Liu Qian, Ni Xueqin, Wang Qiang, Peng Zhirong, Niu Lili, Wang Hengsong, Zhou Yi, Sun Hao, Pan Kangcheng, Jing Bo, Zeng Dong
Animal Microecology Institute, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.
Chengdu Wildlife Institute, Chengdu Zoo, Chengdu, China.
Front Microbiol. 2017 Sep 26;8:1885. doi: 10.3389/fmicb.2017.01885. eCollection 2017.
In this work, we searched for an effective probiotic that can help control intestinal infection, particularly enterotoxigenic K88 (ETEC) invasion, in giant panda (). As a potential probiotic strain, BSGP201683 ( G83) was isolated from the feces of giant panda and proven beneficial . This study was aimed to evaluate the protective effect of G83 in mice challenged with ETEC. The mice were orally administered with 0.2 mL of PBS containing G83 at 0 colony-forming units (cfu) mL (control; negative control, ETEC group), 5.0 × 10 cfu mL (LDLP), 5.0 × 10 cfu mL (MDLP), and 5.0 × 10 cfu mL (HDLP) for 14 consecutive days. At day 15, the mice (LDLP, MDLP, HDLP, and ETEC groups) were challenged with ETEC and assessed at 0, 24, and 144 h. Animal health status; chemical and biological intestinal barriers; and body weight were measured. Results showed that G83 supplementation protected the mouse gut mainly by attenuating inflammation and improving the gut microflora. Most indices significantly changed at 24 h after challenge compared to those at 0 and 144 h. All treatment groups showed inhibited plasma diamine oxidase activity and -lactate concentration. Tight-junction protein expression was down-regulated, and interleukin (IL)-1β, IL-6, IL-8, TLR4, and MyD88 levels were up-regulated in the jejunum in the LDLP and MDLP groups. The number of the family and the heat-labile enterotoxin (LT) gene decreased ( < 0.05) in the colons in the LDLP and MDLP groups. All data indicated that G83 could attenuate acute intestinal inflammation caused by ETEC infection, and the low and intermediate doses were superior to the high dose. These findings suggested that G83 may serve as a protective probiotic for intestinal disease and merits further investigation.
在本研究中,我们寻找一种有效的益生菌,以帮助控制大熊猫的肠道感染,特别是产肠毒素大肠杆菌K88(ETEC)的侵袭。作为一种潜在的益生菌菌株,BSGP201683(G83)从大熊猫粪便中分离出来,并被证明具有益处。本研究旨在评估G83对受ETEC攻击的小鼠的保护作用。连续14天给小鼠口服0.2 mL含G83的PBS,其浓度分别为0菌落形成单位(cfu)/mL(对照组;阴性对照,ETEC组)、5.0×10⁶ cfu/mL(低剂量组,LDLP)、5.0×10⁷ cfu/mL(中剂量组,MDLP)和5.0×10⁸ cfu/mL(高剂量组,HDLP)。在第15天,给小鼠(LDLP、MDLP、HDLP和ETEC组)接种ETEC,并在0、24和144小时进行评估。测量动物健康状况、化学和生物肠道屏障以及体重。结果表明,补充G83主要通过减轻炎症和改善肠道微生物群来保护小鼠肠道。与0小时和144小时相比,大多数指标在攻击后24小时有显著变化。所有治疗组的血浆二胺氧化酶活性和β-乳酸浓度均受到抑制。紧密连接蛋白表达下调,LDLP和MDLP组空肠中的白细胞介素(IL)-1β、IL-6、IL-8、Toll样受体4(TLR4)和髓样分化因子88(MyD88)水平上调。LDLP和MDLP组结肠中的肠杆菌科数量和热不稳定肠毒素(LT)基因数量减少(P<0.05)。所有数据表明,G83可减轻ETEC感染引起的急性肠道炎症,低剂量和中剂量优于高剂量。这些发现表明,G83可能作为肠道疾病的保护性益生菌,值得进一步研究。