ABSTRACT
We present here the complete genome sequences of two newly isolated Pseudoalteromonas tetraodonis and Pseudoalteromonas lipolytica strains, isolated from the gut of the sea cucumber Apostichopus japonicus, to provide a useful means for facilitating the study of antibacterial, bacteriolytic, agarolytic, and algicidal activities of marine Pseudoalteromonas species.
GENOME ANNOUNCEMENT
The genus Pseudoalteromonas belongs to the Gammaproteobacteria class, with 38 recognized species so far. Pseudoalteromonas spp. are heterotrophic Gram-negative flagellated bacteria commonly found in various ocean habitats, including the deep sea, polar sea, and other extreme marine habitats (1–3). Along with these distinct lifestyles, which highlight their diverse roles in marine ecosystems, Pseudoalteromonas species produce biologically active metabolites with antibacterial, bacteriolytic, agarolytic, and algicidal activities (4). Pseudoalteromonas tetraodonis, isolated from puffer fish, secretes the neurotoxin tetrodotoxin (5), and antifouling activities by Pseudoalteromonas lipolytica affect marine invertebrate larval settlement and metamorphosis (6). Here, we report the complete genome sequences of Pseudoalteromonas tetraodonis CSB01KR and Pseudoalteromonas lipolytica CSB02KR strains isolated from the gut of the sea cucumber Apostichopus japonicus (34.1N, 127.18E; Geomun-do, Yeosu, Republic of Korea).
The isolated cells of each strain were harvested in marine broth at room temperature for 1 day, and genomic DNA was extracted using proteinase K digestion and phenol-chloroform extraction. The genomes of these strains were sequenced using the Illumina HiSeq 4000 platform, employing paired-end reads (151 bp × 2) prepared by Accel-NGS 2S PCR-free library kit (Illumina, San Diego, CA, USA), according to the manufacturer’s protocol. A total of 7,155,540 and 7,760,584 raw reads were generated from P. tetraodonis and P. lipolytica, respectively, resulting in 294- and 267-fold coverage of the genomes, respectively. The raw reads were preprocessed and trimmed using the Trimmomatic tool (7), in which reads containing adapter sequences, poly-N sequences, and low-quality bases (below a mean Phred score of 15) were removed. All trimmed reads were de novo assembled using four different genome assemblers, SOAPdenovo2 (8), ABySS version 1.9 (9), Velvet version 1.2 (10), and SPAdes version 3.7 (11), under default parameters with a k-mer range of 33 to 99. Last, qualifying contigs from the four assemblies were integrated using CISA version 1.3 (12). The final assembled contigs were evaluated by QUAST version 4.1 (13). The resulting draft genome for P. tetraodonis CSB01KR consisted of 49 contigs, covering 3,675,392 bp, with 40.3% G+C content and an N50 of 196,947 bp. The draft genome for P. lipolytica CSB02KR also consisted of 49 contigs, covering 4,387,864 bp, with 41.5% G+C content and an N50 of 234,255 bp.
Automatic gene annotation was performed using the program Rapid Annotations using Subsystems Technology (RAST; version 2.0) (14). The annotated P. tetraodonis CSB01KR genome contains 3,567 genes, including 3,479 protein-coding sequences classified in 456 subsystems, 5 5S rRNAs, 5 short subunit (SSU) rRNAs, 3 long subunit (LSU) rRNAs, and 75 tRNAs. In the P. lipolytica CSB02KR genome, 3,984 genes that consist of 3,904 protein-coding sequences classified in 487 subsystems, 2 5S rRNAs, 1 SSU rRNA, 2 LSU rRNAs, and 75 tRNAs were annotated. We believe that the full-genome sequences of the two Pseudoalteromonas strains expand the repertoire of genomic information for the genus Pseudoalteromonas and will provide important insights into their role within microbial communities.
Accession number(s).
The raw data of the two strains have been deposited in the NCBI database under the BioProject accession number PRJNA328511. The assembled draft genomes of P. tetraodonis and P. lipolytica were deposited at GenBank with accession numbers MBMS01000001 to MBMS01000049 and MBSZ01000001 to MBSZ01000049, respectively.
ACKNOWLEDGMENTS
This work was supported by research grants from the Marine Biotechnology Program (PJT200620, Genome Analysis of Marine Organisms and Development of Functional Applications) funded by the Ministry of Oceans and Fisheries of the Republic of Korea, and from the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (NRF-2015R1C1A1A02036896) to C.P. This study was financially supported by Chonnam National University, 2013-2014.
Footnotes
Citation Jo J, Choi H, Lee S-G, Oh J, Lee H-G, Park C. 2017. Draft genome sequences of Pseudoalteromonas tetraodonis CSB01KR and Pseudoalteromonas lipolytica CSB02KR, isolated from the gut of the sea cucumber Apostichopus japonicus. Genome Announc 5:e00627-17. https://doi.org/10.1128/genomeA.00627-17.
REFERENCES
- 1.Baumann L, Baumann P, Mandel M, Allen RD. 1972. Taxonomy of aerobic marine eubacteria. J Bacteriol 110:402–429. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Gauthier G, Gauthier M, Christen R. 1995. Phylogenetic analysis of the genera Alteromonas, Shewanella, and Moritella using genes coding for small-subunit rRNA sequences and division of the genus Alteromonas into two genera, Alteromonas (emended) and Pseudoalteromonas gen. nov., and proposal of twelve new species combinations. Int J Syst Bacteriol 45:755–761. doi: 10.1099/00207713-45-4-755. [DOI] [PubMed] [Google Scholar]
- 3.Holmström C, Kjelleberg S. 1999. Marine Pseudoalteromonas species are associated with higher organisms and produce biologically active extracellular agents. FEMS Microbiol Ecol 30:285–293. [DOI] [PubMed] [Google Scholar]
- 4.Bowman JP. 2007. Bioactive compound synthetic capacity and ecological significance of marine bacterial genus Pseudoalteromonas. Mar Drugs 5:220–241. doi: 10.3390/md504220. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Ivanova EP, Romanenko LA, Matté MH, Matté GR, Lysenko AM, Simidu U, Kita-Tsukamoto K, Sawabe T, Vysotskii MV, Frolova GM, Mikhailov V, Christen R, Colwell RR. 2001. Retrieval of the species Alteromonas tetraodonis Simidu et al. 1990 as Pseudoalteromonas tetraodonis comb. nov. and emendation of description. Int J Syst Evol Microbiol 51:1071–1078. doi: 10.1099/00207713-51-3-1071. [DOI] [PubMed] [Google Scholar]
- 6.Zeng Z, Guo XP, Li B, Wang P, Cai X, Tian X, Zhang S, Yang JL, Wang X. 2015. Characterization of self-generated variants in Pseudoalteromonas lipolytica biofilm with increased antifouling activities. Appl Microbiol Biotechnol 99:10127–10139. doi: 10.1007/s00253-015-6865-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Bolger AM, Lohse M, Usadel B. 2014. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics 30:2114–2120. doi: 10.1093/bioinformatics/btu170. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Luo R, Liu B, Xie Y, Li Z, Huang W, Yuan J, He G, Chen Y, Pan Q, Liu Y, Tang J, Wu G, Zhang H, Shi Y, Liu Y, Yu C, Wang B, Lu Y, Han C, Cheung DW, Yiu SM, Peng S, Xiaoqian Z, Liu G, Liao X, Li Y, Yang H, Wang J, Lam TW, Wang J. 2012. SOAPdenovo2: an empirically improved memory-efficient short-read de novo assembler. Gigascience 1:18. doi: 10.1186/2047-217X-1-18. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Simpson JT, Wong K, Jackman SD, Schein JE, Jones SJ, Birol I. 2009. ABySS: a parallel assembler for short read sequence data. Genome Res 19:1117–1123. doi: 10.1101/gr.089532.108. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Zerbino DR, Birney E. 2008. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res 18:821–829. doi: 10.1101/gr.074492.107. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Bankevich A, Nurk S, Antipov D, Gurevich AA, Dvorkin M, Kulikov AS, Lesin VM, Nikolenko SI, Pham S, Prjibelski AD, Pyshkin AV, Sirotkin AV, Vyahhi N, Tesler G, Alekseyev MA, Pevzner PA. 2012. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J Comput Biol 19:455–477. doi: 10.1089/cmb.2012.0021. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Lin SH, Liao YC. 2013. CISA: contig integrator for sequence assembly of bacterial genomes. PLoS One 8:e60843. doi: 10.1371/journal.pone.0060843. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Gurevich A, Saveliev V, Vyahhi N, Tesler G. 2013. QUAST: quality assessment tool for genome assemblies. Bioinformatics 29:1072–1075. doi: 10.1093/bioinformatics/btt086. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Aziz RK, Bartels D, Best AA, DeJongh M, Disz T, Edwards RA, Formsma K, Gerdes S, Glass EM, Kubal M, Meyer F, Olsen GJ, Olson R, Osterman AL, Overbeek RA, McNeil LK, Paarmann D, Paczian T, Parrello B, Pusch GD, Reich C, Stevens R, Vassieva O, Vonstein V, Wilke A, Zagnitko O. 2008. The RAST server: rapid annotations using subsystems technology. BMC Genomics 9:75. doi: 10.1186/1471-2164-9-75. [DOI] [PMC free article] [PubMed] [Google Scholar]