Comparison of Extracellular Vesicle Isolation Methods for the Study of Exosome Cargo within Toxocara canis and Toxocara cati Excretory Secretory (TES) Products.

Extracellular vesicle Toxocara canis Toxocara cati excretory secretory products exosome

Journal

Experimental parasitology
ISSN: 1090-2449
Titre abrégé: Exp Parasitol
Pays: United States
ID NLM: 0370713

Informations de publication

Date de publication:
26 Apr 2024
Historique:
received: 23 12 2023
revised: 23 04 2024
accepted: 24 04 2024
medline: 29 4 2024
pubmed: 29 4 2024
entrez: 28 4 2024
Statut: aheadofprint

Résumé

Toxocara is a genus of nematodes, which infects a variety of hosts, principally dogs and cats, with potential zoonotic risks to humans. Toxocara spp. larvae are capable of migrating throughout the host tissues, eliciting eosinophilic and granulomatous reactions, while surviving for extended periods of time, unchanged, in the host. It is postulated that larvae are capable of altering the host's immune response through the release of excretory-secretory products, containing both proteins and extracellular vesicles (EVs). The study of EVs has increased exponentially in recent years, largely due to their potential use as a diagnostic tool, and in molecular therapy. To this end, there have been multiple isolation methods described for the study of EVs. Here, we use nanoparticle tracking to compare the yield, size distribution, and % labelling of EV samples acquired through various reported methods, from larval cultures of Toxocara canis and T. cati containing Toxocara excretory-secretory products (TES). The methods tested include ultracentrifugation, polymer precipitation, magnetic immunoprecipitation, size exclusion chromatography, and ultrafiltration. Based on these findings, ultrafiltration produces the best results in terms of yield, expected particle size, and % labelling of sample. Transmission electron microscopy confirmed the presence of EVs with characteristic cup-shaped morphology. These findings can serve as a guide for those investigating EVs, particularly those released from multicellular organisms, such as helminths, for which few comparative analyses have been performed.

Identifiants

pubmed: 38679126
pii: S0014-4894(24)00068-7
doi: 10.1016/j.exppara.2024.108765
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

108765

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of Competing Interest ☐ The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. ☒ The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Timothy Wu reports financial support was provided by Cornell Feline Health Center.

Auteurs

Timothy K Wu (TK)

Cornell University College of Veterinary Medicine, Department of Microbiology and Immunology, 930 Campus Rd, Ithaca, NY, 14853. Electronic address: tkw38@cornell.edu.

Janice L Liotta (JL)

Cornell University College of Veterinary Medicine, Department of Microbiology and Immunology, 930 Campus Rd, Ithaca, NY, 14853.

Dwight D Bowman (DD)

Cornell University College of Veterinary Medicine, Department of Microbiology and Immunology, 930 Campus Rd, Ithaca, NY, 14853.

Classifications MeSH