TY - JOUR
T1 - Validation of the application of gel beads-based single-cell genome sequencing platform to soil and seawater
AU - Nishikawa, Yohei
AU - Kogawa, Masato
AU - Hosokawa, Masahito
AU - Wagatsuma, Ryota
AU - Mineta, Katsuhiko
AU - Takahashi, Kai
AU - Ide, Keigo
AU - Yura, Kei
AU - Behzad, Hayedeh
AU - Gojobori, Takashi
AU - Takeyama, Haruko
N1 - KAUST Repository Item: Exported on 2022-10-03
Acknowledged KAUST grant number(s): URF/1/1976/03/01, URF/1/1976/17/01, URF/1/1976/20/01, FCS/1/3326/01/01
Acknowledgements: This work was supported by JST-PRESTO grant number JPMJPR15FA, MEXT KAKENHI grant numbers 18H01801 and 17H06158, JST ACT-X Grant Number JPMJAX20BE, and the funding from King Abdullah University of Science and Technology (KAUST), under award numbers URF/1/1976/03/01, URF/1/1976/17/01, URF/1/1976/20/01 and FCS/1/3326/01/01. The super-computing resource was provided by the Human Genome Center (University of Tokyo).
PY - 2022/9/29
Y1 - 2022/9/29
N2 - Single-cell genomics is applied to environmental samples as a method to solve the problems of current metagenomics. However, in the fluorescence-activated cell sorting-based cell isolation and subsequent whole genome amplification, the sorting efficiency and the sequence quality are greatly affected by the type of target environment, limiting its adaptability. Here, we developed an improved single-cell genomics platform, named SAG-gel, which utilizes gel beads for single-cell isolation, lysis, and whole genome amplification. To validate the versatility of SAG-gel, single-cell genome sequencing was performed with model bacteria and microbial samples collected from eight environmental sites, including soil and seawater. Gel beads enabled multiple lysis treatments. The genome coverage with model bacteria was improved by 9.1–25%. A total of 734 single amplified genomes were collected from the diverse environmental samples, and almost full-length 16S rRNA genes were recovered from 57.8% of them. We also revealed two marine Rhodobacter strains harboring nearly identical 16S rRNA genes but having different genome contents. In addition, searching for viral sequences elucidated the virus-host linkage over the sampling sites, revealing the geographic distribution and diverse host range of viruses.
AB - Single-cell genomics is applied to environmental samples as a method to solve the problems of current metagenomics. However, in the fluorescence-activated cell sorting-based cell isolation and subsequent whole genome amplification, the sorting efficiency and the sequence quality are greatly affected by the type of target environment, limiting its adaptability. Here, we developed an improved single-cell genomics platform, named SAG-gel, which utilizes gel beads for single-cell isolation, lysis, and whole genome amplification. To validate the versatility of SAG-gel, single-cell genome sequencing was performed with model bacteria and microbial samples collected from eight environmental sites, including soil and seawater. Gel beads enabled multiple lysis treatments. The genome coverage with model bacteria was improved by 9.1–25%. A total of 734 single amplified genomes were collected from the diverse environmental samples, and almost full-length 16S rRNA genes were recovered from 57.8% of them. We also revealed two marine Rhodobacter strains harboring nearly identical 16S rRNA genes but having different genome contents. In addition, searching for viral sequences elucidated the virus-host linkage over the sampling sites, revealing the geographic distribution and diverse host range of viruses.
UR - http://hdl.handle.net/10754/681974
UR - https://www.nature.com/articles/s43705-022-00179-4
U2 - 10.1038/s43705-022-00179-4
DO - 10.1038/s43705-022-00179-4
M3 - Article
SN - 2730-6151
VL - 2
JO - ISME Communications
JF - ISME Communications
IS - 1
ER -