Tang Hui, Xiao Cuihong, Ma Jinzhu, Yu Miao, Li Yumei, Wang Genlin, Zhang Liping
Key Laboratory of Microbial Diversity Research and Application of Heber Province, Hebei University, Baoding, China.
FEMS Microbiol Lett. 2009 Sep;298(2):267-73. doi: 10.1111/j.1574-6968.2009.01730.x. Epub 2009 Jul 16.
In spite of the techniques based on the amplification of 16S rRNA genes (16S rDNA) to compare bacterial communities that are now widely in use in microbial ecology, little is known about the composition of the soybean continuous cropping (CC) and rotational cropping (RC) soil microbial community. To address this, we compared the levels of bacterial community diversity in RC and 5-year CC rhizosphere soil samples. We selected 407 clones in RC and 490 clones in CC for restriction fragment length polymorphism analysis. A total of 123 phylotypes were identified among the 16S rDNA clones, while 78 unique and 21 common phylotypes were identified among the CC soil isolates. Analysis of sequences from a subset of the phylotypes showed that at least 11 bacterial divisions were represented in the clone libraries. The phylotype richness, frequency distribution (evenness), and composition of the two clone libraries were investigated using a variety of diversity indices. Although the analysis of diversity indices and LIBSHUFF comparisons revealed that the compared libraries were not significantly different (P=0.05) between the RC vs. CC soils, some differences could be observed in terms of specific phyla and groups. We concluded that the group variance was not determined immediately by the cropping system's induction, but was a long-term and slow process.
尽管基于16S rRNA基因(16S rDNA)扩增的技术如今在微生物生态学中被广泛用于比较细菌群落,但对于大豆连作(CC)和轮作(RC)土壤微生物群落的组成却知之甚少。为了解决这个问题,我们比较了轮作和5年连作根际土壤样品中细菌群落多样性的水平。我们在轮作中选择了407个克隆,在连作中选择了490个克隆进行限制性片段长度多态性分析。在16S rDNA克隆中总共鉴定出123个系统发育型,而在连作土壤分离物中鉴定出78个独特的和21个常见的系统发育型。对一部分系统发育型的序列分析表明,克隆文库中至少代表了11个细菌门类。使用各种多样性指数研究了两个克隆文库的系统发育型丰富度、频率分布(均匀度)和组成。尽管对多样性指数的分析和LIBSHUFF比较表明,轮作与连作土壤之间比较的文库没有显著差异(P = 0.05),但在特定的门类和类群方面可以观察到一些差异。我们得出结论,群体差异不是由种植系统的诱导立即决定的,而是一个长期而缓慢的过程。