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Cytospora elaeagnicola sp. nov. Associated with Narrow-leaved Oleaster Canker Disease in China

  • Zhang, Linxuan (The Key Laboratory for Silviculture and Conservation of Ministry of Education, Beijing Forestry University) ;
  • Alvarez, Lourdes V. (Department of Biology, College of Science, Polytechnic University of the Philippines) ;
  • Bonthond, Guido (GEOMAR Helmholtz Centre for Ocean Research Kiel) ;
  • Tian, Chengming (The Key Laboratory for Silviculture and Conservation of Ministry of Education, Beijing Forestry University) ;
  • Fan, Xinlei (The Key Laboratory for Silviculture and Conservation of Ministry of Education, Beijing Forestry University)
  • Received : 2018.12.05
  • Accepted : 2019.06.13
  • Published : 2019.09.30

Abstract

Cytospora is a genus including important phytopathogens causing severe dieback and canker diseases distributed worldwide with a wide host range. However, identification of Cytospora species is difficult since the currently available DNA sequence data are insufficient. Aside the limited availability of ex-type sequence data, most of the genetic work is only based on the ITS region DNA marker which lacks the resolution to delineate to the species level in Cytospora. In this study, three fresh strains were isolated from the symptomatic branches of Elaeagnus angustifolia in Xinjiang Uygur Autonomous Region, China. Morphological observation and multi-locus phylogenetic analyses (ITS, LSU, ACT and RPB2) support these specimens are best accommodated as a distinct novel species of Cytospora. Cytospora elaeagnicola sp. nov. is introduced, having discoid, nearly flat, pycnidial conidiomata with hyaline, allantoid conidia, and differs from its relatives genetically and by host association.

Keywords

References

  1. Spielman LJ. Taxonomy and biology of Valsa species on hardwoods in North America, with special reference to species on maples. New York, US: Cornell University; 1983.
  2. Adams GC, Wingfield MJ, Common R, et al. Phylogenetic relationships and morphology of Cytospora species and related teleomorphs (Ascomycota, Diaporthales, Valsaceae) from Eucalyptus. Stud Mycol. 2005;52:1-144.
  3. Ehrenberg CG. Sylvae Mycologicae Berolinenses. Berlin: Formis Theophili Bruschcke;1818.
  4. Wijayawardene NN, Hyde KD, Lumbsch HT, et al. Outline of Ascomycota: 2017. Fungal Divers. 2018;88:167-263. https://doi.org/10.1007/s13225-018-0394-8
  5. Spielman LJ. A monograph of Valsa on hardwoods in North America. Can J Bot. 1985;63:1355-1378. https://doi.org/10.1139/b85-190
  6. Fan XL, Hyde KD, Liu M, et al. Cytospora species associated with walnut canker disease in China, with description of a new species C. gigalocus. Fungal Biol. 2015;119:310-319. https://doi.org/10.1016/j.funbio.2014.12.011
  7. Fan XL, Hyde KD, Yang Q, et al. Cytospora species associated with canker disease of three antidesertification plants in northwestern China. Phytotaxa. 2015;197:227-244. https://doi.org/10.11646/phytotaxa.197.4.1
  8. Rossman AY, Adams GC, Cannon PF, et al. Recommendations of generic names in Diaporthales competing for protection or use. IMA Fungus. 2015;6:145-154. https://doi.org/10.5598/imafungus.2015.06.01.09
  9. Kirk PM, Cannon PF, Minter DW, et al. Ainsworth & Bisby's Dictionary of the Fungi, 10th edn. Wallingford, UK: CABI; 2008.
  10. Deng SQ. Fungi of China. Beijing, China;1963.
  11. Tai FL. Sylloge Fungorum Sinicorum. Beijing, China;1979.
  12. Wei JC. Identification of Fungus Handbook. Shanghai, China; 1979.
  13. Zhang YB, You CJ, Fan XL, et al. Taxonomy and phylogeny of Cytospora in Northeast China. Mycosystema. 2014;33:806-818.
  14. Fan XL, Liang YM, Ma R, et al. Morphological and phylogenetic studies of Cytospora (Valsaceae, Diaporthales) isolates from Chinese scholar tree, with description of a new species. Mycoscience. 2014;55:252-259. https://doi.org/10.1016/j.myc.2013.10.001
  15. Fan XL, Tian CM, Yang Q, et al. Cytospora from Salix in northern China. Mycotaxon. 2014;129:303-315. https://doi.org/10.5248/129.303
  16. Norphanphoun C, Doilom M, Daranagama DA, et al. Revisiting the genus Cytospora and allied species. Mycosphere. 2017;8:51-97. https://doi.org/10.5943/mycosphere/8/1/7
  17. Chang W, Sui X, Fan XX, et al. Arbuscular mycorrhizal symbiosis modulates antioxidant response and ion distribution in salt-stressed Elaeagnus angustifolia seedlings. Front Microbiol. 2018;9:625. https://doi.org/10.3389/fmicb.2018.00625
  18. Mahboubi M. Elaeagnus angustifolia and its therapeutic applications in osteoarthritis. Ind Crops Prod. 2018;121:36-45. https://doi.org/10.1016/j.indcrop.2018.04.051
  19. Rayner RW. A mycological colour chart. Kew, UK: Commonwealth Mycological Institute; 1970.
  20. Doyle JJ, Doyle JL. Isolation of plant DNA from fresh tissue. Focus. 1990;12:13-15.
  21. White TJ, Bruns T, Lee S, et al. Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In: Innis MA, Gelfand DH, Sninsky JJ and White TJ (eds), PCR Protocols: a Guide to Methods and Applications. London: Academic Press; 1990. pp. 315-322.
  22. Vilgalys R, Hester M. Rapid genetic identification and mapping of enzymatically amplified ribosomal DNA from several Cryptococcus species. J Bacteriol. 1990;172:423.
  23. Carbone I, Kohn L. A method for designing primer sets for speciation studies in filamentous ascomycetes. Mycologia. 1999;91:553-556. https://doi.org/10.1080/00275514.1999.12061051
  24. Liu YL, Whelen S, Hall BD. Phylogenetic relationships among ascomycetes: evidence from an RNA polymerase II subunit. Molec Biol Evol. 1999;16:1799-1808. https://doi.org/10.1093/oxfordjournals.molbev.a026092
  25. Katoh K, Standley DM. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Molec Biol Evol. 2013;30:772-780. https://doi.org/10.1093/molbev/mst010
  26. Tamura K, Stecher G, Peterson D, et al. MEGA6: molecular evolutionary genetics analysis version 6.0. Mol Biol and Evol. 2013;30:2725-2729. https://doi.org/10.1093/molbev/mst197
  27. Swofford DL. PAUP*: Phylogenetic analysis using parsimony, *and other methods. Version 4.0b10. Sinauer Associates, Sunderland; 2003.
  28. Hillis DM, Bull JJ. An empirical test of bootstrapping as a method for assessing confidence in phylogenetic analysis. Syst Biol. 1993;42:182-192. https://doi.org/10.1093/sysbio/42.2.182
  29. Stamatakis A. RAxML-VI-HPC: maximum likelihood- based phylogenetic analyses with thousands of taxa and mixed models. Bioinformatics. 2006;22:2688-2690. https://doi.org/10.1093/bioinformatics/btl446
  30. Posada D, Crandall KA. Modeltest: testing the model of DNA substitution. Bioinformatics. 1998;14:817-818. https://doi.org/10.1093/bioinformatics/14.9.817
  31. Ronquist F, Huelsenbeck JP. MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics. 2003;19:1572-1574. https://doi.org/10.1093/bioinformatics/btg180
  32. Rannala B, Yang Z. Probability distribution of molecular evolutionary trees: a new method of phylogenetic inference. J Mol Evol. 1996;43:304-311. https://doi.org/10.1007/BF02338839
  33. Rambaut A, Drummond A. FigTree v.1.3.1. Institute of evolutionary biology. Edinburgh, UK: University of Edinburgh; 2010.
  34. Zhu HY, Fan XL, Tian CM. Multigene phylogeny and morphology reveal Cytospora spiraeae. Phytotaxa. 2018;338:49-62. https://doi.org/10.11646/phytotaxa.338.1.4

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