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首页> 外文期刊>Animal >DGGE and 16S rDNA analysis reveals a highly diverse and rapidly colonising bacterial community on different substrates in the rumen of goats.
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DGGE and 16S rDNA analysis reveals a highly diverse and rapidly colonising bacterial community on different substrates in the rumen of goats.

机译:DGGE和16S rDNA分析揭示了山羊瘤胃中不同底物上高度多样且快速定居的细菌群落。

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In the rumen, plant particles are colonised and degraded by the rumen micro-organisms. Although numerous important findings about fibre-associated bacterial community were obtained using traditional or molecular techniques, little information is available on the dynamics of bacteria associated with feed particles during incubation in the rumen. In the present study, ryegrass leaf, ryegrass stem and rice straw, representing different carbohydrate compositions, were used as substrates and placed in the rumen of goats by using nylon bags, and PCR/DGGE (denaturing gradient gel electrophoresis) with subsequent sequence analysis were used to monitor the dynamics of and identify bacteria associated with the substrates during 24 h of incubation. DGGE results showed that substrate samples collected from 10 min to 6 h had similar DGGE patterns, with up to 24 predominant bands to each sample, including 14 common bands to all samples, suggesting a rapid and stable colonisation by a highly diverse bacterial community. Substrate samples collected at 12 and 24 h showed similar DGGE patterns but had great difference in DGGE patterns from those collected at 10 min to 6 h, suggesting an apparent shift in bacterial community. Sequence analysis indicated that most substrate-associated bacteria were closely related to fibrolytic bacteria. In conclusion, a highly diverse and similar rumen bacterial community could immediately colonise to different substrates and remained stable during the initial 6 h of incubation, but experienced a marked change after 12 h of incubation. Italian ryegrass leaf, Italian ryegrass stem and rice straw were colonised with a similar bacterial community.
机译:在瘤胃中,植物颗粒被瘤胃微生物定殖并降解。尽管使用传统或分子技术获得了许多与纤维相关的细菌群落的重要发现,但在瘤胃中温育期间,与饲料颗粒相关的细菌动力学的信息很少。在本研究中,使用代表不同碳水化合物组成的黑麦草叶,黑麦草茎和稻草作为底物,并使用尼龙袋将其放置在山羊瘤胃中,并进行PCR / DGGE(变性梯度凝胶电泳)及随后的序列分析。用于监测孵育24小时内底物的动态并鉴定与底物相关的细菌。 DGGE结果显示,从10分钟到6 h收集的底物样品具有相似的DGGE模式,每个样品最多具有24条主要谱带,其中所有样品共有14条共同谱带,表明高度多样化的细菌群落可快速稳定地定植。在12和24 h收集的底物样品显示出相似的DGGE模式,但与在10 min至6 h收集到的DGGE模式有很大差异,表明细菌群落有明显变化。序列分析表明,大多数底​​物相关细菌与纤溶细菌密切相关。总之,高度多样化和相似的瘤胃细菌群落可以立即定居到不同的底物上,并在孵育的最初6小时内保持稳定,但是在孵育12小时后发生了显着变化。意大利黑麦草叶,意大利黑麦草茎和稻草均以类似的细菌群落定殖。

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