# The Effects of Recombinant pBD2 on the Growth Performance, Antioxidant Capacity, Immune Function, Intestinal Barrier, and Microbiota of Weaned Piglets

**Authors:** Zhanwei Teng, Qing Meng, Mengting Ren, Bingke Lv, Liping Yuan, Ningning Zhang, Qinghua Wang, Kun Zhang, Chunli Li

PMC · DOI: 10.3390/microorganisms13071443 · 2025-06-20

## TL;DR

This study shows that adding pBD2 to piglet feed improves growth, immunity, and gut health by boosting antioxidants, strengthening the intestinal barrier, and balancing gut bacteria.

## Contribution

The study introduces pBD2 as a novel, effective antibiotic alternative for improving piglet health and performance.

## Key findings

- pBD2 increased weight gain and antioxidant levels in weaned piglets.
- pBD2 improved intestinal barrier function by enhancing tight-junction proteins.
- pBD2 altered gut microbiota to favor beneficial bacteria and reduce harmful ones.

## Abstract

Defensins, one of the members of the antimicrobial peptide family, play a vital role in resisting microbial invasion and immune regulation. Porcine β-defensin 2 possesses excellent stability, making it an ideal antibiotic alternative for feed additives. In this study, a total of 15 piglets were used to investigate the effects of supplementing diets with 2.5 mg/kg (LP group) and 5 mg/kg (HP group) of pBD2 to weaned piglets. The results revealed that pBD2 significantly increased the total weight gain and average daily weight gain (p < 0.05), the contents of T-AOC, SOD, IgM, and IL-10 in serum (p < 0.05), the villus-to-crypt ratios, and the expression of tight-junction proteins ZO-1 and claudin-1 (p < 0.05) in the small intestine. Furthermore, pBD2 increased the abundance of beneficial bacteria related to nutrient and energy metabolism while decreasing the abundance of harmful bacteria associated with intestinal inflammation and diarrhea. Alterations in the gut microbiota were closely associated with the levels of T-AOC, SOD, IgM, and IL-10 in serum. pBD2 primarily enhanced the health of weaned piglets by influencing antioxidant capacity, intestinal barrier function, and the intestinal microbiota. Our research provides a novel perspective for addressing the issue of antibiotic residues in feed.

## Linked entities

- **Proteins:** Pbd2 (peak bone density 2), SOD1 (superoxide dismutase 1), TJP1 (tight junction protein 1), CLDN7 (claudin 7)

## Full-text entities

- **Genes:** CLDN1 (claudin 1) [NCBI Gene 9076] {aka CLD1, ILVASC, SEMP1}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, TJP1 (tight junction protein 1) [NCBI Gene 7082] {aka ZO-1}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}
- **Diseases:** intestinal inflammation (MESH:D007249), diarrhea (MESH:D003967)
- **Chemicals:** LP (MESH:D008070)

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12299929/full.md

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Source: https://tomesphere.com/paper/PMC12299929