Small-molecule metabolome identifies potential therapeutic targets against COVID-19.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
15 06 2022
Historique:
received: 14 01 2022
accepted: 31 05 2022
entrez: 15 6 2022
pubmed: 16 6 2022
medline: 18 6 2022
Statut: epublish

Résumé

Respiratory viruses are transmitted and acquired via the nasal mucosa, and thereby may influence the nasal metabolome composed of biochemical products produced by both host cells and microbes. Studies of the nasal metabolome demonstrate virus-specific changes that sometimes correlate with viral load and disease severity. Here, we evaluate the nasopharyngeal metabolome of COVID-19 infected individuals and report several small molecules that may be used as potential therapeutic targets. Specimens were tested by qRT-PCR with target primers for three viruses: Influenza A (INFA), respiratory syncytial virus (RSV), and SARS-CoV-2, along with unaffected controls. The nasopharyngeal metabolome was characterized using an LC-MS/MS-based screening kit capable of quantifying 141 analytes. A machine learning model identified 28 discriminating analytes and correctly categorized patients with a viral infection with an accuracy of 96% (R

Identifiants

pubmed: 35705626
doi: 10.1038/s41598-022-14050-y
pii: 10.1038/s41598-022-14050-y
pmc: PMC9200216
doi:

Substances chimiques

Lysophosphatidylcholines 0
Carnosine 8HO6PVN24W

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

10029

Informations de copyright

© 2022. The Author(s).

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Auteurs

Sean Bennet (S)

Gastrointestinal Diseases Research Unit (GIDRU), Kingston Health Sciences Centre, 76 Stuart St., Kingston, ON, K7L 2V7, Canada.

Martin Kaufmann (M)

Gastrointestinal Diseases Research Unit (GIDRU), Kingston Health Sciences Centre, 76 Stuart St., Kingston, ON, K7L 2V7, Canada.

Kaede Takami (K)

Gastrointestinal Diseases Research Unit (GIDRU), Kingston Health Sciences Centre, 76 Stuart St., Kingston, ON, K7L 2V7, Canada.

Calvin Sjaarda (C)

Department of Psychiatry, Queen's University, Kingston, ON, Canada.

Katya Douchant (K)

Gastrointestinal Diseases Research Unit (GIDRU), Kingston Health Sciences Centre, 76 Stuart St., Kingston, ON, K7L 2V7, Canada.

Emily Moslinger (E)

Gastrointestinal Diseases Research Unit (GIDRU), Kingston Health Sciences Centre, 76 Stuart St., Kingston, ON, K7L 2V7, Canada.
Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON, Canada.

Henry Wong (H)

Division of Microbiology, Kingston Health Sciences Centre, Kingston, ON, Canada.

David E Reed (DE)

Gastrointestinal Diseases Research Unit (GIDRU), Kingston Health Sciences Centre, 76 Stuart St., Kingston, ON, K7L 2V7, Canada.

Anne K Ellis (AK)

Division of Allergy and Immunology, Department of Medicine, Queen's University, Kingston, ON, Canada.

Stephen Vanner (S)

Gastrointestinal Diseases Research Unit (GIDRU), Kingston Health Sciences Centre, 76 Stuart St., Kingston, ON, K7L 2V7, Canada.

Robert I Colautti (RI)

Department of Biology, Queen's University, Kingston, ON, Canada.

Prameet M Sheth (PM)

Gastrointestinal Diseases Research Unit (GIDRU), Kingston Health Sciences Centre, 76 Stuart St., Kingston, ON, K7L 2V7, Canada. Prameet.sheth@queensu.ca.
Division of Microbiology, Kingston Health Sciences Centre, Kingston, ON, Canada. Prameet.sheth@queensu.ca.
Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON, Canada. Prameet.sheth@queensu.ca.

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Classifications MeSH