Dierick Matthias, Ongena Ruben, Vanrompay Daisy, Devriendt Bert, Cox Eric
Laboratory of Immunology, Department of Translational Physiology, Infectiology and Public Health, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820, Merelbeke, Belgium.
Laboratory for Immunology and Animal Biotechnology, Faculty of Bioscience Engineering, Ghent University, Coupure links 653, 9000, Ghent, Belgium.
J Anim Sci Biotechnol. 2024 Mar 6;15(1):39. doi: 10.1186/s40104-023-00985-3.
Post-weaned piglets suffer from F18 Escherichia coli (E. coli) infections resulting in post-weaning diarrhoea or oedema disease. Frequently used management strategies, including colistin and zinc oxide, have contributed to the emergence and spread of antimicrobial resistance. Novel antimicrobials capable of directly interacting with pathogens and modulating the host immune responses are being investigated. Lactoferrin has shown promising results against porcine enterotoxigenic E. coli strains, both in vitro and in vivo.
We investigated the influence of bovine lactoferrin (bLF) on the microbiome of healthy and infected weaned piglets. Additionally, we assessed whether bLF influenced the immune responses upon Shiga toxin-producing E. coli (STEC) infection. Therefore, 2 in vivo trials were conducted: a microbiome trial and a challenge infection trial, using an F18 STEC strain. BLF did not affect the α- and β-diversity. However, bLF groups showed a higher relative abundance (RA) for the Actinobacteria phylum and the Bifidobacterium genus in the ileal mucosa. When analysing the immune response upon infection, the STEC group exhibited a significant increase in F18-specific IgG serum levels, whereas this response was absent in the bLF group.
Taken together, the oral administration of bLF did not have a notable impact on the α- and β-diversity of the gut microbiome in weaned piglets. Nevertheless, it did increase the RA of the Actinobacteria phylum and Bifidobacterium genus, which have previously been shown to play an important role in maintaining gut homeostasis. Furthermore, bLF administration during STEC infection resulted in the absence of F18-specific serum IgG responses.
断奶仔猪易感染F18大肠杆菌(E. coli),导致断奶后腹泻或水肿病。常用的管理策略,包括使用黏菌素和氧化锌,已促使抗菌药物耐药性的出现和传播。正在研究能够直接与病原体相互作用并调节宿主免疫反应的新型抗菌药物。乳铁蛋白在体外和体内对猪产肠毒素大肠杆菌菌株均显示出有前景的结果。
我们研究了牛乳铁蛋白(bLF)对健康和感染断奶仔猪微生物群的影响。此外,我们评估了bLF是否会影响产志贺毒素大肠杆菌(STEC)感染后的免疫反应。因此,进行了2项体内试验:一项微生物群试验和一项攻毒感染试验,使用F18 STEC菌株。bLF不影响α-和β-多样性。然而,bLF组回肠黏膜中放线菌门和双歧杆菌属的相对丰度(RA)较高。在分析感染后的免疫反应时,STEC组F18特异性IgG血清水平显著升高,而bLF组则无此反应。
综上所述,口服bLF对断奶仔猪肠道微生物群的α-和β-多样性没有显著影响。然而,它确实增加了放线菌门和双歧杆菌属的RA,此前已证明它们在维持肠道稳态中起重要作用。此外,在STEC感染期间给予bLF导致F18特异性血清IgG反应缺失。