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重组抗菌蛋白PIL22-PBD-2在毕赤酵母中的表达及其体外生物学功能验证

Expression of recombination antimicrobial protein PIL22-PBD-2 in Pichia pastoris and verification of its biological function in vitro.

作者信息

Li Xian, Qiu Pengfei, Yue Menglong, Zhang Ying, Lei Congshang, Wang Jingyu, Chen Xiwen, Qi Xuefeng

机构信息

College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi, China.

Key Laboratory of Ruminant Disease Prevention and Control (West), Ministry of Agriculture and Rural Affairs, Yangling, China.

出版信息

Vet Res. 2025 Mar 7;56(1):52. doi: 10.1186/s13567-024-01428-1.

Abstract

Finding suitable alternatives to antibiotics as feed additives is challenging for the livestock industry. Porcine beta-defensin 2 (PBD-2) is an endogenous antimicrobial peptide produced by pigs. Due to its broad-spectrum antibacterial activity against various microorganisms and its low tendency for drug resistance, it is considered a potential substitute for antibiotics. Additionally, given its strong ability to repair intestinal epithelial damage and maintain intestinal mucosal barrier function, porcine interleukin-22 (PIL-22) is a potential feed additive to combat intestinal damage caused by intestinal pathogens in piglets. In this study, the amino acid sequences of PBD-2 and PIL-22 were combined to express the fusion protein in Pichia pastoris, and its biological activity was evaluated in vitro. Our results showed that the PIL22-PBD-2 exhibits broad-spectrum antibacterial activity against multidrug-resistant enterotoxigenic Escherichia coli O8 (ETEC O8), Escherichia coli (E. coli), Salmonella typhimurium, and Staphylococcus aureus (S. aureus). PIL22-PBD-2 demonstrated wound repair capability through a healing assay in the intestinal porcine epithelial cell line-J2 (IPEC-J2). Furthermore, PIL22-PBD-2 significantly enhanced the expression of the major intercellular junction-associated proteins ZO-1 and E-cadherin in IPEC-J2. It is important to note that PIL22-PBD-2 reduced intestinal epithelial cell apoptosis (p < 0.05) considerably and decreased bacterial adhesion (p < 0.05) in ETEC O8-challenged IPEC-J2. We also found that the PIL22-PBD-2 treatment attenuated ETEC O8-induced inflammatory responses in IPEC-J2 by exerting antibacterial activity, increasing the expression of endogenous antimicrobial peptides, and significantly decreasing the mRNA expression levels of IL-6 and TNF-α (p < 0.05). In conclusion, our studies demonstrate that PIL22-PBD-2 has a positive effect on inhibiting pathogenic bacteria and repairing intestinal damage.

摘要

寻找抗生素的合适替代物作为饲料添加剂对畜牧业来说具有挑战性。猪β-防御素2(PBD-2)是猪产生的一种内源性抗菌肽。由于其对多种微生物具有广谱抗菌活性且耐药性低,它被认为是抗生素的潜在替代品。此外,鉴于猪白细胞介素-22(PIL-22)具有强大的修复肠道上皮损伤和维持肠道黏膜屏障功能的能力,它是一种潜在的饲料添加剂,可对抗仔猪肠道病原体引起的肠道损伤。在本研究中,将PBD-2和PIL-22的氨基酸序列进行组合,在毕赤酵母中表达融合蛋白,并在体外评估其生物学活性。我们的结果表明,PIL22-PBD-2对多重耐药产肠毒素大肠杆菌O8(ETEC O8)、大肠杆菌(E. coli)、鼠伤寒沙门氏菌和金黄色葡萄球菌(S. aureus)具有广谱抗菌活性。通过在猪肠道上皮细胞系-J2(IPEC-J2)中的愈合试验,PIL22-PBD-2展示出伤口修复能力。此外,PIL22-PBD-2显著增强了IPEC-J2中主要细胞间连接相关蛋白ZO-1和E-钙黏蛋白的表达。值得注意的是,PIL22-PBD-2在ETEC O8攻击的IPEC-J2中显著降低了肠道上皮细胞凋亡(p < 0.05)并减少了细菌黏附(p < 0.05)。我们还发现,PIL22-PBD-2处理通过发挥抗菌活性、增加内源性抗菌肽的表达以及显著降低IL-6和TNF-α的mRNA表达水平(p < 0.05),减轻了ETEC O8诱导的IPEC-J2中的炎症反应。总之,我们的研究表明,PIL22-PBD-2对抑制病原菌和修复肠道损伤具有积极作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b23/11889930/b9ac9a7fa9ef/13567_2024_1428_Fig1_HTML.jpg

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