Draft Genome Sequence of Dietzia sp. Strain UCD-THP (Phylum Actinobacteria)

Here, we present the draft genome sequence of an actinobacterium, Dietzia sp. strain UCD-THP, isolated from a residential toilet handle. The assembly contains 3,915,613 bp. The genome sequences of only two other Dietzia species have been published, those of Dietzia alimentaria and Dietzia cinnamea.

environments, including Korean food (1), a soda lake (2), and a swab sample from a human patient (3). Dietzia spp. are characterized as Gram positive and can be seen as both cocci and rods. Colonies usually appear orange to coral.
Dietzia sp. strain UCD-THP was isolated from a residential toilet handle in Davis, CA, as part of a project to produce builtenvironment reference genomes. Swabs were incubated overnight at 37°C in Luria broth (LB) and plated on LB agar, and colonies were isolated by serial dilution streaking. Single colonies were grown overnight in a mixture of 1% tryptone, 1% NaCl, 0.5% yeast extract, and 0.4% glucose, adjusted to pH 9. One isolate was identified by sequencing the 16S rRNA gene PCR product produced by the 1391R and 27F primers. Cells were lysed by bead beating and freeze-thawing. DNA was extracted with an equal volume of phenol-chloroform and subjected to ethanol precipitation.
Two Illumina paired-end libraries were generated using a TruSeq DNA sample prep v2 kit (Illumina) and a Nextera DNA sample prep kit (Illumina). Fragments of 300 to 600 bp were selected using a Pippin Prep (Sage Science). Libraries were sequenced on an Illumina MiSeq, with a read length of 250 bp, trimmed to 160 bp prior to assembly. This produced a total of 7,104,230 paired-end reads. Quality trimming and error correction of the reads resulted in 6,516,092 high-quality reads. These steps were performed using the A5 assembly pipeline (4). This pipeline automates data cleaning, error correction, contig assembly, and scaffolding. An additional assembly was generated using the CLC Genomics Workbench. The two assemblies were mapped to each other using progressiveMauve (5), and scaffolds from the CLC assembly that were not present in the A5 assembly were removed. The resulting consensus assembly had 141 scaffolds (minimum, 321 bp; maximum, 506,669 bp; N 50 , 157,523 bp). During scaffolding, some contigs were merged based on short overlaps and read-pair information, yielding a final collection of 219 contigs in 141 scaffolds that were submitted to GenBank. This final assembly had 3,915,613 bp, with a GϩC content of 69.5% and a coverage estimate of 266ϫ. Genome completeness was assessed using the PhyloSift software (A. Darling, G. Jospin, E. Lowe, E. Matsen, H. Bik, and J. Eisen, unpublished data), which searches for a list of 40 highly conserved single-copy marker genes (D. Wu, G. Jospin, and J. Eisen, unpublished data), of which all were found in this assembly.
Annotation was performed using the RAST server (6). Dietzia sp. strain UCD-THP contains 3,614 predicted protein-coding sequences and 50 predicted noncoding RNAs. A phylogenetic tree of all available cultured isolates of Dietzia was produced using the Ribosomal Database Project (RDP), which implements a weighted neighbor-joining algorithm (7). Dietzia sp. strain UCD-THP falls within a poorly resolved paraphyletic clade containing 7 species of Dietzia (http://dx.doi.org/10.6084 /m9.figshare.646178). Because the 16S rRNA gene sequence of Dietzia sp. strain UCD-THP has Ͼ99% identity to homologs from several species of cultured isolates, and the phylogenetic relationships among those species are unclear, we have been unable to assign a species name to this isolate.
Nucleotide sequence accession numbers. This Whole-Genome Shotgun project has been deposited at DDBJ/EMBL/ GenBank under the accession no. AOSR00000000. The version described in this paper is the first version, accession no. AOSR01000000. Illumina reads are available at http://dx.doi.org /10.6084/m9.figshare.644656.

ACKNOWLEDGMENTS
Illumina sequencing was performed at the DNA Technologies Core facility in the Genome Center at the UC Davis, Davis, CA. This work was funded by a grant from the Alfred P. Sloan Foundation as part of their program on the Microbiology of the Built Environment.
We thank John Qingyi Zhang for his help with library preparation.