1887

Abstract

The taxonomic position of a novel actinomycete isolate, designated strain GGCR-6, isolated from the healthy leaves of collected from the botanic garden of Hunan University of Science and Technology in Hunan province, PR China, was determined by a polyphasic approach. GGCR-6 grew well on ISP series media and formed well-developed, branched substrate hyphae and aerial mycelium that differentiated into straight spore chains consisting of cylindrical spores with smooth surfaces. The diagnostic diamino acid was -diaminopimelic acid. The major menaquinones were MK-9(H), MK-9(H), MK-9 and MK-9(H). The polar lipids were diphosphatidylglycerol, phosphatidylethanolamine, phosphotidylinositol and phosphatidylinositol mannosides. The predominant fatty acids were Cω9, iso-C and C. The phenotypic characteristics of GGCR-6 indicated that it represented a member of the genus . Phylogenetic analysis based on the 16S rRNA gene sequence indicated that GGCR-6 was most closely related to NRRL B2296 and NRRL B1818. However, the digital DNA–DNA hybridization, the average nucleotide identity and the multi locus sequence analysis evolutionary distance clearly separate GGCR-6 from the phylogenetically closely related species. Furthermore, the novel isolate was distinctly differentiated from NRRL B2296 and NRRL B1818 by morphological, physiological and biochemical characteristics. Based on these data, strain GGCR-6 should be designated as a representative of a novel species of the genus , for which the name sp. nov. is proposed. The type strain is strain GGCR-6 (=CICC 11055=JCM 33584).

Funding
This study was supported by the:
  • Postgraduate Research and Innovation Project of Hunan Province (Award CX2018B676)
    • Principle Award Recipient: Li Kaiqin
  • Scientific Research Project of Hunan Province Department of Education (Award 16K032)
    • Principle Award Recipient: Gao Jian
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2020-01-22
2024-04-25
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References

  1. Sharma VK, Johnson N, Cizmas L, McDonald TJ, Kim H. A review of the influence of treatment strategies on antibiotic resistant bacteria and antibiotic resistance genes. Chemosphere 2016; 150:702–714 [View Article]
    [Google Scholar]
  2. Lathers CM. Role of veterinary medicine in public health: antibiotic use in food animals and humans and the effect on evolution of antibacterial resistance. J Clin Pharmacol 2001; 41:595–599 [View Article]
    [Google Scholar]
  3. Schulz B, Boyle C. Microbial root endophytes. In Sieber TN. editor What Are Endophytes? Berlin: Springer; 2006 pp 1–13
    [Google Scholar]
  4. Golinska P, Wypij M, Agarkar G, Rathod D, Dahm H et al. Endophytic actinobacteria of medicinal plants: diversity and bioactivity. Antonie van Leeuwenhoek 2015; 108:267–289 [View Article]
    [Google Scholar]
  5. Radha S, Dubey AK. Diversity and applications of endophytic actinobacteria of plants in special and other ecological niches. Front Microbiol 1767; 2018:9
    [Google Scholar]
  6. Masand M, Jose PA, Menghani E, Jebakumar SRD. Continuing hunt for endophytic actinomycetes as a source of novel biologically active metabolites. World J Microbiol Biotechnol 2015; 31:1863–1875 [View Article]
    [Google Scholar]
  7. Verma VC, Gond SK, Kumar A, Mishra A, Kharwar RN et al. Endophytic actinomycetes from Azadirachta indica A. Juss.: isolation, diversity, and anti-microbial activity. Microb Ecol 2009; 57:749–756 [View Article]
    [Google Scholar]
  8. Wang P, Kong F, Wei J, Wang Y, Wang W et al. Alkaloids from the mangrove-derived actinomycete Jishengella endophytica 161111. Mar Drugs 2014; 12:477–490 [View Article]
    [Google Scholar]
  9. Bérdy J. Thoughts and facts about antibiotics: where we are now and where we are heading. J Antibiot 2012; 65:385–395 [View Article]
    [Google Scholar]
  10. Qin S, Li J, Chen H-H, Zhao G-Z, Zhu W-Y et al. Isolation, diversity, and antimicrobial activity of rare actinobacteria from medicinal plants of tropical rain forests in Xishuangbanna, China. Appl Environ Microbiol 2009; 75:6176–6186 [View Article]
    [Google Scholar]
  11. Mo P, Zhao J, Li K, Tang X, Gao J et al. Streptomyces manganisoli sp. nov., a novel actinomycete isolated from manganese-contaminated soil. Int J Syst Evol Microbiol 2018; 68:1890–1895 [View Article]
    [Google Scholar]
  12. Atlas RM. Parks LC. editor Handbook of Microbiological Media Boca Raton, FL: CRC Press; 1993
    [Google Scholar]
  13. Shirling EB, Gottlieb D. Methods for characterization of Streptomyces species. Int J Syst Bacteriol 1966; 16:313–340 [View Article]
    [Google Scholar]
  14. Ridgway R. Color Standards and Color Nomenclature. Published by the Author Washington, DC: 1912 p 1–43, plate I–LII
    [Google Scholar]
  15. Shieh WY, Chen YW, Chaw SM, Chiu HH. Vibrio ruber sp. nov., a red, facultatively anaerobic, marine bacterium isolated from sea water. Int J Syst Evol Microbiol 2003; 53:479–484 [View Article]
    [Google Scholar]
  16. Liu ZH, Jiang CL, LH X, WJ L. Actinomycetes Systematics: Principles, Methods and Practices Beijing, China: Science Press; 2007
    [Google Scholar]
  17. Collins MD, Pirouz T, Goodfellow M, Minnikin DE. Distribution of menaquinones in actinomycetes and corynebacteria. J Gen Microbiol 1977; 100:221–230 [View Article]
    [Google Scholar]
  18. Kroppenstedt RM. Fatty acid and menaquinone analysis of actinomycetes and related organisms. In Goodfellow M, London MinnikinDE. (editors) Chemical Methods in Bacterial Systematics England: Academic Press; 1985 pp 173–199
    [Google Scholar]
  19. Komagata K, Suzuki KI. Lipid and cell-wall analysis in bacterial systematics. Method Microbiol 1987; 19:161–207
    [Google Scholar]
  20. Hasegawa T, Takizawa M, Tanida S. A rapid analysis for chemical grouping of aerobic actinomycetes. J Gen Appl Microbiol 1983; 29:319–322 [View Article]
    [Google Scholar]
  21. Lechevalier MP, Lechevalier H. Chemical composition as a criterion in the classification of aerobic actinomycetes. Int J Syst Bacteriol 1970; 20:435–443 [View Article]
    [Google Scholar]
  22. Orsini M, Romano-Spica V. A microwave-based method for nucleic acid isolation from environmental samples. Lett Appl Microbiol 2001; 33:17–20 [View Article]
    [Google Scholar]
  23. Lane DJ. 16S/23S rRNA sequencing. In Stackebrandt E, Goodfellow M. (editors) Nucleic Acid Techniques in Bacterial Systematics New York, USA: Wiley; 1991 pp 115–175
    [Google Scholar]
  24. Saitou N, Nei M. The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 1987; 4:406–425 [View Article]
    [Google Scholar]
  25. Felsenstein J. Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol 1981; 17:368–376 [View Article]
    [Google Scholar]
  26. Kluge AG, Farris JS. Quantitative phyletics and the evolution of anurans. Syst Zool 1969; 18:1–32 [View Article]
    [Google Scholar]
  27. 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]
    [Google Scholar]
  28. Rong X, Huang Y. Taxonomic evaluation of the Streptomyces hygroscopicus clade using multilocus sequence analysis and DNA–DNA hybridization, validating the MLSA scheme for systematics of the whole genus. Syst Appl Microbiol 2012; 35:7–18 [View Article]
    [Google Scholar]
  29. 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]
    [Google Scholar]
  30. Richter M, Rosselló-Móra R, Glöckner FO, Peplies J. JSpeciesWS: a web server for prokaryotic species circumscription based on pairwise genome comparison. Bioinformatics 2015; 32:btv681–btv931
    [Google Scholar]
  31. Meier-Kolthoff JP, Auch AF, Klenk H-P, Göker M. Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinformatics 2013; 14:60 [View Article]
    [Google Scholar]
  32. Yoon S-H, Ha S-min, 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]
    [Google Scholar]
  33. De Ley J, Cattoir H, Reynaerts A. The quantitative measurement of DNA hybridization from renaturation rates. Eur J Biochem 1970; 12:133–142 [View Article]
    [Google Scholar]
  34. Wright F, Bibb MJ. Codon usage in the G+C-rich Streptomyces genome. Gene 1992; 113:55–65 [View Article]
    [Google Scholar]
  35. Stackebrandt E, Ebers J. Taxonomic parameters revisited: tarnished gold standards. Microbiol Today 2006; 33:152–155
    [Google Scholar]
  36. Richter M, Rosselló-Móra R. Shifting the genomic gold standard for the prokaryotic species definition. Proc Natl Acad Sci USA 2009; 106:19126–19131 [View Article]
    [Google Scholar]
  37. Wayne LG, Brenner DJ, Colwell RR, Grimont PAD, Kandler O et al. International Committee on systematic bacteriology. Report of the ad hoc Committee on reconciliation of approaches to bacterial Systematics. Int J Syst Bacteriol 1987; 37:463–464
    [Google Scholar]
  38. Landwehr W, Kämpfer P, Glaeser SP, Rückert C, Kalinowski J et al. Taxonomic analyses of members of the Streptomyces cinnabarinus cluster, description of Streptomyces cinnabarigriseus sp. nov. and Streptomyces davaonensis sp. nov. Int J Syst Evol Microbiol 2018; 68:382–393 [View Article]
    [Google Scholar]
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