益生菌给药可加重右旋糖酐硫酸钠盐诱导的炎症和断奶仔猪肠上皮破坏。

IF 4.9 Q1 MICROBIOLOGY
Kunhong Xie, Weidong Cai, Lingjie Li, Bing Yu, Yuheng Luo, Zhiqing Huang, Xiangbing Mao, Jie Yu, Ping Zheng, Hui Yan, Hua Li, Jun He
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引用次数: 0

摘要

背景:a . muciniphila (AKK)作为潜在的下一代益生菌引起了广泛的研究兴趣,但其在肠道病理中的作用尚不清楚。本试验旨在研究嗜粘杆菌DSM 22959对葡聚糖硫酸钠(DSS)刺激下断奶仔猪生长性能、肠道屏障功能、微生态和炎症反应的影响。方法:选用24头“杜×长×大”(DLY)断奶仔猪,采用2 × 2因子试验,随机分为4组,每组6头。从1 ~ 15 d, CA组和DA组每天口服1.0 × 1011个嗜黏液芽胞杆菌,CON组和DCON组每天胃内灌注厌氧无菌生理盐水。试验第9天至第16天,分别用DSS灌胃(DCON、DA)或不灌胃(CON、CA),第16天屠宰。结果:在dss攻毒的断奶仔猪中,嗜粘杆菌的存在导致腹泻率、血液中性粒细胞、血清c反应蛋白和免疫球蛋白M水平显著升高,最终体重、平均日采食量和平均日增重显著降低。与DCON组相比,DA组仔猪肠绒毛高度、绒毛高度/隐窝深度比和消化率降低,ZO1、ZO2、Claudin1、DMT1、CAT1、SGLT1和PBD114基因表达降低,肠道碱性磷酸酶、乳糖酶、蔗糖酶和麦芽糖酶活性降低。DA组猪食糜中双歧杆菌、乳酸菌、嗜粘杆菌、暴瘤球菌的丰度显著高于DCON组。同时存在嗜黏液单胞杆菌和DSS显著改变了仔猪的炎症反应:与其他猪组相比,DA猪的IL17A、IL17F、IL23、RORγt、Stat3的表达水平升高。结论:本研究结果表明,口服嗜粘单胞杆菌加重了dss诱导的断奶仔猪健康损害,这可能与肠道形态恶化、微生物群失调和炎症反应紊乱有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Probiotic administration aggravates dextran sulfate sodium salt-induced inflammation and intestinal epithelium disruption in weaned pig.

Background: A. muciniphila (AKK) has attracted extensive research interest as a potential next-generation probiotics, but its role in intestinal pathology is remains unclear. Herein, this study was conducted to investigate the effects of A. muciniphila DSM 22,959 on growth performance, intestinal barrier function, microecology and inflammatory response of weaned piglets stimulated by dextran sulfate sodium salt (DSS).

Method: Twenty-four Duroc × Landrace × Yorkshire (DLY) weaned piglets used for a 2 × 2 factorial arrangement of treatments were divided into four groups with six piglets in each group. From 1 to 15 d, the CA and DA groups were orally fed with 1.0 × 1011 colony-forming units A. muciniphila per day, while the CON and DCON groups were received gastric infusion of anaerobic sterile saline per day. The pigs were orally challenged (DCON, DA) or not (CON, CA) with DSS from day 9 to the end of the experiment and slaughtered on day 16.

Results: Presence of A. muciniphila in DSS-challenged weaned pigs resulted in numerically increased diarrhea rate, blood neutrophilic granulocyte, serum C-reactive protein and immunoglobulin M levels, and numerically reduced final weight, average daily feed intake and average daily gain. The decrease in intestinal villus height, villous height: crypt depth ratio and digestibility was accompanied by lower expression of ZO1, ZO2, Claudin1, DMT1, CAT1, SGLT1 and PBD114 genes, as well as decreased enzyme activities of intestinal alkaline phosphatase, lactase, sucrase and maltase of piglets in DA group compared to piglets in DCON group. The abundance of Bifdobacterium, Lactobacillus, A. muciniphila, Ruminococcus gnavus was numerically higher in digesta of pigs in DA group than those in DCON group. The inflammatory responses of piglets were dramatically changed by the simultaneous presence of A. muciniphila and DSS: expression level of IL17A, IL17F, IL23, RORγt, Stat3 was elevated in DA pigs compared to the other pig groups.

Conclusions: Our result showed that the oral A. muciniphila aggravates DSS-induced health damage of weaned piglet, which may attribute to the deteriorating intestinal morphology, dysbiosis of microbiota and inflammatory response disorders.

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