# Probiotic and antibacterial properties of recombinant Lactococcus lactis expressing the fusion antimicrobial peptides BMAP18-BSN37 in mice and chickens

**Authors:** Ruibiao Wang, Yukai Lin, Yu Xia, Suxian Liu, Doudou Feng, Siyang Li, Tengyue Zhou, Huarun Sun, Jiyuan Shen, Bo Wen, Minghui Li, Chengshui Liao, Baoliang Qin, Jianhe Hu, Yuanfang Ma, Ke Ding, Lei Wang

PMC · DOI: 10.1016/j.psj.2026.106507 · 2026-01-23

## TL;DR

A genetically modified Lactococcus lactis strain was developed to combat Salmonella in animals, showing benefits for gut health and reduced pathogen levels.

## Contribution

A recombinant L. lactis strain expressing fusion antimicrobial peptides was engineered and tested for dual probiotic and antibacterial effects in mice and chickens.

## Key findings

- The recombinant L. lactis NZ-BB strain effectively reduced Salmonella burden in mice and chickens.
- NZ-BB improved intestinal barrier integrity and immune balance through upregulation of tight junction proteins and anti-inflammatory cytokines.
- The strain exhibited stable plasmid maintenance and high peptide expression without metabolic burden.

## Abstract

Antimicrobial resistance poses a serious threat to global food safety and poultry production, prompting the need for effective alternatives to conventional antibiotics in food-producing animals. In this study, a recombinant food-grade strain, L. lactis NZ-BB, was engineered to express a fusion antimicrobial peptide (BMAP18-BSN37), and evaluated its probiotic characteristics and antimicrobial efficacy against Salmonella, a major foodborne pathogen in chicken. The recombinant plasmid pUBB was successfully constructed and introduced into L. lactis NZ9000, with optimal peptide expression achieved following Nisin induction (20 ng/mL, 6 h). NZ-BB demonstrated stable plasmid maintenance, high expression levels, and no detectable metabolic burden. In vivo trials using BALB/c murine and 817 strain avian models showed that NZ-BB enhanced body weight gain, supported immune organ development, and improved intestinal barrier integrity through upregulation of tight junction proteins (occludin, claudin-1, ZO-1) and anti-inflammatory cytokines (TGF-β, IL-4), while reducing pro-inflammatory markers (IL-1β, TNF-α, IL-17a). Importantly, oral administration of NZ-BB significantly reduced intestinal and systemic Salmonella burdens, mitigated tissue damage, and restored immune balance in both mice and chicks. Furthermore, NZ-BB regulated the expression of innate immune receptors (e.g., NLRC3) and matrix metalloproteinases (e.g., MMP-1), highlighting its immunomodulatory potential. These results underscore the dual probiotic and antimicrobial functionality of NZ-BB and support its potential use as a food-safe microbial agent to improve animal health and reduce the risk of Salmonella contamination in the food chain.

## Linked entities

- **Genes:** si:ch73-61d6.3 (uncharacterized si:ch73-61d6.3) [NCBI Gene 103182021], CLDN7 (claudin 7) [NCBI Gene 1366], TJP1 (tight junction protein 1) [NCBI Gene 7082], TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040], IL4 (interleukin 4) [NCBI Gene 3565], IL1B (interleukin 1 beta) [NCBI Gene 3553], TNF (tumor necrosis factor) [NCBI Gene 7124], IL17A (interleukin 17A) [NCBI Gene 3605], NLRC3 (NLR family CARD domain containing 3) [NCBI Gene 197358], MMP1 (matrix metallopeptidase 1) [NCBI Gene 4312]

## Full-text entities

- **Genes:** Blnk (B cell linker) [NCBI Gene 17060] {aka BASH, Bca, Ly-57, Ly57, Lyw-57, SLP-65}, Ocln (occludin) [NCBI Gene 18260] {aka Ocl}, Muc1 (mucin 1, transmembrane) [NCBI Gene 17829] {aka CD227, EMA, Muc-1}, Mmp2 (matrix metallopeptidase 2) [NCBI Gene 17390] {aka Clg4a, GelA, MMP-2}, Nod1 (nucleotide-binding oligomerization domain containing 1) [NCBI Gene 107607] {aka C230079P11, Card4, F830007N14Rik, Nlrc1, mNod1}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Cd8a (CD8 subunit alpha) [NCBI Gene 12525] {aka Ly-2, Ly-35, Ly-B, Lyt-2}, CATHL2 (cathelicidin 2) [NCBI Gene 282165] {aka Bac5}, Usp45 [NCBI Gene 12393281], Mmp3 (matrix metallopeptidase 3) [NCBI Gene 17392] {aka EMS-2, MMP-3, SL-1, SLN-1, SLN1, STR-1}, Il4 (interleukin 4) [NCBI Gene 16189] {aka BSF-1, Il-4}, Cldn1 (claudin 1) [NCBI Gene 12737], Tjp1 (tight junction protein 1) [NCBI Gene 21872] {aka ZO1}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 21803] {aka TGF-beta1, TGFbeta1, Tgfb, Tgfb-1}, Cd3e (CD3 antigen, epsilon polypeptide) [NCBI Gene 12501] {aka CD3, CD3epsilon, T3e}, Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}
- **Diseases:** liver pathological (MESH:D017093), mucosal damage (MESH:D052016), splenomegaly (MESH:D013163), infected (MESH:D007239), tissue damage (MESH:D017695), cytotoxic (MESH:D064420), Thymus atrophy (MESH:D001284), Salmonella (MESH:D012480), hemolysis (MESH:D006461), tumor (MESH:D009369), inflammatory cytokines (MESH:D000080424), villus damage (MESH:D020263), liver steatosis (MESH:D005234), diarrhea (MESH:D003967), Inflammatory (MESH:D007249), weight gain (MESH:D015430), necrosis (MESH:D009336), hypertrophy (MESH:D006984)
- **Chemicals:** AMP (MESH:D000089882), SDS (MESH:D012967), NO (MESH:D009614), peptides (MESH:D010455), Chl (MESH:D002701), Alyteserin (-), PVDF (MESH:C024865), H&amp;E (MESH:D006371), eosin (MESH:D004801), water (MESH:D014867), LPS (MESH:D008070), NaCl (MESH:D012965), hematoxylin (MESH:D006416), PBS (MESH:D007854), agar (MESH:D000362)
- **Species:** Salmonella (genus) [taxon 590], Bacillus subtilis (species) [taxon 1423], Lacticaseibacillus casei (species) [taxon 1582], Gallus gallus (bantam, species) [taxon 9031], Staphylococcus sp. S (species) [taxon 573870], Mus musculus (house mouse, species) [taxon 10090], Bos taurus (bovine, species) [taxon 9913], Salmonella enterica subsp. enterica serovar Typhimurium (no rank) [taxon 90371], Escherichia coli (E. coli, species) [taxon 562], Lactococcus lactis (species) [taxon 1358]
- **Mutations:** A20L, C +- 2  C, C at 300
- **Cell lines:** c — Mus musculus (Mouse), Hepatocellular carcinoma of the mouse, Cancer cell line (CVCL_9103), BALB — Mus musculus (Mouse), Transformed cell line (CVCL_4350), MC1061 — Homo sapiens (Human), Huntington's disease, Finite cell line (CVCL_V036), RAW 264.7 — Mus musculus (Mouse), Mouse leukemia, Cancer cell line (CVCL_0493)

## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12870801/full.md

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Source: https://tomesphere.com/paper/PMC12870801