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Abstract

Four Gram-stain-positive, facultative anaerobic, yellow-pigmented and short rod-shaped strains, designated zg-Y625, zg-Y843, zg-Y1090 and zg-Y1211, were isolated from the intestinal contents of in Qinghai Province, PR China. Strains zg-Y625 and zg-Y1090 showed the highest 16S rRNA gene sequence similarities of 99.7% and 99.9% to DSM 112390, respectively, followed by 99.2% and 99.5% to JCM 14341 and 99.1% and 99.0% to LMG 32277. Phylogenetic analyses based on 16S rRNA gene sequences and phylogenomic analyses using whole-genome sequences revealed that these four strains belong to the genus , forming two separate clades distinct from all other known species. The genome sizes of strains zg-Y625 and zg-Y1090 were 3.26 and 3.07 Mb, respectively, with DNA G+C contents of 70.5 and 70.9 mol%. The average nucleotide identity and digital DNA–DNA hybridization values between each of the novel strains and the available members of the genus were all below the species thresholds. Both type strains contained diphosphatidylglycerol and phosphatidylglycerol as predominant polar lipids with one unidentified glycolipid for zg-Y625 and two unidentified glycolipids for zg-Y1090. The predominant respiratory quinone in zg-Y625 was MK-13, whilst in zg-Y1090, both MK-11 and MK-13 were identified as the major quinones. The major fatty acids (>10%) in strains zg-Y625 and zg-Y843 were anteiso-C, anteiso-C and iso-C, whereas for zg-Y1090 and zg-Y1211, the predominant fatty acids were anteiso-C and anteiso-C. Based on phenotypic, phylogenetic, genomic and chemotaxonomic data, two novel species in the genus are proposed, namely, sp. nov. (zg-Y625=GDMCC 1.3931=JCM 36203) and sp. nov. (zg-Y1090=GDMCC 1.3930=JCM 36205).

Funding
This study was supported by the:
  • the Research Units of Discovery of Unknown Bacteria and Function (Award 2018RU010)
    • Principle Award Recipient: XuJianguo
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2025-06-20
2025-07-10
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References

  1. Orla-Jensen S. The Lactic Acid Bacteria Copenhagen: Høst & Sons; 1919
    [Google Scholar]
  2. Collins MD, Jones D, Kroppenstedt RM. Reclassification of Brevibacterium imperiale (Steinhaus) and “Corynebacterium laevaniformans” (Dias and Bhat) in a redefined genus Microbacterium (Orla-Jensen), as Microbacterium imperiale comb. nov. and Microbacterium laevaniformans nom. rev.; comb. nov. Syst Appl Microbiol 1983; 4:65–78 [View Article] [PubMed]
    [Google Scholar]
  3. Takeuchi M, Hatano K. Union of the genera Microbacterium Orla-Jensen and Aureobacterium Collins et al. in a redefined genus Microbacterium. Int J Syst Bacteriol 1998; 48 Pt 3:739–747 [View Article] [PubMed]
    [Google Scholar]
  4. Krishnamurthi S, Bhattacharya A, Schumann P, Dastager SG, Tang S-K et al. Microbacterium immunditiarum sp. nov., an actinobacterium isolated from landfill surface soil, and emended description of the genus Microbacterium. Int J Syst Evol Microbiol 2012; 62:2187–2193 [View Article] [PubMed]
    [Google Scholar]
  5. Alves A, Correia A, Igual JM, Trujillo ME. Microbacterium endophyticum sp. nov. and microbacterium halimionae sp. nov., endophytes isolated from the salt-marsh plant Halimione portulacoides and emended description of the genus Microbacterium. Syst Appl Microbiol 2014; 37:474–479
    [Google Scholar]
  6. Fidalgo C, Riesco R, Henriques I, Trujillo ME, Alves A. Microbacterium diaminobutyricum sp. nov., isolated from Halimione portulacoides, which contains diaminobutyric acid in its cell wall, and emended description of the genus Microbacterium. Int J Syst Evol Microbiol 2016; 66:4492–4500 [View Article] [PubMed]
    [Google Scholar]
  7. Dong K, Yang J, Lu S, Pu J, Lai X-H et al. Microbacterium wangchenii sp. nov., isolated from faeces of Tibetan gazelles (Procapra picticaudata) on the Qinghai-Tibet Plateau. Int J Syst Evol Microbiol 2020; 70:1307–1314 [View Article] [PubMed]
    [Google Scholar]
  8. Tian Z, Yang J, Lai X-H, Pu J, Jin D et al. Microbacterium caowuchunii sp. nov. and Microbacterium lushaniae sp. nov., isolated from plateau pika (Ochotona curzoniae) on the Qinghai-Tibet Plateau of PR China. Int J Syst Evol Microbiol 2021; 71: [View Article] [PubMed]
    [Google Scholar]
  9. Zhou J, Huang Y, Yang J, Lai X-H, Jin D et al. Microbacterium chengjingii sp. nov. and Microbacterium fandaimingii sp. nov., isolated from bat faeces of Hipposideros and Rousettus species. Int J Syst Evol Microbiol 2021; 71: [View Article]
    [Google Scholar]
  10. Ye L, Zhang G, Yang J, Yang C, Liu Y et al. Taxonomic descriptions of Aeromicrobium duanguangcaii sp. nov., Aeromicrobium wangtongii sp. nov. and Aeromicrobium senzhongii sp. nov. Int J Syst Evol Microbiol 2023; 73: [View Article]
    [Google Scholar]
  11. Jin D, Chen C, Li L, Lu S, Li Z et al. Dynamics of fecal microbial communities in children with diarrhea of unknown etiology and genomic analysis of associated Streptococcus lutetiensis. BMC Microbiol 2013; 13:141–152 [View Article] [PubMed]
    [Google Scholar]
  12. Yoon S-H, 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]
  13. 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]
  14. Saitou N, Nei M. The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 1987; 4:406–425 [View Article] [PubMed]
    [Google Scholar]
  15. Felsenstein J. Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol 1981; 17:368–376 [View Article] [PubMed]
    [Google Scholar]
  16. Kolaczkowski B, Thornton JW. Performance of maximum parsimony and likelihood phylogenetics when evolution is heterogeneous. Nature 2004; 431:980–984 [View Article] [PubMed]
    [Google Scholar]
  17. Kumar S, Stecher G, Li M, Knyaz C, Tamura K. MEGA X: molecular evolutionary genetics analysis across computing platforms. Mol Biol Evol 2018; 35:1547–1549 [View Article] [PubMed]
    [Google Scholar]
  18. Thompson JD, Gibson TJ, Higgins DG. Multiple sequence alignment using ClustalW and ClustalX. Curr Protoc Bioinformatics 2002; Chapter 2:Unit 2.3 [View Article] [PubMed]
    [Google Scholar]
  19. 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]
  20. McCarthy A. Third generation DNA sequencing: pacific biosciences’ single molecule real time technology. Chem Biol 2010; 17:675–676 [View Article]
    [Google Scholar]
  21. Chin C-S, Alexander DH, Marks P, Klammer AA, Drake J et al. Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data. Nat Methods 2013; 10:563–569 [View Article] [PubMed]
    [Google Scholar]
  22. Hyatt D, Chen G-L, Locascio PF, Land ML, Larimer FW et al. Prodigal: prokaryotic gene recognition and translation initiation site identification. BMC Bioinformatics 2010; 11:119–129 [View Article] [PubMed]
    [Google Scholar]
  23. Li W, Godzik A. Cd-hit: a fast program for clustering and comparing large sets of protein or nucleotide sequences. Bioinformatics 2006; 22:1658–1659 [View Article] [PubMed]
    [Google Scholar]
  24. Katoh K, Misawa K, Kuma K, Miyata T. MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform. Nucleic Acids Res 2002; 30:3059–3066 [View Article] [PubMed]
    [Google Scholar]
  25. Price MN, Dehal PS, Arkin AP. FastTree: computing large minimum evolution trees with profiles instead of a distance matrix. Mol Biol Evol 2009; 26:1641–1650 [View Article] [PubMed]
    [Google Scholar]
  26. Huson DH, Scornavacca C. Dendroscope 3: an interactive tool for rooted phylogenetic trees and networks. Syst Biol 2012; 61:1061–1067 [View Article] [PubMed]
    [Google Scholar]
  27. Kanehisa M, Goto S. KEGG: kyoto encyclopedia of genes and genomes. Nucleic Acids Res 2000; 28:27–30 [View Article] [PubMed]
    [Google Scholar]
  28. Auch AF, von Jan M, Klenk H-P, Göker M. Digital DNA-DNA hybridization for microbial species delineation by means of genome-to-genome sequence comparison. Stand Genomic Sci 2010; 2:117–134 [View Article] [PubMed]
    [Google Scholar]
  29. Yoon SH, Ha SM, Lim J, Kwon S, Chun J. A large-scale evaluation of algorithms to calculate average nucleotide identity. Antonie Van Leeuwenhoek 2017; 110:1281–1286 [View Article] [PubMed]
    [Google Scholar]
  30. Cantalapiedra CP, Hernández-Plaza A, Letunic I, Bork P, Huerta-Cepas J. eggNOG-mapper v2: functional annotation, orthology assignments, and domain prediction at the metagenomic scale. Mol Biol Evol 2021; 38:5825–5829 [View Article] [PubMed]
    [Google Scholar]
  31. Huerta-Cepas J, Szklarczyk D, Heller D, Hernández-Plaza A, Forslund SK et al. eggNOG 5.0: a hierarchical, functionally and phylogenetically annotated orthology resource based on 5090 organisms and 2502 viruses. Nucleic Acids Res 2019; 47:D309–D314 [View Article] [PubMed]
    [Google Scholar]
  32. 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]
  33. Blin K, Shaw S, Augustijn HE, Reitz ZL, Biermann F et al. antiSMASH 7.0: new and improved predictions for detection, regulation, chemical structures and visualisation. Nucleic Acids Res 2023; 51:W46–W50 [View Article] [PubMed]
    [Google Scholar]
  34. Huang Y, Jiao Y, Zhang S, Tao Y, Zhang S et al. Description of Ornithinimicrobium cryptoxanthini sp. nov., a novel actinomycete producing β-cryptoxanthin isolated from the tongtian river sediments. J Microbiol 2023; 61:379–388 [View Article] [PubMed]
    [Google Scholar]
  35. Horikoshi K. Discovering novel bacteria, with an eye to biotechnological applications. Curr Opin Biotechnol 1995; 6:292–297 [View Article]
    [Google Scholar]
  36. Sasser M. Identification of bacteria by gas chromatography of cellular fatty acids. MIDI Technical Note 1990
    [Google Scholar]
  37. Minnikin DE, O’Donnell AG, Goodfellow M, Alderson G, Athalye M et al. An integrated procedure for the extraction of bacterial isoprenoid quinones and polar lipids. J Microbiol Methods 1984; 2:233–241 [View Article]
    [Google Scholar]
  38. Collins MD, Pirouz T, Goodfellow M, Minnikin DE. Distribution of menaquinones in actinomycetes and corynebacteria. J Gen Microbiol 1977; 100:221–230 [View Article] [PubMed]
    [Google Scholar]
  39. Kroppenstedt RM. Separation of bacterial menaquinones by HPLC using reverse phase (RP18) and a silver loaded ion exchanger as stationary phases. J Liq Chromatogr 1982; 5:2359–2367 [View Article]
    [Google Scholar]
  40. Schleifer KH, Kandler O. Peptidoglycan types of bacterial cell walls and their taxonomic implications. Bacteriol Rev 1972; 36:407–477 [View Article] [PubMed]
    [Google Scholar]
  41. Schleifer KH. Analysis of the chemical composition and primary structure of murein. Method Microbiol 1985; 18:123–156
    [Google Scholar]
  42. Uchida K, Kudo T, Suzuki K-I, Nakase T. A new rapid method of glycolate test by diethyl ether extraction, which is applicable to a small amount of bacterial cells of less than one milligram. J Gen Appl Microbiol 1999; 45:49–56 [View Article] [PubMed]
    [Google Scholar]
  43. Staneck JL, Roberts GD. Simplified approach to identification of aerobic actinomycetes by thin-layer chromatography. Appl Microbiol 1974; 28:226–231 [View Article] [PubMed]
    [Google Scholar]
  44. Suzuki KI, Hamanda M. Microbacterium. In Bergey’s Manual of Systematics of Archaea and Bacteria John Wiley & Sons, Ltd; 2015
    [Google Scholar]
  45. Schippers A, Bosecker K, Sproer C, Schumann P. Microbacterium oleivorans sp. nov. and Microbacterium hydrocarbonoxydans sp. nov., novel crude-oil-degrading gramram-positive bacteria. Int J Syst Evol Microbiol 2005; 55:655–660 [View Article]
    [Google Scholar]
  46. Kim KK, Lee KC, Oh HM, Lee JS. Microbacterium aquimaris sp. nov., isolated from seawater. Int J Syst Evol Microbiol 2008; 58:1616–1620 [View Article] [PubMed]
    [Google Scholar]
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