques

Anthelmintics 0
Purines 0
Praziquantel 6490C9U457

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0008866

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 108061/Z/15/Z
Pays : United Kingdom
Organisme : Department of Health
ID : 16/136/33
Pays : United Kingdom

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Derick N M Osakunor (DNM)

Institute of Immunology & Infection Research, University of Edinburgh, Ashworth Laboratories, King's Buildings, Edinburgh, United Kingdom.

Takafira Mduluza (T)

Biochemistry Department, University of Zimbabwe, Mount Pleasant, Harare, Zimbabwe.

Douglas Osei-Hyiaman (D)

Laboratory of Physiologic Studies, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland, United States of America.
Metabolomics Research Division, Human Metabolome Technologies Inc., Tsuruoka, Yamagata, Japan.
Department of Systems Neurophysiology, Graduate School of Medical & Dental Science, Tokyo Medical and Dental University, Bunkyo City, Tokyo, Japan.

Karl Burgess (K)

Centre for Synthetic and Systems Biology, University of Edinburgh, CH Waddington Building, King's Buildings, Edinburgh, United Kingdom.

Mark E J Woolhouse (MEJ)

Usher Institute, University of Edinburgh, Ashworth Laboratories, King's Buildings, Edinburgh, United Kingdom.
NIHR Global Health Research Unit Tackling Infections to Benefit Africa (TIBA), University of Edinburgh, Ashworth Laboratories, King's Buildings, Edinburgh, United Kingdom.

Francisca Mutapi (F)

Institute of Immunology & Infection Research, University of Edinburgh, Ashworth Laboratories, King's Buildings, Edinburgh, United Kingdom.
NIHR Global Health Research Unit Tackling Infections to Benefit Africa (TIBA), University of Edinburgh, Ashworth Laboratories, King's Buildings, Edinburgh, United Kingdom.

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