Evidence map›Paper›PMID 33347447›Full record

ArticlePLoS neglected tropical diseases2020

Taenia larvae possess distinct acetylcholinesterase profiles with implications for host cholinergic signalling.

Anja de Lange, Ulrich Fabien Prodjinotho, Hayley Tomes, Jana Hagen, Brittany-Amber Jacobs, Katherine Smith, William Horsnell, Chummy Sikasunge, Dorit Hockman, Murray E Selkirk and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 6 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

12 authors at 4 institutions in 4 countries.

Anja de LangeDivision of Cell Biology, Department of Human Biology and Neuroscience Institute, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.ORCID 0000-0002-7117-8979
Ulrich Fabien ProdjinothoInstitute for Medical Microbiology, Immunology and Hygiene, Centre for Global Health, Technical University Munich (TUM), Munich, Germany.
Hayley TomesDivision of Cell Biology, Department of Human Biology and Neuroscience Institute, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.ORCID 0000-0002-4495-539X
Jana HagenDepartment of Life Sciences, Imperial College London, London, United Kingdom.ORCID 0000-0001-8787-455X
Brittany-Amber JacobsWellcome Centre for Infectious Diseases Research in Africa, Institute of Infectious Disease and Molecular Medicine and Division of Immunology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Katherine SmithWellcome Centre for Infectious Diseases Research in Africa, Institute of Infectious Disease and Molecular Medicine and Division of Immunology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.ORCID 0000-0001-8150-5702
William HorsnellWellcome Centre for Infectious Diseases Research in Africa, Institute of Infectious Disease and Molecular Medicine and Division of Immunology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Chummy SikasungeSchool of Veterinary Medicine, Department of Paraclinicals, University of Zambia, Lusaka, Zambia.ORCID 0000-0002-5564-2655
Dorit HockmanDivision of Cell Biology, Department of Human Biology and Neuroscience Institute, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.ORCID 0000-0003-2613-6216
Murray E SelkirkDepartment of Life Sciences, Imperial College London, London, United Kingdom.ORCID 0000-0002-6274-6014
Clarissa Prazeres da CostaInstitute for Medical Microbiology, Immunology and Hygiene, Centre for Global Health, Technical University Munich (TUM), Munich, Germany.
Joseph Valentino RaimondoDivision of Cell Biology, Department of Human Biology and Neuroscience Institute, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.ORCID 0000-0002-8266-3128
University of Cape Town · ZAImperial College London · GBUniversité d'Orléans · FRUniversity of Zambia · ZM

Funding

Biotechnology and Biological Sciences Research Council BB/R015856/1Wellcome Trust
6 · The paper itself

Abstract

Larvae of the cestodes Taenia solium and Taenia crassiceps infect the central nervous system of humans. Taenia solium larvae in the brain cause neurocysticercosis, the leading cause of adult-acquired epilepsy worldwide. Relatively little is understood about how cestode-derived products modulate host neural and immune signalling. Acetylcholinesterases, a class of enzyme that breaks down acetylcholine, are produced by a host of parasitic worms to aid their survival in the host. Acetylcholine is an important signalling molecule in both the human nervous and immune systems, with powerful modulatory effects on the excitability of cortical networks. Therefore, it is important to establish whether cestode derived acetylcholinesterases may alter host neuronal cholinergic signalling. Here we make use of multiple techniques to profile acetylcholinesterase activity in different extracts of both Taenia crassiceps and Taenia solium larvae. We find that the larvae of both species contain substantial acetylcholinesterase activity. However, acetylcholinesterase activity is lower in Taenia solium as compared to Taenia crassiceps larvae. Further, whilst we observed acetylcholinesterase activity in all fractions of Taenia crassiceps larvae, including on the membrane surface and in the excreted/secreted extracts, we could not identify acetylcholinesterases on the membrane surface or in the excreted/secreted extracts of Taenia solium larvae. Bioinformatic analysis revealed conservation of the functional protein domains in the Taenia solium acetylcholinesterases, when compared to the homologous human sequence. Finally, using whole-cell patch clamp recordings in rat hippocampal brain slice cultures, we demonstrate that Taenia larval derived acetylcholinesterases can break down acetylcholine at a concentration which induces changes in neuronal signalling. Together, these findings highlight the possibility that Taenia larval acetylcholinesterases can interfere with cholinergic signalling in the host, potentially contributing to pathogenesis in neurocysticercosis.

Indexed as

Signal TransductionAcetylcholinesteraseAnimalsFemaleHumansLarvaMice, Inbred C57BLNeurocysticercosisTaenia soliumAcetylcholinesterase

Identifiers

PMID33347447
PMCPMC7785214
OpenAlexW3116405807

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.