TY - JOUR
T1 - Targeted single-cell genomics reveals novel host adaptation strategies of the symbiotic bacteria Endozoicomonas in Acropora tenuis coral
AU - Ide, Keigo
AU - Nishikawa, Yohei
AU - Maruyama, Toru
AU - Tsukada, Yuko
AU - Kogawa, Masato
AU - Takeda, Hiroki
AU - Ito, Haruka
AU - Wagatsuma, Ryota
AU - Miyaoka, Rimi
AU - Nakano, Yoshikatsu
AU - Kinjo, Koji
AU - Ito, Michihiro
AU - Hosokawa, Masahito
AU - Yura, Kei
AU - Suda, Shoichiro
AU - Takeyama, Haruko
N1 - Funding Information:
This work was supported by the “Construction of the environmental risk mathematical model by the meta-omics analyses of marine unculturable microbes based on single cell genome information” grant (JPMJCR12A4) from JST-CREST and by JSPS KAKENHI grant number JP17H06158.
Funding Information:
We would like to thank Dr. Mitsuo Umezu for CT scan analysis, Naoko Okada for 16S rRNA gene sequencing, and Dr. Hisashi Anbutsu and Eisuke Iwamoto for useful suggestions. The super-computing resource was provided by the Human Genome Center (University of Tokyo). This study was supported by the Collaborative Research of Tropical Biosphere Research Center, University of the Ryukyus.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Background: Endozoicomonas bacteria symbiosis with various marine organisms is hypothesized as a potential indicator of health in corals. Although many amplicon analyses using 16S rRNA gene have suggested the diversity of Endozoicomonas species, genome analysis has been limited due to contamination of host-derived sequences and difficulties in culture and metagenomic analysis. Therefore, the evolutionary and functional potential of individual Endozoicomonas species symbiotic with the same coral species remains unresolved. Results: In this study, we applied a novel single-cell genomics technique using droplet microfluidics to obtain single-cell amplified genomes (SAGs) for uncultured coral-associated Endozoicomonas spp. We obtained seven novel Endozoicomonas genomes and quantitative bacterial composition from Acropora tenuis corals at four sites in Japan. Our quantitative 16S rRNA gene and comparative genomic analysis revealed that these Endozoicomonas spp. belong to different lineages (Clade A and Clade B), with widely varying abundance among individual corals. Furthermore, each Endozoicomonas species possessed various eukaryotic-like genes in clade-specific genes. It was suggested that these eukaryotic-like genes might have a potential ability of different functions in each clade, such as infection of the host coral or suppression of host immune pathways. These Endozoicomonas species may have adopted different host adaptation strategies despite living symbiotically on the same coral. Conclusions: This study suggests that coral-associated Endozoicomonas spp. on the same species of coral have different evolutional strategies and functional potentials in each species and emphasizes the need to analyze the genome of each uncultured strain in future coral-Endozoicomonas relationships studies. [MediaObject not available: see fulltext.]
AB - Background: Endozoicomonas bacteria symbiosis with various marine organisms is hypothesized as a potential indicator of health in corals. Although many amplicon analyses using 16S rRNA gene have suggested the diversity of Endozoicomonas species, genome analysis has been limited due to contamination of host-derived sequences and difficulties in culture and metagenomic analysis. Therefore, the evolutionary and functional potential of individual Endozoicomonas species symbiotic with the same coral species remains unresolved. Results: In this study, we applied a novel single-cell genomics technique using droplet microfluidics to obtain single-cell amplified genomes (SAGs) for uncultured coral-associated Endozoicomonas spp. We obtained seven novel Endozoicomonas genomes and quantitative bacterial composition from Acropora tenuis corals at four sites in Japan. Our quantitative 16S rRNA gene and comparative genomic analysis revealed that these Endozoicomonas spp. belong to different lineages (Clade A and Clade B), with widely varying abundance among individual corals. Furthermore, each Endozoicomonas species possessed various eukaryotic-like genes in clade-specific genes. It was suggested that these eukaryotic-like genes might have a potential ability of different functions in each clade, such as infection of the host coral or suppression of host immune pathways. These Endozoicomonas species may have adopted different host adaptation strategies despite living symbiotically on the same coral. Conclusions: This study suggests that coral-associated Endozoicomonas spp. on the same species of coral have different evolutional strategies and functional potentials in each species and emphasizes the need to analyze the genome of each uncultured strain in future coral-Endozoicomonas relationships studies. [MediaObject not available: see fulltext.]
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U2 - 10.1186/s40168-022-01395-9
DO - 10.1186/s40168-022-01395-9
M3 - Article
C2 - 36503599
AN - SCOPUS:85143743829
SN - 2049-2618
VL - 10
JO - Microbiome
JF - Microbiome
IS - 1
M1 - 220
ER -