Protective effects of Mycobacterium vaccae ATCC 15483 against "Western"-style diet-induced weight gain and visceral adiposity in adolescent male mice.

IF 8.8 2区 医学 Q1 IMMUNOLOGY Brain, Behavior, and Immunity Pub Date : 2024-12-19 DOI:10.1016/j.bbi.2024.12.029
Luke W Desmond, Lamya'a M Dawud, Lyanna R Kessler, Tyler Akonom, Elizabeth A H Hunter, Evan M Holbrook, Nathan D Andersen, John D Sterrett, Dennis A Boateng, Barbara J Stuart, Lucas Guerrero, Matthew J Gebert, Pei-San Tsai, Dominik Langgartner, Stefan O Reber, Matthew G Frank, Christopher A Lowry
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Abstract

The prevalence of noncommunicable inflammatory disease is increasing in modern urban societies, posing significant challenges to public health. Novel prevention and therapeutic strategies are needed to effectively deal with this issue. One promising approach is leveraging microorganisms such as Mycobacterium vaccae ATCC 15483, known for its anti-inflammatory, immunoregulatory, and stress-resilience properties. This study aimed to assess whether weekly subcutaneous administrations of a whole-cell, heat-killed preparation of M. vaccae ATCC 15483 (eleven injections initiated one week before the onset of the diet intervention), relative to vehicle injections, in adolescent male C57BL/6N mice can mitigate inflammation associated with Western-style diet-induced obesity, which is considered a risk factor for a number of metabolic and inflammatory diseases. Our results show that treatment with M. vaccae ATCC 15483 prevented Western-style diet-induced excessive weight gain, visceral adipose tissue accumulation, and elevated plasma leptin concentrations. The Western-style diet, relative to a control diet condition, decreased alpha diversity and altered the community composition of the gut microbiome, increasing the Bacillota to Bacteroidota ratio (formerly referred to as the Firmicutes to Bacteroidetes ratio). Despite the finding that M. vaccae ATCC 15483 prevented Western-style diet-induced excessive weight gain, visceral adipose tissue accumulation, and elevated plasma leptin concentrations, it had no effect on the diversity or community composition of the gut microbiome, suggesting that it acts downstream of the gut microbiome to alter immunometabolic signaling. M. vaccae ATCC 15483 reduced baseline levels of biomarkers of hippocampal neuroinflammation and microglial priming, such as Nfkbia and Nlrp3, and notably decreased anxiety-like defensive behavioral responses. The current findings provide compelling evidence supporting the potential for M. vaccae ATCC 15483 as a promising intervention for prevention or treatment of adverse immunometabolic outcomes linked to the consumption of a Western-style diet and the associated dysbiosis of the gut microbiome.

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母牛分枝杆菌ATCC 15483对“西式”饮食诱导的青春期雄性小鼠体重增加和内脏肥胖的保护作用
在现代城市社会中,非传染性炎症疾病的患病率正在上升,对公共卫生构成重大挑战。需要新的预防和治疗策略来有效地处理这一问题。一种很有前景的方法是利用母牛分枝杆菌ATCC 15483等微生物,该微生物以其抗炎、免疫调节和应激恢复特性而闻名。本研究旨在评估相对于载体注射,在青春期雄性C57BL/6N小鼠中,每周皮下注射全细胞、热杀母牛支原体ATCC 15483制剂(在饮食干预开始前一周开始注射11次)是否可以减轻与西式饮食诱导的肥胖相关的炎症,西式饮食诱导的肥胖被认为是许多代谢和炎症疾病的危险因素。我们的研究结果表明,用牛痘芽孢杆菌ATCC 15483治疗可以防止西式饮食引起的过度体重增加、内脏脂肪组织积累和血浆瘦素浓度升高。与对照饮食相比,西式饮食降低了α多样性,改变了肠道微生物群落组成,增加了杆菌门与拟杆菌门的比例(以前称为厚壁菌门与拟杆菌门的比例)。尽管研究发现,牛分枝杆菌ATCC 15483可以防止西式饮食引起的体重过度增加、内脏脂肪组织积累和血浆瘦素浓度升高,但它对肠道微生物组的多样性或群落组成没有影响,这表明它作用于肠道微生物组的下游,改变免疫代谢信号。母牛分枝杆菌ATCC 15483降低了海马神经炎症和小胶质细胞启动的生物标志物(如Nfkbia和Nlrp3)的基线水平,并显著降低了焦虑样防御行为反应。目前的研究结果提供了令人信服的证据,支持母牛分枝杆菌ATCC 15483作为预防或治疗与西式饮食和肠道微生物群相关的不良免疫代谢结果的有希望的干预措施的潜力。
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来源期刊
CiteScore
29.60
自引率
2.00%
发文量
290
审稿时长
28 days
期刊介绍: Established in 1987, Brain, Behavior, and Immunity proudly serves as the official journal of the Psychoneuroimmunology Research Society (PNIRS). This pioneering journal is dedicated to publishing peer-reviewed basic, experimental, and clinical studies that explore the intricate interactions among behavioral, neural, endocrine, and immune systems in both humans and animals. As an international and interdisciplinary platform, Brain, Behavior, and Immunity focuses on original research spanning neuroscience, immunology, integrative physiology, behavioral biology, psychiatry, psychology, and clinical medicine. The journal is inclusive of research conducted at various levels, including molecular, cellular, social, and whole organism perspectives. With a commitment to efficiency, the journal facilitates online submission and review, ensuring timely publication of experimental results. Manuscripts typically undergo peer review and are returned to authors within 30 days of submission. It's worth noting that Brain, Behavior, and Immunity, published eight times a year, does not impose submission fees or page charges, fostering an open and accessible platform for scientific discourse.
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