1887

Abstract

Two Gram-stain-positive, non-motile, strictly aerobic, yellow-coloured, rod-shaped bacterial strains, designated LR1S40 and M4N3S171, were isolated from rhizosphere and bulk saline soil of collected in Inner Mongolia, China. Phylogenetic trees based on 16S rRNA gene and whole genome sequences showed that the two strains clustered tightly with strains of the genus . Strains LR1S40 and M4N3S171 had 95.5% 16S rRNA gene similarity to each other, and strain LR1S40 had 98.8, 98.7, 97.4 and <97.0% similarity to RN3S43, LNNU 22110, YIM 93306 and all other current type strains, while strain M4N3S171 had 98.6 and <97.0% similarity to YIM 93306, and all other current type strains, respectively. The average nucleotide identity based on (ANIb) and digital DNA–DNA hybridization (dDDH) values of LR1S40 and M4N3S171 with each other and to the other type strains of were well below the threshold values (95% for ANIb, 70% for dDDH) for differentiating a species. Diphosphatidylglycerol and phosphatidylglycerol were the major polar lipids in both strains. The predominant menaquinone in both strains was both MK-8. The genome of strain LR1S40 consisted of a 3557440 bp circular chromosome, with a G+C content of 71.1 mol%, while the genome of strain M4N3S171 consisted of 4270413 bp, with a G+C content of 67.6 mol%. The phylogenetic, physiological and phenotypic characteristics allowed discrimination of the two strains from their relatives. The names sp. nov. [type strain LR1S40 (=CGMCC 1.19028=KCTC 49726)] and sp. nov. [type strain M4N3S171 (=CGMCC 1. 19142=KCTC 49727)] are therefore proposed. During the publication of , (type strain T3246-1), which was selected as the reference strain for the identification of , was reclassified as . The two phylogenetic trees showed that HY164 tightly clustered with F300, and had the highest 16S rRNA gene similarity (99.8%) to F300. Based on the phylogenetic analysis and the publication record, should be reclassified as comb. nov.

Funding
This study was supported by the:
  • Natural Science Foundation of Inner Mongolia Autonomous Region of China (Award 2021MS03031)
    • Principle Award Recipient: Ji-QuanSun
Loading

Article metrics loading...

/content/journal/ijsem/10.1099/ijsem.0.005443
2022-06-28
2024-04-27
Loading full text...

Full text loading...

References

  1. Gu Q, Paściak M, Luo H, Gamian A, Liu Z et al. Ruania albidiflava gen. nov., sp. nov., a novel member of the suborder Micrococcineae. Int J Syst Evol Microbiol 2007; 57:809–814 [View Article]
    [Google Scholar]
  2. Schumann P, Kalensee F, Cao J, Criscuolo A, Clermont D et al. Reclassification of Haloactinobacterium glacieicola as Occultella glacieicola gen. nov., comb. nov., of Haloactinobacterium album as Ruania alba comb. nov, with an emended description of the genus Ruania, recognition that the genus names Haloactinobacterium and Ruania are heterotypic synonyms and description of Occultella aeris sp. nov., a halotolerant isolate from surface soil sampled at an ancient copper smelter. Int J Syst Evol Microbiol 2021; 71: [View Article]
    [Google Scholar]
  3. Tang S-K, Zhi X-Y, Wang Y, Wu J-Y, Lee J-C et al. Haloactinobacterium album gen. nov., sp. nov., a halophilic actinobacterium, and proposal of Ruaniaceae fam. nov. Int J Syst Evol Microbiol 2010; 60:2113–2119 [View Article]
    [Google Scholar]
  4. Xu M, Dai Y, Huang Y, Yang J, Lai X-H et al. Identification of Haloactinobacterium kanbiaonis sp. nov. and Ruania zhangjianzhongii sp. nov., two novel species of the family Ruaniaceae isolated from faeces of bats (Hipposideros spp.). Int J Syst Evol Microbiol 2021; 71: [PubMed]
    [Google Scholar]
  5. Lu W-N, Xu Y-Z, Xie Y-G, Gao R, Song J-Q et al. Ruania rhizosphaerae sp. nov., a novel actinobacterium isolated from rhizosphere of Suaeda aralocaspica. Int J Syst Evol Microbiol 2021; 71: [View Article] [PubMed]
    [Google Scholar]
  6. Sun J-Q, Yiayeng PE, Xu L, Huang X-X, Li Y. Ruania alkalisoli sp. nov., isolated from saline-alkaline soil. Curr Microbiol 2021; 78:3285–3291 [View Article]
    [Google Scholar]
  7. Oren A, Garrity GM. Valid publication of new names and new combinations effectively published outside the IJSEM. Int J Syst Evol Microbiol 2021; 71:11 [PubMed]
    [Google Scholar]
  8. Gilroy R, Ravi A, Getino M, Pursley I, Horton DL et al. Extensive microbial diversity within the chicken gut microbiome revealed by metagenomics and culture. PeerJ 2021; 9:e10941 [View Article] [PubMed]
    [Google Scholar]
  9. Wang S, Yang R, Xu L, Xing Y-T, Sun J-Q. Qingshengfaniella alkalisoli gen. nov., sp. nov., a p-hydroxybenzoate-degrading strain isolated from saline soil. Int J Syst Evol Microbiol 2019; 71: [View Article]
    [Google Scholar]
  10. Xing Y-T, Xu L, Wang H-T, Huang X-X, Wang S et al. Echinicola soli sp. nov., isolated from alkaline saline soil. Int J Syst Evol Microbiol 2020; 70:4139–4144 [View Article] [PubMed]
    [Google Scholar]
  11. Xu L, Huang X-X, Fan D-L, Sun J-Q. Lysobacter alkalisoli sp. nov., a chitin-degrading strain isolated from saline-alkaline soil. Int J Syst Evol Microbiol 2020; 70:1273–1281 [View Article] [PubMed]
    [Google Scholar]
  12. Xu L, Sun J-Q, Wang L-J, Gao Z-W, Sun L-Z et al. Sphingobacterium alkalisoli sp. nov., isolated from a saline-alkaline soil. Int J Syst Evol Microbiol 2017; 67:1943–1948 [View Article] [PubMed]
    [Google Scholar]
  13. Xu L, Wang H-T, Zhang J-X, Zhang H, Wang S et al. Flavobacterium alkalisoli sp. nov., isolated from rhizosphere soil of Suaeda salsa. Int J Syst Evol Microbiol 2020; 70:3888–3898 [PubMed]
    [Google Scholar]
  14. Zhang H, Xu L, Zhang J-X, Sun J-Q. Sphingomonas suaedae sp. nov., a chitin-degrading strain isolated from rhizosphere soil of Suaeda salsa. Int J Syst Evol Microbiol 2020; 70:3816–3823 [View Article] [PubMed]
    [Google Scholar]
  15. Sun J-Q, Huang X-X, Xu L, Wei H-M. Luteimonas saliphila sp. nov. and Luteimonas salinisoli sp. nov., two novel strains isolated from saline soils. Int J Syst Evol Microbiol 2022; 72: [View Article] [PubMed]
    [Google Scholar]
  16. Sun J-Q, Xu L, Liu M, Wang X-Y, Wu X-L. Flavobacterium suaedae sp. nov., an endophyte isolated from the root of Suaeda corniculata. Int J Syst Evol Microbiol 2016; 66:1943–1949 [View Article] [PubMed]
    [Google Scholar]
  17. Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG. The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 1997; 25:4876–4882 [View Article] [PubMed]
    [Google Scholar]
  18. Tamura K, Stecher G, Peterson D, Filipski A, Kumar S. MEGA6: Molecular Evolutionary Genetics Analysis version 6.0. Mol Biol Evol 2013; 30:2725–2729 [View Article]
    [Google Scholar]
  19. Ma J-P, Wang Z, Lu P, Wang H, Waseem Ali S et al. Biodegradation of the sulfonylurea herbicide chlorimuron-ethyl by the strain Pseudomonas sp. LW3. FEMS Microbiol Lett 2009; 296:203–209 [View Article] [PubMed]
    [Google Scholar]
  20. 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 [View Article] [PubMed]
    [Google Scholar]
  21. Richter M, Rosselló-Móra R, Oliver Glöckner F, Peplies J. JSpeciesWS: a web server for prokaryotic species circumscription based on pairwise genome comparison. Bioinformatics 2016; 32:929–931 [View Article] [PubMed]
    [Google Scholar]
  22. 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]
  23. Emms DM, Kelly S. OrthoFinder: phylogenetic orthology inference for comparative genomics. Genome Biol 2019; 20:238 [View Article] [PubMed]
    [Google Scholar]
  24. Chaudhari NM, Gupta VK, Dutta C. BPGA- an ultra-fast pan-genome analysis pipeline. Sci Rep 2016; 6:24373 [View Article] [PubMed]
    [Google Scholar]
  25. 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]
  26. Moriya Y, Itoh M, Okuda S, Yoshizawa AC, Kanehisa M. KAAS: an automatic genome annotation and pathway reconstruction server. Nucleic Acids Res 2007; 35:W182–5 [View Article] [PubMed]
    [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. Smibert RM, Krieg NR. Phenotypic characterization. In Methods for General and Molecular Bacteriology Washington, DC: American Society for Microbiology; 1994
    [Google Scholar]
  29. Dong XZ, Cai MY. Determinative Manual for Routine Bacteriology Beijing: Scientific Press; 2001
    [Google Scholar]
  30. Kates M. Techniques of Llipidology, 2nd edn. Amsterdam: Elsevier; 1986
    [Google Scholar]
  31. Sasser M. Identification of Bacteria by Gas Chromatography of Cellular Fatty Acids, MIDI Technical Note 101 Newark, DE: MIDI Inc; 1990
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/ijsem/10.1099/ijsem.0.005443
Loading
/content/journal/ijsem/10.1099/ijsem.0.005443
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