Skip to main content
Microbiology Resource Announcements logoLink to Microbiology Resource Announcements
. 2023 Jan 25;12(2):e01074-22. doi: 10.1128/mra.01074-22

Draft Genome Sequence of Venenivibrio stagnispumantis CP.B2T, Isolated from Champagne Pool, Waiotapu, Aotearoa-New Zealand

Jean F Power a, Holly E Welford b, Carlo R Carere c,d, Ian R McDonald a, S Craig Cary a, Matthew B Stott b,d,
Editor: J Cameron Thrashe
PMCID: PMC9933696  PMID: 36695581

ABSTRACT

Venenivibrio stagnispumantis strain CP.B2T is a thermophilic, chemolithoautotrophic bacterium from the family Hydrogenothermaceae (phylum Aquificota), isolated from Champagne Pool in the Waiotapu geothermal field, Aotearoa-New Zealand. The genome consists of 1.73 Mbp in 451 contigs with a 30.8 mol% G+C content.

ANNOUNCEMENT

The bacterial genus Venenivibrio, within the phylum Aquificota (family Hydrogenothermaceae), is characterized by thermophilic microaerophilic hydrogenotrophs (13). The type strain for the genus, Venenivibrio stagnispumantis CP.B2T, was isolated from Champagne Pool, Waiotapu, Aotearoa-New Zealand, a geothermal system under the kaitiakitanga (guardianship) of Māori iwi (tribe) Ngāti Tahu-Ngāti Whaoa. The V. stagnispumantis genome has previously been sequenced as part of the Genomic Encyclopedia of Bacteria and Archaea (GEBA) project KMG-II (4) (IMG genome ID 2724679818). However, we have resequenced the genome on behalf of Ngāti Tahu-Ngāti Whaoa to recognize indigenous data sovereignty and to assert mana whenua (customary rights) over the bacterium, its genome, and the location in which it was isolated.

Venenivibrio stagnispumantis CP.B2T (obtained from the University of Waikato, Aotearoa-New Zealand) was cultivated using a modified MSH medium (70°C, pH 5.5) within a headspace consisting of N2/H2/CO2/O2 at ratios of 50:40:7.5:2.5 (vol/vol), respectively (1). A total DNA extract (3.5 ng μl−1) of CP.B2T was performed using a NucleoSpin Soil kit (Macherey-Nagel, Düren, Germany) according to the manufacturer’s protocols. Whole-genome sequencing (Macrogen, Inc., Seoul, South Korea) was undertaken using the Illumina HiSeq 2500 platform with TruSeq DNA Nano (550) library preparation for paired-end 101-bp reads (Illumina, Inc., San Diego, CA, USA). Default parameters were used for all assembly, quality control (QC), and annotation software unless otherwise specified. A total of 3.8-Gbp raw sequences (37.32 million reads) were assembled using SPAdes v3.12.0 (5) with the “–careful” option to minimize mismatches and kmer sizes of 21, 33, and 55. The assembly was evaluated using QUAST v5.0.0 (6). The genome was annotated via the NCBI Prokaryotic Genome Annotation Pipeline (PGAP; v6.3 [7]) (GenBank accession no. JAPEIW010000000) using the GeneMarkS-2+ protein reference set. A functionally equivalent annotation of 47 scaffolds using the Integrated Microbial Genomes annotation pipeline v4.16.4 (8) is also available (IMG genome ID 2799112217).

The V. stagnispumantis CP.B2T genome comprised 1,731,156 bp containing 2,034 protein-coding genes, with 1,963 having predicted function. The genome consisted of 451 contigs, with a total G+C content of 30.8% mol. The N50 value was 91,033, the L50 was 8, and genome coverage was ~2,242×. The genome encodes 49 RNAs, including single complete copies of the 5S, 16S, and 23S rRNAs; 36 tRNAs; and 3 noncoding RNAs (ncRNAs).

A pairwise average nucleotide identity (ANI) comparison using FastANI v0.1.3 (9) of the V. stagnispumantis CP.B2T, Sulfurihydrogenibium yellowstonense SS-5T, and Persephonella marina EX-H1T genomes gave <80% similarity for each, confirming the designation of Venenivibrio as a separate genus to sister genera Sulfurihydrogenibium and Persephonella.

Data availability.

Raw sequences for the V. stagnispumantis CP.B2T genome were deposited in the European Nucleotide Archive under the BioProject accession no. PRJEB55610. The assembled genome was deposited in the Genomes Online Database (10) (GOLD analysis ID Ga0591133), for associated annotation with the Integrated Microbial Genomes & Microbiomes platform (8) (IMG genome ID 2799112217). This Whole Genome Shotgun project has been deposited at DDBJ/ENA/GenBank under accession no. JAPEIW010000000. The version described in this paper is version JAPEIW010000000.1.

ACKNOWLEDGMENTS

We wish to acknowledge Ngāti Tahu-Ngāti Whaoa as having mana whenua (customary rights) of the Waiotapu geothermal area and of Venenivibrio stagnispumantis CP.B2T and all associated data (genomic, environmental, phenotypic) linked with this strain. We also thank Ngāti Tahu-Ngāti Whaoa for their continued support and enthusiasm for this and related research projects. The University of Canterbury (HEW), the University of Waikato, and GNS Science are acknowledged for their financial support of this research.

Contributor Information

Matthew B. Stott, Email: matthew.stott@canterbury.ac.nz.

J. Cameron Thrash, University of Southern California

REFERENCES

  • 1.Hetzer A, McDonald IR, Morgan HW. 2008. Venenivibrio stagnispumantis gen. nov., sp. nov., a thermophilic hydrogen-oxidizing bacterium isolated from Champagne Pool, Waiotapu, New Zealand. Int J Syst Evol Microbiol 58:398–403. doi: 10.1099/ijs.0.64842-0. [DOI] [PubMed] [Google Scholar]
  • 2.Hetzer A, Morgan HW, McDonald IR, Daughney CJ. 2007. Microbial life in Champagne Pool, a geothermal spring in Waiotapu, New Zealand. Extremophiles 11:605–614. doi: 10.1007/s00792-007-0073-2. [DOI] [PubMed] [Google Scholar]
  • 3.Power JF, Carere CR, Lee CK, Wakerley GLJ, Evans DW, Button M, White D, Climo MD, Hinze AM, Morgan XC, McDonald IR, Cary SC, Stott MB. 2018. Microbial biogeography of 925 geothermal springs in New Zealand. Nature Comms 9:2876. doi: 10.1038/s41467-018-05020-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Whitman WB, Woyke T, Klenk HP, Zhou Y, Lilburn TG, Beck BJ, De Vos P, Vandamme P, Eisen JA, Garrity G, Hugenholtz P, Kyrpides NC. 2015. Genomic encyclopedia of bacterial and archaeal type strains, phase III: the genomes of soil and plant-associated and newly described type strains. Stand Genomic Sci 10:26. doi: 10.1186/s40793-015-0017-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Prjibelski A, Antipov D, Meleshko D, Lapidus A, Korobeynikov A. 2020. Using SPAdes de novo assembler. Curr Protoc Bioinformatics 70:e102. doi: 10.1002/cpbi.102. [DOI] [PubMed] [Google Scholar]
  • 6.Mikheenko A, Prjibelski A, Saveliev V, Antipov D, Gurevich A. 2018. Versatile genome assembly evaluation with QUAST-LG. Bioinformatics 34:i142–i150. doi: 10.1093/bioinformatics/bty266. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Tatusova T, DiCuccio M, Badretdin A, Chetvernin V, Nawrocki EP, Zaslavsky L, Lomsadze A, Pruitt KD, Borodovsky M, Ostell J. 2016. NCBI prokaryotic genome annotation pipeline. Nucleic Acids Res 44:6614–6624. doi: 10.1093/nar/gkw569. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Chen IA, Chu K, Palaniappan K, Ratner A, Huang J, Huntemann M, Hajek P, Ritter S, Varghese N, Seshadri R, Roux S, Woyke T, Eloe-Fadrosh EA, Ivanova NN, Kyrpides NC. 2021. The IMG/M data management and analysis system v.6.0: new tools and advanced capabilities. Nucleic Acids Res 49:D751–D763. doi: 10.1093/nar/gkaa939. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Jain C, Rodriguez RL, Phillippy AM, Konstantinidis KT, Aluru S. 2018. High throughput ANI analysis of 90K prokaryotic genomes reveals clear species boundaries. Nat Commun 9:5114. doi: 10.1038/s41467-018-07641-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Mukherjee S, Stamatis D, Bertsch J, Ovchinnikova G, Sundaramurthi JC, Lee J, Kandimalla M, Chen IA, Kyrpides NC, Reddy TBK. 2021. Genomes OnLine Database (GOLD) v.8: overview and updates. Nucleic Acids Res 49:D723–D733. doi: 10.1093/nar/gkaa983. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

Raw sequences for the V. stagnispumantis CP.B2T genome were deposited in the European Nucleotide Archive under the BioProject accession no. PRJEB55610. The assembled genome was deposited in the Genomes Online Database (10) (GOLD analysis ID Ga0591133), for associated annotation with the Integrated Microbial Genomes & Microbiomes platform (8) (IMG genome ID 2799112217). This Whole Genome Shotgun project has been deposited at DDBJ/ENA/GenBank under accession no. JAPEIW010000000. The version described in this paper is version JAPEIW010000000.1.


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

RESOURCES