Identifying potential dietary treatments for inherited metabolic disorders using Drosophila nutrigenomics.

CP: Developmental biology CP: Metabolism amino acid metabolism diet fruit fly inherited metabolic disease isolated sulfite oxidase deficiency nutrition

Journal

Cell reports
ISSN: 2211-1247
Titre abrégé: Cell Rep
Pays: United States
ID NLM: 101573691

Informations de publication

Date de publication:
27 Feb 2024
Historique:
received: 16 05 2023
revised: 09 12 2023
accepted: 08 02 2024
medline: 28 2 2024
pubmed: 28 2 2024
entrez: 28 2 2024
Statut: aheadofprint

Résumé

Inherited metabolic disorders are a group of genetic conditions that can cause severe neurological impairment and child mortality. Uniquely, these disorders respond to dietary treatment; however, this option remains largely unexplored because of low disorder prevalence and the lack of a suitable paradigm for testing diets. Here, we screened 35 Drosophila amino acid disorder models for disease-diet interactions and found 26 with diet-altered development and/or survival. Using a targeted multi-nutrient array, we examine the interaction in a model of isolated sulfite oxidase deficiency, an infant-lethal disorder. We show that dietary cysteine depletion normalizes their metabolic profile and rescues development, neurophysiology, behavior, and lifelong fly survival, thus providing a basis for further study into the pathogenic mechanisms involved in this disorder. Our work highlights the diet-sensitive nature of metabolic disorders and establishes Drosophila as a valuable tool for nutrigenomic studies for informing potential dietary therapies.

Identifiants

pubmed: 38416643
pii: S2211-1247(24)00189-X
doi: 10.1016/j.celrep.2024.113861
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

113861

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

Auteurs

Felipe Martelli (F)

School of Biological Sciences, Monash University, Clayton, VIC 3800, Australia.

Jiayi Lin (J)

School of Biological Sciences, Monash University, Clayton, VIC 3800, Australia.

Sarah Mele (S)

School of Biological Sciences, Monash University, Clayton, VIC 3800, Australia.

Wendy Imlach (W)

Department of Physiology, Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.

Oguz Kanca (O)

Department of Molecular and Human Genetics and Duncan Neurological Research Institute at Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.

Christopher K Barlow (CK)

Monash Proteomics & Metabolomics Facility, Monash Biomedicine Discovery Institute & Department of Biochemistry and Molecular Biology, Monash University, Clayton, VIC 3800, Australia.

Jefferson Paril (J)

School of BioSciences, The University of Melbourne, Melbourne, VIC 3052, Australia.

Ralf B Schittenhelm (RB)

Monash Proteomics & Metabolomics Facility, Monash Biomedicine Discovery Institute & Department of Biochemistry and Molecular Biology, Monash University, Clayton, VIC 3800, Australia.

John Christodoulou (J)

Murdoch Children's Research Institute, Parkville, VIC 3052, Australia; Department of Paediatrics, The University of Melbourne, Melbourne, VIC 3052, Australia.

Hugo J Bellen (HJ)

Department of Molecular and Human Genetics and Duncan Neurological Research Institute at Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.

Matthew D W Piper (MDW)

School of Biological Sciences, Monash University, Clayton, VIC 3800, Australia. Electronic address: matthew.piper@monash.edu.

Travis K Johnson (TK)

School of Biological Sciences, Monash University, Clayton, VIC 3800, Australia; Department of Biochemistry and Chemistry and La Trobe Institute for Molecular Science, La Trobe University, Bundoora, VIC 3086, Australia. Electronic address: t.johnson@latrobe.edu.au.

Classifications MeSH