Targeting Lactobacillus johnsonii to reverse chronic kidney disease

肾脏疾病 肾功能 内科学 肌酐 病变 内分泌学 失调 生物 医学 胃肠病学 病理 疾病
作者
Hua Miao,Бо Лю,Yanni Wang,Xiao‐Yong Yu,Shougang Zhuang,Yan Guo,Nosratola D. Vaziri,Shixing Ma,Su Wei,You‐Quan Shang,Ming Gao,Jinhua Zhang,Ming Wang,Ying‐Yong Zhao,Gang Cao
出处
期刊:Signal Transduction and Targeted Therapy [Springer Nature]
卷期号:9 (1)
标识
DOI:10.1038/s41392-024-01913-1
摘要

Abstract Accumulated evidence suggested that gut microbial dysbiosis interplayed with progressive chronic kidney disease (CKD). However, no available therapy is effective in suppressing progressive CKD. Here, using microbiomics in 480 participants including healthy controls and patients with stage 1–5 CKD, we identified an elongation taxonomic chain Bacilli-Lactobacillales-Lactobacillaceae- Lactobacillus - Lactobacillus johnsonii correlated with patients with CKD progression, whose abundance strongly correlated with clinical kidney markers. L. johnsonii abundance reduced with progressive CKD in rats with adenine-induced CKD. L. johnsonii supplementation ameliorated kidney lesion. Serum indole-3-aldehyde (IAld), whose level strongly negatively correlated with creatinine level in CKD rats, decreased in serum of rats induced using unilateral ureteral obstruction (UUO) and 5/6 nephrectomy (NX) as well as late CKD patients. Treatment with IAld dampened kidney lesion through suppressing aryl hydrocarbon receptor (AHR) signal in rats with CKD or UUO, and in cultured 1-hydroxypyrene-induced HK-2 cells. Renoprotective effect of IAld was partially diminished in AHR deficiency mice and HK-2 cells. Our further data showed that treatment with L. johnsonii attenuated kidney lesion by suppressing AHR signal via increasing serum IAld level. Taken together, targeting L. johnsonii might reverse patients with CKD. This study provides a deeper understanding of how microbial-produced tryptophan metabolism affects host disease and discovers potential pathways for prophylactic and therapeutic treatments for CKD patients.
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