Evidence map›Paper›PMID 27762399›Full record

ArticleScientific reports2016

Molecular characterization of host-parasite cell signalling in Schistosoma mansoni during early development.

Margarida Ressurreição, Firat Elbeyioglu, Ruth S Kirk, David Rollinson, Aidan M Emery, Nigel M Page, Anthony J Walker

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Margarida RessurreiçãoMolecular Parasitology Laboratory, School of Life Sciences, Pharmacy and Chemistry, Kingston University, KT1 2EE, United Kingdom.
Firat ElbeyiogluMolecular Parasitology Laboratory, School of Life Sciences, Pharmacy and Chemistry, Kingston University, KT1 2EE, United Kingdom.
Ruth S KirkMolecular Parasitology Laboratory, School of Life Sciences, Pharmacy and Chemistry, Kingston University, KT1 2EE, United Kingdom.
David RollinsonDepartment of Life Sciences, The Natural History Museum, London, SW7 5BD, United Kingdom.
Aidan M EmeryDepartment of Life Sciences, The Natural History Museum, London, SW7 5BD, United Kingdom.
Nigel M PageMolecular Parasitology Laboratory, School of Life Sciences, Pharmacy and Chemistry, Kingston University, KT1 2EE, United Kingdom.
Anthony J WalkerMolecular Parasitology Laboratory, School of Life Sciences, Pharmacy and Chemistry, Kingston University, KT1 2EE, United Kingdom.
Kingston University · GBNatural History Museum · GB

Funding

NIAID NIH HHS HHSN272201000005CNIAID NIH HHS HHSN272201000005I
6 · The paper itself

Abstract

During infection of their human definitive host, schistosomes transform rapidly from free-swimming infective cercariae in freshwater to endoparasitic schistosomules. The 'somules' next migrate within the skin to access the vasculature and are surrounded by host molecules that might activate intracellular pathways that influence somule survival, development and/or behaviour. However, such 'transactivation' by host factors in schistosomes is not well defined. In the present study, we have characterized and functionally localized the dynamics of protein kinase C (PKC) and extracellular signal-regulated kinase (ERK) activation during early somule development in vitro and demonstrate activation of these protein kinases by human epidermal growth factor, insulin, and insulin-like growth factor I, particularly at the parasite surface. Further, we provide evidence that support the existence of specialized signalling domains called lipid rafts in schistosomes and propose that correct signalling to ERK requires proper raft organization. Finally, we show that modulation of PKC and ERK activities in somules affects motility and reduces somule survival. Thus, PKC and ERK are important mediators of host-ligand regulated transactivation events in schistosomes, and represent potential targets for anti-schistosome therapy aimed at reducing parasite survival in the human host.

Indexed as

Host-Pathogen InteractionsSignal TransductionAnimalsEpidermal Growth FactorExtracellular Signal-Regulated MAP KinasesHumansInsulinInsulin-Like Growth Factor ILocomotionMembrane MicrodomainsProtein Kinase CSchistosoma mansoniSurvival AnalysisEpidermal Growth FactorExtracellular Signal-Regulated MAP KinasesInsulinInsulin-Like Growth Factor IProtein Kinase C

Identifiers

PMID27762399
PMCPMC5071895
OpenAlexW2533899091

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.