ABSTRACT
The facultative anaerobic chemoorganoheterotrophic alphaproteobacterium Telmatospirillum siberiense 26-4b1 was isolated from a Siberian peatland. We report here a 6.20-Mbp near-complete high-quality draft genome sequence of T. siberiense that reveals expected and novel metabolic potential for the genus Telmatospirillum, including genes for sulfur oxidation.
GENOME ANNOUNCEMENT
All three validly described strains of Telmatospirillum siberiense were isolated from a mesotrophic Siberian peatland (1). In addition, closely related 16S rRNA gene sequences were recovered from other peatlands (2–8). Uncultured members of the genus Telmatospirillum have been associated with the anaerobic degradation of glucose (2), butyrate (8), acetate, propionate, and lactate (3, 7) in peat soils. Furthermore, in the literature, uncultured Telmatospirillum spp. were stimulated by propionate and butyrate under sulfate-reducing conditions (7), indicating a yet-unresolved role in sulfur cycling.
We obtained the draft genome sequence of Telmatospirillum siberiense 26-4b1 (DSM 18240), the type strain of the only validly described species of this genus (1). DNA was isolated using the DNeasy blood and tissue kit (Qiagen), and sequencing libraries were prepared using the Nextera XT kit (Illumina) and sequenced with the Illumina HiSeq 2000 platform. Raw reads were assembled using SPAdes (version 3.6.2) (9) and subsequently iteratively (n = 4) reassembled with SPAdes (version 3.11.1) using contigs >1 kb from the previous assembly as the “trusted contigs” input. The draft genome sequence consists of 81 scaffolds, with a total size of 6,202,994 bp, a G+C content of 62.3%, and an N50 value of 131,736 bp. Based on CheckM (10), the completeness of the draft genome is 99.5%. The genome was annotated using Rapid Annotation of microbial genomes using Subsystems Technology (RAST) (11) and the NCBI Prokaryotic Genome Annotation Pipeline. The draft genome contains 5,405 coding sequences (CDSs) and 48 tRNAs. Furthermore, the rRNA genes are carried on a small scaffold, with a coverage of 1,210×, although the average genome coverage was 216×, indicating the presence of 5 to 6 rRNA operons.
T. siberiense was reported to grow anaerobically, utilizing organic acids and sugars as energy and carbon sources, with the capability for nitrogen fixation. Autotrophic growth on hydrogen and tolerance to low oxygen pressure (up to 5 kPa) were also observed (1). As expected, the draft genome contains the genetic repertoire for these physiological traits. T. siberiense encodes the Embden-Meyerhof-Parnas (glycolysis) pathway, pentose phosphate pathway, Entner-Doudoroff pathway, and oxidative tricarboxylic acid cycle. It possesses genes of lactate dehydrogenases, for mixed acid fermentation, and several pathways for monosaccharide degradation. Three nitrogenase operons (two [FeMo]nitrogenases and one [FeFe]nitrogenase) and three [NiFe]hydrogenases (groups 1c, 1d, and 2b) (12) were identified. Respiratory complexes I to IV are present, including high-affinity terminal oxidases (cytochrome bd and cbb3 types) that enable the aerobic growth of T. siberiense at low oxygen concentrations. The motility of T. siberiense is explained by flagellar genes and autotrophic growth by genes encoding the complete Calvin-Benson-Bassham cycle. Acidotolerance (1) is reflected by the presence of genes coding for a potassium-transporting ATPase (kdpABCD) and a potassium uptake system (ktrAB) (13).
Surprisingly, the genome analysis revealed a possible metabolic potential of T. siberiense for sulfur oxidation. A partial thiosulfate-oxidizing machinery (soxEFXYZA) and the sulfur-shuttling system DsrEFH were identified. The partial sox operon is syntenic with the operon structure of the alphaproteobacterial thiosulfate oxidizer Starkeya novella (14), in which soxBCD is located separately. No other sox or dsr genes are present in the draft genome. Experimental evidence is needed to confirm a potential role of T. siberiense in sulfur cycling.
Accession number(s).
The draft genome sequence of Telmatospirillum siberiense 26-4b1 was deposited in GenBank under the accession number PIUM00000000.
ACKNOWLEDGMENTS
We are thankful to Michael Pester for his critical review of the manuscript.
This research was supported by the Austrian Science Fund (FWF) (grants P23117-B17 and P25111-B22 to A.L. and grant P27319-B21 to H.D.) and an ERC advanced grant (NITRICARE) (grant 294343 to M.W.).
Footnotes
Citation Hausmann B, Pjevac P, Schreck K, Herbold CW, Daims H, Wagner M, Loy A. 2018. Draft genome sequence of Telmatospirillum siberiense 26-4b1, an acidotolerant peatland alphaproteobacterium potentially involved in sulfur cycling. Genome Announc 6:e01524-17. https://doi.org/10.1128/genomeA.01524-17.
REFERENCES
- 1.Sizova MV, Panikov NS, Spiridonova EM, Slobodova NV, Tourova TP. 2007. Novel facultative anaerobic acidotolerant Telmatospirillum siberiense gen. nov. sp. nov. isolated from mesotrophic fen. Syst Appl Microbiol 30:213–220. doi: 10.1016/j.syapm.2006.06.003. [DOI] [PubMed] [Google Scholar]
- 2.Hamberger A, Horn MA, Dumont MG, Murrell JC, Drake HL. 2008. Anaerobic consumers of monosaccharides in a moderately acidic fen. Appl Environ Microbiol 74:3112–3120. doi: 10.1128/AEM.00193-08. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Pester M, Bittner N, Deevong P, Wagner M, Loy A. 2010. A “rare biosphere” microorganism contributes to sulfate reduction in a peatland. ISME J 4:1591–1602. doi: 10.1038/ismej.2010.75. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Hunger S, Schmidt O, Hilgarth M, Horn MA, Kolb S, Conrad R, Drake HL. 2011. Competing formate- and carbon dioxide-utilizing prokaryotes in an anoxic methane-emitting fen soil. Appl Environ Microbiol 77:3773–3785. doi: 10.1128/AEM.00282-11. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Kanokratana P, Uengwetwanit T, Rattanachomsri U, Bunterngsook B, Nimchua T, Tangphatsornruang S, Plengvidhya V, Champreda V, Eurwilaichitr L. 2011. Insights into the phylogeny and metabolic potential of a primary tropical peat swamp forest microbial community by metagenomic analysis. Microb Ecol 61:518–528. doi: 10.1007/s00248-010-9766-7. [DOI] [PubMed] [Google Scholar]
- 6.Pankratov TA, Ivanova AO, Dedysh SN, Liesack W. 2011. Bacterial populations and environmental factors controlling cellulose degradation in an acidic Sphagnum peat. Environ Microbiol 13:1800–1814. doi: 10.1111/j.1462-2920.2011.02491.x. [DOI] [PubMed] [Google Scholar]
- 7.Hausmann B, Knorr KH, Schreck K, Tringe SG, Glavina del Rio T, Loy A, Pester M. 2016. Consortia of low-abundance bacteria drive sulfate reduction-dependent degradation of fermentation products in peat soil microcosms. ISME J 10:2365–2375. doi: 10.1038/ismej.2016.42. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Schmidt O, Hink L, Horn MA, Drake HL. 2016. Peat: home to novel syntrophic species that feed acetate- and hydrogen-scavenging methanogens. ISME J 10:1954–1966. doi: 10.1038/ismej.2015.256. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Bankevich A, Nurk S, Antipov D, Gurevich AA, Dvorkin M, Kulikov AS, Lesin VM, Nikolenko SI, Pham S, Prjibelski AD, Pyshkin AV, Sirotkin AV, Vyahhi N, Tesler G, Alekseyev MA, Pevzner PA. 2012. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J Comput Biol 19:455–477. doi: 10.1089/cmb.2012.0021. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Parks DH, Imelfort M, Skennerton CT, Hugenholtz P, Tyson GW. 2015. CheckM: assessing the quality of microbial genomes recovered from isolates, single cells, and metagenomes. Genome Res 25:1043–1055. doi: 10.1101/gr.186072.114. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Overbeek R, Olson R, Pusch GD, Olsen GJ, Davis JJ, Disz T, Edwards RA, Gerdes S, Parrello B, Shukla M, Vonstein V, Wattam AR, Xia F, Stevens R. 2014. The SEED and the Rapid Annotation of microbial genomes using Subsystems Technology (RAST). Nucleic Acids Res 42:D206–D214. doi: 10.1093/nar/gkt1226. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Søndergaard D, Pedersen CNS, Greening C. 2016. HydDB: a Web tool for hydrogenase classification and analysis. Sci Rep 6:34212. doi: 10.1038/srep34212. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Baker-Austin C, Dopson M. 2007. Life in acid: pH homeostasis in acidophiles. Trends Microbiol 15:165–171. doi: 10.1016/j.tim.2007.02.005. [DOI] [PubMed] [Google Scholar]
- 14.Kappler U, Davenport K, Beatson S, Lucas S, Lapidus A, Copeland A, Berry KW, Glavina Del Rio T, Hammon N, Dalin E, Tice H, Pitluck S, Richardson P, Bruce D, Goodwin LA, Han C, Tapia R, Detter JC, Chang YJ, Jeffries CD, Land M, Hauser L, Kyrpides NC, Göker M, Ivanova N, Klenk HP, Woyke T. 2012. Complete genome sequence of the facultatively chemolithoautotrophic and methylotrophic alphaproteobacterium Starkeya novella type strain (ATCC 8093T). Stand Genomic Sci 7:44–58. doi: 10.4056/sigs.3006378. [DOI] [PMC free article] [PubMed] [Google Scholar]