Here, the complete genome sequence of sponge-associated Tenacibaculum mesophilum DSM 13764T is presented. T. mesophilum is a close relative of the fish pathogen T. maritimum, which causes significant fish disease outbreaks in aquaculture facilities. The T. mesophilum genome sequence will serve as an important resource for comparative genomics approaches.
ABSTRACT
Here, the complete genome sequence of sponge-associated Tenacibaculum mesophilum DSM 13764T is presented. T. mesophilum is a close relative of the fish pathogen T. maritimum, which causes significant fish disease outbreaks in aquaculture facilities. The T. mesophilum genome sequence will serve as an important resource for comparative genomics approaches.
ANNOUNCEMENT
Tenacibaculum species have often been found in association with marine hosts (1), such as fish and their eggs (e.g., Tenacibaculum soleae and Tenacibaculum ovolyticum) (1, 2), sponges (Tenacibaculum mesophilum) (1), and algae (Tenacibaculum amylolyticum) (1). It has also been reported that Tenacibaculum maritimum is the etiological agent of tenacibaculosis (3, 4), a common fish disease that causes great economic loss in aquaculture facilities around the world. T. mesophilum is a close relative of T. maritimum, and the genome sequence of T. mesophilum will be an important resource for comparative genomics with other Tenacibaculum species, in particular with T. maritimum. T. mesophilum DSM 13764T (isolated from the sponge Halichondria okadai, collected in Numazu, Japan [1]) was obtained from DSMZ (Braunschweig, Germany) and grown in marine broth (BD Difco). Genomic DNA was prepared using two rounds of phenol-chloroform purification (modified according to Sambrook et al. [5]). A total of 10 μg of prepared genomic DNA was purified with AMPure XP magnetic beads, quality checked with a NanoDrop instrument and a Qubit fluorometer (Invitrogen, Carlsbad, CA, USA), and subsequently used for construction of PacBio RS II single-molecule and Illumina MiSeq paired-end (251 × 251-bp) libraries according to the manufacturer’s instructions. PacBio sequencing generated 79,714 reads with a total of 782,889,938 bases. Raw PacBio sequencing reads were corrected, trimmed, and de novo assembled into a single contig using default parameters in Canu 1.8 (6). MiSeq paired-end reads were used for further error correction using Pilon version 1.22 (7). As an initial quality check step of the assembly, RNAmmer version 1.2 (8) was used to annotate and verify the RNA genes. In addition, CheckM version 1.07 (9) was used to assess genome completeness and percent contamination and to find missing single-copy marker genes. The GenBank annotation of the genome was generated by the NCBI Prokaryotic Genome Annotation Pipeline (annotation software revision 4.6). The Pilon-polished assembly of T. mesophilum DSM 13764T yielded a single contig for a total length of 3,358,580 base pairs, with a G+C content of 31.8% and an average coverage of 223× across the genome. A second assembly approach using the SMRT Analysis software (via HGAP4 [10]) with default settings, except that the estimated genome size was set as 3.44 Mb according to the T. maritimum genome available (11), resulted in a highly similar scaffold but remained unclosed, as one repeat region was not fully resolved by HGAP4. Pilon made corrections in 17 different locations of the Canu-assembled genome. The genome has an estimated completeness of 100% and contamination of 0.61% based on 457 marker genes conserved in Flavobacteriaceae, as identified by CheckM. No plasmid was identified. The Canu-assembled genome contained 3,053 genes, of which 75 were RNAs (15 rRNA, 55 tRNA, and 5 noncoding RNA [ncRNA] genes). The central metabolism of T. mesophilum DSM 13764T is similar to that of T. maritimum, whose metabolic potential has been previously reported (11). A comparative analysis with other Tenacibaculum species will further help us to understand the ecological role of Tenacibaculum species in the marine environment and their contribution to fish disease.
Data availability.
This whole-genome shotgun project has been deposited in GenBank under the accession numbers CP045192 (Canu assembly) and CP032544 (HGAP4 assembly). The version of the described Canu assembly in this paper is the first version, CP045192.1. PacBio RS II raw data are available under SRA accession number SRR9020974, and Illumina MiSeq raw data are available under SRA accession number SRR9020973.
ACKNOWLEDGMENTS
We thank Daniela Moses at SCELSE Singapore for performing the PacBio sequencing and Amit Anand and Muhammad Khairillah Bin Nanwi at TLL Biocomputing for bioinformatics support.
This work was funded by Temasek Life Sciences Laboratory.
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Associated Data
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Data Availability Statement
This whole-genome shotgun project has been deposited in GenBank under the accession numbers CP045192 (Canu assembly) and CP032544 (HGAP4 assembly). The version of the described Canu assembly in this paper is the first version, CP045192.1. PacBio RS II raw data are available under SRA accession number SRR9020974, and Illumina MiSeq raw data are available under SRA accession number SRR9020973.