Galbraith Elizabeth A, Antonopoulos Dionysios A, White Bryan A
Department of Animal Sciences, University of Illinois at Urbana-Champaign, 1207 W. Gregory Drive, Urbana, IL 61801, USA.
Environ Microbiol. 2004 Sep;6(9):928-37. doi: 10.1111/j.1462-2920.2004.00575.x.
Molecular techniques previously used for genome comparisons of closely related bacterial species could prove extremely valuable for comparisons of complex microbial communities, or metagenomes. Our study aimed to determine the breadth and value of suppressive subtractive hybridization (SSH) in a pilot-scale analysis of metagenomic DNA from communities of microorganisms in the rumen. Suppressive subtractive hybridization was performed using total genomic DNA isolated from rumen fluid samples of two hay-fed steers, arbitrarily designated as tester or driver. Ninety-six subtraction DNA fragments from the tester metagenome were amplified, cloned and the DNA sequences were determined. Verification of the isolation of DNA fragments unique to the tester metagenome was accomplished through dot blot and Southern blot hybridizations. Tester-specific SSH fragments were found in 95 of 96 randomly selected clones. DNA sequences of subtraction fragments were analysed by computer assisted DNA and amino acid comparisons. Putative translations of 26 (32.1%) subtractive hybridization fragments exhibited significant similarity to Bacterial proteins, whereas 15 (18.5%) distinctive subtracted fragments had significant similarity to proteins from Archaea. The remainder of the subtractive hybridization fragments displayed no similarity to GenBank sequences. This metagenomic approach has exposed an unexpectedly large difference in Archaeal community structure between the rumen microbial populations of two steers fed identical diets and housed together. 16S rRNA dot blot hybridizations revealed similar proportions of Bacteria and Archaea in both rumen samples and suggest that the differences uncovered by SSH are the result of varying community structural composition. Our study demonstrates a novel approach to comparative analyses of environmental microbial communities through the use of SSH.
先前用于密切相关细菌物种基因组比较的分子技术,对于复杂微生物群落(即宏基因组)的比较可能极具价值。我们的研究旨在确定抑制性消减杂交(SSH)在瘤胃微生物群落宏基因组DNA的小规模分析中的广度和价值。使用从两头以干草为食的阉牛的瘤胃液样本中分离的总基因组DNA进行抑制性消减杂交,这两头阉牛被任意指定为测试组或驱动组。从测试组宏基因组中扩增、克隆了96个消减DNA片段,并测定了DNA序列。通过斑点杂交和Southern杂交完成了对测试组宏基因组特有的DNA片段分离的验证。在随机选择的96个克隆中,有95个发现了测试组特异性SSH片段。通过计算机辅助的DNA和氨基酸比较分析了消减片段的DNA序列。26个(32.1%)消减杂交片段的推定翻译产物与细菌蛋白具有显著相似性,而15个(18.5%)独特的消减片段与古菌蛋白具有显著相似性。其余的消减杂交片段与GenBank序列没有相似性。这种宏基因组方法揭示了在相同饮食且饲养在一起的两头阉牛的瘤胃微生物种群中,古菌群落结构存在出乎意料的巨大差异。16S rRNA斑点杂交显示两个瘤胃样本中细菌和古菌的比例相似,这表明SSH揭示的差异是群落结构组成不同的结果。我们的研究展示了一种通过使用SSH对环境微生物群落进行比较分析的新方法。