Variations of Gut Microbiome Profile Under Different Storage Conditions and Preservation Periods: A Multi-Dimensional Evaluation

• Published in: Frontiers in microbiology Vol. 11; p. 972
• Main Authors: Ma, Junli, Sheng, Lili, Hong, Ying, Xi, Chuchu, Gu, Yu, Zheng, Ningning, Li, Mengci, Chen, Linlin, Wu, Gaosong, Li, Yue, Yan, Juan, Han, Ruiting, Li, Bingbing, Qiu, Huihui, Zhong, Jing, Jia, Wei, Li, Houkai
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 27-05-2020
• Subjects: fecal samples; microbial profile; Microbiology; sequencing platform; storage conditions; storage periods; storage conditions; fecal samples; microbial profile; sequencing platform; storage periods
• ISSN: 1664-302X; 1664-302X
• DOI: 10.3389/fmicb.2020.00972

Gut dysbiosis is heavily involved in the development of various human diseases. There are thousands of publications per year for investigating the role of gut microbiota in diseases. However, emerging evidence has indicated the frequent data inconsistency between different studies, which is largely overlooked. There are many factors that can cause data variation and inconsistency during the process of microbiota study, in particular, sample storage conditions and sequencing process. Here, we systemically evaluated the impacts of six fecal sample storage conditions (three non-commercial storage protocols, -80°C, -80°C with 70% ethanol (ET_-80°C), 4°C with 70% ethanol (ET_4°C), and three commercial storage reagents, OMNIgeneGUT OMR-200 (GT) and MGIEasy (MGIE) at room temperature, and Longsee at 4°C (LS) on gut microbiome profile based on 16S rRNA gene sequencing. In addition, we also investigated the impacts of storage periods (1 and 2 weeks, or 6 months) and sequencing platform on microbiome profile. The efficacy of storage conditions was evaluated by DNA yield and quality, α and β diversity, relative abundance of the dominant and functional bacteria associated with short-chain fatty acid (SCFA) production, and BAs metabolism. Our current study suggested that -80°C was acceptable for fecal sample storage, and the addition of 70% ethanol had some benefits in maintaining the microbial community structure. Meanwhile, we found that samples in ET_4°C and GT reagents were comparable, both of them introduced some biases in α or β diversity, and the relative abundance of functional bacteria. Samples stored in MGIE reagent resulted in the least variation, whereas the most obvious variations were introduced by LS reagents. In addition, our results indicated that variations caused by storage condition were larger than that of storage time and sequencing platform. Collectively, our study provided a multi-dimensional evaluation on the impacts of storage conditions, storage time periods, and sequencing platform on gut microbial profile.