Nicholson Matthew J, Evans Paul N, Joblin Keith N
Grasslands Reseach Centre, AgResearch, Private Bag 11008, Palmerston North, New Zealand.
Microb Ecol. 2007 Jul;54(1):141-50. doi: 10.1007/s00248-006-9182-1. Epub 2007 Mar 13.
A temporal temperature gradient gel electrophoresis (TTGE) method was developed to determine the diversity of methanogen populations in the rumen. Tests with amplicons from genomic DNA from 12 cultured methanogens showed single bands for all strains, with only two showing apparently comigrating bands. Fingerprints of methanogen populations were analyzed from DNA extracted from rumen contents from two cattle and four sheep grazing pasture. For one sheep, dilution cultures selective for methanogens were grown and the culturable methanogens in each successive dilution examined by TTGE. A total of 66 methanogen sequences were retrieved from bands in fingerprints and analyzed to reveal the presence of methanogens belonging to the Methanobacteriales, the Methanosarcinales, and to an uncultured archaeal lineage. Twenty-four sequences were most similar to Methanobrevibacter ruminantium, five to Methanobrevibacter smithii, four to Methanosphaera stadtmanae, and for three, the nearest match was Methanimicrococcus blatticola. The remaining 30 sequences did not cluster with sequences from cultured archaea, but when combined with published novel sequences from clone libraries formed a monophyletic lineage within the Euryarchaeota, which contained two previously unrecognized clusters. The TTGE bands from this lineage showed that the uncultured methanogens had significant population densities in each of the six rumen samples examined. In cultures of dilutions from one rumen sample, TTGE examination revealed these methanogens at a level of at least 10(5)g(-1). Band intensities from low-dilution cultures indicated that these methanogens were present at similar densities to Methanobrevibacter ruminantium-like methanogens, the sole culturable methanogens in high dilutions (10(6)-10(-10) g(-1)). It is suggested that the uncultured methanogens together with Methanobrevibacter spp. may be the predominant methanogens in the rumen. The TTGE method presented in this article provides a new opportunity for characterizing methanogen populations in the rumen microbial ecosystem.
开发了一种时间温度梯度凝胶电泳(TTGE)方法来测定瘤胃中产甲烷菌种群的多样性。对来自12种培养产甲烷菌基因组DNA的扩增子进行测试,结果显示所有菌株均为单一条带,只有两条显示出明显的共迁移条带。从两只牛和四只放牧绵羊的瘤胃内容物中提取的DNA分析了产甲烷菌种群的指纹图谱。对于一只绵羊,培养了对产甲烷菌有选择性的稀释培养物,并通过TTGE检查每个连续稀释液中的可培养产甲烷菌。从指纹图谱中的条带中总共检索到66个产甲烷菌序列,并进行分析以揭示属于甲烷杆菌目、甲烷八叠球菌目以及一个未培养古菌谱系的产甲烷菌的存在。24个序列与瘤胃短杆菌最为相似,5个与史氏甲烷短杆菌相似,4个与史氏甲烷球菌相似,3个与布氏甲烷微球菌的匹配度最高。其余30个序列未与培养古菌的序列聚类,但与来自克隆文库的已发表新序列结合后,在广古菌门内形成了一个单系谱系,其中包含两个以前未识别的簇。来自该谱系的TTGE条带表明,在所检查的六个瘤胃样本中的每一个中,未培养的产甲烷菌都具有显著的种群密度。在一个瘤胃样本稀释培养物中,TTGE检查显示这些产甲烷菌的水平至少为10(5)克(-1)。低稀释培养物的条带强度表明,这些产甲烷菌的密度与瘤胃短杆菌样产甲烷菌相似,而瘤胃短杆菌样产甲烷菌是高稀释度(10(6)-10(-10)克(-1))下唯一可培养的产甲烷菌。建议未培养的产甲烷菌与甲烷短杆菌属一起可能是瘤胃中的主要产甲烷菌。本文介绍的TTGE方法为表征瘤胃微生物生态系统中的产甲烷菌种群提供了新的机会。