Meli'sa S Crawford, Arzu Ulu, Briana M Ramirez, Alina N Santos, Pritha Chatterjee, Vinicius Canale, Salomon Manz, Hillmin Lei, Sarah Mae Soriano, Tara M Nordgren, Declan F McCole
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In our previous study, we demonstrated that intranasal exposure of male and female C57BL/6J mice to 12.5% hog dust extract (HDE, containing 22.1-91.1 EU/mL) for 3 weeks resulted in elevated total cell and neutrophil counts in bronchoalveolar lavage fluid and increased intestinal permeability compared to saline controls. Now, we report that 16S and metagenomic analyses of Week 3 stool samples from HDE-treated mice indicate a reduced abundance of the beneficial species Akkermansia muciniphila and Clostridium sp. ASF356 and Lachnospiraceae bacterium. Bacterial alpha diversity showed increased species evenness in fecal samples from HDE-treated mice (Pielou's evenness, p = 0.047, n = 5-6/group). Metabolomic analysis also indicated significant reductions in key metabolites involved in energy metabolism, including riboflavin (p = 0.027, n = 11) and nicotinic acid (p = 0.049, n = 11), as well as essential amino acids, such as inosine (p = 0.043, n = 11) and leucine (p = 0.018, n = 11). While HDE exposure does not robustly alter overall microbial abundance or community structure, it leads to specific reductions in beneficial bacterial species and critical metabolites necessary for maintaining intestinal homeostasis by supporting energy metabolism, gut barrier function, microbiota balance, and immune regulation. 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Metabolomic analysis also indicated significant reductions in key metabolites involved in energy metabolism, including riboflavin (p = 0.027, n = 11) and nicotinic acid (p = 0.049, n = 11), as well as essential amino acids, such as inosine (p = 0.043, n = 11) and leucine (p = 0.018, n = 11). While HDE exposure does not robustly alter overall microbial abundance or community structure, it leads to specific reductions in beneficial bacterial species and critical metabolites necessary for maintaining intestinal homeostasis by supporting energy metabolism, gut barrier function, microbiota balance, and immune regulation. 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引用次数: 0
摘要
接触含有抗菌素抗性病原体的农业粉尘对畜牧业生产工人的健康构成重大风险。除了引起严重的气道炎症外,污染物还与肠道疾病有关。猪场粉尘中含有丰富的超细颗粒、革兰氏阳性菌和革兰氏阴性菌,以及脂多糖(LPS)等细菌成分;木糖醇)。在我们之前的研究中,我们证明了雄性和雌性C57BL/6J小鼠鼻内暴露于12.5%猪粉尘提取物(HDE,含22.1-91.1 EU/mL) 3周,导致支气管肺泡灌洗液中总细胞和中性粒细胞计数升高,肠道通透性增加。现在,我们报告了对hde处理小鼠第3周粪便样本的16S和宏基因组分析表明,有益物种Akkermansia muciniphila和Clostridium sp. ASF356和Lachnospiraceae细菌的丰度降低。细菌α多样性显示,hde处理小鼠粪便样品的物种均匀度增加(Pielou均匀度,p = 0.047, n = 5-6/组)。代谢组学分析还表明,参与能量代谢的关键代谢物显著减少,包括核黄素(p = 0.027, n = 11)和烟酸(p = 0.049, n = 11),以及必需氨基酸,如肌苷(p = 0.043, n = 11)和亮氨酸(p = 0.018, n = 11)。虽然HDE暴露不会显著改变整体微生物丰度或群落结构,但它会导致有益细菌种类和通过支持能量代谢、肠道屏障功能、微生物群平衡和免疫调节来维持肠道稳态所必需的关键代谢物的特异性减少。这项研究的结果强调了吸入农业粉尘对肠道健康造成的潜在风险。
Respiratory Exposure to Agriculture Dust Extract Alters Gut Commensal Species and Key Metabolites in Mice.
Exposure to agricultural dust containing antimicrobial-resistant pathogens poses significant health risks for workers in animal agriculture production. Beyond causing severe airway inflammation, pollutants are linked to intestinal diseases. Swine farm dust is rich in ultrafine particles, gram-positive and gram-negative bacteria, and bacterial components such as lipopolysaccharides (LPS; endotoxins). In our previous study, we demonstrated that intranasal exposure of male and female C57BL/6J mice to 12.5% hog dust extract (HDE, containing 22.1-91.1 EU/mL) for 3 weeks resulted in elevated total cell and neutrophil counts in bronchoalveolar lavage fluid and increased intestinal permeability compared to saline controls. Now, we report that 16S and metagenomic analyses of Week 3 stool samples from HDE-treated mice indicate a reduced abundance of the beneficial species Akkermansia muciniphila and Clostridium sp. ASF356 and Lachnospiraceae bacterium. Bacterial alpha diversity showed increased species evenness in fecal samples from HDE-treated mice (Pielou's evenness, p = 0.047, n = 5-6/group). Metabolomic analysis also indicated significant reductions in key metabolites involved in energy metabolism, including riboflavin (p = 0.027, n = 11) and nicotinic acid (p = 0.049, n = 11), as well as essential amino acids, such as inosine (p = 0.043, n = 11) and leucine (p = 0.018, n = 11). While HDE exposure does not robustly alter overall microbial abundance or community structure, it leads to specific reductions in beneficial bacterial species and critical metabolites necessary for maintaining intestinal homeostasis by supporting energy metabolism, gut barrier function, microbiota balance, and immune regulation. The results of this study underscore the potential risks for gut health posed by inhalation of agricultural dust.
期刊介绍:
Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.