Evidence map›Paper›PMID 25928256›Full record

ArticleScientific reports2015

New insights into the causes of human illness due to consumption of azaspiracid contaminated shellfish.

O P Chevallier, S F Graham, E Alonso, C Duffy, J Silke, K Campbell, L M Botana, C T Elliott

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
6.1field-weighted citation impact, top 4% 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

7 citing papers in PubMed, 34 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

8 authors at 1 institution in 1 country.

O P ChevallierAdvanced Asset Technology Centre, Institute for Global Food Security, Queen's University Belfast, Stranmillis Road, Belfast, BT9 5AG, UK.
S F GrahamBeaumont Research Institute, 3811 W Thirteen Mile Road, Royal Oak, MI, 48073.
E AlonsoDepartment of Pharmacology, Faculty of Veterinary, Campus Lugo, USC, 27002 Lugo, Spain.
C DuffyMarine Institute, Rinville, Oranmore, Co. Galway, Ireland.
J SilkeMarine Institute, Rinville, Oranmore, Co. Galway, Ireland.
K CampbellAdvanced Asset Technology Centre, Institute for Global Food Security, Queen's University Belfast, Stranmillis Road, Belfast, BT9 5AG, UK.
L M BotanaDepartment of Pharmacology, Faculty of Veterinary, Campus Lugo, USC, 27002 Lugo, Spain.
C T ElliottAdvanced Asset Technology Centre, Institute for Global Food Security, Queen's University Belfast, Stranmillis Road, Belfast, BT9 5AG, UK.
Marine Institute · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Azaspiracid (AZA) poisoning was unknown until 1995 when shellfish harvested in Ireland caused illness manifesting by vomiting and diarrhoea. Further in vivo/vitro studies showed neurotoxicity linked with AZA exposure. However, the biological target of the toxin which will help explain such potent neurological activity is still unknown. A region of Irish coastline was selected and shellfish were sampled and tested for AZA using mass spectrometry. An outbreak was identified in 2010 and samples collected before and after the contamination episode were compared for their metabolite profile using high resolution mass spectrometry. Twenty eight ions were identified at higher concentration in the contaminated samples. Stringent bioinformatic analysis revealed putative identifications for seven compounds including, glutarylcarnitine, a glutaric acid metabolite. Glutaric acid, the parent compound linked with human neurological manifestations was subjected to toxicological investigations but was found to have no specific effect on the sodium channel (as was the case with AZA). However in combination, glutaric acid (1 mM) and azaspiracid (50 nM) inhibited the activity of the sodium channel by over 50%. Glutaric acid was subsequently detected in all shellfish employed in the study. For the first time a viable mechanism for how AZA manifests itself as a toxin is presented.

Indexed as

AnimalsBivalviaCarnitineCell LineCell Line, TumorDisease OutbreaksFoodborne DiseasesGlutaratesHEK293 CellsHumansMarine ToxinsPolyether ToxinsShellfishSodium ChannelsSpiro CompoundsazaspiracidCarnitineGlutaratesglutaric acidglutarylcarnitineMarine ToxinsPolyether ToxinsSodium ChannelsSpiro Compounds

Identifiers

PMID25928256
PMCPMC4415421
OpenAlexW1999157056

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.