Sanguin Hervé, Remenant Benoît, Dechesne Arnaud, Thioulouse Jean, Vogel Timothy M, Nesme Xavier, Moënne-Loccoz Yvan, Grundmann Geneviève L
UMR CNRS 5557/USC INRA 1193 Ecologie Microbienne, Université Claude Bernard (Lyon 1), 43 bd du 11 Novembre 1918, F-69622 Villeurbanne Cedex, France.
Appl Environ Microbiol. 2006 Jun;72(6):4302-12. doi: 10.1128/AEM.02686-05.
Bacterial diversity is central to ecosystem sustainability and soil biological function, for which the role of roots is important. The high-throughput analysis potential of taxonomic microarray should match the breadth of bacterial diversity. Here, the power of this technology was evidenced through methodological verifications and analysis of maize rhizosphere effect based on a 16S rRNA-based microarray developed from the prototype of H. Sanguin et al. (Environ. Microbiol. 8:289-307, 2006). The current probe set was composed of 170 probes (41 new probes in this work) that targeted essentially the Proteobacteria. Cloning and sequencing of 16S rRNA amplicons were carried out on maize rhizosphere and bulk soil DNA. All tested clones that had a perfect match with corresponding probes were positive in the hybridization experiment. The hierarchically nested probes were reliable, but the level of taxonomic identification was variable, depending on the probe set specificity. The comparison of experimental and theoretical hybridizations revealed 0.91% false positives and 0.81% false negatives. The microarray detection threshold was estimated at 0.03% of a given DNA type based on DNA spiking experiments. A comparison of the maize rhizosphere and bulk soil hybridization results showed a significant rhizosphere effect, with a higher predominance of Agrobacterium spp. in the rhizosphere, as well as a lower prevalence of Acidobacteria, Bacteroidetes, Verrucomicrobia, and Planctomycetes, a new taxon of interest in soil. In addition, well-known taxonomic groups such as Sphingomonas spp., Rhizobiaceae, and Actinobacteria were identified in both microbial habitats with strong hybridization signals. The taxonomic microarray developed in the present study was able to discriminate and characterize bacterial community composition in related biological samples, offering extensive possibilities for systematic exploration of bacterial diversity in ecosystems.
细菌多样性对于生态系统可持续性和土壤生物功能至关重要,其中根系的作用十分重要。分类微阵列的高通量分析潜力应与细菌多样性的广度相匹配。在此,基于H. Sanguin等人(《环境微生物学》8:289 - 307,2006年)的原型开发的基于16S rRNA的微阵列,通过方法验证和对玉米根际效应的分析证明了该技术的效力。当前的探针集由170个探针组成(本研究中有41个新探针),主要针对变形菌门。对玉米根际和根际外土壤DNA进行了16S rRNA扩增子的克隆和测序。所有与相应探针完全匹配的测试克隆在杂交实验中均呈阳性。分层嵌套探针是可靠的,但分类鉴定水平因探针集特异性而异。实验杂交与理论杂交的比较显示假阳性率为0.91%,假阴性率为0.81%。基于DNA加标实验,微阵列检测阈值估计为给定DNA类型的0.03%。玉米根际和根际外土壤杂交结果的比较显示出显著的根际效应,根际中土壤杆菌属的优势度更高,而酸杆菌门、拟杆菌门、疣微菌门和浮霉菌门(土壤中一个新的重要分类单元)的丰度较低。此外,在两个微生物生境中均鉴定出了具有强杂交信号的知名分类群,如鞘氨醇单胞菌属、根瘤菌科和放线菌。本研究中开发的分类微阵列能够区分和表征相关生物样品中的细菌群落组成,为系统探索生态系统中的细菌多样性提供了广泛的可能性。