Evidence map›Paper›PMID 41023811›Full record

ArticleBMC genomics2025

Coupled transcriptome and proteome analysis of L3 and L4 developmental stages of Anisakis simplex s. s.: insights into target genes under glucose influence.

Iwona Polak, Robert Stryiński, Mateusz Maździarz, Lukasz Paukszto, Mónica Carrera, Iwona Bogacka, Elżbieta Łopieńska-Biernat

Abstract read
In one paragraph

Article in BMC genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Anisakiasis: A Decade of Molecular and Diagnostic Advancements (2015-2026).International journal of molecular sciences · 2026
    Review
  2. International journal of molecular sciences · 2026
    Article
  3. 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

7 authors.

Iwona PolakDepartment of Biochemistry, Faculty of Biology and Biotechnology, University of Warmia and Mazury in Olsztyn, Michała Oczapowskiego 2, 10-719, Olsztyn, Poland.ORCID http://orcid.org/0000-0002-3713-2918
Robert StryińskiDepartment of Biochemistry, Faculty of Biology and Biotechnology, University of Warmia and Mazury in Olsztyn, Michała Oczapowskiego 2, 10-719, Olsztyn, Poland.ORCID http://orcid.org/0000-0001-5518-8854
Mateusz MaździarzDepartment of Biochemistry, Faculty of Biology and Biotechnology, University of Warmia and Mazury in Olsztyn, Michała Oczapowskiego 2, 10-719, Olsztyn, Poland.ORCID http://orcid.org/0000-0002-7278-4604
Lukasz PauksztoDepartment of Botany and Evolutionary Ecology, Faculty of Biology and Biotechnology, University of Warmia and Mazury in Olsztyn, Plac Łódzki 1, 10-721, Olsztyn, Poland.ORCID http://orcid.org/0000-0002-3618-1064
Mónica CarreraDepartment of Food Technology, Institute of Marine Research, Spanish National Research Council, Eduardo Cabello 6, 36-2018, Vigo, Spain.ORCID http://orcid.org/0000-0003-2973-449X
Iwona BogackaDepartment of Animal Anatomy and Physiology, Faculty of Biology and Biotechnology, University of Warmia and Mazury in Olsztyn, Michała Oczapowskiego 2, 10-719, Olsztyn, Poland.ORCID http://orcid.org/0000-0003-3054-0123
Elżbieta Łopieńska-BiernatDepartment of Biochemistry, Faculty of Biology and Biotechnology, University of Warmia and Mazury in Olsztyn, Michała Oczapowskiego 2, 10-719, Olsztyn, Poland. ela.lopienska@uwm.edu.pl.ORCID http://orcid.org/0000-0003-3265-5207

Funding

Narodowe Centrum Nauki 2018/31/B/NZ9/01683
6 · The paper itself

Abstract

Anisakis simplex is a cosmopolitan parasitic nematode of marine organisms with a complex life cycle. Consuming fish infected with its larvae poses a health risk, as the parasites can penetrate gastrointestinal mucosa, damage stomach and intestinal walls, and trigger allergic reactions. The resulting disease is known as anisakiasis. The European Food Safety Authority (EFSA) classifies A. simplex as a biohazard. Most of its developmental stages (L3, L4, and adults) occur under anaerobic conditions, and larvae derive energy mainly from saccharides. However, the effect of glucose on L3 and L4 larvae-stages pathogenic to humans-has not been described. This study aimed to identify genes and pathways involved in glucose (10 mg/mL) response through transcriptomic and proteomic analyses of L3 and L4 larvae. Differentially expressed genes (DEGs), long non-coding RNAs (DELs), and differentially regulated proteins (DRPs) were identified. DEGs were involved in cuticle structure, lyase activity, and metabolic processes. Comparing L3 CTR and L4 CTR (control) to glucose-treated samples revealed 1,969 DEGs; 259 overlapped between L4 GLU vs. L3 GLU, (glucose-treated) with 11 showing reversed expression. Additionally, 84 DELs were identified in L3 GLU vs. control, 40 in L4 GLU vs. control, and 163 between glucose-treated L4 and L3. Larval and glucose-specific alternative splicing events were also analyzed. Proteomic analysis revealed 35 DRPs-5 more abundant in L4, 30 in L3. The data reveal that developmental stage exerts a more substantial influence than glucose exposure on gene and protein expression profiles. However, glucose still modulates several pathways related to translation, cytoskeletal remodeling, extracellular matrix (ECM) reorganization, and energy metabolism.

Indexed as

AnisakisGlucoseProteomeProteomicsTranscriptomeAnimalsGene Expression ProfilingHelminth ProteinsLarvaGlucoseHelminth ProteinsProteomeAnisakis simplexGlucose uptakeProteomicsTranscriptomics

Identifiers

PMID41023811
PMCPMC12482602

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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.