# Effects of chicken hemoglobin antimicrobial peptides on intestinal mucosal immunity under chronic heat stress and vaccination responses in broilers

**Authors:** Decheng Wang, Fengjiao Hu, Hui Liu, Ruiping She, Jijing Tian

PMC · DOI: 10.3389/fvets.2025.1574513 · 2025-06-09

## TL;DR

Chicken hemoglobin antimicrobial peptides (CHAP) improve intestinal immunity and vaccine responses in broilers under chronic heat stress.

## Contribution

CHAP is shown to enhance intestinal health, reduce apoptosis in immune organs, and improve vaccine efficacy in heat-stressed broilers.

## Key findings

- CHAP increased villus height in the duodenum, jejunum, and ileum under chronic heat stress.
- CHAP reduced apoptosis in the bursa by modulating caspase-3, Bax, and Bcl-2 levels.
- CHAP improved antibody titers against NDV and AIV vaccines in broilers.

## Abstract

Heat stress (HS) is a major concern in poultry production worldwide due to its adverse effects on feed intake, weight gain, carcass weight, and metabolic conditions. Several strategies have been explored to ameliorate the negative effects of HS in broiler chickens, among which antimicrobial peptides (AMPs) represent a promising approach. Previously, we isolated chicken hemoglobin antimicrobial peptides (CHAP) and further demonstrated that CHAP has strong bactericidal activity. However, whether CHAP can improve growth performance and maintain intestinal mucosal immunity under chronic HS conditions remains unclear. In the present study, a total of 141 one-day-old broilers were divided into two groups. A total of 36 broilers were used to establish a chronic HS model to evaluate the effects of CHAP on intestinal mucosal immunity, and the remaining 105 birds were used to monitor the inductive effects of CHAP on two vaccines, including Newcastle disease virus (NDV) and avian influenza virus (AIV) vaccines, in broilers. As expected, HS-stimulated broiler chickens supplemented with CHAP showed a significant increase in villus height in the duodenum (p < 0.01), jejunum (p < 0.05), and ileum (p < 0.01) compared to those who did not receive CHAP under chronic HS conditions. The levels of alkaline phosphatase (AKP) and the number of secretory IgA (sIgA)-producing cells were markedly decreased in the chronic HS group (p < 0.01), whereas both significantly recovered after CHAP administration (p < 0.01). CHAP administration improved the birds' body weight and average daily gain (ADG), as well as the feed utilization rate, under HS conditions. Moreover, CHAP effectively mitigated HS-induced bursa injury by inhibiting excessive bursal apoptosis through the downregulation of caspase-3 and Bax, as well as the upregulation of Bcl-2 (p < 0.01). Interestingly, CHAP supplementation enhanced the antibody titer of both NDV and AIV in the broilers. Finally, CHAP administration enhanced the proliferation of splenic lymphocytes. In summary, our data demonstrate that CHAP not only maintains intestinal stability to improve growth performance but also inhibits excessive apoptosis in immune organs and upregulates vaccination effects.

## Linked entities

- **Genes:** Casp3 (caspase 3) [NCBI Gene 12367], BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581], BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596]
- **Diseases:** Newcastle disease (MONDO:0005875), avian influenza (MONDO:0018695)
- **Species:** Gallus gallus (taxon 9031)

## Full-text entities

- **Genes:** CASP3 (caspase 3) [NCBI Gene 836] {aka CPP32, CPP32B, SCA-1}, BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}, LOC102723407 (immunoglobulin heavy variable 4-38-2-like) [NCBI Gene 102723407] {aka IGHV4, IGHV4-30, IGHV4-38-2, IGHV4-39, IGHV4-b, IGVH4-39}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}
- **Diseases:** injury (MESH:D014947)
- **Species:** NDV [taxon 11176], unidentified influenza virus (species) [taxon 11309], Gallus gallus (bantam, species) [taxon 9031]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12183796/full.md

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Source: https://tomesphere.com/paper/PMC12183796