Universite Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, Domaine de Vilvert, 78352, Jouy en Josas, France.
Paris Center for Microbiome Medicine, Fédération Hospitalo-Universitaire, 75012, Paris, France.
Microbiome. 2022 Jun 14;10(1):91. doi: 10.1186/s40168-022-01273-4.
Innate immunity genes have been reported to affect susceptibility to inflammatory bowel diseases (IBDs) and colitis in mice. Dectin-1, a receptor for fungal cell wall β-glucans, has been clearly implicated in gut microbiota modulation and modification of the susceptibility to gut inflammation. Here, we explored the role of Dectin-1 and Dectin-2 (another receptor for fungal cell wall molecules) deficiency in intestinal inflammation.
Susceptibility to dextran sodium sulfate (DSS)-induced colitis was assessed in wild-type, Dectin-1 knockout (KO), Dectin-2KO, and double Dectin-1KO and Dectin-2KO (D-1/2KO) mice. Inflammation severity, as well as bacterial and fungal microbiota compositions, was monitored.
While deletion of Dectin-1 or Dectin-2 did not have a strong effect on DSS-induced colitis, double deletion of Dectin-1 and Dectin-2 significantly protected the mice from colitis. The protection was largely mediated by the gut microbiota, as demonstrated by fecal transfer experiments. Treatment of D-1/2KO mice with opportunistic fungal pathogens or antifungal agents did not affect the protection against gut inflammation, suggesting that the fungal microbiota had no role in the protective phenotype. Amplicon-based microbiota analysis of the fecal bacterial and fungal microbiota of D-1/2KO mice confirmed the absence of changes in the mycobiota but strong modification of the bacterial microbiota. We showed that bacteria from the Lachnospiraceae family were at least partly involved in this protection and that treatment with Blautia hansenii was enough to recapitulate the protection.
Deletion of both the Dectin-1 and Dectin-2 receptors triggered a global shift in the microbial gut environment, affecting, surprisingly, mainly the bacterial population and driving protective effects in colitis. Members of the Lachnospiraceae family seem to play a central role in this protection. These findings provide new insights into the role of the Dectin receptors, which have been described to date as affecting only the fungal population, in intestinal physiopathology and in IBD. Video Abstract.
已有研究报道,固有免疫基因影响小鼠对炎症性肠病(IBD)和结肠炎的易感性。Dectin-1 是真菌细胞壁β-葡聚糖的受体,它明显参与了肠道微生物群的调节,并改变了肠道炎症的易感性。在这里,我们研究了 Dectin-1 和 Dectin-2(真菌细胞壁分子的另一个受体)缺失对肠道炎症的作用。
评估野生型、Dectin-1 敲除(KO)、Dectin-2KO、双重 Dectin-1KO 和 Dectin-2KO(D-1/2KO)小鼠对葡聚糖硫酸钠(DSS)诱导结肠炎的易感性。监测炎症严重程度以及细菌和真菌微生物群组成。
虽然 Dectin-1 或 Dectin-2 的缺失对 DSS 诱导的结肠炎没有强烈影响,但双重缺失 Dectin-1 和 Dectin-2 显著保护了小鼠免受结肠炎的影响。这种保护主要是通过肠道微生物群介导的,粪便转移实验证明了这一点。用机会性真菌病原体或抗真菌剂治疗 D-1/2KO 小鼠不会影响对肠道炎症的保护,这表明真菌微生物群在保护表型中没有作用。D-1/2KO 小鼠粪便细菌和真菌微生物群的扩增子基微生物组分析证实了真菌微生物群没有变化,但细菌微生物群发生了强烈的改变。我们表明,lachnospiraceae 家族的细菌至少部分参与了这种保护,并且布劳特氏菌的治疗足以重现这种保护。
Dectin-1 和 Dectin-2 受体的缺失触发了肠道微生物环境的全面变化,令人惊讶的是,主要影响细菌种群,并在结肠炎中产生保护作用。lachnospiraceae 家族的成员似乎在这种保护中起着核心作用。这些发现为 Dectin 受体的作用提供了新的见解,迄今为止,这些受体被描述为仅影响真菌种群,在肠道生理学和 IBD 中起作用。