# Phytogenic feed additive mitigates necrotic enteritis-associated gut damage and performance loss in broilers

**Authors:** Most Khairunnesa, Alip Kumar, Shu-Biao Wu, Sharmin Akter, Reza Barekatain, Kowsig Palanisamy, Kosar Gharib-Naseri

PMC · DOI: 10.1016/j.psj.2026.106592 · Poultry Science · 2026-02-03

## TL;DR

A phytogenic feed additive helps reduce gut damage and performance loss in chickens caused by a bacterial disease called necrotic enteritis.

## Contribution

The study demonstrates the efficacy of a specific phytogenic blend in mitigating necrotic enteritis in broilers.

## Key findings

- PHB supplementation improved body weight gain and feed intake during the grower and finisher phases.
- PHB reduced intestinal lesions and improved gut morphology in NE-challenged birds.
- PHB lowered excreta inflammation markers and improved liveability in affected chickens.

## Abstract

Necrotic enteritis (NE) remains a major challenge in broiler production following the withdrawal of antibiotic growth promoters. In response, phytogenic feed additives (PFA) have emerged as promising alternatives. This study investigated the efficacy of a phytogenic blend (PHB) containing thymol, oleic acid, capric acid, and refined sunflower fat in mitigating NE-associated compromise in performance, gut health, liveability, oxidative stress, and excreta biomarkers of intestinal inflammation in broilers. A total of 450 Cobb 500 D-old chicks were randomly allocated to three dietary groups: NC (non-challenged control), CC (NE-challenged control), and PHB (NE-challenged birds fed 0.01% phytogenic blend), with 10 replicates of 15 birds each. Birds in the CC and PHB groups were orally inoculated with Eimeria spp. on d9 and Clostridium perfringens at d14 to induce NE. Birds were fed starter (d0-10), grower (d10-24), and finisher (d24-35) diets. During the starter phase (d0-10), birds fed PHB had significantly lower body weight gain (BWG) (P < 0.05) and higher FCR (P < 0.05) compared to the controls. NE challenge significantly (P < 0.05) reduced BWG, feed intake (FI), and increased FCR during d10-24, d10-35, and d0-35. During d10-35, PHB supplementation significantly improved BWG and FI and reduced FCR (P < 0.05) compared with the CC group. While NE challenge impaired gut morphology by reducing villus height (VH), VH/crypt depth (CD), and increasing intestinal lesion scores (P < 0.05), birds in the PHB group showed reduced duodenal lesions and increased VH/CD (P < 0.05) compared to CC birds. Furthermore, NE-related mortality and inflammation markers in excreta, such as calprotectin, fibronectin, and lipocalin-2, were significantly higher (P < 0.05) in NE-challenged birds compared to the NC group. Supplementation with PHB shifted liveability, and excreta calprotectin and fibronectin values towards the NC group (P > 0.05). These findings suggest that PHB supplementation improves intestinal histomorphology and liveability, reduces NE-related mortality, and alleviates inflammation, which together may contribute to the enhanced performance of the PHB-supplemented birds.

## Linked entities

- **Chemicals:** thymol (PubChem CID 6989), oleic acid (PubChem CID 445639), capric acid (PubChem CID 2969), fibronectin (PubChem CID 13085557)

## Full-text entities

- **Genes:** FN1 (fibronectin 1) [NCBI Gene 396133] {aka FN}
- **Diseases:** Jejunal lesion (MESH:D007579), gut damage (MESH:C536735), death (MESH:D003643), Intestinal lesion (MESH:D007410), mucosal damage (MESH:D052016), duodenal lesion (MESH:D004378), NE (MESH:D004751), gut inflammation (MESH:D007249)
- **Chemicals:** thiamine (MESH:D013831), nicotinic acid (MESH:D009525), mineral (MESH:D008903), vitamin K (MESH:D014812), Fatty acids (MESH:D005227), MDA (MESH:D008315), monounsaturated fatty acid (MESH:D005229), Se (MESH:D064586), riboflavin (MESH:D012256), H&amp;E (MESH:D006371), carvacrol (MESH:C073316), Haematoxylin and Eosin (-), Oleic acid (MESH:D019301), oxide (MESH:D010087), folic acid (MESH:D005492), Mn (MESH:D008345), capric acid (MESH:C031071), pantothenic acid (MESH:D010205), cyanocobalamin (MESH:D014805), I (MESH:D007455), vitamin E (MESH:D014810), mineral oil (MESH:D008899), gold (MESH:D006046), vitamin D (MESH:D014807), eucalyptus oil (MESH:D000078122), pyridoxine (MESH:D011736), Zn (MESH:D015032), sulfate (MESH:D013431), formic acid (MESH:C030544), Cu (MESH:D003300), Thymol (MESH:D013943), biotin (MESH:D001710), iodide (MESH:D007454), vitamin A (MESH:D014801), essential oil (MESH:D009822), Fe (MESH:D007501), cinnamaldehyde (MESH:C012843)
- **Species:** Rodentia (rodent, order) [taxon 9989], Gallus gallus (bantam, species) [taxon 9031], Sorghum bicolor (broomcorn, species) [taxon 4558], Eimeria maxima (species) [taxon 5804], Eimeria brunetti (species) [taxon 51314], Eimeria acervulina (species) [taxon 5801], Clostridium perfringens (species) [taxon 1502], Glycine max (soybean, species) [taxon 3847], Salmonella enterica subsp. enterica serovar Typhimurium (no rank) [taxon 90371]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12934304/full.md

## References

77 references — full list in the complete paper: https://tomesphere.com/paper/PMC12934304/full.md

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Source: https://tomesphere.com/paper/PMC12934304