Host-derived nitrate fuels indole production by Escherichia coli to drive chronic kidney disease progression

• 成果类型: Article
• 署名作者: Lee, Jee-Yon; Mahan, Scott P.; Parente de Carvalho, Thaynara; Nguyen, Henry; Singai, Chonikarn; Camacho, Lizbeth; Tekeli, Mert; Kwon, Yu-Jin; Lee, Ji-Won; Santos, Renato L.; Tsolis, Renee M.; Winter, Sebastian E.; Baumler, Andreas J.
• 署名单位: University of California System; University of California Davis; Universidade Federal de Minas Gerais; Yonsei University; Severance Hospital; Yonsei University Health System; Yonsei University; Severance Hospital; Yonsei University Health System; University of California System; University of California Davis
• 刊物名称: SCIENCE
• ISSN/ISSBN: 0036-8075; 1095-9203
• DOI: 10.1126/science.ady5217
• 发表日期: 2026-03-19
• 页码: 1250-1255
• 关键词: INDOXYL SULFATE; microbiota; gene; inhibition; sequence

摘要

Chronic kidney disease (CKD) is linked to an elevated fecal abundance of Enterobacteriaceae, but the ecological drivers of this shift and its impact on disease progression remain unclear. The uremic toxin indoxyl sulfate is produced from microbiota-derived indole in the liver. Here, we found that in mice with adenine-induced CKD, impaired clearance of indoxyl sulfate elevated mucosal expression of the gene encoding inducible nitric oxide synthase (iNOS). The resulting rise in luminal nitrate levels promoted Escherichia coli growth by means of nitrate respiration. Fecal microbiota from CKD patients generated more indole than feces of healthy controls during anaerobic culture, but only in the presence of nitrate. Nitrate enhanced indole production by E. coli, thereby worsening renal pathology in CKD mice, which was mitigated by iNOS inhibition.