生物
厚壁菌
基因组
样品(材料)
门
菌落
芽孢杆菌(形态)
计算生物学
生物技术
16S核糖体RNA
微生物学
细菌
遗传学
基因
色谱法
化学
作者
Hee Sang You,Song Hee Lee,Young Ju Lee,Han B. Lee,Sang Sun Kang,Sung Hee Hyun
出处
期刊:Current Microbiology
[Springer Science+Business Media]
日期:2022-05-07
卷期号:79 (6): 187-187
被引量:2
标识
DOI:10.1007/s00284-022-02865-x
摘要
Next-generation sequencing (NGS) technology has led to innovations in environmental metagenomics and investigations involving humans and microbes. However, it is necessary to analyze the components that will affect analysis of the method upon processing a large amount of information. In particular, the processing method after sample collection affects the NGS results, and it is necessary to check for inaccurate results. Here, we show that the microbial communities obtained from fingertip samples differ from those obtained from fingertips remaining on mobile phones and desks, when cultured or not for 24 h. We also confirmed changes in microbial communities in fingertip samples from desks incubated for 2, 4, 8, 16, and 24 h. Samples of prints from mobile phones that are considerably vulnerable to external factors were not analyzed. Ratios of Firmicutes and Bacillus were, respectively, increased in cultures at the phylum and species levels. Collectively, we identified bacterial species that can aid in determining whether a sample has been cultured. In addition, although microbial communities differed depending on sample types, we confirmed changes after culture for 4 and 8 h. However, since this study is a sample limited to three types, it is necessary to analyze other types of samples in the same way and check whether they are applicable to all types. This strategy can verify the suitability of samples for deriving informative results from cultured or uncultured bacterial communities.
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