Direct Proteomic Detection and Prioritization of 19 Onchocerciasis Biomarker Candidates in Humans.


Journal

Molecular & cellular proteomics : MCP
ISSN: 1535-9484
Titre abrégé: Mol Cell Proteomics
Pays: United States
ID NLM: 101125647

Informations de publication

Date de publication:
Jan 2023
Historique:
received: 19 07 2022
revised: 30 10 2022
accepted: 21 11 2022
pubmed: 27 11 2022
medline: 25 1 2023
entrez: 26 11 2022
Statut: ppublish

Résumé

Onchocerca volvulus, the causative agent of onchocerciasis, infects over 20 million people and can cause severe dermatitis and ocular conditions including blindness. Current treatments employed in mass drug administration programs do not kill adult female worms, and common diagnostic tests cannot reliably assess viability of adult worms. There is an urgent need for better diagnostic tests to facilitate monitoring the efficacy of new treatments and disease elimination efforts. Here, eight plasma samples collected from individuals infected with O. volvulus and seven from uninfected individuals were analyzed by MS/MS spectrometry to directly identify O. volvulus proteins present in infected but absent in uninfected control samples. This direct proteomic approach for biomarker discovery had not been previously employed for onchocerciasis. Among all detected proteins, 19 biomarker candidates were supported by two or more unique peptides, identified in the plasma of at least three O. volvulus-infected human samples and absent in all control samples. Comprehensive analysis and ranking of these candidates included detailed functional annotation and a review of RNA-seq gene expression profiles. Isotope-labeled standard peptides were run in parallel and validated MS/MS peptide identifications for 15 peptides from 11 of the 19 proteins, and two infected urine and one uninfected urine sample was used for additional validation. A major antigen/OVOC11613 was identified as the most promising candidate with eight unique peptides across five plasma samples and one urine sample. Additional strong candidates included OVOC1523/ATP synthase, OVOC247/laminin and OVOC11626/PLK5, and along with OVOC11613, and were also detected in urine samples from onchocerciasis patients. This study has identified a promising novel set of proteins that will be carried forward to develop assays that can be used for diagnosis of O. volvulus infections and for monitoring treatment efficacy.

Identifiants

pubmed: 36435333
pii: S1535-9476(22)00262-6
doi: 10.1016/j.mcpro.2022.100454
pmc: PMC9792368
pii:
doi:

Substances chimiques

Biomarkers 0

Types de publication

Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

100454

Subventions

Organisme : NIGMS NIH HHS
ID : P41 GM103422
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA091842
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000448
Pays : United States
Organisme : Bill & Melinda Gates Foundation
ID : INV-021433
Pays : United States
Organisme : NIGMS NIH HHS
ID : R24 GM136766
Pays : United States

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest The authors declare no competing interests.

Auteurs

Bruce A Rosa (BA)

Division of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA.

Kurt Curtis (K)

Division of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA.

Petra Erdmann Gilmore (P)

Division of Endocrinology, Metabolism and Lipid Research, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA.

John Martin (J)

Division of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA.

Qiang Zhang (Q)

Division of Endocrinology, Metabolism and Lipid Research, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA.

Robert Sprung (R)

Division of Endocrinology, Metabolism and Lipid Research, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA.

Gary J Weil (GJ)

Division of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA.

R Reid Townsend (RR)

Division of Endocrinology, Metabolism and Lipid Research, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA.

Peter U Fischer (PU)

Division of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA.

Makedonka Mitreva (M)

Division of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA; Department of Genetics, Washington University School of Medicine, St Louis, Missouri, USA; McDonnell Genome Institute, Washington University School of Medicine, St Louis, Missouri, USA. Electronic address: mmitreva@wustl.edu.

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Classifications MeSH