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Announcement
8 February 2018

Draft Genome Sequence of Endozoicomonas acroporae Strain Acr-14T, Isolated from Acropora Coral

ABSTRACT

A lacuna exists in our understanding of the genetic makeup of Endozoicomonas bacteria, due to scarcity of genome sequences. We report here the first draft genome sequence of Endozoicomonas acroporae Acr-14, a type strain isolated from the coral Acropora. This sequence will foster an understanding of the genetic makeup and role of hosts in shaping gene repertoires.

GENOME ANNOUNCEMENT

The genus Endozoicomonas belongs to the phylum Proteobacteria, class Gammaproteobacteria, with the type species being Endozoicomonas elysicola (1). Members of this genus form a significant proportion of the bacterial community in diverse marine hosts, including sponges (2), mollusks (1, 35) tubeworms (6), gorgonians (7, 8), and corals (914). Currently, there are only two whole-genome sequences of Endozoicomonas montiporae strains isolated from the Scleractinia coral Montipora aequituberculata (15, 16). Here, we report the first draft genome sequence of strain Acr-14T from the novel species Endozoicomonas acroporae, isolated from Acropora coral off the coast of southern Taiwan. The type strain and taxonomic information have been reported previously (17).
Strain Acr-14T was purified and cultivated as described previously (17), genomic DNA was isolated with the cetyltrimethylammonium bromide (CTAB) method, and the purity of DNA was checked with NanoDrop 1000 (Thermo Scientific, USA). Whole-genome sequencing was performed at the Biodiversity Research Center Academia Sinica (BRCAS) core sequencing facility with a paired-end MiSeq library generated to achieve a 500-bp insert size with an Illumina MiSeq platform. The obtained reads were quality filtered and trimmed (at a Phred score of ≥30) with the NGS QC toolkit (18). Quality-filtered and trimmed reads were de novo assembled using CLC Genomics Workbench version 1.10.1 (Qiagen), with a bubble size of 40, automatic detection of word size enabled, and a minimum contig length of 500 bp (no scaffolding was performed). A total of 309 contigs yielded a genome sequence 6,048,850 bp long, with 448× coverage and a G+C content of 49.16%. The largest contig and N50 value were 161,511 bp and 47,658 bp, respectively. The genome was estimated to be 98.56% complete using CheckM (19).
Open reading frame (ORF) prediction and automatic annotation were performed using the Prokka software (20), with default parameters, obtaining the outputs in GenBank format. The genome contains 5,104 genes, 5,018 coding sequences (CDSs), 79 tRNAs, 5 rRNAs (16S and 5S), and 4 repeat regions.
Furthermore, 5 prophages (2 intact, 2 incomplete, and 1 questionable) were detected in the genome using PHAST (21), and 4 typical clustered regularly interspaced short palindromic repeat (CRISPR) structures were also detected with Prokka (20).
A BLASTn (22) comparison of 16S rRNA obtained after assembly with the NR database gave an identical (100%) match with the already-deposited type strain 16S rRNA (GenBank accession no. LN875493). According to phylogenetic analysis based on 16S rRNA, the closest relative of Acr-14T is Endozoicomonas atrinae WP70T (sequence similarity, 96.7%) (17).

Accession number(s).

This whole-genome shotgun project has been deposited at DDBJ/ENA/GenBank under the accession no. PJPV00000000. The version described in this paper is version PJPV01000000.

ACKNOWLEDGMENTS

K.T. is supported by the Taiwan International Graduate Program for graduate study. This work was supported by the Biodiversity Research Center, Academia Sinica, Taipei, Taiwan, and the National Kaohsiung Marine University, Kaohsiung, Taiwan.

REFERENCES

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Nishijima M, Adachi K, Katsuta A, Shizuri Y, Yamasato K. 2013. Endozoicomonas numazuensis sp. nov., a gammaproteobacterium isolated from marine sponges, and emended description of the genus Endozoicomonas Kurahashi and Yokota 2007. Int J Syst Evol Microbiol 63:709–714.
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Information & Contributors

Information

Published In

cover image Genome Announcements
Genome Announcements
Volume 6Number 68 February 2018
eLocator: 10.1128/genomea.01576-17

History

Received: 20 December 2017
Accepted: 9 January 2018
Published online: 8 February 2018

Contributors

Authors

Kshitij Tandon
Biodiversity Research Center, Academia Sinica, Taipei, Taiwan
Bioinformatics Program, Institute of Information Science, Taiwan International Graduate Program, Academia Sinica, Taipei, Taiwan
Institute of Bioinformatics and Structural Biology, National Tsing Hua University, Hsinchu, Taiwan
Pei-Wen Chiang
Biodiversity Research Center, Academia Sinica, Taipei, Taiwan
Wen-Ming Chen
Laboratory of Microbiology, Department of Seafood Science, National Kaohsiung Marine University, Nantzu, Kaohsiung City, Taiwan
Sen-Lin Tang
Biodiversity Research Center, Academia Sinica, Taipei, Taiwan

Notes

Address correspondence to Sen-Lin Tang, [email protected].

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