Draft genome sequence of Halomonas meridiana R1t3 isolated from the surface microbiota of the Caribbean Elkhorn coral Acropora palmata
© Meyer et al. 2015
Received: 8 May 2015
Accepted: 28 September 2015
Published: 7 October 2015
Members of the gammaproteobacterial genus Halomonas are common in marine environments. Halomonas and other members of the Oceanospirillales have recently been identified as prominent members of the surface microbiota of reef-building corals. Halomonas meridiana strain R1t3 was isolated from the surface mucus layer of the scleractinian coral Acropora palmata in 2005 from the Florida Keys. This strain was chosen for genome sequencing to provide insight into the role of commensal heterotrophic bacteria in the coral holobiont. The draft genome consists of 290 scaffolds, totaling 3.5 Mbp in length and contains 3397 protein-coding genes.
As the name denotes, the first isolated members of the genus Halomonas were acquired from saline environments, and members of this halotolerant genus are increasingly isolated from a wide variety of marine environments. While the type species of Halomonas meridiana was isolated from an Antarctic saline lake , several strains of this species have been isolated from Acropora corals, including strain R001 from Palk Bay, India  and strains R1t3 and R1t4 from A. palmata in the Florida Keys . Halomonas spp. have also been identified in surveys of uncultured bacteria in the surface microbiota of Acropora corals from the Caribbean and Indonesia , while the microbiota of A. millepora corals from the Great Barrier Reef are more commonly dominated by members of another genus in the order Oceanospirillales , Endozoicomonas . Members of the Oceanospirillales are increasingly identified as important components of the stable, commensal coral microbiota, and the loss of commensal bacteria is often correlated with disease symptoms [6–8].
Coral-associated commensal bacteria may inhibit pathogens from colonizing the carbon-rich coral mucus layer by outcompeting non-commensals or through the active production of antimicrobial compounds, as previously demonstrated in Halomonas strain R1t4 . We chose H. meridiana strain R1t3 for whole genome sequencing as a representative coral commensal bacterium from Acropora corals. To date, only one other coral commensal bacterial strain has been sequenced: Endozoicomonas montiporae from the encrusting pore coral, Montipora aequituberculata , isolated from Taiwan .
Classification and features
While the strain was originally isolated using sterile coral mucus as a growth substrate , subsequent growth in both marine broth and Luria broth have been successful. H. meridiana strain R1t3 is aerobic, heterotrophic, and utilizes a wide range of carbon sources, including D-galatonic acid γ-lactone, D-galacturonic acid, D-glucosaminic acid, γ-hydroxybutyric acid, itaconic acid, glycyl-L-glutamic acid, L-phenylalanine, L-serine, L-threonine, phenylethylamine, α-cyclodextrin, Tween 80, N-acetyl-D-glucosamine, D-cellobiose, i-erythritol, α-D-lactose, D-mannitol, putrescine, D,L-α-glycerol phosphate, glucose-1-phosphate, glycogen, Tween 40, and L-asparagine . The carbon sources utilized by the type strains of H. meridiana and H. aquamarina have been previously documented using Biolog GN2 plates  and carbon sources utilized by Halomonas strain R1t3 (33E7) have been previously documented using Biolog Ecoplates . Of the 23 substrates in common between the two types of Biolog plates, strain R1t3 can use 12 more substrates than H. meridiana and 16 more substrates than H. aquamarina (see Additional file 1).
Classification and general features of Halomonas meridiana strain R1t3 
Species Halomonas meridiana
pH range; Optimum
Coral, Marine host
2–10 % NaCl (w/v)
Looe Key Reef, Florida
24° 40′ 48″ N
81° 14′ 24″ W
Halomonas strain R1t3 was isolated from the surface mucus layer of the scleractinian coral Acropora palmata Lamarck 1816 (commonly known as Elkhorn Coral), from the Florida Keys National Marine Sanctuary (Table 1). A. palmata historically dominated shallow Caribbean reefs, but is currently listed as Critically Endangered on the IUCN Red List of Threatened Species due to extensive losses from white-band disease, climate change, and human-related impacts .
Genome sequencing information
Genome project history
Genome sequencing project information
Illumina DNA-seq, PE library (~350 bp insert size)
Gene calling method
IMG: DOE-JGI Genome Annotation Pipeline, NCBI Prokaryotic Genome Annotation Pipeline
IMG: Halo, NCBI: VE30
GenBank Date of Release
04 March 2015
Source Material Identifier
Growth conditions and genomic DNA preparation
A culture of Halomonas meridiana R1t3 (National Center for Marine Algae & Microbiota, Bigelow Laboratory for Ocean Sciences, Accession # NCMA B79) was grown from a single colony at room temperature in 5 ml of Difco™ Marine Broth 2216 for 48 h. Cells were separated from the culture medium using microcentrifugation (12,000 rpm for 5 min) and genomic DNA (gDNA) was extracted from the pelleted cells with a Qiagen AllPrep DNA/RNA Micro Kit (Germantown, MD). The quality of the extracted gDNA was assessed by visualization on a 1 % agarose gel stained with ethidium bromide and with a BioAnalyzer DNA chip, then sent to the University of Maryland Institute for Bioscience and Biotechnology Research for library preparation and sequencing.
Genome sequencing and assembly
A genomic library was prepared with a TruSeq DNA Sample Preparation Kit (Illumina, San Diego, CA) and sequenced on an Illumina HiSeq with the high-output, 100-bp paired-end protocol at the University of Maryland Institute for Bioscience and Biotechnology Research. The average insert size was 337 bp with a DNA concentration of 192 nM. Sequencing reads were quality-filtered by trimming adaptors with cutadapt  and filtering reads for a minimum quality score of 30, minimum length of 100 bp, and discarding all sequences with ambiguous base calls using Sickle . The unassembled, quality-filtered reads (41,481,885 read pairs) are publicly available through the NCBI Sequence Read Archive (SRA) under the accession number SRX800904. Quality-filtered reads were interlaced with the shuffleSequences_fastq.pl script from velvet  and assembled with IDBA-UD  with k-mer sizes of 60, 70, and 80. This assembly yielded 290 contigs greater than 150 bp, a maximum contig length of 173,110 bp, and a total assembly length of 3.5 Mbp. The estimated Illumina sequencing coverage is 23×. To evaluate the quality of the assembly, unassembled reads were mapped to the 290 assembled contigs with bowtie2  and alignment statistics were recovered with samtools . The overall alignment rate was 99.9 %. The coverage of the genome was further assessed from the unassembled reads using nonpareil , which gave an estimated coverage of 100 %, indicating the sequencing effort was more than sufficient to capture all of the genome (4.2 Gbp actual effort, compared to 150 Mbp estimated required effort). Whole genome alignment of the draft genome sequences of Halomonas strain R1t3 and Endozoicomonas montiporae strain LMG 24815 was performed with Mauve v2.4 .
The draft genome assembly was submitted to IMG-ER  for annotation (Taxon ID 2588254266, publicly available) and discussion of genome content here is restricted to the IMG annotation. The 130 contigs greater than 500 bp were also submitted to GenBank (JZEM00000000) and annotated through the NCBI Prokaryotic Genome Annotation Pipeline. Locus tags in IMG are prefaced by “Halo” while locus tags in GenBank are prefaced by “VE30”.
Genome statistics based on the IMG Annotation Pipeline
% of Total
Genome size (bp)
DNA coding (bp)
DNA G + C (bp)
Protein coding genes
Genes in internal clusters
Genes with function prediction
Genes assigned to COGs
Genes with Pfam domains
Genes with signal peptides
Genes with transmembrane helices
Number of genes associated with general COG functional categories, based on the IMG Annotation Pipeline
Translation, ribosomal structure and biogenesis
RNA processing and modification
Replication, recombination and repair
Chromatin structure and dynamics
Cell cycle control, Cell division, chromosome partitioning
Signal transduction mechanisms
Cell wall/membrane biogenesis
Intracellular trafficking and secretion
Posttranslational modification, protein turnover, chaperones
Energy production and conversion
Carbohydrate transport and metabolism
Amino acid transport and metabolism
Nucleotide transport and metabolism
Coenzyme transport and metabolism
Lipid transport and metabolism
Inorganic ion transport and metabolism
Secondary metabolites biosynthesis, transport and catabolism
General function prediction only
Not in COGs
Insights from the genome sequence
Like other members of the Halomonadaceae , strain R1t3 exhibits tolerance to a wide range of salinities that is likely mediated through the production of osmoprotectants, such as glycine betaine. Strain R1t3 has homologues of the two genes needed to produce glycine betaine. These genes, choline dehydrogenase (Halo_00078/VE30_01315) and betaine aldehyde dehydrogenase (Halo_00077/VE30_01310) are part of a operon and are preceded by a choline ABC transporter periplasmic binding protein (Halo_00075/VE30_01300) and a TetR-family transcriptional regulator (Halo_00076/VE30_01305). The genome of strain R1t3 also contains a biosynthetic cluster (ectABC) for the production of the cyclic amino acid osmolyte, ectoine (Halo_01324/01325/01326, VE30_07080/07085/07090) as well as ectoine utilization genes eutED (Halo_01398/01399, VE30_04620/04625).
The genome of strain R1t3 reflects its ability to utilize a wide range of carbon sources, including gene homologues for six different glycoside hydrolases (GH), used for breaking down complex carbohydrates. Four belong to GH family 13 (Halo_01730/VE30_08480, Halo_01736/VE30_08510, Halo_02655/VE30_13740, Halo_02891/VE30_RS10055), used for the breakdown of starch and glycogen. Single genes encode for GH family 3 (Halo_00185/VE30_02710) and GH32 (Halo_01720/VE30_08435) glycosidases, which act on oligosaccharides and fructan, respectively. The genome of strain R1t3 also contains homologues of genes required for glycerol transport across the membrane (glpSTPQV) (Halo_00080/00081/00082/00083/00085. VE30_01325/01330/01335/01340/01350) and glycerol degradation (glpAD) (Halo_00086/VE30_01355). The efficient use of multiple sources of carbon may be mediated through the widely conserved csrA carbon storage regulator (Halo_02194/VE30_11745) that is present in the genome.
Previous work examining the utilization of coral mucus as a carbon source in this strain demonstrated that glucose and galactose are preferred carbon sources for strain R1t3 . The addition of glucose to media containing high-molecular-weight components of coral mucus repressed the enzymatic activity of α-D-fucopyranosidase and the addition of galactose repressed α-L-galactopyranosidase activity. This catabolite repression is likely effected through the tctE/D two-component system (Halo_03014/VE30_14870, Halo_03015/VE30_14875) and tctCBA tricarboxylate transport membrane protein (Halo_03016/03017/03018, VE30_14880/14885/14890) encoded in the genome.
Overall, the average nucleotide identity (ANI) between the IMG annotated draft genomes of H. meridiana strain R1t3 (3.5 Mbp) and Endozoicomonas montiporae LMG 24815 (5.6 Mbp) was 68.64 %. Orthologs shared between the two genomes were identified using a minimum of 60 % sequence identity and 70 % coverage. Despite the similarity of the ecological niches filled by these two Oceanospirillales bacteria, only 11 % of the genes in Halomonas strain R1t3 (392 genes) have orthologs in the Endozoicomonas genome. Reducing the threshold to 30 % sequence similarity only increased the total proportion of orthologs to roughly 12.5 % (442 genes). Of the orthologs with at least 30 % sequence identity, three of the four starch/glycogen-degrading glycoside hydrolases and the single oligosaccharide-degrading GH in Halomonas had orthologs in Endozoicomonas .
The draft genome sequence of Halomonas meridiana strain R1t3 provides insight for the role of a representative strain of the commensal bacterial community associated with the surface mucus layer of an Acropora coral. Strain R1t3 can utilize a wide range of carbon sources, as demonstrated in culture and supported by genome content.
This research was supported by Protect Our Reefs grant 2013–2 and a George E. Burch Fellowship in Theoretical Medicine. This is a contribution #998 of the Smithsonian Marine Station.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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