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A Model to Explain Temperature Dependent Systemic Infection of Potato Plants by Potato virus Y

  • Choi, Kyung San (Research Institute of Climate Change and Agriculture, National Institute of Horticultural and Herbal Science, Rural Development Administration) ;
  • Toro, Francisco del (Biological Research Center, Spanish Council for Scientific Research (CIB-CSIC)) ;
  • Tenllado, Francisco (Biological Research Center, Spanish Council for Scientific Research (CIB-CSIC)) ;
  • Canto, Tomas (Biological Research Center, Spanish Council for Scientific Research (CIB-CSIC)) ;
  • Chung, Bong Nam (Research Institute of Climate Change and Agriculture, National Institute of Horticultural and Herbal Science, Rural Development Administration)
  • Received : 2016.06.16
  • Accepted : 2016.11.22
  • Published : 2017.04.01

Abstract

The effect of temperature on the rate of systemic infection of potatoes (Solanum tuberosum L. cv. Chu-Baek) by Potato virus Y (PVY) was studied in growth chambers. Systemic infection of PVY was observed only within the temperature range of $16^{\circ}C$ to $32^{\circ}C$. Within this temperature range, the time required for a plant to become infected systemically decreased from 14 days at $20^{\circ}C$ to 5.7 days at $28^{\circ}C$. The estimated lower thermal threshold was $15.6^{\circ}C$ and the thermal constant was 65.6 degree days. A systemic infection model was constructed based on experimental data, using the infection rate (Lactin-2 model) and the infection distribution (three-parameter Weibull function) models, which accurately described the completion rate curves to systemic infection and the cumulative distributions obtained in the PVY-potato system, respectively. Therefore, this model was useful to predict the progress of systemic infections by PVY in potato plants, and to construct the epidemic models.

Keywords

References

  1. Broadbent, L. 1948. Aphis migration and the efficiency of the trapping method. Ann. Appl. Biol. 35:379-394.
  2. Chellappan, P., Vanitharani, R., Ogbe, F. and Fauquet, C. M. 2005. Effect of temperature on geminivirus-induced RNA silencing in plants. Plant Physiol. 138:1828-1841. https://doi.org/10.1104/pp.105.066563
  3. Choi, K. S. and Kim, D. S. 2014. Temperature-dependent development of Ascotis selenaria (Lepidoptera: Geometridae) and its stage emergence models with field validation. Crop Prot. 66:72-79. https://doi.org/10.1016/j.cropro.2014.08.020
  4. Chung, B. N., Choi, K. S., Ahn, J. J., Joa, J. H., Do, K. S. and Park, K. S. 2015. Effects of temperature on systemic infection and symptom expression of turnip mosaic virus in Chinese cabbage (Brassica campestris). Plant Pathol. J. 31:363-370. https://doi.org/10.5423/PPJ.NT.06.2015.0107
  5. Close, R. 1964. Some effects of other viruses and of temperature on the multiplication of potato virus X. Ann. Appl. Biol. 53:151-164. https://doi.org/10.1111/j.1744-7348.1964.tb03788.x
  6. Curry, G. L. and Feldman, R. M. 1987. Mathematical foundations of population dynamics. Texas Engineering Experiment Station monograph series, no. 3. Texas A & M University Press, College Station, TX, USA.
  7. Damos, P. T. and Savopoulou-Soultani, M. 2008. Temperaturedependent bionomics and modeling of Anarsia lineatella (Lepidoptera: Gelechiidae) in the laboratory. J. Econ. Entomol. 101:1557-1567. https://doi.org/10.1093/jee/101.5.1557
  8. Del Toro, F. J., Aguilar, E., Hernández-Walias, F. J., Tenllado, F., Chung, B. N. and Canto, T. 2015. High temperature, high ambient $CO_2$ affect the interactions between three positivesense RNA viruses and a compatible host differentially, but not their silencing suppression efficiencies. PLoS One 10: e0136062. https://doi.org/10.1371/journal.pone.0136062
  9. Fajinmi, A. A. and Fajinmi, O. B. 2010. Incidence of okra mosaic virus at different growth stages of okra plants ([Abelmoschus esculentus (L.) Moench) under tropical condition. J. Gen. Mol. Virol. 2:28-31.
  10. Glasa, M., Labonne, G. and Quiot, J. B. 2003. Effect of temperature on plum pox virus infection. Acta Virol. 47:49-52.
  11. Hayes, E. J. and Wall, R. 1999. Age-grading adult insects: a review of techniques. Physiol. Entomol. 24:1-10. https://doi.org/10.1046/j.1365-3032.1999.00104.x
  12. Hull, R. 2002. Matthews' plant virology. 4th ed. Academic Press, San Diego, CA, USA.
  13. Jandel Scientific. 1996. TableCurve 2D. Automated curve fitting and equation discovery: version 4.0. Jandel Scientific, Sam Rafael, CA, USA.
  14. Lactin, D. J., Holliday, N. J., Johnson, D. L. and Craigen, R. 1995. Improved rate model of temperature-dependent development by arthropods. Environ. Entomol. 24:68-75. https://doi.org/10.1093/ee/24.1.68
  15. Llave, C., Martinez, B., Diaz-Ruiz, J. R. and Lopez-Abella, D. 1999. Serological analysis and coat protein sequence determination of Potato virus Y (PVY) pepper pathotypes and differentiation from other PVY strains. Eur. J. Plant Pathol. 105:847-857. https://doi.org/10.1023/A:1008775910680
  16. Radcliffe, E. B. 1982. Insect pests of potato. Ann. Rev. Entomol. 27:173-204. https://doi.org/10.1146/annurev.en.27.010182.001133
  17. Robert, Y., Woodford, J. A. and Ducray-Bourdin, D. G. 2000. Some epidemiological approaches to the control of aphidborne virus diseases in seed potato crops in northern Europe. Virus Res. 71:33-47. https://doi.org/10.1016/S0168-1702(00)00186-6
  18. Roberts, A. G., Cruz, S. S., Roberts, I. M., Prior, D., Turgeon, R. and Oparka, K. J. 1997. Phloem unloading in sink leaves of Nicotiana benthamiana: comparison of a fluorescent solute with a fluorescent virus. Plant Cell 9:1381-1396. https://doi.org/10.1105/tpc.9.8.1381
  19. SAS Institute. 1999. SAS OnlineDoc. Version 8. SAS Institute, Cary, NC, USA.
  20. Shepard, J. F. and Uyemoto, J. K. 1976. Influence of elevated temperatures on the isolation and proliferation of mesophyll protoplasts from PVX-and PVY-infected tobacco tissue. Virology 70:558-560. https://doi.org/10.1016/0042-6822(76)90299-3
  21. Syller, J. 1987. The influence of temperature on transmission of potato leaf roll virus by Myzus persicae Sulz. Potato Res. 30:47-58. https://doi.org/10.1007/BF02357683
  22. Szittya, G., Silhavy, D., Molnar, A., Havelda, Z., Lovas, A., Lakatos, L., Banfalvi, Z. and Burgyan, J. 2003. Low temperature inhibits RNA silencing-mediated defence by the control of siRNA generation. EMBO J. 22:633-640. https://doi.org/10.1093/emboj/cdg74
  23. Valkonen, J. P. T. 1997. Novel resistances to four potyviruses in tuber-bearing potato species, and temperature-sensitive expression of hypersensitive resistance to potato virus Y. Ann. Appl. Biol. 130:91-104. https://doi.org/10.1111/j.1744-7348.1997.tb05785.x
  24. Valkonen, J. P. T., Puurand, U., Slack, S. A., Mäkinen, K. and Saarma, M. 1995. Three strain groups of potato A potyvirus based on the hypersensitive responses in potato, serological properties, and coat protein sequences. Plant Dis. 79:748-753. https://doi.org/10.1094/PD-79-0748
  25. Wagner, T. L., Wu, H. I., Feldman, R. M., Sharpe, P. J. H. and Coulson, R. N. 1985. Multiple-cohort approach for simulating development of insect populations under variable temperatures. Ann. Entomol. Soc. Am. 78:691-704. https://doi.org/10.1093/aesa/78.6.691
  26. Wagner, T. L., Wu, H. I., Sharpe, P. J. H. and Coulson, R. N. 1984. Modeling distribution of insect development time: a literature review and application of Weibull function. Ann. Entomol. Soc. Am. 77:475-483. https://doi.org/10.1093/aesa/77.5.475
  27. Watson, M. A. and Roberts, F. M. 1939. A comparative study of the transmission of Hyoscyamus virus 3, potato virus Y, and cucumber virus 1 by the vectors Myzus persicae (Sulz.), M. circumflexus (Buckton), and Macrosiphum gei (Koch). Proc. R. Soc. Lond. B Biol. Sci. 127:543-576. https://doi.org/10.1098/rspb.1939.0039