Derakshani M, Lukow T, Liesack W
Max-Planck-Institut für terrestrische Mikrobiologie, D-35043 Marburg, Germany.
Appl Environ Microbiol. 2001 Feb;67(2):623-31. doi: 10.1128/AEM.67.2.623-631.2001.
Using a newly developed 16S rRNA gene (rDNA)-targeted PCR assay with proposed group specificity for planctomycetes, we examined anoxic bulk soil of flooded rice microcosms for the presence of novel planctomycete-like diversity. For comparison, oxic rice roots were included as an additional sample in this investigation. The bacterial diversity detectable by this PCR assay was assessed by using a combined approach that included terminal restriction fragment length polymorphism (T-RFLP) analysis and comparative sequence analysis of cloned 16S rDNA. T-RFLP fingerprint patterns generated from rice roots contained 12 distinct terminal restriction fragments (T-RFs). In contrast, the T-RFLP fingerprint patterns obtained from the anoxic bulk soil contained 33 distinct T-RFs, a clearly higher level of complexity. A survey of 176 bulk soil 16S rDNA clone sequences permitted correlation of 20 T-RFs with phylogenetic information. The other 13 T-RFs remained unidentified. The predominant T-RFs obtained from rice roots could be assigned to members of the genus Pirellula within the Planctomycetales, while most of the T-RFs obtained from the bulk soil corresponded to novel lines of bacterial descent. Using a level of 16S rDNA sequence dissimilarity to cultured microorganisms of approximately 20% as a threshold value, we detected 11 distinct bacterial lineages for which pure-culture representatives are not known. Four of these lineages could be assigned to the order Planctomycetales, while one lineage was affiliated with the division Verrucomicrobia and one lineage was affiliated with the spirochetes. The other five lineages either could not be assigned to any of the main lines of bacterial descent or clearly expanded the known diversity of division level lineages WS3 and OP3. Our results indicate the presence of bacterial diversity at a subdivision and/or division level that has not been detected previously by the so-called universal 16S rDNA PCR assays.
我们使用一种新开发的针对16S rRNA基因(rDNA)的PCR检测方法,该方法对浮霉菌具有拟群组特异性,检测了淹水水稻微观世界的缺氧土壤中是否存在新型浮霉菌样多样性。作为比较,本研究还纳入了有氧水稻根作为额外样本。通过使用包括末端限制性片段长度多态性(T-RFLP)分析和克隆16S rDNA的比较序列分析在内的综合方法,评估了该PCR检测方法可检测到的细菌多样性。水稻根产生的T-RFLP指纹图谱包含12个不同的末端限制性片段(T-RFs)。相比之下,从缺氧土壤中获得的T-RFLP指纹图谱包含33个不同的T-RFs,复杂性明显更高。对176个土壤16S rDNA克隆序列的调查使20个T-RFs与系统发育信息相关联。其他13个T-RFs仍未鉴定。从水稻根获得的主要T-RFs可归属于浮霉菌目中的皮氏菌属成员,而从土壤中获得的大多数T-RFs对应于新的细菌谱系。以与培养微生物的16S rDNA序列差异水平约20%作为阈值,我们检测到11个不同的细菌谱系,其纯培养代表未知。其中四个谱系可归属于浮霉菌目,一个谱系隶属于疣微菌门,一个谱系隶属于螺旋体。其他五个谱系要么无法归属于任何主要细菌谱系,要么明显扩展了已知的WS3和OP3门水平谱系的多样性。我们的结果表明,存在着以前通过所谓的通用16S rDNA PCR检测方法未检测到的细分和/或门水平的细菌多样性。