Skip to main content
Genome Announcements logoLink to Genome Announcements
. 2013 Jan 24;1(1):e00114-12. doi: 10.1128/genomeA.00114-12

Genome Sequence of the Sulfate-Reducing Bacterium Desulfotomaculum hydrothermale Lam5T

Oulfat Amin a, Marie-Laure Fardeau a, Odile Valette b, Agnès Hirschler-Réa a, Valérie Barbe c, Claudine Médigue d, Benoit Vacherie c, Bernard Ollivier a, Philippe N Bertin e, Alain Dolla b,✉
PMCID: PMC3569332  PMID: 23405336

Abstract

Here, we report the draft genome sequence of Desulfotomaculum hydrothermale, a sulfate-reducing, spore-forming bacterium isolated from a Tunisian hot spring. The genome is composed of 2.7 Mb, with a G+C content of 49.48%, and it contains 2,643 protein-coding sequences.

GENOME ANNOUNCEMENT

Members of the genus Desulfotomaculum are sulfate-reducing, spore-forming Gram-positive bacteria that are widely distributed within mesothermic and thermal ecosystems (1). Evidence of their presence in terrestrial geothermal hot springs has been obtained several times using molecular approaches (2), but only three species of this genus have been isolated so far, the most recent being Desulfotomaculum hydrothermale (3). Here, we report the first draft genome sequence of a Desulfotomaculum species isolated from a terrestrial hot spring in Tunisia: D. hydrothermale. The strain was shown to reductively detoxify arsenate [As(V)], in the presence of pyruvate as an electron donor, without evidence for any respiration using As(V) as a terminal electron acceptor (3). Because arsenic is known to be present in hot springs (4), information regarding the genome sequence of D. hydrothermale may be useful in understanding the As-detoxifying process developed in Desulfotomaculum species.

A Sanger/pyrosequencing hybrid approach was used for the whole-genome sequencing. A shotgun library was constructed with 10-kb fragments of genomic DNA in vector pCNS (derived from pSU). Sequencing with vector-based primers was carried out using the ABI 3730 Applera sequencer, and a total of 6,421 reads (~1.6-fold coverage) were analyzed and assembled with Newbler (a Roche assembler), with 341,086 single reads (~26-fold coverage) and 106,386 mate-paired 8-kb reads obtained with Genome Sequencer version FLX and Titanium (Roche Applied Science), respectively. The finishing step was achieved by using primer walks, PCRs, and in vitro transposition technologies. For quality assessment, 5,501,511 (36-nucleotide) Illumina reads (~70-fold coverage) were mapped using Soap1 (http://soap.genomics.org.cn/) on the 16 consensus contigs. The draft genome sequence consists of 2,706,432 bases with a G+C content of 49.48%, and it contains 2,643 candidate protein-encoding genes, in addition to 60 tRNA and 3 16S rRNA genes.

The mechanism of microbe-mediated metal reduction, studied mainly in Geobacter and Shewanella species, involves c-type cytochromes (5, 6). For Desulfotomaculum reducens, it has been hypothesized that an integral membrane multiheme c-type cytochrome (Dred_0700-0701) is involved in the reduction of metals such as Fe(III) and U(VI) (7). Inspection of the draft genome sequence of D. hydrothermale suggests the absence of c-type cytochromes and the absence of an identified ortholog of Dred_0700-0701, even though the strain is able to reduce Fe(III) to Fe(II) (3). Metal reduction in this strain would use a different pathway, which needs to be specified. The D. hydrothermale genome encodes an arsenite resistance protein (DESHYv2_110039) that exhibits homology to the intrinsic membrane protein ArsB (8). A gene (DESHYv2_110038) encoding a transcriptional regulator belonging to the AsrR family (9) was found immediately upstream from asrB. Even if no homolog to the arsenate reductase gene asrC (10) has been identified so far, this gene cluster could be of great importance for arsenite reduction and for the tolerance capacity of this strain.

Insights into the arsenite resistance process of Desulfotomaculum species could be gained through comparative genomics and biochemical analyses of the arsenite resistance mechanisms, which are in progress in our laboratories.

Nucleotide sequence accession numbers.

The whole-genome shotgun project has been deposited at DDBL/EMBL/Genbank under the accession no. CAOS01000001 to CAOS01000016.

ACKNOWLEDGMENTS

Financial support came from the Université de Strasbourg (UDS), the Consortium National de Recherche en Génomique (CNRG), and the CNRS.

Footnotes

Citation Amin O, Fardeau M-L, Valette O, Hirschler-Réa A, Barbe V, Médigue C, Vacherie B, Ollivier B, Bertin PN, Dolla A. 2013. Genome sequence of the sulfate-reducing bacterium Desulfotomaculum hydrothermale LAM5T. Genome Announc. 1(1):e00114-12. doi:10.1128/genomeA.00114-12.

REFERENCES

  • 1. Kuever J, Rainey FA. 2009. Genus II. Desulfotomaculum C, Postgate. 1965. 361AL, p 989–996 De Vos P, Garrity GM, Jones D, Krieg NR, Ludwig W, Rainey FA, Schleifer KH, Whitman WB. Bergey’s manual of systematic bacteriology, vol 3, 2nd ed. Springer Verlag, New York, NY. [Google Scholar]
  • 2. Fishbain S, Dillon JG, Gough HL, Stahl DA. 2003. Linkage of high rates of sulfate reduction in Yellowstone hot springs to unique sequence types in the dissimilatory sulfate respiration pathway. Appl. Environ. Microbiol. 69(6):3663–3667 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Haouari O, Fardeau ML, Cayol JL, Casiot C, Elbaz-Poulichet F, Hamdi M, Joseph M, Ollivier B. 2008. Desulfotomaculum hydrothermale sp. nov., a thermophilic sulfate-reducing bacterium isolated from a terrestrial Tunisian hot spring. Int. J. Syst. Evol. Microbiol. 58(Pt 11):2529–2535 [DOI] [PubMed] [Google Scholar]
  • 4. Mandal BK, Suzuki KT. 2002. Arsenic round the world: a review. Talanta 58(1):201–235 [PubMed] [Google Scholar]
  • 5. Weber KA, Achenbach LA, Coates JD. 2006. Microorganisms pumping iron: anaerobic microbial iron oxidation and reduction. Nat. Rev. Microbiol. 4(10):752–764 [DOI] [PubMed] [Google Scholar]
  • 6. Beliaev AS, Saffarini DA, McLaughlin JL, Hunnicutt D. 2001. MtrC, an outer membrane decahaem c cytochrome required for metal reduction in Shewanella putrefaciens MR-1. Mol. Microbiol. 39(3):722–730 [DOI] [PubMed] [Google Scholar]
  • 7. Junier P, Junier T, Podell S, Sims DR, Detter JC, Lykidis A, Han CS, Wigginton NS, Gaasterland T, Bernier-Latmani R. 2010. The genome of the gram-positive metal- and sulfate-reducing bacterium Desulfotomaculum reducens strain MI-1. Environ. Microbiol. 12(10):2738–2754 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Prakash S, Cooper G, Singhi S, Saier MH., Jr 2003. The ion transporter superfamily. Biochim. Biophys. Acta 1618(1):79–92 [DOI] [PubMed] [Google Scholar]
  • 9. Wu J, Rosen BP. 1991. The ArsR protein is a trans-acting regulatory protein. Mol. Microbiol. 5(6):1331–1336 [DOI] [PubMed] [Google Scholar]
  • 10. Messens J, Silver S. 2006. Arsenate reduction: thiol cascade chemistry with convergent evolution. J. Mol. Biol. 362(1):1–17 [DOI] [PubMed] [Google Scholar]

Articles from Genome Announcements are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES