Higher growth induced upon Potato Virus X invasion in Messenger treated tomato plants

Yıl 2017, Cilt: 34 Sayı: 3, 74 - 81, 29.12.2017

Mohamed Husseın Muharrem Arap Kamberoğlu

https://doi.org/10.13002/jafag4329

Öz

This investigation aimed to examine the possible role of foliar Messenger (a bio-product based on harpin protein) application in reducing the Potato virus X (PVX) development on tomato plants treated with 3 different doses of Messenger (M1: 0.5g l-1, M2: 1g l-1, M3: 0.25g l-1). For that reason, seventy-two hours post treatment (hpt) a group of tomato plants was inoculated with PVX. Besides, another group of tomato plants were inoculated 24 hours afterwards to check the effect of plant age on PVX infection. Plants treated with M1 at 72h prior to the PVX inoculation showed the maximum recovery as an increase in chlorophyll content (25.78±0.67), plant height (31±4.58) cm and leaf area (361.07±76.15) cm2. However, M1-enhancement in plant height (27±0.4) cm and leaf area (289.83±45.04) cm2 of the non-inoculated tomato plants was lower than that in the inoculated ones. This indicated that M1 induction was most distinct after viral inoculation with higher growth of tomato plants than before introducing the virus. Furthermore, mature plant resistance against PVX was developed with as short plant age increase as to 24 hours.

Anahtar Kelimeler

Chlorophyll content, harpin, leaf area, messenger, plant height

Kaynakça

• Afreen B, Gulfishan M, Baghel G, Fatma M, Khan AA, Naqvi QA (2011). Molecular detection of a virus infecting carrot and its effect on some cytological and physiological parameters. African Journal of Plant Science, 5(7):407-11.
• Bald JG (1937). Investigations on" Spotted Wilt" of Tomatoes: III.-Infection in Field Plots. Council for Scientific and IndustriaL Research, Australia 106:32.
• Balogun OS, Xu L, Teraoka T, Hosokawa D (2002). Effects of single and double infections with Potato virus X and Tobacco mosaic virus on disease development, plant growth, and virus accumulation in tomato. Fitopatologia Brasileira, 27(3):241-8.
• Beemster AB (1987). Virus translocation and mature-plant resistance in potato plants. in: Viruses of potatoes and seed-potato production. edited by JA de Bokx and JPH van der Want. Published by Wageningen Pudoc. (2) 116-125.
• Buiel AA, Parlevliet JE (1996). Mature plant and tissue resistance in the groundnut-peanut bud necrosis virus system. Euphytica, 91(2):213-7.
• Clark MF, Adams AN (1977). Characteristics of the microplate method of enzyme-linked immunosorbent assay for the detection of plant viruses. Journal of general virology, 34(3):475-83.
• Crowley NC (1967). Factors affecting the local lesion response of Nicotiana glutinosa to lettuce necrotic yellows virus. Virology, 31(1):107-13.
• El-Dougdoug KA, Mohamed H, Abo-Senna A (2007). Effect of PVY viral infection on alkaloid contents of cultivated medicinal plants. Journal of Applied Science Research 3:558-63.
• Gibson RW (1991). The development of mature plant resistance in four potato cultivars against aphid-inoculated potato virus Y O and Y N in four potato cultivars. Potato Research, 34(2):205-10.
• Goncalves MC, Vega J, Oliveira JG, Gomes M (2005). Sugarcane yellow leaf virus infection leads to alterations in photosynthetic efficiency and carbohydrate accumulation in sugarcane leaves. Fitopatologia Brasileira, 30(1):10-6.
• Guest D, Brown J (1997). Plant defences against pathogens. In Plant pathogens and plant diseases (edited by J.F. Brown and H.J. Ogle endorsed by the Australasian Plant Pathology Society Inc.) Rockvale Publications for the Division of Botany, School of Rural Science and Natural Resources, University of New England, 263-286.
• Guo DP, Guo YP, Zhao JP, Liu H, Peng Y, Wang QM, Chen JS, Rao GZ (2005). Photosynthetic rate and chlorophyll fluorescence in leaves of stem mustard (Brassica juncea var. tsatsai) after turnip mosaic virus infection. Plant Science, 168(1):57-63.
• Hooks CR, Wright MG, Kabasawa DS, Manandhar R, Almeida RP (2008). Effect of banana bunchy top virus infection on morphology and growth characteristics of banana. Annals of Applied Biology, 153(1):1-9.
• Khalil RR, Bassiouny FM, El-Dougdoug KA, Abo-Elmaty S, Yousef MS (2014). A dramatic physiological and anatomical changes of tomato plants infecting with tomato yellow leaf curl germinivirus. International Journal of Agricultural Sustainability, 10:1213-29.
• Kucharek T, Purcifull D, Hiebert E (2003). Viruses that have occurred naturally in agronomic and vegetable crops in Florida. Plant Pathology Department Document. in: PP/PPP7. University of Florida/IFAS, Gainesville, FL ;32611.
• Lapierre H, Signoret PA (2004). Viruses and virus diseases of Poaceae (Gramineae). INRA editions, Paris, France, 381-383.
• Loebenstein G, Berger PH, Brunt AA, Lawson RH, (2013). Virus and virus-like diseases of potatoes and production of seed-potatoes. Springer Science & Business Media, 87-94.
• Mofunanya AAJ, Edu EA (2015). Physiological and Biochemical Changes in Cucurbita moschata Duch. Ex. Poir Inoculated with a Nigerian Strain of Moroccan Watermelon Mosaic Virus (MWMV): Lagenaria breviflora Isolate. International Journal of Plant Pathology, 6(2):36-47.
• Nandi P, Raychaudhuri SP (1966). Effect of iron on the concentration of potato virus X in tomato. American Journal of Potato Research, 43(1):6-9.
• Naylor M, Murphy AM, Berry JO, Carr JP (1998). Salicylic acid can induce resistance to plant virus movement. Molecular Plant-Microbe Interactions, 11(9):860-8.
• Pazarlar S, Gümüş M, Öztekin GB (2013). The effects of Tobacco mosaic virus infection on growth and physiological parameters in some pepper varieties. Notulae Botanicae Horti Agrobotanici Cluj-Napoca, 41(2):427.
• Plattt SG, Henriques F, Rand L (1979). Effects of virus infection on the chlorophyll content, photosynthetic rate and carbon metabolism of Tolmiea menziesii. Physiological Plant Pathology, 15(3):351-65.
• Palanisamy P, Michael PI, Krishnaswamy M (2009). Physiological response of yellow vein mosaic virus-infected bhendi (Abelmoschus esculentus) leaves. Physiological and Molecular Plant Pathology, 74(2):129-33.
• Rahman H, Alam MM, Bhyan SB, Akanda AM (2008). Alteration of cellular pigments of papaya leaves infected with seven symptomatic isolates of PRSV-P. Journal of Plant Sciences, 3(1):69-76.
• Rivas-San Vicente M, Plasencia J (2011). Salicylic acid beyond defence: its role in plant growth and development. Journal of experimental botany, 62(10):3321-38.
• Ryšlavá H, Müller K, Semorádová Š, Synková H, Čeřovská N (2003). Photosynthesis and activity of phosphoenolpyruvate carboxylase in Nicotiana tabacum L. leaves infected by Potato virus A and Potato virus Y. Photosynthetica, 41(3):357-63.
• Schein RD (1965). Age-correlated changes in susceptibility of bean leaves to Uromyces phaseoli and tobacco mosaic virus. Phytopathology,55(4):454.
• Sigvald R (1985). Mature-plant resistance of potato plants against potato virus Y O (PVY O). Potato Research, 28(2):135-43.
• Singh V, Shukla K (2009). Effect of PRSV infection on pigment content and assimilation of carbohydrate in Carica papaya L. Annals of Plant Protection Sciences, 17(1):152-6.
• Smit G, Parlevliet JE (1990). Mature plant resistance of barley to barley leaf rust, another type of resistance. Euphytica, 50(2):159-62.
• Song XS, Wang YJ, Mao WH, Shi K, Zhou YH, Nogués S, Yu JQ (2009). Effects of cucumber mosaic virus infection on electron transport and antioxidant system in chloroplasts and mitochondria of cucumber and tomato leaves. Physiologia Plantarum, 135(3):246-57.
• Spoustová P, Synková H, Valcke R, Čeřovská N (2013). Chlorophyll a fluorescence as a tool for a study of the Potato virus Y effects on photosynthesis of nontransgenic and transgenic Pssu-ipt tobacco. Photosynthetica, 51(2):191-201.
• Strand L (2006). Integrated pest management for potatoes in the western United States. UCANR Publications; p95.
• Vance VB, Berger PH, Carrington JC, Hunt AG, Shi XM (1995). 5′ proximal potyviral sequences mediate potato virus X/potyviral synergistic disease in transgenic tobacco. Virology, 206(1):583-90.
• Venekamp JH, Beemster AB (1980). Mature plant resistance of potato against some virus diseases. I. Concurrence of development of mature plant resistance against Potato virus X, and decrease of ribosome and RNA content. Netherlands Journal of Plant Pathology, 86(1):1-0.
• Walters D, Newton A, Lyon G (2007). Induced Resistance for Plant Defence. in: A Sustainable Approach to Crop Protection, Publ. by Blackwell Publishing, 9-28.
• Wei ZM, Laby RJ, Zumoff CH, Bauer DW, He SY, Collmer H, Beer SV (1992). Harpin, elicitor of the hypersensitive response produced by the plant pathogen Erwinia amylovora. Science(Washington), 257(5066):85-8.
• Wislocka M (1984). Influence of weather factors on the increase of mature plant resistance to PVY. The Potato (1983–1984),105-16.