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Description of the structural diversity of rumen microbial communities in vitro using single-strand conformation polymorphism profiles

机译:利用单链构象多态性描述体外瘤胃微生物群落的结构多样性

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Changes of the rumen microbial community structure, as it can be established with a rumen simulation technique (RUSITEC) were studied using PCR and single-strand conformation polymorphism (SSCP) of small subunit rDNA genes (SSU rDNA). Four total mixed rations were incubated and two ammonia levels in the artificial saliva were applied. Three replicated vessels were used for each treatment. Mixed microbial fractions were isolated by stepwise centrifugation from the liquid fraction (reference microbes, RM) and from the solids of the feed residues (solid-associated microbes, SAM). PCR-primers targeting archaea, fibrobacter, clostridia, and bacteria, respectively, were applied to represent the individual taxonomic groups by SSCP profiles. These SSCP profiles were converted into a binary matrix and distances among treatments were visualised by non-metric multidimensional scaling. Between replicates belonging to one treatment only small differences were found, indicating a high reproducibility of the RUSITEC and the chosen SSCP method. The ammonia concentration seems to be affecting the SSCP profiles. Great differences occurred between RM and SAM, especially for profiles targeting bacteria and clostridia. Differences in the profiles of RM were also found between mixed rations that contained the same feedstuffs in different ratios and between rations with similar nutrient content but based on different feedstuffs. In conclusion, the PCR-SSCP-based technique in conjunction with non-metric multidimensional scaling was sufficiently sensitive to detect and compare changes in composition of rumen microbial community structure in vitro as affected by diet and other environmental factors.
机译:利用小亚基rDNA基因(SSU rDNA)的PCR和单链构象多态性(SSCP),研究了可以通过瘤胃模拟技术(RUSITEC)建立的瘤胃微生物群落结构的变化。总共孵育四个混合日粮,并在人造唾液中添加两个氨水平。每个处理使用三个复制的容器。通过逐步离心从液体部分(参考微生物,RM)和进料残渣的固体(固体相关微生物,SAM)中分离出混合的微生物部分。分别针对古细菌,纤维杆菌,梭菌和细菌的PCR引物用于通过SSCP谱图代表各个分类组。将这些SSCP配置文件转换为二进制矩阵,并通过非度量多维标度可视化处理之间的距离。在属于一种处理的重复样本之间,仅发现了很小的差异,表明RUSITEC和所选SSCP方法具有很高的重现性。氨浓度似乎正在影响SSCP曲线。 RM和SAM之间存在很大差异,尤其是针对细菌和梭状芽胞杆菌的谱图。在包含相同比例不同饲料的混合日粮之间,以及在营养成分相似但基于不同饲料的日粮之间,RM的分布也存在差异。总之,基于PCR-SSCP的技术与非度量多维标度相结合,足以敏感地检测和比较受饮食和其他环境因素影响的瘤胃微生物群落结构的体外变化 。

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