16S核糖体RNA
生物
放大器
UniFrac公司
DNA提取
操作分类学单元
冷库
核糖体RNA
食品科学
细菌
遗传学
聚合酶链反应
基因
园艺
作者
Hiroto Furuhashi,Lena Takayasu,Kimio Isshi,Yuko Hara,Shingo Ono,Masayuki Kato,Kazuki Sumiyama,Wataru Suda
摘要
Abstract The sample storage environment affects gut microbial profiles as assessed using 16S rRNA sequencing. However, the influence of storage condition on human salivary microbial profiles has not been well characterized. Here, we performed an observational study to assess the robustness of microbiota profiles in three different storage environments (−80°C after flash‐freezing, −80°C, and −15°C; all for 14 days) compared to immediate DNA extraction using the MiSeq Illumina platform. Notably, the 16S rRNA V1–V2 region amplicon sequencing revealed no difference in microbiota profiles between the immediate extraction and each of three storage conditions. An almost perfect correlation was shown between the immediate extraction and the −15°C storage group for relative abundance at the genus and operational taxonomic unit levels. The intraindividual UniFrac distances among storage methods were significantly shorter than those of interindividual distances. None of the amount of extracted DNA, the α‐diversity indices, or the relative abundance at the phylum/genus/operational taxonomic unit level differed among storage methods. These findings indicate that a storage temperature of −15°C without flash‐freezing may be optimal in terms of cost advantage and simplicity in 16S rRNA sequencing‐based salivary microbial research.
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