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. 2016 Nov 18;15:44–45. doi: 10.1016/j.nmni.2016.11.012

Draft genome sequence of a human-associated isolate of Haloferax alexandrinus strain Arc-hr, an extremely halophilic archaea

S Khelaifia 1,2,, A Caputo 1, F Djossou 3, D Raoult 1,2
PMCID: PMC5167240  PMID: 28018603

Abstract

We report the draft genome sequence of Haloferax alexandrinus strain Arc-hr (CSUR P798), isolated from the human gut of a 10-year-old Amazonian individual. Its 3 893 626 bp genome exhibits a 66.00% GC content. The genome of the strain Arc-hr contains 37 genes identified as ORFans, seven genes associated to halocin and 11 genes associated with polyketide synthases or nonribosomal peptide synthetases.

Keywords: Culturomics, genome sequence, genomics, Haloferax alexandrinus, halophilic archaea


Haloferax alexandrinus is an extremely halophilic archaea initially isolated from a solar saltern in Alexandria, Egypt. This Gram-negative halophilic archaea is highly pleomorphic, nonmotile and strictly aerobic, and it requires at least 10 g/L NaCl for growth [1]. Interestingly, DNA related to halophilic archaea from Halorubrum and Halobacterium genera was detected by PCR in colon mucous biopsy samples collected from patients with inflammatory bowel disease [2], but no isolate was made from any of these specimens. Recently we reported the first isolation of H. alexandrinus strain Arc-hr (Collection de Souches de l'Unité des Rickettsies (CSUR) P798) from a human stool specimen as part of a culturomics study of intestinal microflora of a 10-year-old Amazonian individual using media containing high salt concentrations [3]. H. alexandrinus strain Arc-hr is a Gram-negative archaeon, highly pleomorphic and strictly aerobic, with optimal growth observed at 37°C, pH 7.5 and 100 g/L NaCl. Sequencing the 16S ribosomal DNA confirmed the affiliation of the strain Arc-hr (GenBank accession no. HG931927) to the genus Haloferax and yielded a 99.9% sequence similarity with the reference H. alexandrinus JCM 10717T (GenBank accession no. NR_113438). Strain Arc-hr therefore represents the first H. alexandrinus isolate cultured from the human gut.

The complete genome of H. alexandrinus strain Arc-hr was sequenced on the MiSeq Technology (Illumina, San Diego, CA, USA) with the mate-pair strategy as previously described [4]. Open reading frames (ORFs) were predicted using Prodigal [5] with default parameters, but the predicted ORFs were excluded if they spanned a sequencing gap region (containing N) [6]. Noncoding genes and miscellaneous features were predicted using RNAmmer [7], ARAGORN [8], Rfam [9], PFAM [10] and Infernal [11]. Coding DNA sequences were predicted using Prodigal [5], and functional annotation was achieved using BLAST+ [6] and HMMER3 [12] against the UniProtKB database [13].

The genome the strain Arc-hr is 3 893 626 bp long with 66.00% GC content. It is composed of one scaffold (composed of five contigs); of the 3770 predicted genes, 3679 were protein-coding genes and 58 were RNAs (two genes are 5S rRNA, three genes are 16S rRNA, two genes are 23S rRNA and 51 genes are tRNA genes). A total of 2019 genes (65.38%) were assigned a putative function. The remaining genes were annotated as hypothetical proteins (924 genes, 29.92%). Moreover, the H. alexandrinus strain Arc-hr genome contains 37 genes identified as ORFans, seven genes associated to halocin and 11 genes associated with polyketide synthases or nonribosomal peptide synthetases.

Deposit in a culture collection

Strain Arc-hr was deposited in CSUR (WDCM 875) under number CSUR P974.

Nucleotide sequence accession number

The H. alexandrinus strain Arc-hr genome sequence has been deposited in European Molecular Biology Laboratory under the accession number CCDK010000001:CCDK010000010.

Acknowledgements

This study was funded by the Fondation Méditerranée Infection. We thank M. Lardière for English-language review.

Conflict of Interest

None declared.

References

  • 1.Asker D., Ohta Y. Haloferax alexandrinus sp. nov., an extremely halophilic canthaxanthin-producing archaeon from a solar saltern in Alexandria (Egypt) Int J Syst Evol Microbiol. 2002;52:729–738. doi: 10.1099/00207713-52-3-729. [DOI] [PubMed] [Google Scholar]
  • 2.Oxley A.P., Lanfranconi M.P., Würdemann D., Ott S., Schreiber S., McGenity T.J. Halophilic archaea in the human intestinal mucosa. Environ Microbiol. 2010;12:2398–2410. doi: 10.1111/j.1462-2920.2010.02212.x. [DOI] [PubMed] [Google Scholar]
  • 3.Lagier J.C., Khelaifia S., Alou M.T., Ndongo S., Dione N., Hugon P. Culture of previously uncultured members of the human gut microbiota by culturomics. Nat Microbiol. 2016;7(1):16203. doi: 10.1038/nmicrobiol.2016.203. [DOI] [PubMed] [Google Scholar]
  • 4.Khelaifia S., Lagier J.C., Bibi F., Azhar E.I., Croce O., Padmanabhan R. Microbial culturomics to map halophilic bacterium in human gut: genome sequence and description of Oceanobacillus jeddahense sp. nov. Omics. 2016;20:248–258. doi: 10.1089/omi.2016.0004. [DOI] [PubMed] [Google Scholar]
  • 5.Hyatt D., Chen G.L., Locascio P.F., Land M.L., Larimer F.W., Hauser L.J. Prodigal: prokaryotic gene recognition and translation initiation site identification. BMC Bioinformatics. 2010;8:119. doi: 10.1186/1471-2105-11-119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Camacho C., Coulouris G., Avagyan V., Ma N., Papadopoulos J., Bealer K. BLAST+: architecture and applications. BMC Bioinformatics. 2009;15(10):421. doi: 10.1186/1471-2105-10-421. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Lagesen K., Hallin P., Rodland E.A., Staerfeldt H.H., Rognes T., Ussery D.W. RNAmmer: consistent and rapid annotation of ribosomal RNA genes. Nucleic Acids Res. 2007;35:3100–3108. doi: 10.1093/nar/gkm160. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Laslett D., Canback B. ARAGORN, a program to detect tRNA genes and tmRNA genes in nucleotide sequences. Nucleic Acids Res. 2004;32:11–16. doi: 10.1093/nar/gkh152. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Griffiths-Jones S., Bateman A., Marshall M., Khanna A., Eddy S.R. Rfam: an RNA family database. Nucleic Acids Res. 2003;31:439–441. doi: 10.1093/nar/gkg006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Punta M., Coggill P.C., Eberhardt R.Y., Mistry J., Tate J., Boursnell C. The Pfam protein families database. Nucleic Acids Res. 2012;40:D290–D301. doi: 10.1093/nar/gkr1065. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Nawrocki E.P., Kolbe D.L., Eddy S.R. Infernal 1.0: inference of RNA alignments. Bioinformatics. 2009;25:1335–1337. doi: 10.1093/bioinformatics/btp157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Eddy S.R. Accelerated profile HMM searches. PLoS Comp Biol. 2011;7:e1002195. doi: 10.1371/journal.pcbi.1002195. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.UniProt Consortium Ongoing and future developments at the Universal Protein Resource. Nucleic Acids Res. 2011;39:D214–D219. doi: 10.1093/nar/gkq1020. [DOI] [PMC free article] [PubMed] [Google Scholar]

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