Barbieri Elena, Bertini Luana, Rossi Ismaela, Ceccaroli Paola, Saltarelli Roberta, Guidi Chiara, Zambonelli Alessandra, Stocchi Vilberto
Istituto di Chimica Biologica Giorgio Fornaini, University of Urbino Carlo Bo, Urbino (PU), Italy.
FEMS Microbiol Lett. 2005 Jun 1;247(1):23-35. doi: 10.1016/j.femsle.2005.04.027.
The microbial community associated with ascocarps of the ectomycorrhizal fungus Tuber borchii Vittad. was studied by both cultivation and direct extraction of bacterial 16S rRNA gene (rDNA) sequence approaches. The inner part of six T. borchii ascoma collected in North-Central Italy was used to establish a bacterial culture collection and to extract the total genomic DNA to obtain a library of 16S rDNAs representative of the truffle bacterial community. Most of the isolates were affiliated to the gamma-Proteobacteria, mainly Fluorescent pseudomonads; some isolates were members of the Bacteroidetes group and Gram-positive bacteria, mostly Bacillaceae. The majority of the clones from the library were alpha-Proteobacteria showing significant similarity values, of greater than 97%, with members of the Sinorhizobium/Ensifer Group, Rhizobium and Bradyrhizobium spp. not previously identified as Tuber-associated bacteria. Only a few bacterial strains belonging to this bacterial subclass were found in the culture collection and isolated on a medium specific for Rhizobium-like organisms. A few clones were members of the beta- and gamma-Proteobacteria; as well as low and high G+C Gram-positive bacteria. Our findings clearly indicate that a dual approach increases the information obtained on the structural composition of a truffle bacterial community as compared to that derived via cultivation or direct recovery of 16S rDNA sequences alone.
采用培养法和直接提取细菌16S rRNA基因(rDNA)序列的方法,对与外生菌根真菌波氏块菌(Tuber borchii Vittad.)子囊果相关的微生物群落进行了研究。利用在意大利中北部采集的6个波氏块菌子实体的内部建立细菌培养物库,并提取总基因组DNA,以获得代表松露细菌群落的16S rDNA文库。大多数分离菌株属于γ-变形菌纲,主要是荧光假单胞菌;一些分离菌株是拟杆菌群和革兰氏阳性菌的成员,大多属于芽孢杆菌科。文库中的大多数克隆属于α-变形菌纲,与中华根瘤菌/剑菌属(Sinorhizobium/Ensifer Group)、根瘤菌属(Rhizobium)和慢生根瘤菌属(Bradyrhizobium spp.)的成员具有大于97%的显著相似性值,这些菌以前未被鉴定为与块菌相关的细菌。在培养物库中仅发现少数属于该细菌亚类的菌株,并且是在针对类根瘤菌的培养基上分离得到的。少数克隆属于β-和γ-变形菌纲,以及低G+C和高G+C革兰氏阳性菌纲。我们的研究结果清楚地表明,与单独通过培养或直接回收16S rDNA序列相比,采用双重方法可增加关于松露细菌群落结构组成的信息。