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Streptomyces Spinosirectus sp. nov., Isolated From the Medicinal Plant Xanthium Sibiricum

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Abstract

A novel actinobacterium, designated strain CRSS-Y-16T, was isolated from the healthy leaves of Xanthium sibiricum, in China and characterized by a polyphasic approach. This strain produced abundant aerial mycelia that generated rod-shaped spores with spiny surfaces. The cell wall contained ll-diaminopimelic acid. The major cellular fatty acids (>10.0%) were C16:0, iso-C16:0, and C18:1 ω9c. The predominant menaquinones were MK-9(H2) and MK-9(H4). The detected polar lipids were diphosphatidylglycerol, hydroxyl phosphatidylethanolamine, phosphatidylethanolamine, phosphatidylinositolmannoside, phospholipids of unknown structure containing glucosamine and unidentified phospholipids. The genomic G+C content was 70.7%. The full-length 16S rRNA gene sequence analysis indicated that strain CRSS-Y-16T belonged to the genus Streptomyces and shared <98.7% sequence similarities with all recognized type species of the genus. Phylogenetic analysis based on 16S rRNA gene sequences showed that this strain formed a distinct branch. Phylogenomic analysis demonstrated that it was closely related to Streptomyces panaciradicis 1MR-8T. However, the clustering patterns resulting from phylogenomic tree verified that strain CRSS-Y-16T represented a novel Streptomyces species. This result was further confirmed by low average nucleotide identity and digital DNA–DNA hybridization values (87.54% and 30.1%) between them. Based on all these data, it is concluded that strain CRSS-Y-16T represents a novel Streptomyces species, for which the name Streptomyces spinosirectus sp. nov. is proposed. The type strain is CRSS-Y-16T (=MCCC 1K06950T=JCM 35007T).

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References

  1. Bérdy J (2005) Bioactive microbial metabolites, a personal view. J Antibiot 58:1–26. https://doi.org/10.1038/ja.2005.1

    Article  Google Scholar 

  2. Bérdy J (2012) Thoughts and facts about antibiotics: where we are now and where we are heading. J Antibiot 65:385–395. https://doi.org/10.1038/ja.2012.54

    Article  CAS  Google Scholar 

  3. Waksman SA, Henrici AT (1943) The nomenclature and classification of the actinomycetes. J Bacteriol 46:337–341. https://doi.org/10.1128/jb.46.4.337-341.1943

    Article  CAS  Google Scholar 

  4. Kumbhar C, Mudliar P, Bhatia L, Kshirsagar A, Watve M (2014) Widespread predatory abilities in the genus Streptomyces. Arch Microbiol 196:235–248. https://doi.org/10.1007/s00203-014-0961-7

    Article  CAS  Google Scholar 

  5. Stone JK, Bacon CW, White JF (2000) An overview of endophytic microbes: endophytism defined. In: Bacon CW, White JF (eds) Microbial endophytes. Marcel Dekker Inc, New York, pp 3–29

    Google Scholar 

  6. Janso JE, Carter GT (2010) Biosynthetic potential of phylogenetically unique endophytic actinomycetes from tropical plants. Appl Environ Microbiol 76:4377–4386. https://doi.org/10.1128/AEM.02959-09

    Article  CAS  Google Scholar 

  7. Masand M, Jose PA, Menghani E, Jebakumar SRD (2015) Continuing hunt for endophytic actinomycetes as a source of novel biologically active metabolites. World J Microbiol Biotechnol 31:1863–1875. https://doi.org/10.1007/s11274-015-1950-y

    Article  CAS  Google Scholar 

  8. Hu SR, Wang YF, Wang JZ, Liu KY, Tang XK, Gao J (2021) Streptomyces xanthii sp. Nov. and Streptomyces roseirectus sp. Nov. isolated from a Chinese medicinal plant. Int J Syst Evol Microbiol. https://doi.org/10.1099/ijsem.0.004962

    Article  Google Scholar 

  9. Atlas RM (1993). In: Parks LC (ed) Handbook of Microbiological Media. CRC Press, Boca Raton

    Google Scholar 

  10. Shirling EB, Gottlieb D (1966) Methods for characterization of Streptomyces species. Int J Syst Bacteriol 16:313–340. https://doi.org/10.1099/00207713-16-3-313

    Article  Google Scholar 

  11. Ridgway R (1912) Color standards and color nomenclature. Published by the author, Washington, DC

    Book  Google Scholar 

  12. Xu LH, Li WJ, Liu ZH, Jiang CL (2007) Actinomycetes systematics: principles, methods and practices. Science Press, Beijing, China (in Chinese)

    Google Scholar 

  13. Lechevalier MP, Lechevalier H (1970) Chemical composition as a criterion in the classification of aerobic actinomycetes. Int J Syst Bacteriol 20:433–435. https://doi.org/10.1099/00207713-20-4-435

    Article  Google Scholar 

  14. Hasegawa T, Takizawa M, Tanida S (1983) A rapid analysis for chemical grouping of aerobic actinomycetes. J Gen Appl Microbiol 29:319–322

    Article  CAS  Google Scholar 

  15. Collins MD, Pirouz T, Goodfellow M, Minnikin DE (1977) Distribution of menaquinones in actinomycetes and corynebacteria. J Gen Microbiol 100:221–230. https://doi.org/10.1099/00221287-100-2-221

    Article  CAS  Google Scholar 

  16. Kates M (1986) Techniques of lipidology, 2nd edn. Elsevier, Amsterdam

    Google Scholar 

  17. Richter M, Rosselló-Móra R, Glöckner FO, Peplies J (2016) JSpeciesWS: a web server for prokaryotic species circumscription based on pairwise genome comparison. Bioinformatics 32:929–931. https://doi.org/10.1093/bioinformatics/btv681

    Article  CAS  Google Scholar 

  18. Aziz RK, Bartels D, Best AA, DeJongh M, Disz T, Edwards RA, Formsma K, Gerdes S, Glass EM, Kubal M et al (2008) The RAST server: rapid annotations using subsystems technology. BMC Genomics 9:75. https://doi.org/10.1186/1471-2164-9-75

    Article  CAS  Google Scholar 

  19. Blin K, Shaw S, Kloosterman AM, Charlop-Powers Z, van Wezel GP, Medema MH, Weber T (2021) antiSMASH 6.0: improving cluster detection and comparison capabilities. Nucleic Acids Res. https://doi.org/10.1093/nar/gkab335

    Article  Google Scholar 

  20. Alcock BP, Raphenya AR, Lau TTY, Tsang KK, Bouchard M, Edalatmand A, Huynh W, Nguyen AV, Cheng AA, Liu S et al (2020) CARD 2020: antibiotic resistome surveillance with the comprehensive antibiotic resistance database. Nucleic Acids Res 48(D1):D517–D525. https://doi.org/10.1093/nar/gkz935

    Article  CAS  Google Scholar 

  21. Makarova KS, Wolf YI, Iranzo J, Shmakov SA, Alkhnbashi OS, Brouns SJJ, Charpentier E, Cheng D, Haft DH, Horvath P et al (2019) Evolutionary classification of CRISPR–Cas systems: a burst of class 2 and derived variants. Nat Rev Microbiol 18:67–83. https://doi.org/10.1038/s41579-019-0299-x

    Article  CAS  Google Scholar 

  22. Claire B, Laird MR, Williams KP, Lau BY, Hoad G, Winsor GL, Brinkman FSL, Simon Fraser University Research Computing Group (2017) IslandViewer 4: expanded prediction of genomic islands for larger-scale datasets. Nucleic Acids Res. https://doi.org/10.1093/nar/gkx343

    Article  Google Scholar 

  23. Weisburg WG, Barns SM, Pelletier DA, Lane DJ (1991) 16S ribosomal DNA amplification for phylogenetic study. J Bacteriol 173:697–703. https://doi.org/10.1128/jb.173.2.697-703.1991

    Article  CAS  Google Scholar 

  24. Lane DJ (1991) 16S/23S rRNA sequencing. In: Stackebrandt E, Goodfellow M (eds) Nucleic acid techniques in bacterial systematics. Wiley, New York, pp 115–175

    Google Scholar 

  25. Yoon SH, Ha SM, Kwon S, Lim J, Kim Y, Seo H, Chun J (2017) Introducing EzBioCloud: a taxonomically united database of 16S rRNA and whole genome assemblies. Int J Syst Evol Microbiol 67:1613–1617. https://doi.org/10.1099/ijsem.0.001755

    Article  CAS  Google Scholar 

  26. Saitou N, Nei M (1987) The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 4:406–425. https://doi.org/10.1093/oxfordjournals.molbev.a040454

    Article  CAS  Google Scholar 

  27. Felsenstein J (1981) Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol 17:368–376. https://doi.org/10.1007/BF01734359

    Article  CAS  Google Scholar 

  28. Kluge AG, Farris FS (1969) Quantitative phyletics and the evolution of anurans. Syst Zool 18:1–32

    Article  Google Scholar 

  29. Tamura K, Stecher G, Kumar S (2021) MEGA11: molecular evolutionary genetics analysis version 11. Mol Biol Evol 38:3022–3027. https://doi.org/10.1093/molbev/msab120

    Article  CAS  Google Scholar 

  30. Meier-Kolthoff JP, Sardà Carbasse J, Peinado-Olarte RL, Göker M (2022) TYGS and LPSN: a database tandem for fast and reliable genome-based classification and nomenclature of prokaryotes. Nucleic Acid Res 50:D801–D807. https://doi.org/10.1093/nar/gkab902

    Article  CAS  Google Scholar 

  31. Meier-Kolthoff JP, Auch AF, Klenk HP, Göker M (2013) Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinformatics 14:60. https://doi.org/10.1186/1471-2105-14-60

    Article  Google Scholar 

  32. Wright F, Bibb MJ (1992) Codon usage in the G+C-rich Streptomyces genome. Gene 113:55–65. https://doi.org/10.1016/0378-1119(92)90669-g

    Article  CAS  Google Scholar 

  33. Stackebrandt E, Ebers J (2006) Taxonomic parameters revisited: the tarnished “gold standard.” Microbiol Today 33:152–155

    Google Scholar 

  34. Hu SR, Li KQ, Zhang YF, Wang YF, Li Fu, Yan X, Tang XK, Gao J (2022) New insights into the threshold values of multi-locus sequence analysis, average nucleotide identity and digital DNA–DNA hybridization in delineating Streptomyces species. Front Microbiol 13:910277. https://doi.org/10.3389/fmicb.2022.910277

    Article  Google Scholar 

  35. Wayne LG, Brenner DJ, Colwell RR, Grimont PAD, Kandler O, Krichevsky MI, Moore LH, Moore WEC, Murray RGE, Stackebrandt E et al (1987) International Committee on Systematic Bacteriology. Report of the ad hoc committee on the reconciliation of approaches to bacterial systematics. Int J Syst Bacteriol 37:463–464. https://doi.org/10.1099/00207713-37-4-463

    Article  Google Scholar 

  36. Vincent L, Richard D, Olivier G (2015) FastME 2.0: a comprehensive, accurate, and fast distance-based phylogeny inference program. Mol Biol Evol 32:2798–2800. https://doi.org/10.1093/molbev/msv150

    Article  CAS  Google Scholar 

  37. Farris JS (1972) Estimating Phylogenetic Trees from Distance Matrices. Am Nat 106:645–668

    Article  Google Scholar 

  38. Lee HJ, Cho GY, Chung SH, Whang KS (2014) Streptomyces panaciradicis sp. nov., a b-glucosidase-producing bacterium isolated from ginseng rhizoplane. Int J Syst Evol Microbiol 64:3816–3820. https://doi.org/10.1099/ijs.0.061705-0

    Article  CAS  Google Scholar 

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Acknowledgements

The authors are grateful to Prof. Aharon Oren (The Hebrew University of Jerusalem, Israel) for helping with the etymology.

Funding

This work was supported by the Hunan Provincial Natural Science Foundation of China and Xiangtan Science and Technology Bureau (2022JJ50125) and Scientific Research Project of Hunan Province Department of Education (20A200).

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YFW and SRH carried out the polyphasic taxonomy, data analysis and wrote the manuscript. LF and XKT prepared figures and tables. YX provided the samples. JG corrected and reviewed the paper and takes full responsibility for the final submission. All authors reviewed and approved the final version of the paper.

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Correspondence to Jian Gao.

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Wang, YF., Hu, SR., Fu, L. et al. Streptomyces Spinosirectus sp. nov., Isolated From the Medicinal Plant Xanthium Sibiricum. Curr Microbiol 80, 27 (2023). https://doi.org/10.1007/s00284-022-03134-7

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