Genome sequence of a commensal bacterium, Enterococcus faecalis CBA7120, isolated from a Korean fecal sample

Enterococcus faecalis CBA7120 was isolated from the feces of an 81-year-old healthy female living in the Republic of Korea and cultivated on modified Eggerth–Gagnon (EG) medium [containing per liter of distilled water: peptone 10 g, Na₂HPO₄ 4 g, porcine gastric mucin 2 g, sheep blood 50 ml, agar 15 g] at 37 °C for 24 h in an anaerobic chamber (Coy Laboratory Products). Once a pure culture was obtained, strain CBA7120 was preserved at −80 °C in a suspension of 20% glycerol for long-term storage. Genomic DNA for sequencing was prepared using QuickGene DNA tissue kit S (Kurabo, Japan) and QIAamp DNA extraction Kits (Qiagen, USA).

A SMRTbell library was constructed according to the Pacific Biosciences protocol “20-kb Template Preparation Using BluePippin Size-selection system (15-kb Size Cutoff)”. The library was sequenced using P6-C4 chemistry on a Pacific Biosciences RS II instrument. The PacBio RS II sequencing system generated 150,292 reads, with an average read length of 8095 bp from one SMRT cell. For the assembly, filtering was performed by Hierarchical Genome Assembly Process (HGAP) version 2 protocol with default parameter. Assembly was performed using the HGAP 2 protocol with default parameters in SMRT Analysis version 2.3 [4]. The assembly was polished with three successive passes through Quiver to reach a final consensus accuracy of >99.988% at 232.798 × coverage. Finally, finished assembly consisted of four contigs. Using RS_Modification_and_Motif_analysis protocol with default parameter in PacBio SMRT analysis pipeline, 4 N6-methyladenine and other six unidentified methylated motifs were identified. Gene prediction was accomplished using Glimmer3 [5] on the Rapid Annotation using Subsystem Technology (RAST; http://​rast.​nmpdr.​org/​) server [6], and gene annotation was performed using the SEED and Clusters of Orthologous Groups (COG; http://​www.​ncbi.​nlm.​nih.​gov/​COG/​) databases [7, 8]. RNAmmer 1.2 [9] and tRNAscan-SE 1.21 [10] were used to identify rRNA and tRNA sequences, respectively.

MLST was performed using the following seven housekeeping genes: glucose-6-phosphate dehydrogenase (gdh), glyceraldehyde-3-phosphate dehydrogenase (gyd), phosphate ATP binding cassette transporter (pstS), glucokinase (gki), shikimate-5-dehydrogenase (aroE), xanthine phosphoribosyltransferase (xpt), and acetyl-CoA acetyltransferase (yiqL) using PubMLST (http://​pubmlst.​org/​efaecalis/​).

Using data in the NCBI genome database (http://​www.​ncbi.​nlm.​nih.​gov/​genome/​), four E. faecalis strains were selected as the closest neighbors of strain CBA7120 (>89% symmetric identity): E. faecalis strain 12107, T13, OG1RF, and T20, and these genomes were used for comparative genomic analysis. The genome of E. faecalis TX0031 also showed high symmetric identity, but it was excluded from further analysis because the genome contains a large number of contigs. For whole-genome comparison, the genomes of strain CBA7120 and the other related strains were aligned using the progressive MAUVE algorithm in the MAUVE multiple genome alignment software 2.4.0 [11]. The OrthoANI algorithm was used to assess overall similarity between two genome sequences [12]. OrthoANI values were obtained and a phylogenetic tree was constructed based on OrthoANI analysis of the E. faecalis strains CBA7120, 12107, T13, OG1RF, and T20 using the orthologous average nucleotide identity tool [12]. Orthologs in the genomes of strain CBA7120 and other related strains were identified using reciprocal best hit (RBH) in the UBLAST program [13]. Pan-genome orthologous groups (POGs) were constructed using the EzBioCloud Comparative Genomics Database (http://​cg.​ezbiocloud.​net/​). For the visualization heat map and the dendrogram based on the gene content (presence or absence) of the genomes of strain CBA7120 and the other four strains, Jaccard coefficients and UPGMA clustering were used to calculate the presence of POGs and genome clustering, respectively. The Venn diagram based on POGs shared between strain CBA7120 and related strains was constructed using the jvenn program [14].

To obtain pure cultures, a single colony of strain CBA7120 was repeatedly transferred to fresh modified EG medium more than three times, and confirmed using electron microscopy (Fig. 1). Genomic DNA of strain CBA7120 was purified using an MG Genomic DNA purification kit (Doctor Protein) and the 16S rRNA gene sequence from the draft genome was used to check for contamination.

General genome features of E. faecalis CBA7120 are shown in Table 1. The genome sequence of strain CBA7120 is 3,134,087 bp in length, with a G + C content of 37.35 mol%, and is comprised of four contigs with an N50 value of 2,922,046 bp. Using BLAST in the NCBI, we found that contig 1, 2 and 4 represented plasmid sequences and contig 3 represented chromosome sequence. The genome contains 3018 coding DNA sequences (CDSs), 60 tRNA genes, and four 16S-23S-5S rRNA operons. The distribution of COGs and SEED subsystems is illustrated in Fig. 2. The most abundant COG categories were G (carbohydrate transport and metabolism), R (general function prediction only), K (transcription), L (replication, recombination and repair), E (amino acid transport and metabolism), J (translation, ribosomal structure and biogenesis), and P (inorganic ion transport and metabolism); the S category (function unknown) was also abundant (Fig. 2a). The SEED subsystems “Carbohydrates”, “Amino Acids and Derivatives”, “Protein Metabolism”, “DNA Metabolism”, “Cell Wall and Capsule”, “Cofactors, Vitamins, Prosthetic Groups, Pigments”, “RNA Metabolism”, and “Nucleosides and Nucleotides” subsystems were most abundant (Fig. 2b).

Enterococcus faecalis CBA7120 was typed with MLST at loci gdh 1, gyd 7, pstS 9, gki 1, aroE 1, xpt 3, and yqiL 1, and was classified as sequence type 5 (ST 5) containing solely strain B343 that was isolated from a chicken product in Spain.

Whole-genome comparison of strain CBA7120 with E. faecalis 12107, T13, OG1RF, and T20 showed that most of the locally collinear blocks (LCBs) are highly homologous between the five assemblies, although the genome of strain CBA7120 contains large gaps in three LCBs (Fig. 3). E. faecalis CBA7120 showed 99.24, 99.55, 99.62 and 99.64% orthoANI values with E. faecalis strains OG1RF, T13, 12107, and T20, respectively. The phylogenetic tree based on orthoANI values for strain CBA7120 and the four reference strains indicated that strain CBA7120 is closely related to the E. faecalis reference strains (Fig. 4a). Based on analysis of the gene presence or absence heat map, strain CBA7120 possesses different POGs from the other four strains. In the dendrogram based on presence of POGs, strain CBA7120 was located as an outgroup to the other E. faecalis strains (Fig. 4b). As shown in Fig. 5, strain CBA7120 and the other four strains share 2341 POGs. The genome of strain CBA7120 contains only 374 POGs as singletons, contained in a single genome. Without the POGs that had no match in the SEED database, most of the 91 POGs identified belong to the “Phages, Prophages, Transposable elements, Plasmids” (20 POGs), “Carbohydrates” (12 POGs), “DNA metabolism” (11 POGs), and “Virulence, Disease and Defense” subsystems (9 POGs).

Based on comparison with the SEED database, 28 CDS were annotated as belonging to the “Virulence, Disease, Defense” category (Table 2). Strain CBA7120 was found to contain genes related to multidrug resistance efflux pumps, such as multidrug resistance efflux pump PmrA, multi antimicrobial extrusion protein, multidrug and toxin extrusion (MATE) family efflux pump YdhE/NorM, and multidrug-efflux transporter.

Genomic analysis based on ortholog analysis may be a powerful comparative genomics tool. Additional study of the virulence factors present in E. faecalis CBA7120 will guide further research on E. faecalis virulence.