Skip to main content
Log in

Modelling the interaction between early blight epidemics and host dynamics of tomato

  • Published:
Tropical Plant Pathology Aims and scope Submit manuscript

Abstract

A model describing an early blight epidemic and the growth dynamics of tomato interacting together is developed. The model is formulated as a set of differential equations for the rate of change in the amount of healthy H, diseased Y and defoliated D area in the disease situation, and healthy H DF and defoliated D DF in the disease-free situation. Model parameters were estimated through fitting the model to experimental data obtained from glasshouse experiments which comprised tomato plants inoculated with A. solani at three inoculation times; early (t INOC  = 23 days after transplanting (DAT)), intermediate (33 DAT) and late (43 DAT) in experiment 1 and t INOC  = 22, 30 and 38 DAT in experiment 2. Defoliation rates were 2.5 times higher for late inoculated (older) plants compared with the early inoculated (younger) plants. Values of the logistic rate parameter for disease increase were about three-fold higher in the late inoculations (0.380, 0.305 day−1) when compared with the early inoculations (0.151, 0.095 day−1). Based on the good fit of the model outputs to observed data with R 2 > 0.995, the model can be considered as offering a good description of the dynamic interaction between the early blight epidemic and growth of tomato.

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

  • Allorent D, Savary S (2005) Epidemiological characteristics of angular leaf spot of bean: a systems analysis. Eur J Plant Pathol 113:329–341

    Article  Google Scholar 

  • Allorent D, Willocquet L, Sartorato A, Savary S (2005) Quantifying and modelling the mobilisation of inoculum from diseased leaves and infected defoliated tissues in epidemics of angular leaf spot of bean. Eur J Plant Pathol 113:377–394

    Article  Google Scholar 

  • Aust HJ, Hoyningen-Huene JV (1986) Microclimate in relation to epidemics of powdery mildew. Annu Rev Phytopathol 24:491–510

    Article  Google Scholar 

  • Barnwal MK, Kotasthane A, Magculia N, Mukherjee PK, Savary S, Sharma AK, Singh HB, Singh US, Sparks AH, Variar M, Zaidi N (2013) A review on crop losses, epidemiology and disease management of rice brown spot to identify research priorities and knowledge gaps. Eur J Plant Pathol 136:443–457

    Article  Google Scholar 

  • Basu PK (1974) Measuring early blight, its progress and influence on fruit losses in nine tomato cultivars. Can Plant Dis Surv 54:45–51

    Google Scholar 

  • Bennett FG (1981) The expression of resistance to powdery mildew infection in winter wheat cultivars. II. Adult plant resistance. Ann Appl Biol 98:305–317

    Article  Google Scholar 

  • Blanco FF, Folegatti MV (2005) Estimation of leaf area for greenhouse cucumber by linear measurements under salinity and grafting. Sci Agric 62:305–309

    Article  Google Scholar 

  • Calonnec A, Cartolaro P, Naulin JM, Bailey D, Langlais M (2008) A host–pathogen simulation model: powdery mildew of grapevine. Plant Pathol 57:493–508

    Article  Google Scholar 

  • Chaerani R, Voorrips RE (2006) Tomato early blight (Alternaria solani): the pathogen, genetics, and breeding for resistance. J Gen Plant Pathol 72:335–347

    Article  Google Scholar 

  • Chaerani R, Groenwold R, Stam P, Voorrips RE (2007a) Assessment of early blight (Alternaria solani) resistance in tomato using a drop inoculation method. J Gen Plant Pathol 73:96–103

    Article  Google Scholar 

  • Chaerani R, Smulders MJM, van der Linden CG, Vosman B, Stam P, Voorrips RE (2007b) QTL identification for early blight resistance (Alternaria solani) in a Solanum lycopersicum × S. Arcanum cross. Theor Appl Genet 114:439–450

    Article  CAS  PubMed  Google Scholar 

  • Cook RJ, Yarham DJ (1998) Epidemiology in sustainable systems. In: Jones DG (ed) The epidemiology of plant diseases. Kluwer Academic Publishers, Dordrecht, The Netherlands, pp 260–277

    Chapter  Google Scholar 

  • Datar VV, Mayee CD (1981) Assessment of losses in tomato yield due to early blight. Indian Phytopathol 34:191–195

    Google Scholar 

  • De Wolf ED, Isard SA (2007) Disease cycle approach to plant disease prediction. Annu Rev Phytopathol 45:203–220

    Article  PubMed  Google Scholar 

  • Denissen CJM (1993) Components of adult plant resistance to leaf rust in wheat. Euphytica 70:131–140

    Article  Google Scholar 

  • Gleason ML, Ricker MD, MacNab AA, East DA, Pitblado RE, Latin RX (1995) Disease-warning systems for processing tomatoes in eastern North America: Are we there yet? Plant Dis 79:113–121

    Article  Google Scholar 

  • Godoy CV, Amorim L, Bergamin Filho A, Silva HP, Silva WJ, Berger RD (2003) Temporal progress of southern rust in maize under different environmental conditions. Fitopatol Bras 28:273–278

    Article  Google Scholar 

  • Jasinski J (1999) TOMCAST for Ohio, Indiana and Michigan. Available at: www.2.ag.ohiostate.edu/~vegnet/tomcats/tomfrm.htm. Accessed on April 10 2013

  • Jeger MJ (1986) The potential of analytic compared with simulation approaches to modeling in plant disease epidemiology. In: Leonard KJ, Fry WE (eds) Plant disease epidemiology. Population dynamics and management, vol 1. MacMillan Publishing Co, New York, USA, pp 255–281

    Google Scholar 

  • Johnson KB, Teng PS (1990) Coupling a disease progress model for early blight to a model of potato growth. Phytopathology 80:416–425

    Article  Google Scholar 

  • Jones JP (1991) Early blight. In: Jones JB, Jones JP, Stall RE, Zitter TA (eds) Compendium of tomato diseases. APS Press, St. Paul MN, USA, pp 13–14

    Google Scholar 

  • Koo J (2002) Modeling the impacts of climate variability on tomato disease management and production. Available at: www.etd.fcla.edu/UF/UFE1000136/koo_j.pdf. Accessed on July 15 2013

  • Kranz J, Jörg E (1989) The synecological approach in plant disease epidemiology. Rev Trop Plant Pathol 6:27–38

    Google Scholar 

  • Lawrence CB, Singh NP, Qiu J, Gardener RG, Tuzun S (2000) Constitutive hydrolytic enzymes are associated with polygenic resistance of tomato to Alternaria solani and may function as elicitor release mechanism. Physiol Mol Plant Pathol 57:211–220

    Article  CAS  Google Scholar 

  • Ma H, Singh RP (1996) Expression of adult resistance to stripe rust at different growth stages of wheat. Plant Dis 80:375–379

    Article  Google Scholar 

  • Madden L, Pennypacker SP, MacNab AA (1978) FAST, a forecast system for Alternaria solani on tomato. Phytopathology 68:1354–1358

    Article  Google Scholar 

  • Majid RF, Heather LM, Hamid A (2008) Genetics, genomics and breeding of late blight and early blight resistance in tomato. Crit Rev Plant Sci 27:75–107

    Article  Google Scholar 

  • Melching JS, Dowler WM, Koogle DL, Royer MH (1988) Effect of plant and leaf age on susceptibility of soybean to soybean rust. Can J Plant Pathol 10:30–35

    Article  Google Scholar 

  • Mersha Z, Hau B (2008) Effects of bean rust (Uromyces appendiculatus) epidemics on host dynamics of common bean (Phaseolus vulgaris). Plant Pathol 57:674–686

    Article  Google Scholar 

  • Mersha Z, Hau B (2011) Reciprocal effects of host and disease dynamics in the bean rust pathosystems. J Plant Dis Protect 118:54–62

    Google Scholar 

  • Nash AF, Gardner RG (1988) Tomato early blight resistance in a breeding line derived from Lycopersicon hirsutum PI 126445. Plant Dis 72:206–209

    Article  Google Scholar 

  • Nelson SC, Campbell CL (1993) Disease progress, defoliation and spatial pattern in a multiple-pathogen disease complex on white clover. Phytopathology 83:419–429

    Article  Google Scholar 

  • Ojiambo PS, Scherm H (2005) Temporal progress of Septoria leaf spot on rabbiteye blueberry (Vaccinium ashei). Plant Dis 89:1090–1096

    Article  Google Scholar 

  • Pandey KK, Pandey PK, Kallo G, Banerjee MK (2003) Resistance to early blight of tomato with respect to various parameters of disease epidemics. J Gen Plant Pathol 69:364–371

    Article  Google Scholar 

  • Pretorius ZA, Rijkenberg FHJ, Wilcoxson RD (1988) Effects of growth stage, leaf position and temperature on adult plant resistance of wheat infected by Puccinia recondita f. sp. tritici. Plant Pathol 37:36–44

    Article  Google Scholar 

  • Rossi V, Racca P, Giosuè S, Pancaldi D, Alberti I (1997) A simulation model for the development of brown rust epidemics in winter wheat. Eur J Plant Pathol 103:453–465

    Article  Google Scholar 

  • Rotem J (1994) The genus Alternaria: biology, epidemiology, and pathogenicity. APS Press, St. Paul MN, USA

    Google Scholar 

  • Rotem J, Reichert I (1964) Dew–a principal moisture factor enabling early blight epidemics in a semi arid region of Israel. Plant Dis Rep 48:211–215

    Google Scholar 

  • Savary S, Willocquet L, Teng PS (1997) Modelling sheath blight epidemics on rice tillers. Agric Syst 55:359–384

    Article  Google Scholar 

  • Schwarz D, Klaring HP (2001) Allometry to estimate leaf area tomato. J Plant Nutr 24:1291–1309

    Article  CAS  Google Scholar 

  • Sherf AF, MacNab AA (1986) Vegetable diseases and their control. Wiley Interscience, New York NY, USA

    Google Scholar 

  • Sinden SL, Goth RW, O’brien MJ (1972) Effect of potato alkaloids on the growth of Alternaria solani and their possible role as resistance factors in potatoes. Phytopathology 63:303–307

    Article  Google Scholar 

  • Thal WM, Campbell CL (1988) Analysis of progress of alfalfa leaf spot epidemics. Phytopathology 78:389–395

    Article  Google Scholar 

  • Van Maanen A, Xu M (2003) Modelling plant disease epidemics. Eur J Plant Pathol 109:669–682

    Article  Google Scholar 

  • Vloutoglou I, Kalogerakis SN (2000) Effects of inoculum concentration, wetness duration and plant age on development of early blight (Alternaria solani) and on shedding of leaves in tomato plants. Plant Pathol 49:339–345

    Article  Google Scholar 

  • Waggoner PE (1986) Progress curves of foliar diseases: their interpretation and use. In: Leonard KJ, Fry WE (eds) Plant disease epidemiology. Population dynamics and management, vol 1. MacMillan Publishing Co, New York NY, USA, pp 3–37

    Google Scholar 

  • Waggoner PE, Berger RD (1987) Defoliation, disease, and growth. Phytopathology 77:393–398

    Google Scholar 

  • Waggoner PE, Horsfall JG (1969) EPIDEM: a simulator of plant disease written for a computer. Conn Agric Exp Station Bull 698:1–80

    Google Scholar 

  • Walker JC (1957) Plant pathology. McGraw-Hill Book Co, New York NY, USA

    Google Scholar 

  • Willocquet L, Allorent D, Savary S (2004) Quantitative analysis of two important epidemiological features in the common bean – Phaeoisariopsis griseola pathosystem. Fitopatol Bras 29:676–679

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Bernhard Hau.

Additional information

Section Editor: Harald Scherm

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Chelal, J., Al Masri, A. & Hau, B. Modelling the interaction between early blight epidemics and host dynamics of tomato. Trop. plant pathol. 40, 77–87 (2015). https://doi.org/10.1007/s40858-015-0021-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40858-015-0021-0

Keywords

Navigation