Microbial pathogenesis · 2026
Autophagy induced by Trichinella spiralis infection alleviate TNBS-induced colitis in mice through inhibiting the NLRP3 inflammasome.
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Zhang Yanan, Wang Yuxin, Zhang Zhiyuan, Liu Xuanrui, Kang Xinyi, Yang Wentao, Cao Xin, Jiang Yanlong, Wang Jianzhong, Zeng Yan, Shi Chunwei, Huang Haibin, Wang Chunfeng, Yang Guilian, Zhang Jingwei, Wang Nan
Аннотация
BACKGROUND: Inflammatory bowel disease (IBD), including Crohn's disease and ulcerative colitis, is a group of chronic intestinal inflammatory disorders with diverse etiologies and limitations in current treatments. Trichinella spiralis, a foodborne parasitic nematode, has been reported to alleviate colitis in mouse models, but its specific mechanism remains unclear.
METHODS: This study aims to investigate whether T. spiralis-induced autophagy can alleviate IBD by inhibiting the NLRP3 inflammasome. Experimental colitis was induced by 2,4,6-trinitrobenzene sulfonic acid (TNBS) in mice 21 days after T. spiralis infection. Experimental groups were treated with 3-methyladenine (3-MA, autophagy inhibitor), rapamycin (Rapa, autophagy activator), or MCC950 (NLRP3 inhibitor), respectively. The severity of enteritis, the levels of autophagy and NLRP3 inflammasome activity, were evaluated using colon length, body weight, disease activity index (DAI) scores, hematoxylin-eosin (H&E) staining, myeloperoxidase (MPO) activity assay, flow cytometry, qPCR, and Western blot.
RESULTS: The results revealed that T. spiralis infection alleviated colitis, concurrent with enhanced autophagy and suppressed NLRP3 inflammasome activation. Notably, inhibition of autophagy led to aggravated colitis symptoms and concomitant activation of the NLRP3 inflammasome. In contrast, autophagy activation resulted in attenuated colitis manifestations and inhibition of the NLRP3 inflammasome. Moreover, direct inhibition of the NLRP3 inflammasome was capable of alleviating colitis.
CONCLUSIONS: This study reveals that T. spiralis can alleviate IBD by inducing autophagy to inhibit the NLRP3 inflammasome, providing new insights into the treatment of IBD.
METHODS: This study aims to investigate whether T. spiralis-induced autophagy can alleviate IBD by inhibiting the NLRP3 inflammasome. Experimental colitis was induced by 2,4,6-trinitrobenzene sulfonic acid (TNBS) in mice 21 days after T. spiralis infection. Experimental groups were treated with 3-methyladenine (3-MA, autophagy inhibitor), rapamycin (Rapa, autophagy activator), or MCC950 (NLRP3 inhibitor), respectively. The severity of enteritis, the levels of autophagy and NLRP3 inflammasome activity, were evaluated using colon length, body weight, disease activity index (DAI) scores, hematoxylin-eosin (H&E) staining, myeloperoxidase (MPO) activity assay, flow cytometry, qPCR, and Western blot.
RESULTS: The results revealed that T. spiralis infection alleviated colitis, concurrent with enhanced autophagy and suppressed NLRP3 inflammasome activation. Notably, inhibition of autophagy led to aggravated colitis symptoms and concomitant activation of the NLRP3 inflammasome. In contrast, autophagy activation resulted in attenuated colitis manifestations and inhibition of the NLRP3 inflammasome. Moreover, direct inhibition of the NLRP3 inflammasome was capable of alleviating colitis.
CONCLUSIONS: This study reveals that T. spiralis can alleviate IBD by inducing autophagy to inhibit the NLRP3 inflammasome, providing new insights into the treatment of IBD.