Division of Gastroenterology and Hepatology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.
Division of Infectious Diseases, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.
Cell Rep. 2022 Jul 19;40(3):111093. doi: 10.1016/j.celrep.2022.111093.
Pathobionts employ unique metabolic adaptation mechanisms to maximize their growth in disease conditions. Adherent-invasive Escherichia coli (AIEC), a pathobiont enriched in the gut mucosa of patients with inflammatory bowel disease (IBD), utilizes diet-derived L-serine to adapt to the inflamed gut. Therefore, the restriction of dietary L-serine starves AIEC and limits its fitness advantage. Here, we find that AIEC can overcome this nutrient limitation by switching the nutrient source from the diet to the host cells in the presence of mucolytic bacteria. During diet-derived L-serine restriction, the mucolytic symbiont Akkermansia muciniphila promotes the encroachment of AIEC to the epithelial niche by degrading the mucus layer. In the epithelial niche, AIEC acquires L-serine from the colonic epithelium and thus proliferates. Our work suggests that the indirect metabolic network between pathobionts and commensal symbionts enables pathobionts to overcome nutritional restriction and thrive in the gut.
病原生物利用独特的代谢适应机制,在疾病条件下最大限度地生长。黏附侵袭性大肠杆菌(AIEC)是一种在炎症性肠病(IBD)患者肠道黏膜中丰富的病原生物,利用饮食中衍生的 L-丝氨酸来适应发炎的肠道。因此,限制饮食中的 L-丝氨酸会使 AIEC 饥饿并限制其适应性优势。在这里,我们发现,在黏液溶解细菌存在的情况下,AIEC 可以通过将营养来源从饮食切换到宿主细胞来克服这种营养限制。在饮食衍生的 L-丝氨酸限制下,黏液溶解共生菌阿克曼氏菌促进 AIEC 侵袭上皮细胞龛,通过降解黏液层。在上皮细胞龛中,AIEC 从结肠上皮细胞获取 L-丝氨酸并因此增殖。我们的工作表明,病原生物和共生共生体之间的间接代谢网络使病原生物能够克服营养限制并在肠道中茁壮成长。