Paßlack Nadine, Büttner Kathrin, Vahjen Wilfried, Zentek Jürgen
Small Animal Clinic, Faculty of Veterinary Medicine, Justus-Liebig-University Giessen, 35392 Giessen, Germany.
Unit for Biomathematics and Data Processing, Justus-Liebig-University Giessen, 35392 Giessen, Germany.
Metabolites. 2025 Mar 22;15(4):215. doi: 10.3390/metabo15040215.
BACKGROUND/OBJECTIVES: The dietary fat supply might interact with the intestinal microbiota via different mechanisms. Research on this topic, however, remains scarce in cats. For this reason, the present study was conducted to evaluate the impact of the fat concentration and fatty acid profile in the diet on the fecal microbiota of healthy cats.
A low-fat basal diet was fed to ten healthy adult cats. The diet was offered without or with the daily addition of 0.5 g or 1 g of sunflower oil, fish oil or lard per kg body weight of the cats, using a randomized cross-over design. Each feeding period lasted for 21 days, and the fecal samples were collected on the last days of each period. The fecal microbiota was analyzed by 16S rDNA sequencing. Additionally, microbial metabolites (short-chain fatty acids, lactate, ammonium, biogenic amines) were measured in the fecal samples.
The dietary treatment had no impact on the alpha-diversity of the fecal microbiota or on the relative abundance of bacterial phyla in the samples. Only a few changes were observed in the relative abundance of bacterial genera and the concentrations of microbial metabolites in the feces, probably being of minor physiological relevance.
The balanced intestinal microbiota of cats seems to be relatively resistant to moderate variations in the dietary fat supply over a short feeding period. Longer-term treatments and higher dietary fat levels should be evaluated in future studies to further clarify the relevance of fat intake for the feline gut microbiome.
背景/目的:膳食脂肪供应可能通过不同机制与肠道微生物群相互作用。然而,关于这一主题的研究在猫身上仍然很少。因此,本研究旨在评估日粮中脂肪浓度和脂肪酸谱对健康猫粪便微生物群的影响。
给十只健康成年猫喂食低脂基础日粮。采用随机交叉设计,日粮不添加或每天每千克猫体重添加0.5克或1克向日葵油、鱼油或猪油。每个喂食期持续21天,并在每个时期的最后一天收集粪便样本。通过16S rDNA测序分析粪便微生物群。此外,还测量了粪便样本中的微生物代谢产物(短链脂肪酸、乳酸、铵、生物胺)。
日粮处理对粪便微生物群的α多样性或样本中细菌门的相对丰度没有影响。在粪便中细菌属的相对丰度和微生物代谢产物的浓度方面仅观察到一些变化,可能具有较小的生理相关性。
在短时间喂食期内,猫的肠道微生物群平衡似乎对膳食脂肪供应的适度变化具有相对抗性。未来的研究应评估长期处理和更高的日粮脂肪水平,以进一步阐明脂肪摄入对猫肠道微生物组的相关性。