1887

Abstract

Three bacterial strains, designated Red330, Red736 and Red745, were isolated from forest and paddy soils in Japan. Strains Red330, Red736 and Red745 are flagella-harbouring and strictly anaerobic bacteria forming red colonies. A 16S rRNA gene sequence-based phylogenetic tree showed that all three strains were located in a cluster, including the type strains of species, which were recently separated from the genus within the family . Similarities of the 16S rRNA gene sequences among the three strains and S43, the type species of the genus , were 96.3–98.5 %. The genome-related indexes, average nucleotide identity, digital DNA–DNA hybridization, and average amino acid identity, among the three strains and e S43 were 74.7–86.8 %, 21.2–33.3 % and 70.4–89.8 %, respectively, which were lower than the species delineation thresholds. Regarding the phylogenetic relationships based on genome sequences, the three strains clustered with the type strains of species, which were independent from the type strains of species. The distinguishableness of the three isolated strains was supported by physiological and chemotaxonomic properties, with the profile of availability of electron donors and cellular fatty acids composition being particularly different among them. Based on genetic, phylogenetic and phenotypic properties, the three isolates represent three novel independent species in the genus , for which the names sp. nov., sp. nov. and sp. nov. are proposed. The type strains are Red330 (=NBRC 114028=MCCC 1K03949), Red736 (=NBRC 114029=MCCC 1K03950) and Red745 (=NBRC 114030=MCCC 1K03951), respectively.

Funding
This study was supported by the:
  • Japan Society for the Promotion of Science (Award JP18K14366)
    • Principle Award Recipient: YokoMasuda
  • Japan Society for the Promotion of Science (Award JP18K19165)
    • Principle Award Recipient: KeishiSenoo
  • Japan Society for the Promotion of Science (Award JP18K19165)
    • Principle Award Recipient: HideomiItoh
  • Japan Society for the Promotion of Science (Award JP17H01464)
    • Principle Award Recipient: KeishiSenoo
  • Japan Society for the Promotion of Science (Award JP17H01464)
    • Principle Award Recipient: HideomiItoh
Loading

Article metrics loading...

/content/journal/ijsem/10.1099/ijsem.0.004607
2020-12-09
2024-04-19
Loading full text...

Full text loading...

/deliver/fulltext/ijsem/71/1/ijsem004607.html?itemId=/content/journal/ijsem/10.1099/ijsem.0.004607&mimeType=html&fmt=ahah

References

  1. Xu Z, Masuda Y, Itoh H, Ushijima N, Shiratori Y et al. Geomonas oryzae gen. nov., sp. nov., Geomonas edaphica sp. nov., Geomonas ferrireducens sp. nov., Geomonas terrae sp. nov., four Ferric-reducing bacteria isolated from paddy soil, and reclassification of three species of the genus Geobacter as members of the genus Geomonas gen. nov. Front Microbiol 2019; 10:2201 [View Article][PubMed]
    [Google Scholar]
  2. Masuda Y, Itoh H, Shiratori Y, Isobe K, Otsuka S et al. Predominant but previously-overlooked prokaryotic drivers of reductive nitrogen transformation in paddy soils, revealed by metatranscriptomics. Microbes Environ 2017; 32:180–183 [View Article][PubMed]
    [Google Scholar]
  3. Masuda Y, Itoh H, Shiratori Y, Senoo K. Metatranscriptomic insights into microbial consortia driving methane metabolism in paddy soils. Soil Sci Plant Nutr 2018; 64:455–464 [View Article]
    [Google Scholar]
  4. Holmes DE, Finneran KT, O'Neil RA, Lovley DR. Enrichment of members of the family Geobacteraceae associated with stimulation of dissimilatory metal reduction in uranium-contaminated aquifer sediments. Appl Environ Microbiol 2002; 68:2300–2306 [View Article][PubMed]
    [Google Scholar]
  5. Hori T, Aoyagi T, Itoh H, Narihiro T, Oikawa A et al. Isolation of microorganisms involved in reduction of crystalline iron(III) oxides in natural environments. Front Microbiol 2015; 6:386 [View Article][PubMed]
    [Google Scholar]
  6. Mei R, Nobu MK, Narihiro T, Yu J, Sathyagal A et al. Novel Geobacter species and diverse methanogens contribute to enhanced methane production in media-added methanogenic reactors. Water Res 2018; 147:403–412 [View Article][PubMed]
    [Google Scholar]
  7. Xu Z, Masuda Y, Hayakawa C, Ushijima N, Kawano K et al. Description of three novel members in the family Geobacteraceae, Oryzomonas japonicum gen. nov., sp. nov., Oryzomonas sagensis sp. nov., and Oryzomonas ruber sp. nov. Microorganisms 2020; 8:634 [View Article][PubMed]
    [Google Scholar]
  8. Masuda Y, Yamanaka H, Xu Z-X, Shiratori Y, Aono T et al. Diazotrophic Anaeromyxobacter Isolates from Soils. Appl Environ Microbiol 2020; 86:e00956–20 [View Article][PubMed]
    [Google Scholar]
  9. Kawano K, Ushijima N, Kihara M, Itoh H. Patiriisocius marinistellae gen. nov., sp. nov., isolated from the starfish Patiria pectinifera, and reclassification of Ulvibacter marinus as a member of the genus Patiriisocius comb. nov. Int J Syst Evol Microbiol 2020; 70:4119–4129 [View Article][PubMed]
    [Google Scholar]
  10. Yoon SH, Ha S-M, Kwon S, Lim J, Kim Y et al. Introducing EzBioCloud: a taxonomically united database of 16S rRNA gene sequences and whole-genome assemblies. Int J Syst Evol Microbiol 2017; 67:1613–1617 [View Article][PubMed]
    [Google Scholar]
  11. Cole JR, Wang Q, Fish JA, Chai B, McGarrell DM et al. Ribosomal database project: data and tools for high throughput rRNA analysis. Nucleic Acids Res 2014; 42:D633–D642 [View Article][PubMed]
    [Google Scholar]
  12. Kimura M. A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. J Mol Evol 1980; 16:111–120 [View Article][PubMed]
    [Google Scholar]
  13. Kumar S, Stecher G, Tamura K. mega7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol 2016; 33:1870–1874 [View Article][PubMed]
    [Google Scholar]
  14. Kim M, Oh H-S, Park S-C, Chun J. Towards a taxonomic coherence between average nucleotide identity and 16S rRNA gene sequence similarity for species demarcation of prokaryotes. Int J Syst Evol Microbiol 2014; 64:346–351 [View Article][PubMed]
    [Google Scholar]
  15. Yarza P, Yilmaz P, Pruesse E, Glöckner FO, Ludwig W et al. Uniting the classification of cultured and uncultured bacteria and archaea using 16S rRNA gene sequences. Nat Rev Microbiol 2014; 12:635–645 [View Article][PubMed]
    [Google Scholar]
  16. Itoh H, Kawano K, Kihara M. Draft genome sequence of Agarivorans sp. strain Toyoura001, isolated from an abalone gut. Microbiol Resour Announc 2019; 8:e00169–00119 [View Article][PubMed]
    [Google Scholar]
  17. Zerbino DR, Birney E. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res 2008; 18:821–829 [View Article][PubMed]
    [Google Scholar]
  18. Tanizawa Y, Fujisawa T, Nakamura Y. DFAST: a flexible prokaryotic genome annotation pipeline for faster genome publication. Bioinformatics 2018; 34:1037–1039 [View Article]
    [Google Scholar]
  19. Kanehisa M, Sato Y, Morishima K. BlastKOALA and GhostKOALA: KEGG tools for functional characterization of genome and metagenome sequences. J Mol Biol 2016; 428:726–731 [View Article][PubMed]
    [Google Scholar]
  20. Lu S, Wang J, Chitsaz F, Derbyshire MK, Geer RC et al. CDD/SPARCLE: the conserved domain database in 2020. Nucleic Acids Res 2020; 48:D265–D268 [View Article][PubMed]
    [Google Scholar]
  21. Meier-Kolthoff JP, Auch AF, Klenk HP, Göker M. Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinformatics 2013; 14:60 [View Article][PubMed]
    [Google Scholar]
  22. Rodriguez-R LM, Konstantinidis KT. The enveomics collection: atoolbox for specialized analyses of microbial genomes and meta-genomes. PeerJ 2016e1900v1
    [Google Scholar]
  23. Na S-I, Kim YO, Yoon S-H, Ha S-M, Baek I, SI N et al. UBCG: up-to-date bacterial core gene set and pipeline for phylogenomic tree reconstruction. J Microbiol 2018; 56:280–285 [View Article][PubMed]
    [Google Scholar]
  24. Aklujkar M, Young ND, Holmes D, Chavan M, Risso C et al. The genome of Geobacter bemidjiensis, exemplar for the subsurface clade of Geobacter species that predominate in Fe(III)-reducing subsurface environments. BMC Genomics 2010; 11:490–18 [View Article]
    [Google Scholar]
  25. Lu X, Liu Y, Johs A, Zhao L, Wang T et al. Anaerobic mercury methylation and demethylation by Geobacter bemidjiensis Bem. Environ Sci Technol 2016; 50:4366–4373 [View Article][PubMed]
    [Google Scholar]
  26. Schmelling NM, Lehmann R, Chaudhury P, Beck C, Albers SV et al. Minimal tool set for a prokaryotic circadian clock. BMC Evol Biol 2017; 17:1–20 [View Article]
    [Google Scholar]
  27. Chun J, Oren A, Ventosa A, Christensen H, Arahal DR et al. Proposed minimal standards for the use of genome data for the taxonomy of prokaryotes. Int J Syst Evol Microbiol 2018; 68:461–466 [View Article][PubMed]
    [Google Scholar]
  28. Richter M, Rosselló-Móra R. Shifting the genomic gold standard for the prokaryotic species definition. Proc Natl Acad Sci U S A 2009; 106:19126–19131 [View Article][PubMed]
    [Google Scholar]
  29. Luo C, Rodriguez-R LM, Konstantinidis KT. MyTaxa: an advanced taxonomic classifier for genomic and metagenomic sequences. Nucleic Acids Res 2014; 42:e73 [View Article][PubMed]
    [Google Scholar]
  30. Suzuki D, Ueki A, Shizuku T, Ohtaki Y, Ueki K. Desulfovibrio butyratiphilus sp. nov., a gram-negative, butyrate-oxidizing, sulfate-reducing bacterium isolated from an anaerobic municipal sewage sludge digester. Int J Syst Evol Microbiol 2010; 60:595–602 [View Article][PubMed]
    [Google Scholar]
  31. Lovley DR, Giovannoni SJ, White DC, Champine JE, Phillips EJ et al. Geobacter metallireducens gen. nov. sp. nov., a microorganism capable of coupling the complete oxidation of organic compounds to the reduction of iron and other metals. Arch Microbiol 1993; 159:336–344 [View Article][PubMed]
    [Google Scholar]
  32. Kuykendall LD, Roy MA, O'neill JJ, Devine TE. Fatty acids, antibiotic resistance, and deoxyribonucleic acid homology groups of Bradyrhizobium japonicum . Int J Syst Bacteriol 1988; 38:358–361 [View Article]
    [Google Scholar]
  33. Nevin KP, Holmes DE, Woodard TL, Hinlein ES, Ostendorf DW et al. Geobacter bemidjiensis sp. nov. and Geobacter psychrophilus sp. nov., two novel Fe(III)-reducing subsurface isolates. Int J Syst Evol Microbiol 2005; 55:1667–1674 [View Article][PubMed]
    [Google Scholar]
  34. Straub KL, Buchholz-Cleven BE. Geobacter bremensis sp. nov. and Geobacter pelophilus sp. nov., two dissimilatory ferric-iron-reducing bacteria. Int J Syst Evol Microbiol 2001; 51:1805–1808 [View Article][PubMed]
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/ijsem/10.1099/ijsem.0.004607
Loading
/content/journal/ijsem/10.1099/ijsem.0.004607
Loading

Data & Media loading...

Supplements

Supplementary material 1

PDF
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error