Extracellular vesicles from Heligmosomoides bakeri and Trichuris muris contain distinct microRNA families and small RNAs that could underpin different functions in the host.


Journal

International journal for parasitology
ISSN: 1879-0135
Titre abrégé: Int J Parasitol
Pays: England
ID NLM: 0314024

Informations de publication

Date de publication:
08 2020
Historique:
received: 07 05 2020
revised: 18 06 2020
accepted: 19 06 2020
pubmed: 14 7 2020
medline: 22 6 2021
entrez: 14 7 2020
Statut: ppublish

Résumé

Extracellular vesicles (EVs) have emerged as a ubiquitous component of helminth excretory-secretory products that can deliver parasite molecules to host cells to elicit immunomodulatory effects. RNAs are one type of cargo molecule that can underpin EV functions, hence there is extensive interest in characterising the RNAs that are present in EVs from different helminth species. Here we outline methods for identifying all of the small RNAs (sRNA) in helminth EVs and address how different methodologies may influence the sRNAs detected. We show that different EV purification methods introduce relatively little variation in the sRNAs that are detected, and that different RNA library preparation methods yielded larger differences. We compared the EV sRNAs in the gastrointestinal nematode Heligmosomoides bakeri with those in EVs from the distantly related gastrointestinal nematode Trichuris muris, and found that many of the sRNAs in both organisms derive from repetitive elements or intergenic regions. However, only in H. bakeri do these RNAs contain a 5' triphosphate, and Guanine (G) starting nucleotide, consistent with their biogenesis by RNA-dependent RNA polymerases (RdRPs). Distinct microRNA (miRNA) families are carried in EVs from each parasite, with H. bakeri EVs specific for miR-71, miR-49, miR-63, miR-259 and miR-240 gene families, and T. muris EVs specific for miR-1, miR-1822 and miR-252, and enriched for miR-59, miR-72 and miR-44 families, with the miR-9, miR-10, miR-80 and let-7 families abundant in both. We found a larger proportion of miRNA reads derive from the mouse host in T. muris EVs, compared with H. bakeri EVs. Our report underscores potential biases in the sRNAs sequenced based on library preparation methods, suggests specific nematode lineages have evolved distinct sRNA synthesis/export pathways, and highlights specific differences in EV miRNAs from H. bakeri and T. muris that may underpin functional adaptation to their host niches.

Identifiants

pubmed: 32659276
pii: S0020-7519(20)30164-8
doi: 10.1016/j.ijpara.2020.06.002
pmc: PMC7435682
pii:
doi:

Substances chimiques

MicroRNAs 0
RNA, Helminth 0
RNA, Small Interfering 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

719-729

Subventions

Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/J004243/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : Z03128/Z/16/Z/WT
Pays : United Kingdom
Organisme : National Centre for the Replacement, Refinement and Reduction of Animals in Research
ID : NC/P001521/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : Z10661/Z/18/Z/WT
Pays : United Kingdom
Organisme : Wellcome Trust
ID : WT104915MA
Pays : United Kingdom
Organisme : Wellcome Trust
ID : WT 097394/Z/11/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/K001744/1
Pays : United Kingdom

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.

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Auteurs

Ruby White (R)

Institute of Immunology & Infection Research, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK.

Sujai Kumar (S)

Institute of Immunology & Infection Research, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK.

Franklin Wang-Ngai Chow (FW)

Institute of Immunology & Infection Research, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK.

Elaine Robertson (E)

Institute of Immunology & Infection Research, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK.

Kelly S Hayes (KS)

Lydia Becker Institute of Immunology and Inflammation, Wellcome Trust Centre for Cell Matrix Research and Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.

Richard K Grencis (RK)

Lydia Becker Institute of Immunology and Inflammation, Wellcome Trust Centre for Cell Matrix Research and Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.

María A Duque-Correa (MA)

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton CB10 1SA, UK.

Amy H Buck (AH)

Institute of Immunology & Infection Research, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK. Electronic address: a.buck@ed.ac.uk.

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Classifications MeSH