Evidence map›Paper›PMID 31292008›Full record

ArticleParasites & vectors2019

Characterisation of a niche-specific excretory-secretory peroxiredoxin from the parasitic nematode Teladorsagia circumcincta.

Daniel R G Price, Alasdair J Nisbet, David Frew, Yvonne Bartley, E Margaret Oliver, Kevin McLean, Neil F Inglis, Eleanor Watson, Yolanda Corripio-Miyar, Tom N McNeilly

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 8 citations in OpenAlex.

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  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Daniel R G PriceMoredun Research Institute, Pentlands Science Park, Edinburgh, EH26 0PZ, UK. daniel.price@moredun.ac.uk.ORCID http://orcid.org/0000-0002-4819-0654
Alasdair J NisbetMoredun Research Institute, Pentlands Science Park, Edinburgh, EH26 0PZ, UK.
David FrewMoredun Research Institute, Pentlands Science Park, Edinburgh, EH26 0PZ, UK.
Yvonne BartleyMoredun Research Institute, Pentlands Science Park, Edinburgh, EH26 0PZ, UK.
E Margaret OliverMoredun Research Institute, Pentlands Science Park, Edinburgh, EH26 0PZ, UK.
Kevin McLeanMoredun Research Institute, Pentlands Science Park, Edinburgh, EH26 0PZ, UK.
Neil F InglisMoredun Research Institute, Pentlands Science Park, Edinburgh, EH26 0PZ, UK.
Eleanor WatsonMoredun Research Institute, Pentlands Science Park, Edinburgh, EH26 0PZ, UK.
Yolanda Corripio-MiyarMoredun Research Institute, Pentlands Science Park, Edinburgh, EH26 0PZ, UK.
Tom N McNeillyMoredun Research Institute, Pentlands Science Park, Edinburgh, EH26 0PZ, UK.
Moredun Research Institute · GB

Funding

Horizon 2020 635408Scottish Government Rural Affairs, Food and the Environment (RAFE) Strategic Research Portfolio 2016-2021
6 · The paper itself

Abstract

backgroundThe primary cause of parasitic gastroenteritis in small ruminants in temperate regions is the brown stomach worm, Teladorsagia circumcincta. Host immunity to this parasite is slow to develop, consistent with the ability of T. circumcincta to suppress the host immune response. Previous studies have shown that infective fourth-stage T. circumcincta larvae produce excretory-secretory products that are able to modulate the host immune response. The objective of this study was to identify immune modulatory excretory-secretory proteins from populations of fourth-stage T. circumcincta larvae present in two different host-niches: those associated with the gastric glands (mucosal-dwelling larvae) and those either loosely associated with the mucosa or free-living in the lumen (lumen-dwelling larvae).

resultsIn this study excretory-secretory proteins from mucosal-dwelling and lumen-dwelling T. circumcincta fourth stage larvae were analysed using comparative 2-dimensional gel electrophoresis. A total of 17 proteins were identified as differentially expressed, with 14 proteins unique to, or enriched in, the excretory-secretory proteins of mucosal-dwelling larvae. One of the identified proteins, unique to mucosal-dwelling larvae, was a putative peroxiredoxin (T. circumcincta peroxiredoxin 1, Tci-Prx1). Peroxiredoxin orthologs from the trematode parasites Schistosoma mansoni and Fasciola hepatica have previously been shown to alternatively activate macrophages and play a key role in promoting parasite induced Th2 type immunity. Here we demonstrate that Tci-Prx1 is expressed in all infective T. circumcincta life-stages and, when produced as a recombinant protein, has peroxidase activity, whereby hydrogen peroxide (H

conclusionsIn this study, we identified differences in the excretory-secretory proteome of mucosal-dwelling and lumen-dwelling infective fourth-stage T. circumcincta larvae, and demonstrated the utility of this comparative proteomic approach to identify excretory-secretory proteins of potential importance for parasite survival and/or host immune modulation.

Indexed as

AnimalsElectrophoresis, Gel, Two-DimensionalHelminth ProteinsHost-Parasite InteractionsHydrogen PeroxideIntestinal Diseases, ParasiticLarvaMiceMucous MembranePeroxiredoxinsProteomeProteomicsSheepSheep DiseasesTrichostrongyloideaHelminth ProteinsHydrogen PeroxidePeroxiredoxinsProteomeAnti-oxidantExcretory–secretoryNichePeroxidasePeroxiredoxin

Identifiers

PMID31292008
PMCPMC6617597
OpenAlexW2958496303

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.