# Enhancement of Disease Resistance in Pengze Crucian Carp (Carassius auratus var. Pengze) by Carvacrol Through Modulation of Intestinal Microbiota and Serum Metabolism

**Authors:** Yuzhu Wang, Xiaoze Guo, Jingjing Lu, Lingya Li, Yanqiang Tang, Haihong Xiao, Siming Li, Wenshu Liu

PMC · DOI: 10.3390/metabo16030151 · Metabolites · 2026-02-25

## TL;DR

Carvacrol improves disease resistance in Pengze crucian carp by changing gut bacteria and serum metabolism.

## Contribution

This study shows carvacrol's novel role in modulating fish gut microbiota and serum metabolism to enhance disease resistance.

## Key findings

- Carvacrol at 600 mg/kg reduces pathogenic bacteria and increases beneficial Cetobacterium in fish intestines.
- Carvacrol modulates serum metabolism pathways like lipid metabolism and autophagy.
- Carvacrol maintains microbial diversity and reduces pathogen proliferation after disease challenge.

## Abstract

What are the main findings?
Microencapsulated carvacrol at 600 mg/kg reduces the abundance of intestinal pathogenic bacteria and increases the levels of beneficial bacteria such as Cetobacterium in Pengze crucian carp.Carvacrol modulates metabolites in serum lipid metabolism, autophagy and other related pathways.

Microencapsulated carvacrol at 600 mg/kg reduces the abundance of intestinal pathogenic bacteria and increases the levels of beneficial bacteria such as Cetobacterium in Pengze crucian carp.

Carvacrol modulates metabolites in serum lipid metabolism, autophagy and other related pathways.

What are the implications of the main findings?
This study provides a research reference for the effects of carvacrol on intestinal microbiota and serum metabolism in fish.It offers experimental evidence for the application of plant-derived immunostimulants as antibiotic alternatives in the green aquaculture of freshwater fish.

This study provides a research reference for the effects of carvacrol on intestinal microbiota and serum metabolism in fish.

It offers experimental evidence for the application of plant-derived immunostimulants as antibiotic alternatives in the green aquaculture of freshwater fish.

Objectives: This study aimed to investigate the regulatory effects of dietary carvacrol on intestinal micro biota composition, serum metabolic profiles, and their association with increased resistance to Aeromonas hydrophila in Pengze crucian carp. Methods: Juvenile fish (5.63 ± 0.35 g) were randomly allocated into two experimental groups: a control group (CK) fed a basal diet and a treatment group (CA) supplemented with 600 mg/kg microencapsulated carvacrol. Following an 8-week feeding trial, nine specimens per group were sampled for venous blood and intestinal tract collection. Remaining individuals were subjected to a 12-h A. hydrophila challenge prior to identical sample collection. Results: Key findings revealed that carvacrol supplementation induced significant microbial modulations, notably reducing Firmicutes abundance while enhancing Cetobacterium populations by 33.25% compared to controls. Post-challenge analysis demonstrated marked declines in intestinal microbial diversity indices (Observed ASV, Chao1, ACE, and PD whole tree) in the CK group, whereas the CA group maintained stable microbial diversity. Pathogenic genera including Aeromonas, Shewanella, and Vibrio showed significant proliferation in challenged controls, contrasting with maintained microbial homeostasis in carvacrol-fed specimens. Serum metabolomic profiling identified the most significantly altered metabolic pathways associated with carvacrol administration: glycerophospholipid metabolism, linoleic acid metabolism, arachidonic acid metabolism, α-linolenic acid metabolism, GPI-anchor biosynthesis, and autophagy-animal pathways. Conclusions: Our results demonstrate that dietary carvacrol may reinforce intestinal microbial barrier function by optimizing beneficial microbial composition and reducing the proportion of pathogens, and modulate immune-related metabolic pathways critical for host defense, which might be involved in enhanced disease resistance.

## Linked entities

- **Chemicals:** carvacrol (PubChem CID 10364)

## Full-text entities

- **Diseases:** breast cancer (MESH:D001943), inflammatory (MESH:D007249), AKI (MESH:D058186), toxicity (MESH:D064420), gastrointestinal diseases (MESH:D005767), Edwardsiella tarda (MESH:D010009), A. hydrophila infection (MESH:D007239), injury to (MESH:D014947)
- **Chemicals:** cobalamin (MESH:D014805), Phosphatidylethanolamine (MESH:C483858), alpha-linolenic acid (MESH:D017962), ascorbic acid (MESH:D001205), Dodecanoic acid (MESH:C030358), prephenic acid (MESH:C005550), DPPH (MESH:C004931), ATP (MESH:D000255), vitamin D (MESH:D014807), lithocholic acid (MESH:D008095), essential fatty acid (MESH:D005228), water (MESH:D014867), glycerophospholipid (MESH:D020404), nicotinamide (MESH:D009536), formic acid (MESH:C030544), Ca-lactate (MESH:C110051), vitamin E (MESH:D014810), acetonitrile (MESH:C032159), thiamin (MESH:D013831), unsaturated fatty acid (MESH:D005231), 5-isopropyl-2-methylphenol (MESH:C073316), PC (MESH:D010713), hydroxyl radicals (MESH:D017665), folate (MESH:D005492), glycerides (MESH:D005989), KI (MESH:C066186), CuCl2 (MESH:C029892), methanol (MESH:D000432), omega-3 fatty acids (MESH:D015525), L-leucine (MESH:D007930), arachidonic acid (MESH:D016718), MC (MESH:C061001), phospholipids (MESH:D010743), amino acids (MESH:D000596), calcium pantothenate (MESH:D010205), Bile acids (MESH:D001647), inositol (MESH:D007294), Gramine (MESH:C007884), Alanylphenylalanine (MESH:C014309), 3beta-Hydroxy-5-cholenoic acid (MESH:C014596), 2-Hexyldecanoic acid (MESH:C400263), DHA (MESH:C027493), L-arginine (MESH:D001120), CaCO3 (MESH:D002119), 25-Hydroxycholesterol (MESH:C007997), biotin (MESH:D001710), menadione (MESH:D024483), lipid (MESH:D008055), free radicals (MESH:D005609), B12 (MESH:C034730), prostaglandins (MESH:D011453), Asiatic acid (MESH:C017032), GPI (MESH:D017261), linoleic acid (MESH:D019787), cholesterol (MESH:D002784), riboflavin (MESH:D012256), nitrate (MESH:D009566), 1,3,4-trihydroxy-5-oxocyclohexane-1-carboxylic acid (-), agarose (MESH:D012685), CTAB (MESH:D000077286)
- **Species:** Aeromonas (genus) [taxon 642], Enterococcus (genus) [taxon 1350], Paenalcaligenes (genus) [taxon 1100891], Carassius auratus ssp. 'Pengze' (Pengze crucian carp, subspecies) [taxon 564874], Actinomycetota (actinobacteria, phylum) [taxon 201174], Carassius auratus (goldfish, species) [taxon 7957], Shewanella (genus) [taxon 22], Cyanobacteriota (blue-green algae, phylum) [taxon 1117], Mycoplasma (genus) [taxon 2093], Carassius carassius (crucian carp, species) [taxon 217509], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Aeromonas salmonicida (species) [taxon 645], Aeromonas hydrophila (species) [taxon 644], Vibrio (genus) [taxon 662], Plesiomonas (C 27 Group, genus) [taxon 702], Homo sapiens (human, species) [taxon 9606], Cetobacterium (genus) [taxon 180162], Pseudomonadota (proteobacteria, phylum) [taxon 1224], Streptococcus lutetiensis (species) [taxon 150055], Oncorhynchus mykiss (rainbow trout, species) [taxon 8022], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Bacteroidota (Bacteroides-Cytophaga-Flexibacter group, phylum) [taxon 976], Danio rerio (leopard danio, species) [taxon 7955], Fusobacteriota (phylum) [taxon 32066], Timonella (genus) [taxon 1465824], Actinopterygii (fishes, superclass) [taxon 7898]
- **Cell lines:** SCK0 — Homo sapiens (Human), Cholangiocarcinoma, Cancer cell line (CVCL_M271)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13028411/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13028411/full.md

## References

62 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028411/full.md

---
Source: https://tomesphere.com/paper/PMC13028411