The combination of Clostridium butyricum and Akkermansia muciniphila mitigates DSS-induced colitis and attenuates colitis-associated tumorigenesis by modulating gut microbiota and reducing CD8+ T cells in mice.

IF 5 2区 生物学 Q1 MICROBIOLOGY mSystems Pub Date : 2025-01-22 DOI:10.1128/msystems.01567-24
Dengxiong Hua, Qin Yang, Xiaowei Li, Xuexue Zhou, Yingqian Kang, Yan Zhao, Daoyan Wu, Zhengrong Zhang, Boyan Li, Xinxin Wang, Xiaolan Qi, Zhenghong Chen, Guzhen Cui, Wei Hong
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Abstract

The gut microbiota is closely associated with inflammatory bowel disease (IBD) and colorectal cancer (CRC). Probiotics such as Clostridium butyricum (CB) or Akkermansia muciniphila (AKK) have the potential to treat inflammatory bowel disease (IBD) or colorectal cancer (CRC). However, research on the combined therapeutic effects and immunomodulatory mechanisms of CB and AKK in treating IBD or CRC has never been studied. This study evaluates the potential of co-administration of CB and AKK in treating DSS/AOM-induced IBD and colitis-associated CRC. Our results indicate that compared to mono-administration, the co-administration of CB and AKK not only significantly alleviates symptoms such as weight loss, colon shortening, and increased Disease Activity Index in IBD mice but also regulates the gut microbiota composition and effectively suppresses colonic inflammatory responses. In the colitis-associated CRC mice model, a combination of CB and AKK significantly alleviates weight loss and markedly reduces inflammatory infiltration of macrophages and cytotoxic T lymphocytes (CTLs) in the colon, thereby regulating anti-tumor immunity and inhibiting the occurrence of inflammation-induced CRC. In addition, we found that the combined probiotic therapy of CB and AKK can enhance the sensitivity of colitis-associated CRC mice to the immune checkpoint inhibitor anti-mouse PD-L1 (aPD-L1), significantly improving the anti-tumor efficacy of immunotherapy and the survival rate of colitis-associated CRC mice. Furthermore, fecal microbiota transplantation therapy showed that transplanting feces from CRC mice treated with the co-administration of CB and AKK into other CRC mice alleviated the tumor loads in the colon and significantly extended their survival rate. Our study suggests that the combined use of two probiotics, CB and AKK, can not only alleviate chronic intestinal inflammation but also inhibit the progression to CRC. This may be a natural and relatively safe method to support the gut microbiota and enhance the host's immunity against cancer.

Importance: Our study suggests that the combined administration of CB and AKK probiotics, as opposed to a single probiotic strain, holds considerable promise in preventing the advancement of IBD to CRC. This synergistic effect is attributed to the ability of this probiotic combination to more effectively modulate the gut microbiota, curb inflammatory reactions, bolster the efficacy of immunotherapeutic approaches, and optimize treatment results via fecal microbiota transplantation.

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在小鼠中,丁酸梭菌和嗜黏液阿克曼氏菌联合使用可通过调节肠道微生物群和减少CD8+ T细胞来减轻dss诱导的结肠炎和减轻结肠炎相关的肿瘤发生。
肠道微生物群与炎症性肠病(IBD)和结直肠癌(CRC)密切相关。益生菌如丁酸梭菌(CB)或嗜粘杆菌(AKK)具有治疗炎症性肠病(IBD)或结直肠癌(CRC)的潜力。然而,CB和AKK联合治疗IBD或CRC的疗效及免疫调节机制的研究尚未见报道。本研究评估了CB和AKK联合用药治疗DSS/ aom诱导的IBD和结肠炎相关CRC的潜力。我们的研究结果表明,与单给药相比,CB和AKK联合给药不仅能显著缓解IBD小鼠体重减轻、结肠缩短、疾病活动指数升高等症状,还能调节肠道菌群组成,有效抑制结肠炎症反应。在结肠炎相关结直肠癌小鼠模型中,CB和AKK联合使用可显著缓解体重减轻,并显著降低结肠内巨噬细胞和细胞毒性T淋巴细胞(ctl)的炎症浸润,从而调节抗肿瘤免疫,抑制炎症性结直肠癌的发生。此外,我们发现CB和AKK联合益生菌治疗可增强结肠炎相关结直肠癌小鼠对免疫检查点抑制剂抗小鼠PD-L1 (aPD-L1)的敏感性,显著提高免疫治疗的抗肿瘤效果和结肠炎相关结直肠癌小鼠的生存率。此外,粪便微生物群移植治疗表明,将CB和AKK联合处理的结直肠癌小鼠粪便移植到其他结直肠癌小鼠体内,可减轻结肠内的肿瘤负荷,显著延长其存活率。我们的研究表明,联合使用两种益生菌,CB和AKK,不仅可以缓解慢性肠道炎症,还可以抑制CRC的进展。这可能是一种自然和相对安全的方法来支持肠道微生物群和增强宿主对癌症的免疫力。重要性:我们的研究表明,CB和AKK益生菌联合施用,而不是单一的益生菌菌株,在预防IBD向CRC进展方面具有相当大的希望。这种协同效应归因于这种益生菌组合能够更有效地调节肠道微生物群,抑制炎症反应,增强免疫治疗方法的疗效,并通过粪便微生物群移植优化治疗结果。
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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
期刊最新文献
Correction for Taylor et al., "Depression in Individuals Coinfected with HIV and HCV Is Associated with Systematic Differences in the Gut Microbiome and Metabolome". Discovery of viruses and bacteria associated with swine respiratory disease on farms at a nationwide scale in China using metatranscriptomic and metagenomic sequencing. Exploration of the genetic landscape of bacterial dsDNA viruses reveals an ANI gap amid extensive mosaicism. With a little help from my friends: importance of protist-protist interactions in structuring marine protistan communities in the San Pedro Channel. Biodiversity within phytoplankton-associated microbiomes regulates host physiology, host community ecology, and nutrient cycling.
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