Department of Poultry Science, College of Agricultural, Food and Life Sciences, University of Arkansas, Fayetteville, AR, 72701, USA.
Cell and Molecular Biology Program, University of Arkansas, Fayetteville, AR, 72701, USA.
BMC Res Notes. 2020 Jun 3;13(1):269. doi: 10.1186/s13104-020-05113-2.
Microbial community profiling using 16S rRNA gene has provided invaluable insights into diverse microbial communities. Recently a few studies have attempted to use 16S rRNA gene microbiota profiling in combination with the conventional culture methods to explore bacterial communities. In this "culture-enriched microbiota profiling" approach, microbes in a sample are cultured on solid media, and the resulting colonies are combined and subjected to 16S rRNA gene microbiota profiling. Here we investigated the effect of cell densities as determined by varying levels of sample dilution on the culture-enriched microbiota profiles using De Man, Rogosa and Sharpe (MRS) agar medium as a model system.
Cecal samples collected from 10 healthy chickens were serially diluted to 10 fold (M-LOW), 10 fold (M-MEDIUM), and 10 fold (M-HIGH), and the dilutions were plated on MRS agar. 16S rRNA gene profiling showed that the relative abundance of certain genera showed gradual increase (Pediococcus and Enterococcus) or decrease (Lactobacillus and Turicibacter) with higher dilutions, though it was significant only for Pediococcus (p < 0.05). The result indicates that the dilution levels of the samples can alter the resulting microbiota profiles via unknown density-dependent mechanisms and thus should be considered for designing experiments using culture-enriched microbiota profiling.
使用 16S rRNA 基因进行微生物群落分析为研究各种微生物群落提供了宝贵的见解。最近,一些研究试图将 16S rRNA 基因微生物组分析与传统的培养方法结合起来,以探索细菌群落。在这种“培养富集微生物组分析”方法中,将样品中的微生物在固体培养基上培养,然后将得到的菌落混合并进行 16S rRNA 基因微生物组分析。在这里,我们研究了通过改变样品稀释度来确定细胞密度对以 De Man、Rogosa 和 Sharpe (MRS) 琼脂培养基为模型系统的培养富集微生物组谱的影响。
从 10 只健康鸡的盲肠中采集样本,分别以 10 倍稀释(M-LOW)、10 倍稀释(M-MEDIUM)和 10 倍稀释(M-HIGH)的比例进行稀释,然后将稀释液涂在 MRS 琼脂上。16S rRNA 基因分析显示,某些属的相对丰度随着稀释度的增加呈逐渐增加(肠球菌和魏斯氏菌)或减少(乳杆菌和图里西杆菌)趋势,尽管仅对肠球菌具有统计学意义(p < 0.05)。结果表明,样品的稀释水平可以通过未知的密度依赖性机制改变最终的微生物组谱,因此在设计使用培养富集微生物组分析的实验时应考虑这一点。