Literature DB >> 24874683

Complete Genome Sequence of the Subsurface, Mesophilic Sulfate-Reducing Bacterium Desulfovibrio aespoeensis Aspo-2.

Karsten Pedersen1, Andreas Bengtsson2, Johanna Edlund2, Lisa Rabe2, Terry Hazen, Romy Chakraborty3, Lynne Goodwin4, Nicole Shapiro4.   

Abstract

Desulfovibrio aespoeensis Aspo-2, DSM 10631(T), is a mesophilic, hydrogenotrophic sulfate-reducing bacterium sampled from a 600-m-deep subsurface aquifer in hard rock under the island of Äspö in southeastern Sweden. We report the genome sequence of this bacterium, which is a 3,629,109-bp chromosome; plasmids were not found.
Copyright © 2014 Pedersen et al.

Entities:  

Year:  2014        PMID: 24874683      PMCID: PMC4038888          DOI: 10.1128/genomeA.00509-14

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Desulfovibrio aespoeensis was isolated from a borehole (KAS03) that intersected a water-conducting aquifer at 600-m depth (1). Knowledge about subsurface sulfate-reducing bacteria (SRB) is essential for evaluating adverse effects of their sulfide production on future spent nuclear fuel (SNF) waste repositories planned to be built 500 to 1,000 m underground. This is because metal canisters will be in use to encapsulate the SNF and many metals are susceptible to corrosion by sulfide (2). The safety case may consequently be challenged by subsurface SRB. Because D. aespoeensis readily reduces sulfate to sulfide with a very low K for hydrogen (3), this species and other hydrogenotropic SRB may increase anaerobic corrosion rates of iron in SNF repositories (4). It has previously been shown that D. aespoeensis forms biofilms of metallic copper (5), which indicates the presence of genes involved in copper homeostasis (6). Since the isolation, this species and closely related strains (>98% 16S rRNA gene identity) have been found repeatedly in deep groundwater, strongly suggesting the deep biosphere as the natural habitat for D. aespoeensis (7, 8). The draft genome of Desulfovibrio aespoeensis Aspo-2 was generated at the U.S. Department of Energy (DOE) Joint Genome Institute (JGI) using a combination of Illumina and 454 technologies (project 4086336 [NCBI project 37869], principal investigator [PI] Terry C. Hazen). An Illumina GAii shotgun library was constructed which generated 36,973,545 reads totaling 1,331 Mb, a 454 Titanium standard library which generated 226,344 reads, and a paired-end 454 library with average insert sizes of 12 kbp which generated 58,898 reads totaling 208.3 Mb of 454 data. The initial draft assembly contained 73 contigs in 1 scaffold. The 454 Titanium standard data and the 454 paired-end data were assembled together with Newbler, version 2.3. Illumina sequencing data were assembled with VELVET, version 0.7.63. The genome consists of one contig of 3,629,109 bp. The GC content is 62.6%, which agrees well with the previous melting point determination of 61 ± 0.5 mol% (1). Annotation predicted a total of 3,405 coding DNA sequences, as well as 39 pseudogenes, 2 rRNA genes, 53 tRNA genes, and 902 genes without identified functions. Phylogenetic analysis based on completed genomes shows that the closest sequenced genomes to D. aespoeensis are those of Desulfovibrio piezophilus (9), Desulfovibrio hydrothermalis (10), and Desulfovibrio salexigens. These three species were isolated from marine habitats of which at least two are under considerable hydrostatic pressure (i.e., 26 and 17 MPa). D. salexigens was isolated from shallow sediments. Ji et al. (10) found that D. aespoeensis shares 2,069 orthologous proteins with D. hydrothermalis and 1974 proteins are common between these species and D. salexigens. Further analysis results by Ji et al. (10) suggest that D. aespoeensis has a phylogenetic position between marine and piezophilic species and nonmarine species such as Desulfovibrio desulfuricans and Desulfovibrio alaskensis. Comparative genomic analyses, including those of other Desulfovibrio species, will give insights into the adaptation of D. aespoeensis to subsurface habitats in hard rock aquifers and future SNF repositories.

Nucleotide sequence accession number.

The complete annotated genome of D. aespoeensis is available in Genbank under the accession no. CP002431.1.
  9 in total

1.  Genome sequence of Desulfovibrio sp. A2, a highly copper resistant, sulfate-reducing bacterium isolated from effluents of a zinc smelter at the Urals.

Authors:  Stefano Mancini; Helge K Abicht; Olga V Karnachuk; Marc Solioz
Journal:  J Bacteriol       Date:  2011-12       Impact factor: 3.490

2.  Abundance and diversity of biofilms in natural and artificial aquifers of the Äspö Hard Rock Laboratory, Sweden.

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Journal:  Microb Ecol       Date:  2010-12-04       Impact factor: 4.552

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Journal:  FEMS Microbiol Ecol       Date:  2012-07-09       Impact factor: 4.194

4.  Desulfovibrio aespoeensis sp. nov., a mesophilic sulfate-reducing bacterium from deep groundwater at Aspö hard rock laboratory, Sweden.

Authors:  M Motamedi; K Pedersen
Journal:  Int J Syst Bacteriol       Date:  1998-01

5.  Analysis of copper corrosion in compacted bentonite clay as a function of clay density and growth conditions for sulfate-reducing bacteria.

Authors:  K Pedersen
Journal:  J Appl Microbiol       Date:  2009-11-18       Impact factor: 3.772

6.  Bacteriophage lytic to Desulfovibrio aespoeensis isolated from deep groundwater.

Authors:  Hallgerd S C Eydal; Sara Jägevall; Malte Hermansson; Karsten Pedersen
Journal:  ISME J       Date:  2009-06-11       Impact factor: 10.302

7.  Marine sulfate-reducing bacteria cause serious corrosion of iron under electroconductive biogenic mineral crust.

Authors:  Dennis Enning; Hendrik Venzlaff; Julia Garrelfs; Hang T Dinh; Volker Meyer; Karl Mayrhofer; Achim W Hassel; Martin Stratmann; Friedrich Widdel
Journal:  Environ Microbiol       Date:  2012-05-23       Impact factor: 5.491

8.  Complete Genome Sequence of the Piezophilic, Mesophilic, Sulfate-Reducing Bacterium Desulfovibrio hydrothermalis AM13(T.).

Authors:  Boyang Ji; Gregory Gimenez; Valérie Barbe; Benoît Vacherie; Zoé Rouy; Amira Amrani; Marie-Laure Fardeau; Philippe Bertin; Didier Alazard; Sabine Leroy; Emmanuel Talla; Bernard Ollivier; Alain Dolla; Nathalie Pradel
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Journal:  PLoS One       Date:  2013-01-30       Impact factor: 3.240

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