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Prokaryotes

Genome Sequence of the Piezophilic, Mesophilic Sulfate-Reducing Bacterium Desulfovibrio indicus J2T

Junwei Cao, Lois Maignien, Zongze Shao, Karine Alain, Mohamed Jebbar
Junwei Cao
aUniversité de Bretagne Occidentale (UBO, UEB), Institut Universitaire Européen de la Mer (IUEM) – UMR 6197, Laboratoire de Microbiologie des Environnements Extrêmes (LMEE), Place Nicolas Copernic, Plouzané, France
bCNRS, IUEM–UMR 6197, Laboratoire de Microbiologie des Environnements Extrêmes (LMEE), Place Nicolas Copernic, Plouzané, France
cIfremer, UMR 6197, Laboratoire de Microbiologie des Environnements Extrêmes (LMEE), Technopôle Pointe du diable, Plouzané, France
dSchool of Municipal and Environmental Engineering, Harbin Institute of Technology, Harbin, China
eState Key Laboratory Breeding Base of Marine Genetic Resources, Key Laboratory of Marine Genetic Resources, The Third Institute of State Oceanic Administration, Collaborative Innovation Center of Marine Biological Resources, Key Laboratory of Marine Genetic Resources of Fujian Province, Xiamen, China
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Lois Maignien
aUniversité de Bretagne Occidentale (UBO, UEB), Institut Universitaire Européen de la Mer (IUEM) – UMR 6197, Laboratoire de Microbiologie des Environnements Extrêmes (LMEE), Place Nicolas Copernic, Plouzané, France
bCNRS, IUEM–UMR 6197, Laboratoire de Microbiologie des Environnements Extrêmes (LMEE), Place Nicolas Copernic, Plouzané, France
cIfremer, UMR 6197, Laboratoire de Microbiologie des Environnements Extrêmes (LMEE), Technopôle Pointe du diable, Plouzané, France
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Zongze Shao
eState Key Laboratory Breeding Base of Marine Genetic Resources, Key Laboratory of Marine Genetic Resources, The Third Institute of State Oceanic Administration, Collaborative Innovation Center of Marine Biological Resources, Key Laboratory of Marine Genetic Resources of Fujian Province, Xiamen, China
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Karine Alain
bCNRS, IUEM–UMR 6197, Laboratoire de Microbiologie des Environnements Extrêmes (LMEE), Place Nicolas Copernic, Plouzané, France
aUniversité de Bretagne Occidentale (UBO, UEB), Institut Universitaire Européen de la Mer (IUEM) – UMR 6197, Laboratoire de Microbiologie des Environnements Extrêmes (LMEE), Place Nicolas Copernic, Plouzané, France
cIfremer, UMR 6197, Laboratoire de Microbiologie des Environnements Extrêmes (LMEE), Technopôle Pointe du diable, Plouzané, France
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Mohamed Jebbar
aUniversité de Bretagne Occidentale (UBO, UEB), Institut Universitaire Européen de la Mer (IUEM) – UMR 6197, Laboratoire de Microbiologie des Environnements Extrêmes (LMEE), Place Nicolas Copernic, Plouzané, France
bCNRS, IUEM–UMR 6197, Laboratoire de Microbiologie des Environnements Extrêmes (LMEE), Place Nicolas Copernic, Plouzané, France
cIfremer, UMR 6197, Laboratoire de Microbiologie des Environnements Extrêmes (LMEE), Technopôle Pointe du diable, Plouzané, France
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DOI: 10.1128/genomeA.00214-16
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ABSTRACT

The complete genome sequence of Desulfovibrio indicus J2T, a member of the family Desulfovibrionaceae, consists of 3,966,573-bp in one contig and encodes 3,461 predicted genes, 5 noncoding RNAs, 3 rRNAs operons, and 52 tRNA-encoding genes. The genome is consistent with a heterotrophic, anaerobic lifestyle including the sulfate reduction pathway.

GENOME ANNOUNCEMENT

Sulfate-reducing prokaryotes are those bacteria and archaea that are key players in sulfur cycle on Earth; they can obtain energy by oxidizing organic compounds or molecular hydrogen (H2) while reducing sulfate (SO42−) to hydrogen sulfide (H2S).

Desulfovibrio indicus J2T was isolated from a deep-sea serpentinized peridotite sample collected at a depth of 3173 m in a hydrothermal vent area of the Indian Ocean (27°88′ S, 63°53′ E; site 30I-TVG05) (1). D. indicus, with Desulfovibrio hydrothermalis (2) are the only known sulfate-reducing bacteria (SRB) isolated from deep sea hydrothermal area samples. D. indicus is meso-piezophilic growing optimally at 10 MPa (range 0 to 30 MPa). This anaerobic, motile vibrio can use lactate, malate, pyruvate, formate, and hydrogen as energy sources when using sulfate, thiosulfate, sulfite, fumarate, and nitrate as terminal electron acceptors.

Genomic DNA was extracted with the QIAGEN genomic-tip 20/G (QIAGEN, Düsseldorf, Germany) kit following the manufacturer's standard protocol. Whole-genome shotgun sequencing was carried out using PacBio (Pacific Biosciences, Menlo Park, CA) single-molecule-real-time (SMRT) sequencing technology (Duke University) (3). The genome was sequenced with two PacBio SMRT cells. For the genome assembly, we used the HGAP assembler included in a local installation of the PacBio SMRT portal (V. 2.3.0) with default parameters, This resulted in a single 3,970,855 bp circular genome with a 32× coverage and a G+C content of 63.5%.

Genome was annotated using the NCBI Prokaryotic Genome Annotation Pipeline (http://www.ncbi.nlm.nih.gov/genome/annotation_prok/). A total of 3,461 coding DNA sequences (CDSs) were identified, as well as 90 pseudogenes, 5 noncoding RNAs (ncRNA), 3 rRNAs (5S, 16S, and 23S) operons, and 52 tRNA genes. Additionally, the genome contains one clustered regularly interspaced short palindromic repeat (CRISPR) array associated with seven cas (cas 1, cas 2, cas 3, cas 4, cas 5d, csd 1, and csd 2/csh 2) genes.

Phylogenetic analysis based on 16S rRNA gene sequences showed that strain J2T falls into the genus Desulfovibrio within the class Deltaproteobacteria, with highest sequence similarity of 98.05% to Desulfovibrio dechloracetivorans SF3T (1).

Genes involved in sulfate reduction (4) were identified in the genome, for example, sulfate adenylyltransferase gene (sat, AWY79_04190 and AWY79_13965); adenosine phosphosulfate reductase genes (aprBA, AWY79_04195 and AWY79_04200); dissimilatory sulfite reductase genes (dsrAB, AWY79_17895 and AWY79_17900; dsrC, AWY79_11020); sulfate transporter gene (AWY79_06665, AWY79_10840, and AWY79_14480); Genes that mediate the electron transport between the cytoplasmic AprBA and DsrAB and the membrane-integral quinol/quinone pool (4, 5) were also found, for instance, quinone-interacting membrane-bound oxidoreductase genes (qmoABC, AWY79_04205 AWY79_04210 and AWY79_04215); sulfite reduction-associated complex protein genes (dsrMKJOP, AWY79_04535, AWY79_04540, AWY79_04545, AWY79_04550, and AWY79_04555). The genome also contains a large number of genes encoding hydrogenases, cytochromes c and cytochrome c-associated membrane redox complexes, which may be possibly involved in electron-transfer and energy conserving pathways (5).

Previous study indicated that energy metabolism of SRB is far more versatile than we considered, so that SRB can use different alternative strategies for energy conservation (5, 6). The genome sequence analysis will allow comprehensive comparisons with other SRB and pave the way for further understanding of SRB lifestyle in anaerobic deep sea environments.

Nucleotide sequence accession number.The genome sequence has been deposited in GenBank under the accession no. CP014206.

ACKNOWLEDGMENTS

We are very grateful to the R/V “Da Yang Yi Hao” operation teams for helping us to collect the hydrothermal samples.

This work was supported by the EU program MaCuMBA, the PICS-InEE Phypress, the PHC Cai Yuanpei Pandore (30412wg), the PHC Cai Yuanpei Provirvent (34634we), the National Program on Key Basic Research Project (973 Program 2012CB417304), and the National Natural Science Foundation of China (41411130113).

FOOTNOTES

    • Received 15 February 2016.
    • Accepted 24 February 2016.
    • Published 7 April 2016.
  • Copyright © 2016 Cao et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

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Genome Sequence of the Piezophilic, Mesophilic Sulfate-Reducing Bacterium Desulfovibrio indicus J2T
Junwei Cao, Lois Maignien, Zongze Shao, Karine Alain, Mohamed Jebbar
Genome Announcements Apr 2016, 4 (2) e00214-16; DOI: 10.1128/genomeA.00214-16

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Genome Sequence of the Piezophilic, Mesophilic Sulfate-Reducing Bacterium Desulfovibrio indicus J2T
Junwei Cao, Lois Maignien, Zongze Shao, Karine Alain, Mohamed Jebbar
Genome Announcements Apr 2016, 4 (2) e00214-16; DOI: 10.1128/genomeA.00214-16
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