Ben-Amor Kaouther, Heilig Hans, Smidt Hauke, Vaughan Elaine E, Abee Tjakko, de Vos Willem M
Laboratory of Microbiology, Wageningen University, Hesselink van Suchtelenweg 4, 6703 CT Wageningen, The Netherlands.
Appl Environ Microbiol. 2005 Aug;71(8):4679-89. doi: 10.1128/AEM.71.8.4679-4689.2005.
A novel approach combining a flow cytometric in situ viability assay with 16S rRNA gene analysis was used to study the relationship between diversity and activity of the fecal microbiota. Simultaneous staining with propidium iodide (PI) and SYTO BC provided clear discrimination between intact cells (49%), injured or damaged cells (19%), and dead cells (32%). The three subpopulations were sorted and characterized by denaturing gradient gel electrophoresis (DGGE) of 16S rRNA gene amplicons obtained from the total and bifidobacterial communities. This analysis revealed that not only the total community but also the distinct subpopulations are characteristic for each individual. Cloning and sequencing of the dominant bands of the DGGE patterns showed that most of clones retrieved from the live, injured, and dead fractions belonged to Clostridium coccoides, Clostridium leptum, and Bacteroides. We found that some of the butyrate-producing related bacteria, such as Eubacterium rectale and Eubacterium hallii, were obviously viable at the time of sampling. However, amplicons affiliated with Bacteroides and Ruminococcus obeum- and Eubacterium biforme-like bacteria, as well as Butyrivibrio crossotus, were obtained especially from the dead population. Furthermore, some bacterial clones were recovered from all sorted fractions, and this was especially noticeable for the Clostridium leptum cluster. The bifidobacterial phylotypes identified in total samples and sorted fractions were assigned to Bifidobacterium adolescentis, Bifidobacterium longum, Bifidobacterium infantis, Bifidobacterium pseudocatenulatum, and Bifidobacterium bifidum. Phylogenetic analysis of the live, dead, and injured cells revealed a remarkable physiological heterogeneity within these bacterial populations; B. longum and B. infantis were retrieved from all sorted fractions, while B. adolescentis was recovered mostly from the sorted dead fraction.
一种将流式细胞术原位活力测定与16S rRNA基因分析相结合的新方法被用于研究粪便微生物群的多样性与活性之间的关系。用碘化丙啶(PI)和SYTO BC同时染色能够清晰区分完整细胞(49%)、受损或损伤细胞(19%)以及死亡细胞(32%)。这三个亚群被分选出来,并通过对从总群落和双歧杆菌群落获得的16S rRNA基因扩增子进行变性梯度凝胶电泳(DGGE)来进行表征。该分析表明,不仅总群落,而且不同的亚群对于每个个体都是独特的。对DGGE图谱中优势条带进行克隆和测序显示,从活细胞、损伤细胞和死亡细胞组分中获得的大多数克隆属于球状梭菌、纤细梭菌和拟杆菌属。我们发现,一些与丁酸产生相关的细菌,如直肠真杆菌和哈氏真杆菌,在采样时明显具有活性。然而,与拟杆菌属、瘤胃球菌属、类双歧真杆菌以及交叉丁酸弧菌相关的扩增子尤其从死亡细胞组分中获得。此外,一些细菌克隆从所有分选中的组分中都能回收,这在纤细梭菌簇中尤为明显。在总样本和分选中的组分中鉴定出的双歧杆菌系统型被归类为青春双歧杆菌、长双歧杆菌、婴儿双歧杆菌、假链状双歧杆菌和两歧双歧杆菌。对活细胞、死亡细胞和损伤细胞的系统发育分析揭示了这些细菌群体中显著的生理异质性;长双歧杆菌和婴儿双歧杆菌从所有分选中的组分中都能回收,而青春双歧杆菌大多从分选出的死亡细胞组分中回收。