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. 2019 Jul 11;8(28):e00607-19. doi: 10.1128/MRA.00607-19

Complete Genome Sequence of Kocuria indica CE7, Isolated from Human Skin

Kyoung Lee a,, Munkhtsatsral Ganzorig a, Ji Yoon Jung a, Sachin Kumar Badaya b, Jae Yun Lim c
Editor: Steven R Gilld
PMCID: PMC6624770  PMID: 31296687

Here, we report the complete genome sequence of Kocuria indica CE7, isolated from human skin. This strain possesses a 2,809-kbp chromosome and a 32-kbp plasmid with 2,507 coding sequences. In particular, the genome contains multiple genes potentially involved in adaptations in pH homeostasis and salt tolerance.

ABSTRACT

Here, we report the complete genome sequence of Kocuria indica CE7, isolated from human skin. This strain possesses a 2,809-kbp chromosome and a 32-kbp plasmid with 2,507 coding sequences. In particular, the genome contains multiple genes potentially involved in adaptations in pH homeostasis and salt tolerance.

ANNOUNCEMENT

Kocuria indica is a high-GC-content Gram-positive aerobic nonmotile and coccus-type bacterium belonging to the family Micrococcaceae in the phylum Actinobacteria. K. indica NIO-1021T was first isolated from a sediment sample from Chorao Island, India (1). K. indica strain NIO-1021T is known to grow in the presence of 0 to 15% NaCl and in the pH range of 4.0 to 10. In the comparative analysis of 16S rRNA gene sequences, K. indica forms a monophyletic clade with Kocuria marina with 100% bootstrap values compared to 17 other species (1). Two incomplete genome sequences each of K. indica and K. marina are currently available in the NCBI database. Here, we report the complete genome sequence of K. indica CE7, an isolate from human skin.

K. indica CE7 (KCTC 49187) was isolated from the forehead of a male college student using swab sampling and direct streaking onto Difco nutrient agar. The agar medium was incubated for 3 days under aerobic conditions at 28°C. Ethical approval for subject sampling was granted by the institutional review board of Changwon National University. The phenol extraction method (2) was used to extract total DNA from K. indica CE7 cells, which were cultured for 2 days in a shaking incubator (140 rpm) for 48 h at 28°C. The genomic SMRTbell library using a total of 5 μg of purified DNA was constructed with the SMRTbell template prep kit v1.0 (product number 100-259-100) following the manufacturer’s instructions (Pacific Biosciences). The fragments of the template smaller than 20 kbp were removed using the BluePippin size selection system, and the constructed library was validated using an Agilent 2100 bioanalyzer. The SMRTbell library was sequenced using 1 single-molecule real-time (SMRT) cell using C4 chemistry, and 240-minute movies were captured for each SMRT cell using the MagBead OneCellPerWell v1 protocol (Pacific Biosciences) of the PacBio RS II sequencing platform (DNA Link, Seoul, South Korea). De novo assembly was conducted according to the Hierarchical Genome Assembly Process (HGAP) v2.3 workflow, including consensus polishing with Quiver (3). Control filtering (RemoveControlReads.1.xml) and a seed read length of 13,000 bp were used as options for the HGAP workflow. After filtering the subreads, a pool of 1,312,238,763 bp from 168,966 reads with an N50 value of 2,820,133 bp was produced, yielding a 124-fold genome coverage. In order to check if the contigs were circular, bioinformatics programs such as NUCmer and MUMmer v3.5 (4) were used to identify overlapped sequences of both ends for manual genome closure. Gene predictions and annotations were provided by NCBI using the NCBI Prokaryotic Genome Annotation Pipeline (5).

The CE7 assembly consists of a circular chromosome of 2,809,846 bp (68.7% GC content) and a circular plasmid (pCE7) of 32,758 bp (64.5% GC content). The chromosome contains 2,472 coding sequences (CDSs), 3 copies of rRNA genes (5S, 16S, and 23S), 46 coding regions of tRNAs, 2 noncoding RNAs (ncRNAs), and 1 transfer-messenger RNA (tmRNA). Compared to the K. indica NIO-1021T reference genome, the chromosome sequence of K. indica CE7 showed 97.10% (82.82% coverage) average nucleotide identity based on BLAST average nucleotide identity (ANIb), as determined by the JSpeciesWS server (6). The pCE7 plasmid carries 35 CDSs, including 17 hypothetical proteins. Since K. indica has been known to be salt tolerant and grows in a wide range of pH values, the genes related to the niche were sought in the genome. The CE7 genome contains genes encoding two NhaA and one Mrp protein complex for Na+:H+ antiporters, a Ca2+:H+ antiporter, and a cation:H+ antiporter, which are known to play critical roles in alkaline pH homeostasis in cells (7). In addition, the CE7 genome possesses the genes encoding trehalose biosynthesis, the amino acid:cation symporter family proteins, the Na+:solute symporter, and the K+ uptake system, which confer resistance to osmotic stress.

Data availability.

The complete genome sequences of the chromosome and plasmid pCE7 of the K. indica CE7 strain were deposited in GenBank under the accession numbers CP035504 and CP035505, respectively. The raw sequencing data have been deposited in the SRA under the accession number PRJNA517384.

ACKNOWLEDGMENT

This research was financially supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science, and Technology (grant number 2016R1D1A1B01007775).

REFERENCES

  • 1.Dastager SG, Tang SK, Srinivasan K, Lee JC, Li WJ. 2014. Kocuria indica sp. nov., isolated from a sediment sample. Int J Syst Evol Microbiol 64:869–874. doi: 10.1099/ijs.0.052548-0. [DOI] [PubMed] [Google Scholar]
  • 2.Ausubel FM, Brent R, Kingston RE, Moore DD, Seidman JG, Smith JA, Struhl K. 1990. Current protocols in molecular biology. John Wiley and Sons, New York, NY. [Google Scholar]
  • 3.Chin CS, Alexander DH, Marks P, Klammer AA, Drake J, Heiner C, Clum A, Copeland A, Huddleston J, Eichler EE, Turner SW, Korlach J. 2013. Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data. Nat Methods 10:563–569. doi: 10.1038/nmeth.2474. [DOI] [PubMed] [Google Scholar]
  • 4.Kurtz S, Phillippy A, Delcher AL, Smoot M, Shumway M, Antonescu C, Salzberg SL. 2004. Versatile and open software for comparing large genomes. Genome Biol 5:R12. doi: 10.1186/gb-2004-5-2-r12. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Tatusova T, DiCuccio M, Badretdin A, Chetvernin V, Nawrocki EP, Zaslavsky L, Lomsadze A, Pruitt KD, Borodovsky M, Ostell J. 2016. NCBI Prokaryotic Genome Annotation Pipeline. Nucleic Acids Res 44:6614–6624. doi: 10.1093/nar/gkw569. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Richter M, Rosselló-Móra R, Oliver Glöckner F, Peplies J. 2016. JSpeciesWS: a Web server for prokaryotic species circumscription based on pairwise genome comparison. Bioinformatics 32:929–931. doi: 10.1093/bioinformatics/btv681. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Padan E, Bibi E, Ito M, Krulwich TA. 2005. Alkaline pH homeostasis in bacteria: new insights. Biochim Biophys Acta 1717:67–88. doi: 10.1016/j.bbamem.2005.09.010. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The complete genome sequences of the chromosome and plasmid pCE7 of the K. indica CE7 strain were deposited in GenBank under the accession numbers CP035504 and CP035505, respectively. The raw sequencing data have been deposited in the SRA under the accession number PRJNA517384.


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