Animal Microecology Research Center, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.
Central Station of Animal Feed Affairs of Sichuan Province, Sichuan Provincial Department of Agriculture and Rural Affairs, Chengdu, China.
Front Immunol. 2021 Dec 8;12:747045. doi: 10.3389/fimmu.2021.747045. eCollection 2021.
Intestinal diseases are one of the main causes of captive giant panda death. Their special dietary habits and gastrointestinal tract structure often lead to intestinal epithelium damage and secondary intestinal infection. The captive giant panda is predisposed to suffer from microbiota dysbiosis due to long-term artificial feeding and antibiotic misuse. However, there are few reported probiotics to treat giant panda enteritis and the associated dysbiosis. This study aims to elucidate the mechanism by which G201683 ( G83), a promising panda-derived probiotic, exerts a protective effect on intestinal inflammation in the dextran sulfate sodium- (DSS) induced panda microbiota-associated (DPMA) mouse model. The DPMA mouse was generated by antibiotic treatment and 5% DSS drinking water administration to assess the effect of G83 on intestinal inflammation and microbiota . Our results demonstrated the successful generation of a DPMA mouse model with enrichment, consistent with the giant panda intestinal microbiota. G83 decreased clinical and histological severity of intestinal inflammation, enhanced intestinal tight junction protein expression (ZO-1, Occludin) and alleviated inflammatory cytokine production (TNF-) in the colon of DPMA mice. The administration of G83 altered the microbiota composition by decreasing pathogen associated taxa such as and increasing abundance of beneficial bacteria including spp. These changes in microbiota composition were associated with an increased concentration of short chain fatty acids (SCFA), reduced NF-κB signaling, and an altered balance of T helper cell subsets. Our findings support G83 as a promising probiotic to treat intestinal inflammation in the giant panda.
肠道疾病是圈养大熊猫死亡的主要原因之一。它们特殊的饮食习惯和胃肠道结构常常导致肠道上皮细胞损伤和继发性肠道感染。由于长期人工饲养和抗生素滥用,圈养大熊猫易发生微生物群落失调。然而,用于治疗大熊猫肠炎和相关失调的益生菌却很少有报道。本研究旨在阐明一种有前景的大熊猫源益生菌 G201683(G83)对葡聚糖硫酸钠(DSS)诱导的大熊猫微生物群相关(DPMA)小鼠模型中肠道炎症的保护作用机制。通过抗生素处理和 5% DSS 饮用水给药来生成 DPMA 小鼠,以评估 G83 对肠道炎症和微生物群的影响。我们的结果成功地生成了一种 DPMA 小鼠模型,其肠道微生物群与大熊猫的肠道微生物群相一致。G83 降低了 DPMA 小鼠肠道炎症的临床和组织学严重程度,增强了肠道紧密连接蛋白的表达(ZO-1、Occludin),并减轻了结肠中炎症细胞因子的产生(TNF-)。G83 通过减少与病原体相关的分类群(如)和增加有益细菌(如 spp.)的丰度来改变微生物群落组成。这些微生物群落组成的变化与短链脂肪酸(SCFA)浓度增加、NF-κB 信号降低以及辅助性 T 细胞亚群平衡改变有关。我们的研究结果支持 G83 作为一种有前途的益生菌,用于治疗大熊猫的肠道炎症。