Mayorga Olga L, Kingston-Smith Alison H, Kim Eun J, Allison Gordon G, Wilkinson Toby J, Hegarty Matthew J, Theodorou Michael K, Newbold Charles J, Huws Sharon A
Institute of Biological, Environmental and Rural Sciences, Aberystwyth University Aberystwyth, UK.
Department of Animal Science, Kyungpook National University Sangju, Korea.
Front Microbiol. 2016 Nov 18;7:1854. doi: 10.3389/fmicb.2016.01854. eCollection 2016.
Understanding the relationship between ingested plant material and the attached microbiome is essential for developing methodologies to improve ruminant nutrient use efficiency. We have previously shown that perennial ryegrass (PRG) rumen bacterial colonization events follow a primary (up to 4 h) and secondary (after 4 h) pattern based on the differences in diversity of the attached bacteria. In this study, we investigated temporal niche specialization of primary and secondary populations of attached rumen microbiota using metagenomic shotgun sequencing as well as monitoring changes in the plant chemistry using mid-infrared spectroscopy (FT-IR). Metagenomic Rapid Annotation using Subsystem Technology (MG-RAST) taxonomical analysis of shotgun metagenomic sequences showed that the genera , and dominated the attached microbiome irrespective of time. MG-RAST also showed that , and rDNA increased in read abundance during secondary colonization, whilst decreased in read abundance. MG-RAST Clusters of Orthologous Groups (COG) functional analysis also showed that the primary function of the attached microbiome was categorized broadly within "metabolism;" predominantly amino acid, carbohydrate, and lipid metabolism and transport. Most sequence read abundances (51.6, 43.8, and 50.0% of COG families pertaining to amino acid, carbohydrate and lipid metabolism, respectively) within these categories were higher in abundance during secondary colonization. Kyoto encyclopedia of genes and genomes (KEGG) pathways analysis confirmed that the PRG-attached microbiota present at 1 and 4 h of rumen incubation possess a similar functional capacity, with only a few pathways being uniquely found in only one incubation time point only. FT-IR data for the plant residues also showed that the main changes in plant chemistry between primary and secondary colonization was due to increased carbohydrate, amino acid, and lipid metabolism. This study confirmed primary and secondary colonization events and supported the hypothesis that functional changes occurred as a consequence of taxonomical changes. Sequences within the carbohydrate metabolism COG families contained only 3.2% of cellulose activities, on average across both incubation times (1 and 4 h), suggesting that degradation of the plant cell walls may be a key rate-limiting factor in ensuring the bioavailability of intra-plant nutrients in a timely manner to the microbes and ultimately the animal. This suggests that a future focus for improving ruminant nutrient use efficiency should be altering the recalcitrant plant cell wall components and/or improving the cellulolytic capacity of the rumen microbiota.
了解摄入的植物材料与附着的微生物群之间的关系对于开发提高反刍动物营养利用效率的方法至关重要。我们之前已经表明,基于附着细菌多样性的差异,多年生黑麦草(PRG)瘤胃细菌定殖事件遵循初级(长达4小时)和次级(4小时后)模式。在本研究中,我们使用宏基因组鸟枪法测序研究了附着瘤胃微生物群初级和次级群体的时间生态位特化,并使用中红外光谱(FT-IR)监测植物化学变化。使用子系统技术的宏基因组快速注释(MG-RAST)对鸟枪宏基因组序列进行的分类分析表明,无论时间如何,属、和在附着的微生物群中占主导地位。MG-RAST还表明,在次级定殖期间,、和rDNA的读取丰度增加,而的读取丰度下降。MG-RAST直系同源群(COG)功能分析还表明,附着微生物群的主要功能大致归类为“代谢”;主要是氨基酸、碳水化合物和脂质代谢及转运。在这些类别中,大多数序列读取丰度(分别占与氨基酸、碳水化合物和脂质代谢相关COG家族的51.6%、43.8%和50.0%)在次级定殖期间丰度更高。京都基因与基因组百科全书(KEGG)通路分析证实,瘤胃培养1小时和4小时时存在的附着于PRG的微生物群具有相似的功能能力,只有少数通路仅在一个培养时间点独特存在。植物残渣的FT-IR数据还表明,初级和次级定殖之间植物化学的主要变化是由于碳水化合物、氨基酸和脂质代谢增加。本研究证实了初级和次级定殖事件,并支持了功能变化是分类学变化结果的假设。在两个培养时间(1小时和4小时)内,碳水化合物代谢COG家族中的序列平均仅含有3.2%的纤维素活性,这表明植物细胞壁的降解可能是确保植物内营养物质及时向微生物乃至动物提供生物可利用性的关键限速因素。这表明,未来提高反刍动物营养利用效率的重点应该是改变顽固的植物细胞壁成分和/或提高瘤胃微生物群的纤维素分解能力。