Evidence map›Paper›PMID 34069371›Full record

ArticleMicroorganisms2021

Metagenomics Analysis Reveals an Extraordinary Inner Bacterial Diversity in Anisakids (Nematoda: Anisakidae) L3 Larvae.

Susana C Arcos, Felipe Lira, Lee Robertson, María Rosa González, Noelia Carballeda-Sangiao, Isabel Sánchez-Alonso, Laura Zamorano, Mercedes Careche, Yolanda Jiménez-Ruíz, Ricardo Ramos and 5 more

Open access · goldAbstract read
In one paragraph

Article in Microorganisms, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
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 1 country.

Susana C ArcosMuseo Nacional de Ciencias Naturales, Dpto Biodiversidad y Biología Evolutiva, CSIC, 28006 Madrid, Spain.
Felipe LiraCentro Nacional de Biotecnología, Departamento de Biotecnología Microbiana, CSIC, 28049 Madrid, Spain.
Lee RobertsonMuseo Nacional de Ciencias Naturales, Dpto Biodiversidad y Biología Evolutiva, CSIC, 28006 Madrid, Spain.ORCID 0000-0002-4628-5596
María Rosa GonzálezMuseo Nacional de Ciencias Naturales, Dpto Biodiversidad y Biología Evolutiva, CSIC, 28006 Madrid, Spain.
Noelia Carballeda-SangiaoServicio de Immunología, Hospital Universitario La Paz, 28046 Madrid, Spain.
Isabel Sánchez-AlonsoInstituto de Ciencia y Tecnología de Alimentos y Nutrición, CSIC, 28040 Madrid, Spain.ORCID 0000-0003-0003-2080
Laura ZamoranoServicio de Microbiología y Unidad de Investigación, Hospital Son Espases, (IdISPa), 07120 Palma de Mallorca, Spain.
Mercedes CarecheInstituto de Ciencia y Tecnología de Alimentos y Nutrición, CSIC, 28040 Madrid, Spain.ORCID 0000-0003-1769-374X
Yolanda Jiménez-RuízMuseo Nacional de Ciencias Naturales, Dpto Biodiversidad y Biología Evolutiva, CSIC, 28006 Madrid, Spain.ORCID 0000-0002-1458-8082
Ricardo RamosUnidad de Genómica, "Scientific Park of Madrid", Campus de Cantoblanco, 28049 Madrid, Spain.
Carlos LlorensBiotechvana, "Scientific Park", University of Valencia, 46980 Valencia, Spain.
Miguel González-MuñozServicio de Immunología, Hospital Universitario La Paz, 28046 Madrid, Spain.ORCID 0000-0002-3957-4955
Antonio OliverServicio de Microbiología y Unidad de Investigación, Hospital Son Espases, (IdISPa), 07120 Palma de Mallorca, Spain.
José L MartínezCentro Nacional de Biotecnología, Departamento de Biotecnología Microbiana, CSIC, 28049 Madrid, Spain.ORCID 0000-0001-8813-7607
Alfonso NavasMuseo Nacional de Ciencias Naturales, Dpto Biodiversidad y Biología Evolutiva, CSIC, 28006 Madrid, Spain.ORCID 0000-0003-2493-8530
Museo Nacional de Ciencias Naturales · ESCentro Nacional de Biotecnología · ESHospital Universitario La Paz · ESHospital Universitario Son Espases · ESInstituto de Ciencia y Tecnología de Alimentos y Nutrición · ESParc Científic de la Universitat de València · ES

Funding

Laboratorio de Nematología, MNCN-CSIC Ref. 202030E054Ministerio de Ciencia e Innovación, Spain. AGL2015-68248-C2-1-R
6 · The paper itself

Abstract

L3 larvae of anisakid nematodes are an important problem for the fisheries industry and pose a potential risk for human health by acting as infectious agents causing allergies and as potential vectors of pathogens and microrganisms. In spite of the close bacteria-nematode relationship very little is known of the anisakids microbiota. Fresh fish could be contaminated by bacteria vectored in the cuticle or in the intestine of anisakids when the L3 larvae migrate through the muscles. As a consequence, the bacterial inoculum will be spread, with potential effects on the quality of the fish, and possible clinical effects cannot be discarded. A total of 2,689,113 16S rRNA gene sequences from a total of 113 L3 individuals obtained from fish captured along the FAO 27 fishing area were studied. Bacteria were taxonomically characterized through 1803 representative operational taxonomic units (OTUs) sequences. Fourteen phyla, 31 classes, 52 orders, 129 families and 187 genera were unambiguously identified. We have found as part of microbiome an average of 123 OTUs per L3 individual. Diversity indices (Shannon and Simpson) indicate an extraordinary diversity of bacteria at an OTU level. There are clusters of anisakids individuals (samples) defined by the associated bacteria which, however, are not significantly related to fish hosts or anisakid taxa. This suggests that association or relationship among bacteria in anisakids, exists without the influence of fishes or nematodes. The lack of relationships with hosts of anisakids taxa has to be expressed by the association among bacterial OTUs or other taxonomical levels which range from OTUs to the phylum level. There are significant biological structural associations of microbiota in anisakid nematodes which manifest in clusters of bacteria ranging from phylum to genus level, which could also be an indicator of fish contamination or the geographic zone of fish capture. Actinobacteria, Aquificae, Firmicutes, and Proteobacteria are the phyla whose abundance value discriminate for defining such structures.

Indexed as

anisakidsmicrobiotanematode-bacteria association

Identifiers

PMID34069371
PMCPMC8158776
OpenAlexW3108190729

What Socratic holds

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LicenceCC BY
Read underepoch 390

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 Socratic graph.