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Draft Genome Sequence of Phoma arachidicola Wb2 Causing Peanut Web Blotch in China

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Abstract

Peanut web blotch, a peanut disease with both web and blotch symptom leaflets, is an emerging threat for peanut cultivation worldwide and one of the most important fungal diseases in China. However, the limited pieces of information in genomic resources and pathogenesis are the major constraints to integrated disease management. The genome contains a large number of pathogenicity-related genes, but the genomic information of the pathogen is still blank. Considering this fact, current study presented the draft genome sequence of a Phoma arachidicola isolate named Wb2. Strain Wb2 was isolated from peanut leaves with typical web blotch symptoms, and identified as Phoma arachidicola based on morphological characteristics and phylogenic analysis using ITS sequence. The draft genome of Wb2 is about 34.11 Mb and contains 37330 open reading frames (ORFs), with G + C content 49.23%. The strain Wb2 has an abundance of secreted oxidases, peroxidases, and carbohydrate-active enzymes for degrading cell wall polysaccharides and penetrating into the host tissue. The genome information of Wb2 will help to better understand the mechanisms of interaction between P. arachidicola and peanuts. Furthermore, the genome-based plant–pathogen interaction analysis will provide clues for disease control, which is essential to ensure peanut production and food security.

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References

  1. Jiang L, Hua D, Wang Z, Xu S (2010) Aqueous enzymatic extraction of peanut oil and protein hydrolysates. Food Bioprod Process 88:233–238

    Article  CAS  Google Scholar 

  2. Vargas Gil S, Meriles JM, Haro R, Casini C, March GJ (2008) Crop rotation and tillage systems as a proactive strategy in the control of peanut fungal soilborne diseases. Biocontrol 53:685–698

    Article  Google Scholar 

  3. Fávero AP, Santos RFD, Simpson CE, Valls JFM, Vello NA (2015) Successful crosses between fungal-resistant wild species of Arachis (section Arachis) and Arachis hypogaea. Genet Mol Biol 38:353–365

    Article  PubMed  PubMed Central  Google Scholar 

  4. Manamgoda DS, Rossman AY, Castlebury LA, Crous PW, Madrid H, Chukeatirote E, Hyde KD (2014) The genus Bipolaris. Stud Mycol 79:221–288

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Subrahmanyam P, Van Wyk PS, Kisyombe CT, Cole DL, Hildebrand GL, Chiyembekeza AJ, Van Der Merwe PJA (1997) Diseases of groundnut in the Southern African Development Community (SADC) region and their management. Int J Pest Manage 43:261–273

    Article  Google Scholar 

  6. Taber RA, Pettit RE, Philley GL (1984) Peanut Web Blotch: I. Cultural Characteristics and Identity of Causal Fungus. Peanut Sci 11:109–114

    Article  Google Scholar 

  7. Fávero AP, Moraes SAD, Garcia AAF, Valls JFM, Vello NA (2009) Characterization of rust, early and late leaf spot resistance in wild and cultivated peanut germplasm. Sci Agr 66:110–117

    Article  Google Scholar 

  8. Liu N, Xu S, Yao X, Zhang G, Mao W, Hu Q, Feng Z, Gong Y (2016) Studies on the Control of Ascochyta Blight in Field Peas (Pisum sativum L.) Caused by Ascochyta pinodes in Zhejiang Province, China. Front Microbiol 7:481–494

    PubMed  PubMed Central  Google Scholar 

  9. Edwards JE, Forster RJ, Callaghan TM et al (2017) PCR and Omics Based Techniques to Study the Diversity, Ecology and Biology of Anaerobic Fungi: Insights, Challenges and Opportunities. Front Microbiol 8:1657–1684

    Article  PubMed  PubMed Central  Google Scholar 

  10. Vu D, Groenewald M, de Vries M et al (2019) Large-scale generation and analysis of filamentous fungal DNA barcodes boosts coverage for kingdom fungi and reveals thresholds for fungal species and higher taxon delimitation. Stud Mycol 92:135–154

    Article  CAS  PubMed  Google Scholar 

  11. Chen K, Pachter L (2005) Bioinformatics for whole-genome shotgun sequencing of microbial communities. PLoS Comput Biol 1:106–112

    Article  CAS  PubMed  Google Scholar 

  12. de Wit PJ, van der Burgt A, Okmen B et al (2012) The genomes of the fungal plant pathogens Cladosporium fulvum and Dothistroma septosporum reveal adaptation to different hosts and lifestyles but also signatures of common ancestry. PLoS Genet 8:e1003088–e1003110

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Op De Beeck M, Lievens B, Busschaert P, Declerck S, Vangronsveld J, Colpaert JV (2014) Comparison and validation of some ITS primer pairs useful for fungal metabarcoding studies. PLoS ONE 9:e97629–e97640

    Article  PubMed  PubMed Central  Google Scholar 

  14. Zerbino DR, Birney E (2008) Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res 18:821–829

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Delcher AL, Bratke KA, Powers EC, Salzberg SL (2007) Identifying bacterial genes and endosymbiont DNA with Glimmer. Bioinformatics 23:673–679

    Article  CAS  PubMed  Google Scholar 

  16. Conesa A, Gotz S, Garcia-Gomez JM, Terol J, Talon M, Robles M (2005) Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research. Bioinformatics 21:3674–3676

    Article  CAS  PubMed  Google Scholar 

  17. Lagesen K, Hallin P, Rodland EA, Staerfeldt HH, Rognes T, Ussery DW (2007) RNAmmer: consistent and rapid annotation of ribosomal RNA genes. Nucleic Acids Res 35:3100–3108

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Yin Y, Mao X, Yang J, Chen X, Mao F, Xu Y (2012) dbCAN: a web resource for automated carbohydrate-active enzyme annotation. Nucleic Acids Res 40:W445–W451

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Petersen TN, Brunak S, von Heijne G, Nielsen H (2011) SignalP 4.0: discriminating signal peptides from transmembrane regions. Nat Methods 8:785–786

    Article  CAS  PubMed  Google Scholar 

  20. Mukherjee S, Stamatis D, Bertsch J, Ovchinnikova G, Verezemska O, Isbandi M, Thomas AD, Ali R, Sharma K, Kyrpides NC, Reddy TB (2017) Genomes OnLine Database (GOLD) v.6: data updates and feature enhancements. Nucleic Acids Res 45:D446–D456

    Article  CAS  PubMed  Google Scholar 

  21. Fleck CB, Schöbel F, Brock M (2011) Nutrient acquisition by pathogenic fungi: nutrient availability, pathway regulation, and differences in substrate utilization. Int J Med Microbiol 301(5):400–407

    Article  CAS  PubMed  Google Scholar 

  22. Amich J, Bignell E (2016) Amino acid biosynthetic routes as drug targets for pulmonary fungal pathogens: what is known and why do we need to know more? Curr Opin Microbiol 32:151–158

    Article  CAS  PubMed  Google Scholar 

  23. Mammeri H, Galleni M, Nordmann P (1998) The role of the Aspergillus fumigatus areA gene in invasive pulmonary aspergillosis. Mol Gen Genet 258(5):553–557

    Article  Google Scholar 

  24. Lee IR, Chow EW, Morrow CA, Djordjevic JT, Fraser JA (2011) Nitrogen metabolite repression of metabolism and virulence in the human fungal pathogen Cryptococcus neoformans. Genetics 188(2):309–323

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Krappmann S, Bignell EM, Reichard U, Rogers T, Haynes K, Braus GH (2010) The Aspergillus fumigatus transcriptional activator CpcA contributes significantly to the virulence of this fungal pathogen. Mol Microbiol 52(3):785–799

    Article  CAS  Google Scholar 

  26. Amich J, Schafferer L, Haas H, Krappmann S (2013) Regulation of Sulphur Assimilation Is Essential for Virulence and Affects Iron Homeostasis of the Human-Pathogenic Mould Aspergillus fumigatus. Plos Pathog 9(8):e1003573

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Marzluf GA (1997) Molecular genetics of sulfur assimilation in filamentous fungi and yeast. Ann Rev Microbiol 51(51):73

    Article  CAS  Google Scholar 

  28. Menino JF, Saraiva M, Gomesrezende J, Sturme M, Pedrosa J, Castro AG, Ludovico P, Goldman GH, Rodrigues F (2013) P. brasiliensis Virulence Is Affected by SconC, the Negative Regulator of Inorganic Sulfur Assimilation. Plos ONE 8(9):e74725

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Dezwaan TM, Carroll AM, Valent B, Sweigard JA (1999) Magnaporthe grisea pth11p is a novel plasma membrane protein that mediates appressorium differentiation in response to inductive substrate cues. Plant Cell 11(10):2013–2030

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. O’Rourke SM, Herskowitz I (2002) A third osmosensing branch in Saccharomyces cerevisiae requires the Msb2 protein and functions in parallel with the Sho1 branch. Mol Cell Biol 22(13):4739–4749

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Pitoniak A, Birkaya B, Dionne HM, Vadaie N, Cullen PJ (2009) The signaling mucins Msb2 and Hkr1 differentially regulate the filamentation mitogen-activated protein kinase pathway and contribute to a multimodal response. Mol Biol Cell 20(13):3101

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Liu W, Zhou X, Li G, Li L, Kong L, Wang C, Zhang H, Xu JR (2011) Multiple plant surface signals are sensed by different mechanisms in the rice blast fungus for appressorium formation. Plos Pathog 7(1):e1001261

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  33. Kolattukudy PE (1985) Enzymatic penetration of the plant cuticle by fungal pathogens. Ann Rev Phytopathol 23:27

    Article  Google Scholar 

  34. VC A, Wilhelm S, Siegfried S (2005) A secreted lipase of Fusarium graminearum is a virulence factor required for infection of cereals. Plant J 42:364–375

    Article  CAS  Google Scholar 

  35. Zhao Z, Liu H, Wang C, Xu JR (2013) Comparative analysis of fungal genomes reveals different plant cell wall degrading capacity in fungi. BMC Genom 14:274–289

    Article  CAS  Google Scholar 

  36. Hittalmani S, Mahesh HB, Mahadevaiah C, Prasannakumar MK (2016) De novo genome assembly and annotation of rice sheath rot fungus Sarocladium oryzae reveals genes involved in Helvolic acid and Cerulenin biosynthesis pathways. BMC Genom 17:271–284

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank the anonymous reviewers for their constructive and helpful comments. This research was funded by Natural Science Foundation of Shandong Province (ZR2017PC015, ZR2018LC015); Agricultural Scientific and Technological Innovation Project of Shandong Academy of Agricultural Sciences (CXGC2018E21, 06210214442019, 2-18-43); Qingdao Foundation (17-3-3-70-nsh); Shandong Agriculture Research System (SDAIT-04-07); National key scientific and technological project (2017YFD0201608, 2016YFD0200504).

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Correspondence to Yucheng Chi.

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Zhang, X., Xu, M., Wu, J. et al. Draft Genome Sequence of Phoma arachidicola Wb2 Causing Peanut Web Blotch in China. Curr Microbiol 76, 200–206 (2019). https://doi.org/10.1007/s00284-018-1612-z

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  • DOI: https://doi.org/10.1007/s00284-018-1612-z

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