Schwarzenbach Kaspar, Enkerli Jürg, Widmer Franco
Molecular Ecology, Agroscope Reckenholz-Tänikon Research Station ART, Reckenholzstrasse 191, CH-8046 Zürich, Switzerland.
J Microbiol Methods. 2007 Feb;68(2):358-66. doi: 10.1016/j.mimet.2006.09.015. Epub 2006 Nov 3.
Soil fungal community structures are often highly heterogeneous even among samples taken from small field plots. Sample pooling is widely used in order to overcome this heterogeneity, however, no objective criteria have yet been defined on how to determine the number of samples to be pooled for representatively profiling a field plot. In the present study PCR/RFLP and T-RFLP analysis of fungal 18S rDNA in ten soil samples obtained from a grassland plot of 400 m(2) also revealed this known heterogeneity in fungal community structures. Based on these data a three-step approach to assess representativity of fungal community profiles was established. First, soil DNA quantities needed for robust community profiling were determined. Second, profiles of single or multiple samples were theoretically averaged to test for statistically significant clustering in order to determine the minimal number of samples to be pooled to achieve representativity. Third, DNA extracts of single or multiple samples were pooled prior to profiling in order to test for statistically significant clustering. Analyses revealed robust profiles for 50 ng soil DNA but not for 5 ng. Averaged T-RFLP profiles from five or more soil samples and experimental T-RFLP profiles from pools of seven or more samples formed one significant branch. Theoretical averaging and experimental pooling revealed that five to seven samples have to be pooled for robustly representing the field plot. Our results demonstrate that representativity of soil fungal community profiles can objectively be determined for a field plot with only little deviation between theoretical and experimental approaches. This three-step approach will be of assistance for designing sampling and pooling strategies for comparative analyses of soil fungal communities in ecological studies.
即使在从小块田间地块采集的样本中,土壤真菌群落结构通常也具有高度的异质性。为了克服这种异质性,样本合并被广泛使用,然而,对于如何确定合并样本的数量以代表性地描绘田间地块,尚未定义客观标准。在本研究中,对从一块400平方米草地地块获得的10个土壤样本中的真菌18S rDNA进行PCR/RFLP和T-RFLP分析,也揭示了真菌群落结构中这种已知的异质性。基于这些数据,建立了一种三步法来评估真菌群落图谱的代表性。首先,确定稳健的群落图谱所需的土壤DNA量。其次,理论上对单个或多个样本的图谱进行平均,以测试统计上显著的聚类,从而确定为实现代表性而合并的最小样本数量。第三,在进行图谱分析之前,将单个或多个样本的DNA提取物合并,以测试统计上显著的聚类。分析表明,50 ng土壤DNA可得到稳健的图谱,而5 ng则不行。来自五个或更多土壤样本的平均T-RFLP图谱和来自七个或更多样本池的实验T-RFLP图谱形成一个显著分支。理论平均和实验合并表明,必须合并五到七个样本才能稳健地代表田间地块。我们的结果表明,对于田间地块,可以客观地确定土壤真菌群落图谱的代表性,理论方法和实验方法之间的偏差很小。这种三步法将有助于设计采样和合并策略,用于生态研究中土壤真菌群落的比较分析。