Zhou Dong, Zhu Yao-Hong, Zhang Wei, Wang Meng-Ling, Fan Wen-Yi, Song Dan, Yang Gui-Yan, Jensen Bent Borg, Wang Jiu-Feng
College of Veterinary Medicine, China Agricultural University, Beijing, 100193, China.
Division of Microbiology and Immunology, Danish Center for Food and Agriculture, Aarhus University, DK 8830, Tjele, Denmark.
Vet Res. 2015 Sep 17;46(1):95. doi: 10.1186/s13567-015-0223-y.
Although breeding of F4 receptor - negative (F4R(-)) pigs may prevent post-weaning diarrhea, the underlying immunity is poorly understood. Here, various doses of a Bacillus licheniformis and Bacillus subtilis mixture (BLS-mix) were orally administered to F4ab/acR(-) pigs for 1 week before F4 (K88) - positive ETEC/VTEC/EPEC challenge. Administration of BLS-mix increased the percentage of Foxp3(-)IL-10(+) T cells but not of Foxp3(+)IL-10(+) regulatory T (Treg) cells among peripheral blood CD4(+) T cells. A low dose of BLS-mix feeding resulted in increased the expression of IL-6, TNF-α, IL-10, and the transcription factors Foxp3 and T-bet mRNAs in the jejunum. Administration of either a low or high dose BLS-mix also led to an increase in the percentage of CD4(+)Foxp3(+) Treg cells among intraepithelial lymphocytes and CD4(+)IL-10(+) T cells in the small intestinal Peyer's patches and the lamina propria of F4ab/acR(-) pigs following F4(+) ETEC/VTEC/EPEC challenge. The increased number of IL-10-producing CD4(+) T cells was attributed to an increase in the proportion of Foxp3(-)IL-10(+) Treg cells rather than Foxp3(+)IL-10(+) Treg cells. Our data indicate that oral administration of BLS-mix to newly weaned F4ab/acR(-) pigs ameliorates enteritis in an F4(+) ETEC/VTEC/EPEC model; however, induction of IL-10-producing Foxp3(-) Treg cells by BLS-mix administration cannot account for the protection of newly weaned F4ab/acR(-) pigs from F4(+) ETEC/VTEC/EPEC infection, and that excessive generation of CD4(+)IL-10(+) T cells following consumption of BLS-mix during episodes of intestinal inflammation that is caused by enteric pathogens might prohibit clearance of the pathogen. Select probiotic mixtures may allow for tailoring strategies to prevent infectious diseases.
尽管培育F4受体阴性(F4R(-))猪可能预防断奶后腹泻,但其潜在的免疫机制仍知之甚少。在此,在F4(K88)阳性肠毒素大肠杆菌/产志贺毒素大肠杆菌/肠致病性大肠杆菌攻击前1周,给F4ab/acR(-)猪口服不同剂量的地衣芽孢杆菌和枯草芽孢杆菌混合物(BLS混合物)。给予BLS混合物增加了外周血CD4(+) T细胞中Foxp3(-)IL-10(+) T细胞的百分比,但未增加Foxp3(+)IL-10(+)调节性T(Treg)细胞的百分比。低剂量BLS混合物喂养导致空肠中IL-6、TNF-α、IL-10以及转录因子Foxp3和T-bet mRNA的表达增加。在F4(+)肠毒素大肠杆菌/产志贺毒素大肠杆菌/肠致病性大肠杆菌攻击后,给予低剂量或高剂量BLS混合物也导致F4ab/acR(-)猪的上皮内淋巴细胞、小肠派尔集合淋巴结和固有层中CD4(+)Foxp3(+) Treg细胞以及CD4(+)IL-10(+) T细胞的百分比增加。产生IL-10的CD4(+) T细胞数量增加归因于Foxp3(-)IL-10(+) Treg细胞比例的增加,而非Foxp3(+)IL-10(+) Treg细胞。我们的数据表明,给刚断奶的F4ab/acR(-)猪口服BLS混合物可在F4(+)肠毒素大肠杆菌/产志贺毒素大肠杆菌/肠致病性大肠杆菌模型中改善肠炎;然而,给予BLS混合物诱导产生IL-10的Foxp3(-) Treg细胞并不能解释刚断奶的F4ab/acR(-)猪免受F4(+)肠毒素大肠杆菌/产志贺毒素大肠杆菌/肠致病性大肠杆菌感染的保护作用,并且在由肠道病原体引起的肠道炎症发作期间,食用BLS混合物后过量产生的CD4(+)IL-10(+) T细胞可能会阻止病原体的清除。选择益生菌混合物可能有助于制定预防传染病的策略。