Open access
Announcement
16 February 2017

Complete Genome Sequence of the Hyperthermophilic Piezophilic Archaeon Pyrococcus kukulkanii NCB100 Isolated from the Rebecca’s Roost Hydrothermal Vent in the Guaymas Basin

ABSTRACT

Members of the order Thermococcales are common inhabitants of high-temperature hydrothermal vent systems (black smokers) that are represented in clone libraries mostly by isolates from the Thermococcus genus. We report the complete sequence of a novel species from the Pyrococcus genus, P. kukulkanii strain NCB100, which has been isolated from a flange fragment of the Rebecca’s Roost hydrothermal vent system in the Guaymas Basin.

GENOME ANNOUNCEMENT

Pyrococcus kukulkanii strain NCB100T was isolated from a flange fragment collected at the Rebecca’s Roost hydrothermal vent in the Guaymas Basin at a depth of 2004 m by cultivation in SME medium at 100°C (1). P. kukulkanii is the most hyperthermophilic Thermococcales known to date, with an optimum growth temperature of 105°C. This species is a piezophilic, obligately anaerobic chemoorganotroph, growing best by fermentation of proteinaceaous substrates, such as peptone, in the presence of sulfur.
DNA was extracted from cells grown in SME medium to late exponential phase as described in Barbier et al (2). For determination of the complete genome sequence, a first 800 bp fragment library was sequenced with Ion Torrent PGM using a 316 chip and the HiQ, which generated 583 k reads with a mean 389 bp length after QC check and trimming (http://www.bioinformatics.babraham.ac.uk/projects/ ) (3). A second 500 bp paired-end library was sequenced (2 × 100 bp) as part of a HiSeq run, which generated 13 million paired 100 bp reads after QC check and trimming (3). The IonTorrent data were assembled de novo with Newbler 2.8. The paired-end Illumina data was assembled de novo with velvet (4). The pooled IonTorrent and Illumina data was assembled de novo with MIRA (5) and Newbler. The resulting assemblies generated 27, 11, 2, and 2 contigs for IonTorrent, Illumina, and both hybrid assemblies, respectively. The scaffolds were connected by Sanger sequencing of PCR amplified fragments. The total size of the assembly is a single circular chromosome of 1,977,126 bp with an average G+C content of 44.6%. The sequence was automatically annotated by the NCBI (6) and is available on the MaGe platform for genomic comparisons (7, 8).
The genome consists of 2,207 protein-coding genes, 47 tRNAs, two copies of the 5S rRNA, and one copy of the 16S-23S genes. With inclusion of strain NCB100, the new core- and pan-genome of the Pyrococcus genome contains 1,086 and 4,539 genes families, respectively. Most (393/427) of the P. kukulkanii specific genome comprises open reading frames (ORFs) with no known functions. Strain NCB100 is most closely related to Pyrococcus sp. strain ST04, which has been isolated from the Juan de Fuca Ridge (9). In silico hybridization yielded an average nucleotide identity (ANI) value (of protein-coding genes shared at ≥60% nucleotide identity and ≥70% coverage) of 78%, over 1,318 genes conserved between the two species, which indicate phylogenetically close but distinct species (10). Genomic comparisons reveal an organotrophic potential comparable in both species (6, 7). In contrast to other Pyrococcus species, P. kukulkanii encodes the locus for formate-driven hydrogenogenesis growth described so far only in Thermococcus onnurineus, T. gammatoelrans, and T. barophilus (1113) and present only in the other piezophile Pyrococcus yayanosii (14). However, it lacks the CO dehydrogenase which allows hydrogenogenic lithoheterotrophic growth on CO as in these three Thermococcus species (15).

Accession number(s).

The final annotated genome of Pyrococcus kukulkanii NCB100 is available in GenBank under accession number CP010835 .

ACKNOWLEDGMENTS

This work was supported in part by the Agence Nationale de la Recherche (ANR-10-BLAN-Living deep) to P.M.O. and M.J. and by a program of the FR41 to C.O.-D. and P.M.O.
Sequencing was performed in part at the DTAMB (Université Claude Bernard Lyon 1) and at the sequencing platform of the Institut de Génomique Fonctionelle de Lyon as part of a series of tests of the HiQ kit from IonTorrent.

REFERENCES

1.
Callac N, Oger P, Lesongeur F, Rattray JE, Vannier P, Michoud G, Beauverger M, Gayet N, Rouxel O, Jebbar M, and Godfroy A. 2016. Pyrococcus kukulkanii sp. nov., a hyperthermophilic, piezophilic archaeon isolated from a deep-sea hydrothermal vent. Int J Syst Evol Microbiol66:3142–3149.
2.
Barbier G, Godfroy A, Meunier JR, Quérellou J, Cambon MA, Lesongeur F, Grimont PAD, and Raguénès G. 1999. Pyrococcus glycovorans, sp. nov., a hyperthermophilic archaeon isolated from the East Pacific Rise. Int J Syst Bacteriol49:1829–1837.
3.
Bolger AM, Lohse M, and Usadel B. 2014. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics30:2114–2120.
4.
Zerbino DR and Birney E. 2008. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res18:821–829.
5.
Chevreux B, Wetter T, and Suhai S. 1999. Genome sequence assembly using trace signals and additional sequence information, p. 45–56. InComputer science and biology. Proceedings of the German Conference on Bioinformatics (GCB) ‘99. GCB, Hannover, Germany.
6.
Angiuoli SV, Gussman A, Klimke W, Cochrane G, Field D, Garrity G, Kodira CD, Kyrpides N, Madupu R, Markowitz V, Tatusova T, Thomson N, and White O. 2008. Toward an online repository of standard operating procedures (SOPs) for (meta)genomic annotation. Omics12:137–141.
7.
Vallenet D, Belda E, Calteau A, Cruveiller S, Engelen S, Lajus A, Le Fèvre F, Longin C, Mornico D, Roche D, Rouy Z, Salvignol G, Scarpelli C, Thil Smith AAT, Weiman M, and Médigue C. 2013. MicroScope—An integrated microbial resource for the curation and comparative analysis of genomic and metabolic data. Nucleic Acids Res41:D636–D647.
8.
Vallenet D, Engelen S, Mornico D, Cruveiller S, Fleury L, Lajus A, Rouy Z, Roche D, Salvignol G, Scarpelli C, and Médigue C. 2009. MicroScope: a platform for microbial genome annotation and comparative genomics. Database J Biol Databases Curation2009:bap021.
9.
Jung JH, Lee JH, Holden JF, Seo DH, Shin H, Kim HY, Kim W, Ryu S, and Park CS. 2012. Complete genome sequence of the hyperthermophilic archaeon Pyrococcus sp. strain ST04, isolated from a deep-sea hydrothermal sulfide chimney on the Juan de Fuca Ridge. J Bacteriol194:4434–4435.
10.
Goris J, Konstantinidis KT, Klappenbach JA, Coenye T, Vandamme P, and Tiedje JM. 2007. DNA-DNA hybridization values and their relationship to whole-genome sequence similarities. Int J Syst Evol Microbiol57:81–91.
11.
Lee HS, Kang SG, Bae SS, Lim JK, Cho Y, Kim YJ, Jeon JH, Cha SS, Kwon KK, Kim HT, Park CJ, Lee HW, Kim SI, Chun J, Colwell RR, Kim SJ, and Lee JH. 2008. The complete genome sequence of Thermococcus onnurineus NA1 reveals a mixed heterotrophic and carboxydotrophic metabolism. J Bacteriol190:7491–7499.
12.
Kim YJ, Lee HS, Kim ES, Bae SS, Lim JK, Matsumi R, Lebedinsky AV, Sokolova TG, Kozhevnikova DA, Cha SS, Kim SJ, Kwon KK, Imanaka T, Atomi H, Bonch-Osmolovskaya EA, Lee JH, and Kang SG. 2010. Formate-driven growth coupled with H2 production. Nature467:352–355.
13.
Oger P, Sokolova TG, Kozhevnikova DA, Taranov EA, Vannier P, Lee HS, Kwon KK, Kang SG, Lee J-H, Bonch-Osmolovskaya EA, and Lebedinsky AV. 2015. Complete genome sequence of the hyperthermophilic and piezophilic archaeon Thermococcus barophilus Ch5 capable of growth at the expense of hydrogenogenesis from carbon monoxide and formate. Genome Announc4(1):e01534-15.
14.
Jun X, Lupeng L, Minjuan X, Oger P, Fengping W, Jebbar M, and Xiang X. 2011. Complete genome sequence of the obligate piezophilic hyperthermophilic archaeon Pyrococcus yayanosii CH1. J Bacteriol193:4297–4298.
15.
Sokolova TG, Jeanthon C, Kostrikina NA, Chernyh NA, Lebedinsky AV, Stackebrandt E, and Bonch-Osmolovskaya EA. 2004. The first evidence of anaerobic CO oxidation coupled with H2 production by a hyperthermophilic archaeon isolated from a deep-sea hydrothermal vent. Extremophiles8:317–323.

Information & Contributors

Information

Published In

cover image Genome Announcements
Genome Announcements
Volume 5Number 716 February 2017
eLocator: 10.1128/genomea.01667-16
PubMed: 28209839

History

Received: 8 December 2016
Accepted: 11 December 2016
Published online: 16 February 2017

Contributors

Authors

Philippe M. Oger
CNRS, UMR 5276, Laboratoire de Géologie de Lyon, Lyon, France
Nolwenn Callac
Université de Brest, UEB, IUEM, Laboratoire de Microbiologie des Environnements Extrêmes, UMR 6197, Plouzané, France
Ifremer, Laboratoire de Microbiologie des Environnements Extrêmes, UMR 6197, Technopôle Brest Iroise, Plouzané, France
CNRS, Laboratoire de Microbiologie des Environnements Extrêmes, UMR 6197, Plouzané, France
Université de Brest, Domaines Océaniques IUEM, UMR 6538, Plouzané, France
Christine Oger-Desfeux
Pôle Rhône Alpes de Bioinformatique, Université Claude Bernard Lyon 1, Villeurbanne, France
Sandrine Hughes
École Normale Supériure de Lyon, Institut de Génomique Fonctionnelle de Lyon, Lyon, France
Benjamin Gillet
École Normale Supériure de Lyon, Institut de Génomique Fonctionnelle de Lyon, Lyon, France
Université de Brest, UEB, IUEM, Laboratoire de Microbiologie des Environnements Extrêmes, UMR 6197, Plouzané, France
Ifremer, Laboratoire de Microbiologie des Environnements Extrêmes, UMR 6197, Technopôle Brest Iroise, Plouzané, France
CNRS, Laboratoire de Microbiologie des Environnements Extrêmes, UMR 6197, Plouzané, France
Anne Godfroy
Université de Brest, UEB, IUEM, Laboratoire de Microbiologie des Environnements Extrêmes, UMR 6197, Plouzané, France
Ifremer, Laboratoire de Microbiologie des Environnements Extrêmes, UMR 6197, Technopôle Brest Iroise, Plouzané, France
CNRS, Laboratoire de Microbiologie des Environnements Extrêmes, UMR 6197, Plouzané, France

Notes

Address correspondence to Philippe M. Oger, [email protected], or Anne Godfroy, [email protected].

Metrics & Citations

Metrics

Note:

  • For recently published articles, the TOTAL download count will appear as zero until a new month starts.
  • There is a 3- to 4-day delay in article usage, so article usage will not appear immediately after publication.
  • Citation counts come from the Crossref Cited by service.

Citations

If you have the appropriate software installed, you can download article citation data to the citation manager of your choice. For an editable text file, please select Medlars format which will download as a .txt file. Simply select your manager software from the list below and click Download.

View Options

Figures and Media

Figures

Media

Tables

Share

Share

Share the article link

Share with email

Email a colleague

Share on social media

American Society for Microbiology ("ASM") is committed to maintaining your confidence and trust with respect to the information we collect from you on websites owned and operated by ASM ("ASM Web Sites") and other sources. This Privacy Policy sets forth the information we collect about you, how we use this information and the choices you have about how we use such information.
FIND OUT MORE about the privacy policy