Abstract
Here, we report the draft genome sequence of radiation-resistant Rhodococcus erythropolis strain P27, isolated from leaves of Deschampsia antarctica Desv. (Poaceae) in the Admiralty Bay area, Antarctica.
GENOME ANNOUNCEMENT
It is becoming increasingly clear that global warming influences the climate and affects living beings in many ways (1). This global phenomenon also affects the ozone layer (2). The resulting depletion of the ozone layer usually leads to deleterious effects, mainly due to high UV incidence, which may pose a special threat for organisms living in Antarctica. In our survey of the epiphytic bacteria associated with Deschampsia antarctica Desv. (Poaceae), one of only two native flowering plants occurring throughout maritime Antarctica, we recovered an actinomycete isolate moderately to highly resistant to gamma rays and UVC radiation.
Members of the Rhodococcus genus have been intensively studied owing to their ability to survive under extreme conditions (3, 4), and these bacteria seem to be interesting targets for screening radiation-resistant genes (5). Furthermore, although many investigations have demonstrated the resistance of Rhodococcus bacteria to UVC exposure, there is a lack of information on their resistance to gamma radiation. To gain insight into the genes related to the resistance to ionizing and nonionizing radiation of strain P27, we performed whole-genome sequencing using the Ion Torrent (PGM) platform.
Sequencing was carried out on the Ion 316 chip provided in the Ion sequencing kit 200 v.2.0, following the manufacturer’s protocol. The genome sequence was de novo assembled using the MIRA v.3.4, CLC Genomics Workbench v.5.5.1, and SeqMan NGen v.4.0.0 packages, and the obtained contigs were integrated by using CISA (6). The taxonomic position of strain P27 was further evaluated by using the JSpecies package (7).
The total number of reads (>Q20) generated using R. erythropolis PR4 (GenBank accession no. AP008957.1) as a reference was 2,972,204, which were allocated into 60 contigs with 85.3× coverage and a mean length of 123.25 bp. The assembled data were analyzed by RAST annotation (8), and the genome size was found to be 6,262,348 bp, comprising 6,852 open reading frames (ORFs). The G+C content was estimated to be 62.4 mol%. The genome contains 78 copies of 12 genes annotated as DNA repair mechanisms usually associated with radiation resistance, mainly DNA repair base excision and DNA repair bacterial recBCD and recFOR pathways. 16S rRNA gene analysis revealed that strain P27 (CMAA 1247) shares high identity with the type strain of Rhodococcus erythropolis (9). The average nucleotide identity (ANI) of P27 and its phylogenetically closely related neighbor was 98.5%, suggesting that P27 is a member of the R. erythropolis species.
Nucleotide sequence accession numbers.
The R. erythropolis strain P27 genome sequence and annotation data have been deposited at DDBJ/EMBL/GenBank under the accession number AVCO00000000. The version described in this paper is version AVCO01000000.
ACKNOWLEDGMENTS
We are grateful to PROANTAR and FAPESP for providing the funding for developing this research.
Footnotes
Citation Gouvêa Taketani R, Domingues Zucchi T, Soares de Melo I, Mendes R. 2013. Whole-genome shotgun sequencing of Rhodococcus erythropolis strain P27, a highly radiation-resistant actinomycete from Antarctica. Genome Announc. 1(5):e00763-13. doi:10.1128/genomeA.00763-13.
REFERENCES
- 1. Hughes I. 2000. Biological consequences of global warming: is the signal already apparent? Trends Ecol. Evol. 15:56–61 [DOI] [PubMed] [Google Scholar]
- 2. Steig EJ. 2012. Climage change: brief but warm Antarctic summer. Nature 489:39–40 [DOI] [PubMed] [Google Scholar]
- 3. Bej AK, Saul D, Aislabie J. 2000. Cold-tolerant alkane-degrading Rhodococcus species from Antarctica. Polar Biol. 23:100–105 [Google Scholar]
- 4. Burchell MJ, Mann JR, Bunch AW. 2004. Survival of bacteria and spores under extreme shock pressures. Mon. Not. R. Astron. Soc. 352:1273–1278 [Google Scholar]
- 5. Santos SC, Alviano DS, Alviano CS, Goulart FR, de Pádula M, Leitão AC, Martins OB, Ribeiro CM, Sassaki MY, Matta CP, Bevilaqua J, Sebastián GV, Seldin L. 2007. Comparative studies of phenotypic and genetic characteristics between two desulfurizing isolates of Rhodococcus erythropolis and the well-characterized R. erythropolis strain IGTS8. J. Ind. Microbiol. Biotechnol. 34:423–431 [DOI] [PubMed] [Google Scholar]
- 6. Lin SH, Liao YC. 2013. CISA: contig integrator for sequence assembly of bacterial genomes. PLOS One 8:e60843 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Richter M, Rosselló-Móra R. 2009. Shifting the genomic gold standard for the prokaryotic species definition. Proc. Natl. Acad. Sci. U. S. A. 106:19126–19131 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8. 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] [PMC free article] [PubMed] [Google Scholar]
- 9. Goodfellow M, Alderson G. 1977. The actinomycete-genus Rhodococcus: a home for the “rhodochrous” complex. J. Gen. Microbiol. 100:99–122 [DOI] [PubMed] [Google Scholar]