Evidence map›Paper›PMID 30086708›Full record

ArticleBMC genomics2018

Functional insights into the infective larval stage of Anisakis simplex s.s., Anisakis pegreffii and their hybrids based on gene expression patterns.

C Llorens, S C Arcos, L Robertson, R Ramos, R Futami, B Soriano, S Ciordia, M Careche, M González-Muñoz, Y Jiménez-Ruiz and 5 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC genomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 38 citations in OpenAlex.

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  9. Hybrid Genotype ofAnimals : an open access journal from MDPI · 2021
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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

15 authors at 6 institutions in 2 countries.

C LlorensBiotechvana, Scientific Park, University of Valencia, Calle Catedrático José Beltrán 2, 46980, Paterna, Valencia, Spain.
S C ArcosDepartamento Biodiversidad y Biología Evolutiva, Museo Nacional de Ciencias Naturales, CSIC, Calle José Gutiérrez Abascal, 2, 28006, Madrid, Spain.
L RobertsonDepartamento Biodiversidad y Biología Evolutiva, Museo Nacional de Ciencias Naturales, CSIC, Calle José Gutiérrez Abascal, 2, 28006, Madrid, Spain.
R RamosUnidad de Genómica, Campus de Cantoblanco, Scientific Park of Madrid, Calle Faraday, 7, Campus de Cantoblanco, 28049, Madrid, Spain.
R FutamiBiotechvana, Scientific Park, University of Valencia, Calle Catedrático José Beltrán 2, 46980, Paterna, Valencia, Spain.
B SorianoBiotechvana, Scientific Park, University of Valencia, Calle Catedrático José Beltrán 2, 46980, Paterna, Valencia, Spain.
S CiordiaUnidad de Proteomica Centro Nacional de Biotecnología, CSIC, Calle Darwin, 3, 28049, Madrid, Spain.
M CarecheInstituto de Ciencia y Tecnología de Alimentos y Nutrición (ICTAN), Calle José Antonio Novais, 10, 28040, Madrid, Spain.
M González-MuñozServicio de Immunología, Hospital Universitario La Paz, Paseo de la Castellana, 261, 28046, Madrid, Spain.
Y Jiménez-RuizDepartamento Biodiversidad y Biología Evolutiva, Museo Nacional de Ciencias Naturales, CSIC, Calle José Gutiérrez Abascal, 2, 28006, Madrid, Spain.
N Carballeda-SangiaoServicio de Immunología, Hospital Universitario La Paz, Paseo de la Castellana, 261, 28046, Madrid, Spain.
I MoneoServicio de Immunología, Hospital Universitario La Paz, Paseo de la Castellana, 261, 28046, Madrid, Spain.
J P AlbarUnidad de Proteomica Centro Nacional de Biotecnología, CSIC, Calle Darwin, 3, 28049, Madrid, Spain.
M BlaxterEdinburgh Genomics, and Institute of Evolutionary Biology, School of Biological Sciences, The King's Buildings, The University of Edinburgh, Edinburgh, EH9 3JT, UK.
A NavasDepartamento Biodiversidad y Biología Evolutiva, Museo Nacional de Ciencias Naturales, CSIC, Calle José Gutiérrez Abascal, 2, 28006, Madrid, Spain. anavas@mncn.csic.es.ORCID http://orcid.org/0000-0003-2493-8530
Museo Nacional de Ciencias Naturales · ESHospital Universitario La Paz · ESParc Científic de la Universitat de València · ESCentro Nacional de Biotecnología · ESEdinburgh Genomics · GBInstituto de Ciencia y Tecnología de Alimentos y Nutrición · ES

Funding

European Union FP7-312068Ministerio de Economía, Industria y Competitividad, Gobierno de España AGL2009-2485-C03-02
6 · The paper itself

Abstract

backgroundAnisakis simplex sensu stricto and Anisakis pegreffii are sibling species of nematodes parasitic on marine mammals. Zoonotic human infection with third stage infective larvae causes anisakiasis, a debilitating and potentially fatal disease. These 2 species show evidence of hybridisation in geographical areas where they are sympatric. How the species and their hybrids differ is still poorly understood.

resultsThird stage larvae of Anisakis simplex s.s., Anisakis pegreffii and hybrids were sampled from Merluccius merluccius (Teleosti) hosts captured in waters of the FAO 27 geographical area. Specimens of each species and hybrids were distinguished with a diagnostic genetic marker (ITS). RNA was extracted from pools of 10 individuals of each taxon. Transcriptomes were generated using Illumina RNA-Seq, and assembled de novo. A joint assembly (here called merged transcriptome) of all 3 samples was also generated. The inferred transcript sets were functionally annotated and compared globally and also on subsets of secreted proteins and putative allergen families. While intermediary metabolism appeared to be typical for nematodes in the 3 evaluated taxa, their transcriptomes present strong levels of differential expression and enrichment, mainly of transcripts related to metabolic pathways and gene ontologies associated to energy metabolism and other pathways, with significant presence of excreted/secreted proteins, most of them allergens. The allergome of the 2 species and their hybrids has also been thoroughly studied; at least 74 different allergen families were identified in the transcriptomes.

conclusionsA. simplex s.s., A. pegreffi and their hybrids differ in gene expression patterns in the L3 stage. Strong parent-of-origin effects were observed: A. pegreffi alleles dominate in the expression patterns of hybrids albeit the latter, and A. pegreffii also display significant differences indicating that hybrids are intermediate biological entities among their parental species, and thus of outstanding interest in the study of speciation in nematodes. Analyses of differential expression based on genes coding for secreted proteins suggests that co-infections presents different repertoires of released protein to the host environment. Both species and their hybrids, share more allergen genes than previously thought and are likely to induce overlapping disease responses.

Indexed as

AllergensAnimalsAnisakisBreedingEnergy MetabolismFish DiseasesGadiformesGene Expression ProfilingGene Expression RegulationHelminth ProteinsLarvaMolecular Sequence AnnotationSequence Analysis, RNAVirulence FactorsAllergensHelminth ProteinsVirulence FactorsAllergensAnisakis simplexA. PegreffiiGene expressionTranscriptome

Identifiers

PMID30086708
PMCPMC6080401
OpenAlexW2887596614

What Socratic 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 Socratic graph.