Objective

Enterococci are Gram-positive lactic acid bacteria with a wide environmental distribution, encompassing many species from a wide variety of ecological niches [1]. Enterococcus faecium is a major nosocomial pathogen often causing neonatal meningitis or endocarditis [2]. However, certain strains of E. faecium have beneficial effects on human health due to their probiotic activity [3]. For example, E. faecium T-110 is a syndicate member in several probiotic products including BIO-THREER which is widely prescribed for human, animal and aquacultural use [3] and E. faecium strain L-3 is the principle organism in the probiotic Laminolact [4]. E. faecium is well known for its ability to produce bacteriocins, but there are relatively few reports in the literature on the genome sequence of E. faecium from non-clinical sources [5, 6] and there are no current NCBI database genome entries for E. faecium isolated from natural water sources.

Data description

Enterococcus faecium SP15 was isolated from spring water in Rawalakot (Azad Kashmir, Pakistan), a site of relative isolation with little waste water contamination. The strain exhibited strong antimicrobial activity against a panel of seven indicator strains, including Listeria monocytogenesis, indicative of enterocin production. E. faecium SP15 genomic DNA was extracted using a GeneJET genomic DNA purification kit (Thermofisher Scientific) as recommended by the vendor and assessed using a NanoDrop ND-1000 spectrophotometer and 0.7% agarose gel electrophoresis. Genome sequencing was performed by MicrobesNG (University of Birmingham, UK) using Illumina MiSeq and HiSeq 2500 platforms (Illumina, UK) with 2 × 250 bp paired-end reads. The reads were trimmed using Trimmomatic version 0.30 [7] and the quality was assessed using in-house scripts combined with BWA-MEM software 0.7.16 [8]. De novo assembly was performed with SPAdes software version 3.9.0 [9] and assembly metrics were calculated using QUAST version 2.0 [10]. Gene prediction and annotation were carried out using the Pathosystems Resources Integration Center (PATRIC) web server [11], RAST version 2.0 [12] and the NCBI, PGAP version 4.6 [13]. The tRNA genes were predicted by tRNA scan-SE 2.0 [14]. Antimicrobial mechanisms (e.g. enterocin production) were explored with BAGEL 3 [15] and anti-SMASH V4 [16]. Virulence factors were identified using the virulence factor database, VFDB [17]. Antibiotic resistance gene were identified using the Comprehensive Antibiotic Resistance Database, CARD [18], and acquired resistance genes were predicted by Resistance Finder 3.0 [19]. Contigs were ordered by alignment against the most closely related sequence in GenBank [20] (E. faecium T110, CP006030; 99% identity) using progressive Mauve version 2.4.0 [21]. Intact and incomplete prophage regions were identified through the integrated search and annotation tool, PHAST [22]. Clustered regularly interspaced short palindromic repeat (CRISPR) arrays were identified using CRISPR finder [23].

The draft genome assembly consisted of 121 contigs with a total size of 2,783,033 bp (Table 1). The genome sequence data was at 30× coverage with an N50 of 102,590 bp and mean GC content 38.08%. A total of 2900 protein-encoding genes were predicted of which 2063 were assigned putative functions while 837 remain hypothetical. A total of 63 tRNA structural genes were identified. BAGLE 3 predicted five bacteriocin biosynthetic gene clusters (enterocin-HF, enterocin-P, enterocin SE-K4, enterocin L50A/L50B and enterolysin). No virulence factors (AS, Ace, Acm, Scm, EfaA, EcbA, Esp, Cyl, GelE and SprE) were detected. Two antibiotic resistance genes aac (6′)-li and msrC (98 and 97% identity, respectively) were identified conferring resistance to aminoglycosides, and macrolides and streptogramin B antibiotics, but no acquired resistance determinants were found. Four prophage loci were predicted of which three were intact (Strept_9871, Lactob_phig1e and Staphy_SPbeta (40, 36.9 and 32.7 kb, respectively) and one incomplete (Salmon_SJ46, 17.4 kb). One CRISPR array was identified of 190 bp, containing three spacers with a highly conserved 24 bp DR region, and although two cas gene clusters (cas3_typeI, cas4_typeI-II) were found, these were not associated with the CRISPR array.

Table 1 Overview of data files
Full size table

Two major replicons are apparent: a chromosome of ~ 2,545,000 bp and a plasmid of ~ 149,300 bp (related to plasmid pNB2354 from E. faecium NRRL-B-2354, CP004064).

Limitations

Current data is based on the draft level genome such that the exact length of the genome, and the number of rRNA genes and repetitive elements, cannot be absolutely determined. Furthermore, the genome includes extrachromosomal elements that cannot be predicted precisely.