Evidence map›Paper›PMID 41401155›Full record

ArticlePloS one2025

The innate immune IMD pathway is a key regulator of gut microbiome and metabolic homeostasis in the black tiger shrimp (Penaeus monodon).

Premruethai Supungul, Sureerat Tang, Tanaporn Uengwetwanit, Umaporn Uawisetwathana, Pacharaporn Angthong, Sopacha Arayamethakorn, Phimsucha Bunphimpapha, Panyisa Potibut, Waraporn Jangsutthivorawat, Virak Visudtiphole and 2 more

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Premruethai SupungulAquatic Molecular Genetics and Biotechnology Research Team, Integrative Aquaculture Biotechnology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Development Agency, Pathum Thani, Thailand.
Sureerat TangAquatic Molecular Genetics and Biotechnology Research Team, Integrative Aquaculture Biotechnology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Development Agency, Pathum Thani, Thailand.
Tanaporn UengwetwanitAdvanced Diagnostics and Biomarker Discovery Research Team, Biosensing and Bioprospecting Technology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Development Agency, Pathum Thani, Thailand.ORCID https://orcid.org/0000-0003-4710-2613
Umaporn UawisetwathanaAdvanced Diagnostics and Biomarker Discovery Research Team, Biosensing and Bioprospecting Technology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Development Agency, Pathum Thani, Thailand.
Pacharaporn AngthongAdvanced Diagnostics and Biomarker Discovery Research Team, Biosensing and Bioprospecting Technology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Development Agency, Pathum Thani, Thailand.
Sopacha ArayamethakornAdvanced Diagnostics and Biomarker Discovery Research Team, Biosensing and Bioprospecting Technology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Development Agency, Pathum Thani, Thailand.
Phimsucha BunphimpaphaAquatic Molecular Genetics and Biotechnology Research Team, Integrative Aquaculture Biotechnology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Development Agency, Pathum Thani, Thailand.
Panyisa PotibutAquaculture Service Development Research Team, Integrative Aquaculture Biotechnology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Development Agency, Pathum Thani, Thailand.
Waraporn JangsutthivorawatAquaculture Service Development Research Team, Integrative Aquaculture Biotechnology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Development Agency, Pathum Thani, Thailand.
Virak VisudtipholeAdvanced Diagnostics and Biomarker Discovery Research Team, Biosensing and Bioprospecting Technology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Development Agency, Pathum Thani, Thailand.
Sage ChaiyapecharaAquaculture Service Development Research Team, Integrative Aquaculture Biotechnology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Development Agency, Pathum Thani, Thailand.
Wanilada RungrassameeAdvanced Diagnostics and Biomarker Discovery Research Team, Biosensing and Bioprospecting Technology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Development Agency, Pathum Thani, Thailand.ORCID https://orcid.org/0000-0002-5802-4342

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gut microbiome plays a fundamental role in host health and homeostasis, yet immune mechanisms regulating this relationship remain poorly understood in commercially important invertebrate such as the black tiger shrimp (Penaeus monodon). We employed a multiomics approach, combining RNA interference (RNAi) with transcriptomic, metabolomic, and 16S rRNA gene profiling, to investigate how the innate immune Toll and IMD pathways regulate gut health. We systematically suppressed key signaling components, MyD88 (Toll) and Relish (IMD), under non-pathogenic conditions. Knockdown of the IMD pathway transcription factor, Relish, triggered a profound and selective response across all measured biological layers. We observed a disproportionately large transcriptomic change, with 1,362 differentially expressed genes (DEGs) in the Relish knockdown group compared to only 333 DEGs in the MyD88 knockdown group. This was accompanied by a targeted alteration in immune effectors, including the upregulation of lysozyme C-like (log2 fold change = 2.44) and a strong suppression of penaeidin 5 (log2 fold change = -3.62). At the microbial level, while overall community structure remained stable, a selective shift was observed, the abundance of specific Gram-negative genera, particularly Photobacterium and Shewanella, was significantly reduced, yet Pseudoalteromonas were enriched in the Relish knockdown group. Metabolomic analysis further revealed that the Relish-suppressed shrimp had a distinct metabolic signature, marked by a decrease in bacterial-associated metabolites like D-alanyl-D-alanine and an increase in pro-inflammatory markers such as succinic acid and 8-HETE. Our findings showed that in P. monodon, the IMD pathway is the primary and central regulator of gut microbiome and metabolic homeostasis. This study provides novel insights into the dynamic interplay between innate immunity and the gut microbiome in a crustacean, identifying the IMD pathway as a promising target for developing strategies to enhance shrimp health and the sustainability of the global aquaculture industry.

Indexed as

Gastrointestinal MicrobiomeHomeostasisImmunity, InnatePenaeidaeAnimalsGene Expression ProfilingMyeloid Differentiation Factor 88RNA, Ribosomal, 16SSignal TransductionTranscriptomeMyeloid Differentiation Factor 88RNA, Ribosomal, 16S

Identifiers

PMID41401155
PMCPMC12707661

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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.