Skip to main content
Log in

Influence of surface characteristics on germination and early growth of Botryosphaeriaceae species

  • Published:
European Journal of Plant Pathology Aims and scope Submit manuscript

Abstract

This study investigated the effect of surface wettability, hardness and surface contact on the germination and subsequent development of Botryosphaeriaceae species conidia. Mean percent germination for isolates Neofusicoccum luteum MM558, N. luteum CC445, N. parvum G652 and Botryosphaeria dothidea 007 was highest on cellulose which was the most hydrophilic surface (72.2%, 76.9%, 52.4% and 74.9%, respectively), but did not differ between the other surfaces tested (glass, polystyrene and Parafilm M™). Germ tube growth for all isolates was least on cellulose and similar on the other surfaces. Cellulose agar assays indicated that mycelia could be utilising the cellulose as a food source. Germination assays on surfaces of different hardness showed no discernible patterns of germination or growth related to hardness. Further, there was no effect on germination of surface contact versus continuous shaking of conidial suspensions for isolate N. luteum MM558. These assays demonstrated that conidia of the Botryosphaeriaceae were able to germinate on a variety of surfaces with this flexibility indicative of their reported pathogenicity of different host tissues.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  • Adebayo, A. A., & Harris, R. F. (1971). Fungal growth responses to osmotic as compared to matric water potential. Proceedings Soil Science Society of America, 35, 465–469.

    Article  Google Scholar 

  • Amiri, A., Cholodowski, D., & Bompeix, G. (2005). Adhesion and germination of waterborne and airborne conidia of Penicillium expansum to apple and inert surfaces. Physiological and Molecular Plant Pathology, 67(1), 40–48.

    Article  CAS  Google Scholar 

  • Amponsah, N. T., Jones, E. E., Ridgway, H. J., & Jaspers, M. V. (2009). Rainwater dispersal of Botryosphaeria conidia from infected grapevines. New Zealand Plant Protection, 62, 228–233.

    Article  Google Scholar 

  • Amponsah, N. T., Jones, E. E., Ridgway, H. J., & Jaspers, M. V. (2012a). Microscopy of some interactions between Botryosphaeriaceae species and grapevine tissues. Australasian Plant Pathology, 41(6), 665–673.

    Article  Google Scholar 

  • Amponsah, N. T., Jones, E. E., Ridgway, H. J., & Jaspers, M. V. (2012b). Susceptibility of grapevine tissues to Neofusicoccum luteum conidial infection. Plant Pathology, 61(4), 719–729.

    Article  Google Scholar 

  • Apoga, D., Jansson, H.-B., & Tunlid, A. (2001). Adhesion of conidia and germlings of the plant pathogenic fungus Bipolaris sorokiniana to solid surfaces. Mycological Research, 105(10), 1251–1260.

    Article  CAS  Google Scholar 

  • Baskarathevan, J. (2011). Botryosphaeriaceous infection in New Zealand vineyards: Identification population structure and genetic diversity. PhD Thesis: Lincoln University, Lincoln, New Zealand.

  • Carver, T. L. W., & Ingerson, S. M. (1987). Responses of Erysiphe graminis germlings to contact with artificial and host surfaces. Physiological and Molecular Plant Pathology, 30, 359–372.

    Article  Google Scholar 

  • Chaky, J., Anderson, K., Moss, M., & Vaillancourt, L. (2001). Surface hydrophobicity and surface rigidity induce spore germination in Colletotrichum graminicola. Phytopathology, 91(6), 558–564.

    Article  CAS  PubMed  Google Scholar 

  • Doehlemann, G., Berndt, P., & Hahn, M. (2006). Different signalling pathways involving a Gαprotein, cAMP and a MAP kinase control germination of Botrytis cinerea conidia. Molecular Microbiology, 59(3), 821–835.

    Article  CAS  PubMed  Google Scholar 

  • Egley, G. H. (1994). Substrate surface influences upon germination of Colletotrichum truncatum conidia. Canadian Journal of Botany, 72(12), 1758–1765.

    Article  Google Scholar 

  • Espinoza, J. G., Briceño, E. X., Chávez, E. R., Úrbez-Torres, J. R., & Latorre, B. A. (2009). Neofusicoccum spp. associated with stem canker and dieback of blueberry in Chile. Plant Disease, 93(11), 1187–1194.

    Article  CAS  PubMed  Google Scholar 

  • Guest, D., & Brown, J. (1997). Infection processes. In J. F. Brown & H. J. Ogle (Eds.), Plant pathogens and plant diseases (pp. 245–262). Armidale: Rockvale Publications.

    Google Scholar 

  • Ilmén, M., Saloheimo, A., Onnela, M. L., & Penttilä, M. E. (1997). Regulation of cellulase gene expression in the filamentous fungus Trichoderma reesei. Applied and Environmental Microbiology, 63(4), 1298–1306.

    PubMed  PubMed Central  Google Scholar 

  • Jelitto, T. C., Page, H. A., & Read, N. D. (1994). Role of external signals in regulating the pre-penetration phase of infection by the rice blast fungus Magnaporthe grisea. Planta, 194(4), 471–477.

    Article  CAS  Google Scholar 

  • Jo, W.-S., Bae, S.-H., Cho, D.-H., Park, S.-D., Yoo, Y.-B., & Park, S.-C. (2009). Optimal medium conditions for the detection of cellulolytic activity in Ganoderma lucidum. Mycobiology, 37(4), 313–316.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Jones, E. E., Stewart, A., & Whipps, J. M. (2011). Water potential affects Coniothyrium minitans growth, germination and parasitism of Sclerotinia sclerotiorum sclerotia. Fungal Biology, 115(9), 871–881.

    Article  PubMed  Google Scholar 

  • Kasana, R. C., Salwan, R., Dhar, H., Dutt, S., & Gulati, A. (2008). A rapid and easy method for the detection of microbial cellulases on agar plates using Gram’s iodine. Current Microbiology, 57(5), 503–507.

    Article  CAS  PubMed  Google Scholar 

  • Kunoh, H., Yamaoka, N., Yoshioka, H., & Nicholson, R. L. (1988). Preparation of the infection court by Erysiphe graminis: I. Contact-mediated changes in morphology of the conidium surface. Experimental Mycology, 12(4), 325–335.

    Article  Google Scholar 

  • Kuo, K., & Hoch, H. C. (1996). Germination of Phyllosticta ampelicida pycnidiospores: Prerequisite of adhesion to the substratum and the relationship of substratum wettability. Fungal Genetics and Biology, 20(1), 18–29.

    Article  CAS  PubMed  Google Scholar 

  • Li, M., Gao, Z., Hui, M., Zhou, S., Yang, D., Yang, B., Yi, J., & Yang, F. (2012). Pathogenicity of cell wall degrading enzymes produced by Botryodiplodia theobromae pat. Against mangoes. Agricultural Biotechnology, 1(6), 18–21.

    CAS  Google Scholar 

  • Magan, N., & Lynch, J. M. (1986). Water potential, growth and cellulolysis of fungi involved in decomposition of cereal residues. Journal of General Microbiology, 132(5), 1181–1187.

    CAS  Google Scholar 

  • Meguro, A., Fujita, K., Kunoh, H., Carver, T. W., & Nicholson, R. (2001). Release of the extracellular matrix from conidia of Blumeria graminis in relation to germination. Mycoscience, 42(2), 201–209.

    Article  Google Scholar 

  • Nadeau, M. P., Dunphy, G. B., & Boisvert, J. L. (1995). Effects of physical factors on the development of secondary conidia of Erynia conica (Zygomycetes: Entomophthorales), a pathogen of adult black flies (Diptera: Simuliidae). Experimental Mycology, 19, 324–329.

    Article  Google Scholar 

  • Nesci, A., Etcheverry, M., & Magan, N. (2004). Osmotic and matric potential effects on growth, sugar alcohol and sugar accumulation by Aspergillus section Flavi strains from Argentina. Journal of Applied Microbiology, 96(5), 965–972.

    Article  CAS  PubMed  Google Scholar 

  • Ritz, K., & Young, I. M. (2004). Interactions between soil structure and fungi. Mycologist, 18(02), 52–59.

    Article  Google Scholar 

  • Sammonds, J., Jaspers, M. V., & Jones, E. E. (2016). Pre-infection processes of Botryosphaeriaceae spp. conidia: Adhesion to different substrata. Plant Pathology, 65, 1142–1152.

    Article  Google Scholar 

  • Shafi, A., Ridgway, H. J., Jaspers, M. V., & Jones, E. E. (2017). Conidial production by Botryosphaeriaceae species from grapevine shoot lesions in Marlborough vineyards. New Zealand Plant Protection, 70, 295–300.

    Article  Google Scholar 

  • Shafi, A., Ridgway, H. J., Jaspers, M. V., & Jones, E. E. (2019). Variability and influence of temperature and relative humidity on sporulation of Neofusicoccum species on grapevine shoots. European Journal of Plant Pathology In press.

  • Shahriarinour, M., Mohd Noor, A. W., Ariff, A., & Mohamad, R. (2011). Screening, isolation and selection of cellulolytic fungi from oil palm empty fruit bunch fibre. Biotechnology, 10(1), 108–113.

    Article  Google Scholar 

  • Shaw, B. D., Carroll, G. C., & Hoch, H. C. (2006). Generality of the prerequisite of conidium attachment to a hydrophobic substratum as a signal for germination among Phyllosticta species. Mycologia, 98(2), 186–194.

    Article  CAS  PubMed  Google Scholar 

  • Slippers, B., & Wingfield, M. J. (2007). Botryosphaeriaceae as endophytes and latent pathogens of woody plants: Diversity, ecology and impact. Fungal Biology Reviews, 21(2–3), 90–106.

    Article  Google Scholar 

  • Staples, R. C., & Hoch, H. C. (1997). Physical and chemical cues for spore germination and appressorium formation by fungal pathogens. In G. C. Carroll & P. Tudzynski (Eds.), Plant Relationships (pp. 27–40), The Mycota (A Comprehensive Treatise on Fungi as Experimental Systems for Basic and Applied Research) (Vol. 5). Berlin: Springer.

    Google Scholar 

  • Takikawa, Y., Xu, L., Kakutani, K., Nonomura, T., Sameshima, T., Matsuda, Y., & Toyoda, H. (2011). Conidia of the tomato powdery mildew Oidium neolycopersici initiate germ tubes at a predetermined site. Mycoscience, 52(3), 198–203.

    Article  Google Scholar 

  • ten Have, A., Tenberge, K., Benen, J.A.E., Tudzynski, P., Visser, J., & van Kan, J.A.L. (2002). The contribution of cell wall degrading enzymes to pathogenesis of fungal plant pathogens. In Agricultural Applications (11 ed., pp. 341–358): Springer Berlin Heidelberg. Retrieved from https://doi.org/10.1007/978-3-662-03059-2_17.

  • Tucker, S. L., & Talbot, N. J. (2001). Surface attachment and pre-penetration stage development by plant pathogenic fungi. Annual Review of Phytopathology, 39(1), 385–417.

    Article  CAS  PubMed  Google Scholar 

  • Úrbez-Torres, J. R. (2011). The status of Botryosphaeriaceae species infecting grapevines (Vol. 50, pp. S5–S45). Phytopathologica Mediterranea.

  • Úrbez-Torres, J. R., & Gubler, W. D. (2011). Susceptibility of grapevine pruning wounds to infection by Lasiodiplodia theobromae and Neofusicoccum parvum. Plant Pathology, 60(2), 261–270.

    Article  Google Scholar 

  • Úrbez-Torres, J. R., Battany, M., Bettiga, L. J., Gispert, C., McGourty, G., Roncoroni, J., & Gubler, W. D. (2010). Botryosphaeriaceae species spore-trapping studies in California vineyards. Plant Disease, 94(6), 717–724.

    Article  PubMed  Google Scholar 

  • van Niekerk, J. M., Calitz, F., Halleen, F., & Fourie, P. H. (2010). Temporal spore dispersal patterns of grapevine trunk pathogens in South Africa. European Journal of Plant Pathology, 127(3), 375–390.

    Article  Google Scholar 

  • Warwar, V., & Dickman, M. B. (1996). Effects of calcium and calmodulin on spore germination and appressorium development in Colletotrichum trifolii. Applied and Environmental Microbiology, 62(1), 74–79.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Wright, A. J., Carver, T. L. W., Thomas, B. J., Fenwick, N. I. D., Kunoh, H., & Nicholson, R. L. (2000). The rapid and accurate determination of germ tube emergence site by Blumeria graminis conidia. Physiological and Molecular Plant Pathology, 57(6), 281–301.

    Article  Google Scholar 

  • Wunderlich, N., Ash, G. J., Steel, C. C., Raman, H., & Savocchia, S. (2011). Association of Botryosphaeriaceae grapevine trunk disease fungi with the reproductive structures of Vitis vinifera. Vitis, 50(2), 89–96.

    Google Scholar 

Download references

Acknowledgements

The authors would like to thank Lincoln University for funding this research.

Funding

Funding was provided by Lincoln University.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to E. Eirian Jones.

Ethics declarations

Conflict of interest

None of the authors declare a conflict of interest, with all authors consenting to publication.

Ethical approval

This article does not contain any studies with human participants or animals performed by any of the authors.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sammonds, J., Jaspers, M.V. & Jones, E.E. Influence of surface characteristics on germination and early growth of Botryosphaeriaceae species. Eur J Plant Pathol 154, 1125–1134 (2019). https://doi.org/10.1007/s10658-019-01733-y

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10658-019-01733-y

Keywords

Navigation