Skip to main content
Genome Announcements logoLink to Genome Announcements
. 2017 Jul 6;5(27):e00081-17. doi: 10.1128/genomeA.00081-17

Complete Genome Sequence of the Lytic Giant Bacteriophage pT24 Infecting Tenacibaculum spp., Isolated from a Shrimp Culture Pond

Ho Viet Khoa a, Yuki Midorikawa a, Tsubasa Uchino a, Toshihiro Nakai b, Goshi Kato a, Hidehiro Kondo a, Ikuo Hirono a, Matthura Labaiden c, Sataporn Direkbusarakom c, Motohiko Sano a,
PMCID: PMC5502841  PMID: 28684560

ABSTRACT

The lytic bacteriophage pT24, which infects Tenacibaculum spp., was isolated from the water of a whiteleg shrimp (Litopenaeus vannamei) culture pond in Thailand. This giant bacteriophage with myovirus morphology comprised 234,670 bp with 296 predicted genes.

GENOME ANNOUNCEMENT

The genus Tenacibaculum is a member of the family Flavobacteriaceae and is an abundant and important component of marine bacterial ecosystems (13). We isolated Tenacibaculum sp. T24—a Gram-negative, aerobic, gliding motile, long-rod bacterium that produces yellow pigment—from the water of a whiteleg shrimp (Litopenaeus vannamei) culture pond in Thailand. The lytic bacteriophage pT24 with myovirus morphology was isolated from the water of a shrimp-rearing pond in Thailand by screening on T24. Here, we report the complete genome sequence of phage pT24, which can infect the species T. mesophilum and T. discolor.

DNA of the phage was sequenced with the Illumina MiSeq platform using the Nextera XT library preparation kit and the MiSeq version 3 reagent kit (600 cycles). The sequence reads were imported into CLC Genomics Workbench version 9 (CLC bio) and de novo assembled. The obtained linear DNA sequences were confirmed by PCR, with a primer set designed at both ends of the sequence, followed by Sanger sequencing. The coding sequences (CDSs) were predicted by GeneMarkS (4), followed by annotation using Blast2GO (5); tRNAs were found using tRNAscan-SE version 2.0 (6).

In total, 1,182,866 reads were generated (1,290× coverage of the genome), and their average length was 255.84 bp. Phage pT24 had 234,670 bp of linear genomic DNA with a GC content of 28.85% and 4 tRNAs identified. A total of 296 CDSs were predicted, and among the 41 annotated genes were those encoding for DNA ligase, DNA helicase, DNA polymerase, large terminase protein, ribonucleotide reductase, DNA topoisomerase, RNA ligase, and thymidylate synthase. Twenty of the 41 annotated proteins revealed similarities to those of the “giant phage” Sphingomonas phage PAU (GenBank accession no. NC_019521) (7) at 42.9 to 59.7% identity.

This is the first report of a Tenacibaculum phage genome sequence. This newly sequenced genome information will be useful for studies on the dynamics of phage-infecting environmental bacteria in shrimp culture ponds and on the interactions between phages and their hosts, as well as to clarify the impact of lytic phages on the microbial community structure in the pond.

Accession number(s).

The complete genome sequence of bacteriophage pT24 was submitted to DDBJ/GenBank under the accession number LC168164.

ACKNOWLEDGMENTS

This work was supported in part by a grant from the Japan Science and Technology Agency/Japan International Cooperation Agency, Science and Technology Research Partnership for Sustainable Development (JST/JICA, SATREPS), and by JSPS KAKENHI grant 26660170.

Footnotes

Citation Khoa HV, Midorikawa Y, Uchino T, Nakai T, Kato G, Kondo H, Hirono I, Labaiden M, Direkbusarakom S, Sano M. 2017. Complete genome sequence of the lytic giant bacteriophage pT24 infecting Tenacibaculum spp., isolated from a shrimp culture pond. Genome Announc 5:e00081-17. https://doi.org/10.1128/genomeA.00081-17.

REFERENCES

  • 1.Kirchman DL. 2002. The ecology of CytophagaFlavobacteria in aquatic environments. FEMS Microbiol Ecol 39:91–100. doi: 10.1111/j.1574-6941.2002.tb00910.x. [DOI] [PubMed] [Google Scholar]
  • 2.Habib C, Houel A, Lunazzi A, Bernardet JF, Olsen AB, Nilsen H, Toranzo AE, Castro N, Nicolas P, Duchaud E. 2014. Multilocus sequence analysis of the marine bacterial genus Tenacibaculum suggests parallel evolution of fish pathogenicity and endemic colonization of aquaculture systems. Appl Environ Microbiol 80:5503–5514. doi: 10.1128/AEM.01177-14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Suzuki M, Nakagawa Y, Harayama S, Yamamoto S. 2001. Phylogenetic analysis and taxonomic study of marine Cytophaga-like bacteria: proposal for Tenacibaculum gen. nov. with Tenacibaculum maritimum comb. nov. and Tenacibaculum ovolyticum comb. nov., and description of Tenacibaculum mesophilum sp. nov. and Tenacibaculum amylolyticum sp. nov. Int J Syst Evol Microbiol 51:1639–1652. doi: 10.1099/00207713-51-5-1639. [DOI] [PubMed] [Google Scholar]
  • 4.Besemer J, Borodovsky M. 2005. GeneMark: Web software for gene finding in prokaryotes, eukaryotes and viruses. Nucleic Acids Res 33:W451–W454. doi: 10.1093/nar/gki487. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. 1990. Basic local alignment search tool. J Mol Biol 215:403–410. doi: 10.1016/S0022-2836(05)80360-2. [DOI] [PubMed] [Google Scholar]
  • 6.Lowe TM, Eddy SR. 1997. TRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res 25:955–964. doi: 10.1093/nar/25.5.955. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Ackermann HW, Auclair P, Basavarajappa S, Konjin HP, Savanurmath C. 1994. Bacteriophages from Bombyx mori. Arch Virol 137:185–190. doi: 10.1007/BF01311186. [DOI] [PubMed] [Google Scholar]

Articles from Genome Announcements are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES