تأثیر باکتری‌های محرک رشد بر شاخص‌های رشدی و بیوشیمیایی کاهو تحت تنش زیستی سفیدک پودری

نوع مقاله : مقالات پژوهشی

نویسندگان

گروه علوم باغبانی، دانشکده کشاورزی، دانشگاه زنجان، زنجان، ایران

چکیده

به‌منظور ارزیابی تأثیر باکتری­‌های محرک رشد بر شاخص‌­های رشدی و بیوشیمیایی کاهو در شرایط تنش زیستی قارچ سفیدک پودری، آزمایشی به‌صورت طرح کاملا تصادفی با سه تکرار در گلخانه تحقیقاتی دانشگاه زنجان، در سال 1399 اجرا شد. گیاهان در شرایط تنش زیستی قارچ سفیدک پودری با پنج سطح از باکتری­‌های محرک رشد شامل سودوموناس­کورینسیس، سودوموناس­ونکورنسیس، سودوموناس­پوتیدا، پانتوآگلومرانس و ترکیب چهار گونه باکتری محرک رشد (سودوموناس­کورینسیس + سودوموناس­ونکورنسیس + سودوموناس­پوتیدا + پانتوآگلومرانس) و یک سطح کود شیمیایی NPK تیمار شدند. دو تیمار شاهد (بدون تلقیح باکتری ریزوسفری و بدون افزودن کود شیمیایی) در شرایط بدون تنش و تحت تنش زیستی بود. نتایج نشان داد، حداکثر وزن تازه، درصد ماده خشک بوته و تعداد برگ در کاربرد تیمار باکتری ترکیبی حاصل شد، به­‌طوری‌که نسبت به گیاهان شاهد با تنش، 5/59 درصد وزن تازه بوته، 8/34 درصد ماده خشک بوته و 2/42 درصد تعداد برگ افزایش یافت. بیشترین محتوای کلروفیل کل (افزایش 5/38 درصد) با کاربرد باکتری سودوموناس کورینسیس و پانتوآگلومرانس نسبت به گیاهان شاهد تحت تنش بدست آمد. همچنین با کاربرد باکتری پانتوآگلومرانس کاهش 100 درصدی لکه­‌های نکروزه و 2/25 درصدی لکه‌­های کلروزه مشاهده شد. افزایش لکه­‌های کلروزه (8/55 درصد)، لکه­‌های نکروزه (8/88 درصد)، فعالیت آنزیم کاتالاز (4/28 درصد)، آنزیم پراکسیداز (1/49 درصد)، محتوای فنول کل (52 درصد) و فلاونوئید کل (3/39 درصد) نسبت به گیاهان شاهد تحت تنش، در کاربرد تیمار کود شیمیایی NPK حاصل شد. کاربرد باکتری­‌های محرک رشد و کود شیمیایی NPK اثر معنی­داری بر فعالیت آنتی‌­اکسیدانی گیاه کاهو تحت تنش زیستی نداشت. حداکثر محتوای آنتوسیانین (افزایش 6/55 درصد) با کاربرد باکتری کورینسیس نسبت به گیاهان شاهد تحت تنش بدست آمد. به‌طور کلی تلقیح بذر کاهو با باکتری­‌های محرک رشد موجب افزایش معنی­دار رنگیزه آنتوسیانین در برگ، محتوای کلروفیل کل، ترکیبات فنولی، مقاومت گیاه میزبان به تنش زیستی سفیدک پودری و متعاقباً بهبود شاخص­های رشدی و عملکرد (وزن تازه بوته قابل برداشت) گردید. با توجه به نتایج این پژوهش، پیش تیمار بذر کاهو با باکتری‌­های محرک رشد برای بهبود عملکرد و کیفیت کاهو در شرایط قارچ سفیدک پودری توصیه می‌­شود.

کلیدواژه‌ها

موضوعات


عنوان مقاله [English]

Effect of Plant Growth Promoting Bacteria on Growth and Biochemical Indices of Lettuce under Powdery Mildew Biotic Stress

نویسندگان [English]

  • Parastoo Molaei
  • Fatemeh Nekounam
Department of Horticultural Science, Faculty of Agriculture, University of Zanjan, Zanjan, Iran
چکیده [English]

Introduction
Lettuce (Lactuca sativa L.) from the Asteraceae family is one of the most important vegetables due to its rapid growth and commercial value. Currently, the market share of organic vegetables is constantly increasing due to customer demand for safer and healthier food. Excessive use of pesticides and chemical fertilizers threatens the environment and leads to the production of unsafe food products. Therefore, it is important to find alternatives instead of using pesticides chemical methods to manage powdery mildew. Generally, biotic and abiotic stresses are among the factors that have a destructive effect on growth and development, performance, and production of plant biomass. Fungicides can be the most effective method of controlling the powdery mildew disease, but this pathogen can develop resistance to fungicides. Rhizosphere bacteria are among the living agents that, by producing some allelochemicals, cause the dissolution of soil nutrients, increase the availability of nutrients, and induce plant resistance to biotic and abiotic stresses. In addition, they enhance host plant growth through an indirect mechanism, including the inhibition of disease-causing pathogens by releasing some allelochemical substances. The biological control of powdery mildew disease with the use of rhizospheric bacteria in lettuce and zucchini has been reported.
 
Material and Methods
To evaluate the biological control of powdery mildew fungus with plant growth promoting rhizobacteria (PGPR) and effects on yield and quality of New Red Fire greenhouse lettuce, an experiment was carried out in a completely randomized design with three replications in the Research greenhouse of University of Zanjan during 2020. Experiment treatments consisted of five levels of PGPR (Pseudomonas vancouverensis- VPM, Pseudomonas Koreensis- KPM, Pantoea agglomerans- PAPM, Pseudomonas putida- PPM, and one level of combined bacteria (Pantoea agglomerans+ Pseudomonas Koreensis+ Pseudomonas putida+ Pseudomonas vancouverensis- MBPM, one level of chemical fertilizer 100% N, P and, K according to soil test results- NPK, and two control treatment without powdery mildew condition (C) and under powdery mildew conditions (CPM).
The “New Red Fire” lettuce seeds were surface sterilized with 0.5% (v/v) sodium hypochlorite for 10 min and germinated at 20ºC. After germination, seedlings with similar size were transplanted into pots. Plants were grown under greenhouse condition with 60/70 % (day/night) relative humidity, 15/18 °C (day/night) temperature. Inoculation of pathogenic fungi was done 40 days after seed germination. Plants were harvested after 75 days. The chlorosis and necrosis spots number on each plant, plant fresh weight, plant dry weight, leaf number, total chlorophyll, total phenol and flavonoids contents, antioxidant activity, anthocyanin content, and catalase and peroxidase enzyme activity were measured.
 
Results
The results showed that the application of potassium and phosphorus solubilizing bacteria and NPK fertilizer significantly increased plant growth compared to control plants under the stress of powdery mildew fungus. The highest plant fresh weight, percentage of plant dry weight, and leaf number were obtained with the application of combined potassium and phosphorus solubilizing bacteria treatment and 100% N fertilizer under the biostress. The maximum total chlorophyll was obtained with the application of Pseudomonas koreensis and Pantoea agglomerans bacteria. 100% reduction of necrosis spots was obtained by using the Pantoea agglomerans bacteria. The maximum of chlorosis spots (increase of 55.8%) and necrosis spots (an increase of 88.8%), total phenol (an increase of 52%), total flavonoids (an increase of 39.3%), catalase (an increase of 28.4%) and peroxidase enzymes activity (49.1%) were obtained with application of NPK fertilizer. No significant effect on antioxidant activity was observed with the application of chemical fertilizer and rhizosphere bacteria under the Biostress. The maximum anthocyanin contents were obtained with the application of Pseudomonas koreensis.
 
Conclusion
According to the results, the application of NPK chemical fertilizer and seed pretreatment of lettuce with PGPR increased the value of antioxidant compounds including total phenol, flavonoid, and anthocyanin contents and catalase and peroxidase enzymes activity under powdery mildew conditions. Inoculation of lettuce seeds with PGPR, in addition to improve plant growth under biological stress conditions, increased anthocyanin contents and induced the resistance of lettuce plants to powdery mildew. Seed pretreatment with PGPR reduced chlorosis and necrosis spots in leaves. Therefore, pretreatment of lettuce seeds with PGPR instead of chemical compounds (fertilizers, pesticides and plant growth regulators) is recommended to improve the yield and quality of lettuce under powdery mildew conditions.

کلیدواژه‌ها [English]

  • Anthocyanin
  • Biological control
  • Biostress
  • Necrotic spots
  • Powdery mildew

©2022 The author(s). This is an open access article distributed under Creative Commons Attribution 4.0 International License (CC BY 4.0), which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source.

1- Ahemad, M., & Kibret, M. (2014). Mechanisms and application s of plant growth promoting rhizobacteri a: Current perspective. Journal of King Saud University Science, 26, 1-20. https://doi.org/10.1016/j.jksus.2013.05.001
2- Arnon, A.N. (1967). Method of extraction of chlorophyll in the plants. Agronomy Journal, 23, 112-121.
3- Babu, S., Prasanna, R., Bidyarani, N., Nain, L., & Shivay, Y.S. (2015). Synergistic action of PGP agents and Rhizobium spp. for improved plant growth, nutrient mobilization and yields in different leguminous crops. Biocatal Agric Biotechnol, 4, 456-464. https://doi.org/10.1016/j.bcab.2015.09.004
4- Bahrami, N., Jalali, M., & Zare, A.K. (2020). The effect of various sources of iron on the nitrate accumulation in lettuce (Lactuca sativa L.). Iranian Journal of Soil and Water Research, 51, 2953-2963. (In Persian with English abstract). https://doi.org/10.22059/ijswr.2020.306193.668669
5- Basu, S., Roychoudhury, A., Saha, P.P., & Sengupta, D.N. (2010). Differential antioxidative responses of indica rice cultivars to drought stress. Plant Growth Regulation, 60, 51-59. https://doi.org/10.1007/s10725-009-9418-4 
6- Cappellari, L.D.R., Santoro, M.V., Nievas, F., Giordano, W., & Banchio, E. (2013). Increase of secondary metabolite content in marigold by inoculation with plant growth-promoting rhizobacteria. Applied Soil Ecology, 70, 16-22. https://doi.org/10.1016/j.apsoil.2013.04.001
7- Cézard, C., Farvacques, N., & Sonnet, P. (2015). Chemistry and biology of pyoverdines, Pseudomonas primary siderophores. Current Medicinal Chemistry, 22, 165-186. https://doi.org/10.2174/0929867321666141011194624
8- Chang, C., Yang, M., Wen, H., & Chern, J. (2002). Estimation of total flavonoid content in propolis by two complementary colorimetric methods. Journal of Food and Drug Analysis, 10, 178-182. https://doi.org/10.38212/2224-6614.2748
9- Chen, Y., Cao, S., Chai, Y., Clardy, J., Kolter, R., Gue, J., & Losick, R. (2012). A Bacillus subtilis sensor kinase involved in triggering biofilm formation on the roots of tomato plants. Molecular Microbiology, 85, 418-430. https://doi.org/10.1111/j.1365-2958.2012.08109.x
10- Chithrashree, C., & Srinivas, C. (2012). Role of antioxidant scavenging enzymes and extracellular polysaccharide in pathogenicity of rice bacterial blight pathogen Xanthomonas oryzae pv. Oryzae. African Journal of Biotechnology, 11, 13186-13193. https://doi.org/10.5897/AJB12.1670
11- Demiray, S., Pintado, M.E., & Castro, P.M.L. (2009). Evaluation of phenolic profiles and antioxidant activities of Turkish medicinal plants: Tilia argentea, Crataegi folium leaves and Polygonum bistorta roots. World Academy of Science Engineering and Technology, 54, 312-317. https://doi.org/10.5281/zenodo.1075066
12- Derikvand, F., Bazgir, E., Darvishnia, M., & Mirzaei Najafgholi, H. (2020). A study on the changes of some enzymes related to antioxidant defense system in common bean against Xanthomonas axonopodis pv. Phaseoli. Nova Biologica Reperta, 6, 424-434. (In Persian with English abstract). https://doi.org/10.29252/nbr.6.4.424
13-Dinesh, R., Anandaraj, M., Kumar, A., Bini, Y.K., Subila, K.P., & Aravind, R. (2015). Isolation, characterization, and evaluation of multi-trait plant growth promoting rhizobacteria for their growth promoting and disease suppressing effects on ginger. Microbiological Research, 173, 34-43. https://doi.org/10.1016/j.micres.2015.01.014
14- Farahani, A.S., & Taghavi, M. (2016). Changes of antioxidant enzymes of mung bean [Vigna radiata (L.) R. Wilczek] in response to host and non -host bacterial pathogens. Journal of Plant Protection Research, 56, 95-99. https://doi.org/10.1515/jppr-2016-0016
15- Fernandez, O., Theocharis, A., Bordiec, S., Feil, R., Jacquens, L., & Clement, C. (2012). Burkholderia phytofirmans PsJN acclimates grapevine to cold by modulating carbohydrate metabolism. Molecular Plant-Microbe Interactions, 25, 496-504. https://doi.org/10.1094/MPMI-09-11-0245
16- Glick, B.R. (2012). Plant growth-promoting bacteria: mechanisms and applications. Hindawi Publishing Corporation Scientifica. https://doi.org/10.6064/2012/963401
17- Itako, A.T., Tolentino Júnior, J.B., Júnior, S., Soman, J.M., & Maringoni, A.C. (2015). Chemical products induce resistance to Xanthomonas perforans in tomato. Brazilian Journal of Microbiology, 46, 701-706. https://doi.org/10.1590/S1517-838246320140177
18- Jamali Zavareh, A.H., Sharifi Tehrani, A., Hejarood, GH.A., Zad, S.J., Mohammadi, M., & Talebi Jahromi, K.J. (2004). An investigation of the effectiveness of acibenzolar S methyl for the control of cucumber powdery mildew. Iranian Journal of Agriculture Science, 35, 2. (In Persian with English abstract)
19- Jayaprakashvel, M., & Mathivanan, N. (2011). Management of plant diseases by microbial metabolites. In, Maheshwari DK (ed) Bacteria in agrobiology, plant nutrient management. Springer Berlin Heidelberg, 237-265.
20- Kara, M., & Mishra, E. (1976). Catalse, peroxidase and polyphenol oxidase activities rice leaf senescence. Plant Physiology, 57, 315-319. https://doi.org/10.1104/pp.57.2.315
21- Koc, E., İslek, C., & Üstun, A.S. (2010). Effect of cold on protein, proline, phenolic compounds and chlorophyll content of two pepper (Capsicum annuum L.) varieties. Gazi University Journal of Science, 23, 1-6.
22- Kumar, M., Mishra, S., Dixit, V., Kumar, M., Agarwal, L., Singh Chauhan, P., & Shekhar Nautiyal, C. (2015). Synergistic effect of Pseudomonas putida and Bacillus amyloliquefaciens ameliorates drought stress in chickpea (Cicer arietinum L.). Plant Signaling and Behavior, 11, e1071004. https://doi.org/10.1080/15592324.2015.1071004
23- Lindenthal, M., Steiner, U., Dehne, H.W., & Oerke, E.C. (2005). Effect of downy mildew development on transpiration of cucumber leaves visualized by digital infrared thermography. Phytopathology, 95, 233-240. https://doi.org/10.1094/PHYTO-95-0233
24- Liu, F., Zhuge, Y.Y., Yang, C.Y., Jin, S.X., Chen, J., Li, H., & Dai, G.H. (2010). Control effects of some plant extracts against cucumber powdery mildew (Sphaerotheca fuliginea) and their Stability Study. Europ, Journal of Horticultural Science, 75, 147-152. https://doi.org/10.2307/24127045
25- Mahfouz, S.A., & Sharaf- Eldin, A. (2007). Effect of mineral vs. biofertilizer on growth, yield and essential oil content of fennel (Foeniculum vulgare Mill.). International Agrophysics, 2, 361-366. https://doi.org/10.1055/s-2007-987419
26- Mampholo, B.M., Maboko, M.M., Soundy, P., & Sivakumar, D. (2016). Phytochemicals and overall quality of leafy lettuce (Lactuca sativa L.) varieties grown in closed hydroponic system. Journal of Food Quality, 39, 805-815. https://doi.org/10.1111/jfq.12234
27- Martins, S.J., Medeiros, F.H.V., Souza, R.M., & Resende, M.L.V. (2013). Biological control of bacterial wilt of common bean by plant growth-promoting rhizobacteria. Biological Control, 66, 65-71. https://doi.org/10.1016/j.biocontrol.2013.03.009
28- McGrath, M.T. (2017). Vegetable crops: powdery mildew of Cucurbits, Cooperative extension. https://vegetablemdonline.ppath.cornell.edu/fact sheets/Cucurbits_PM.htm
29- Miliauskas, G., Venskutonis, P.R., & Vanbeek, T.A. (2004). Screening of radical scavenging activity of some medicinal and aromatic plant extracts. Food Chemistry, 85, 231-237. https://doi.org/10.1016/j.foodchem.2003.05.007
30- Molaei, P., Barzegar, T., Baba Akbari Sari, M., Nekounam, F., & Ghahremani, Z. (2023). The effect of bio and chemical fertilizers on yield and quality of lettuce (Lactuca sativa cv. New Red Fire). Journal of Horticultural Science, 37(3), 685-697. (In Persian with English abstract). https://doi.org/10.22067/jhs.2022.76893.1175
31- Narendra Babu, A., Jogaiah, S., Ito, S., Kestur Nagaraj, A., & Tran, L.S.P. (2015). Improvement of growth, fruit weight and early blight disease protection of tomato plants by rhizosphere bacteria is correlated with their beneficial traits and induced biosynthesis of antioxidant peroxidase and polyphenol oxidase. Journal of Plant Sciences, 231, 62-73. https://doi.org/10.1016/j.plantsci.2014.11.006
32- Radhakrishnan, R., Hashem, A., & Abd-Allah, E.F. (2017). Bacillus: a biological tool for crop improvement through bio- molecular changes in adverse environments. Frontiers in Physiology, 8, 667. https://doi.org/10.3389/fphys.2017.00667
33- Saharan, B.S., & Nehra, V. (2011). Plant growth promoting rhizobacteria. Life Sciences and Medicine Research, 21, 1-30.
34- Saraf, M., Pandya, U., & Thakkar, A. (2014). Role of allelochemicals in plant growth promoting rhizobacteria for biocontrol of phytopathogens. Microbiological Research, 169, 18-29. https://doi.org/10.1016/j.micres.2013.08.009
35- Shariatifar, N., Kamakar, A., Shams Ardakani, M.R., Misaghi, A., Jamshidi, A.H., & Khaniki, J. (2012). Quantitative and qualitative study of phenilic compounds and antioxidant activity of plant pulicaria gnaphalodes. Journal of Gonabad University of Medical Sciences, 18, 35-42. (In Persian with English abstract)
36- Singla, J., & Krattinger, S.G. (2016). Biotic stress resistance genes in wheat. In: Wrigley, C.W., Faubion, J., Corke, H., Seetharaman, K. (Eds.). Encyclopedia of Food Grains Elsevier Oxford, 388-392. https://doi.org/10.1016/B978-0-12-394437-5.00229-1
37- Singleton, V.L., & Rossi J.A. (1965). Colorimetry of total phenolics with phosphomolybdic-phosphotungstic acid reagents. American journal of Enology and Viticulture, 16(3), 144-158.‏ https://doi.org/10.5344/ajev.1965.16.3.144
38- Sirous, A., & Jamali Zavareh, A.H. (2014). Effectiveness of celery leaf extract on the induction of resistance against cucumber powdery mildew. Iranian Journal of Plant Pathology, 50(2), 151-161. (In Persian with English abstract)
39- Spaepen, S., & Vanderleyden, J. (2011). Auxin and plant-microbe interactions, Cold Spring Harb Perspect Biol. https://doi.org/10.1101/cshperspect.a001438
40- Taiz, L., & Zeiger, E. (2010). Plant Physiology (5th ed.), Sinauer Associates, Inc., Sunderland.
41- Turan, M., Ekinci, M., Yildirim, E., Güneş, A., Karagöz, K., Kotan, R., & Dursun, A. (2014). Plant growth-promoting rhizobacteria improved growth, nutrient, and hormone content of cabbage (Brassica oleracea) seedlings. Turkish Journal of Agriculture and Forestry, 38, 327-333. https://doi.org/10.3906/tar-1308-62
42- Vlot, A.C., Dempsey, D.A., & Klessig, D.F. (2009). Salicylic acid, a multifaceted hormone to combat disease. Annual Review of Phytopathology, 47, 177-206. https://doi.org/10.1146/annurev.phyto.050908.135202
43- Vurukonda, S.S.K.P., Vardharajula, S., Shrivastava, M., & SkZ, A. (2015). Enhancement of drought stress tolerance in crops by plant growth promoting rhizobacteria. Microbiological Research, 184, 13-24. https://doi.org/10.1016/j.micres.2015.12.003
44- Wagner, G.J. (1979). Content and vacuole/ extra vacuole distribution of neutral sugars, free amino acids and anthocyanins in protoplasts. Plant Physiology, 64, 88-93. https://doi.org/10.1104/pp.64.1.88
45- Zhang, H., Murzello, C., Sun, Y., Kim, X., Mi, S.R., Jeter, R.M., Zak, J.C., Scot Dowd, E., & Pare, P.W. (2010). Choline and osmotic-stress tolerance induced in Arabidopsis by the soil microbe Bacillus subtilis (GB03). Molecular Plant-Microbe Interactions, 23, 1097-1104. https://doi.org/10.1094/MPMI-23-8-1097
46- Zhang, K.M., Yu, H.J., Shi, K., Zhou, Y.H., Yu, J.Q., & Xia, X.J. (2010). Photoprotective roles of anthocyanins in Begonia semperflorens. Plant Science, 179, 202-208. https://doi.org/10.1016/j.plantsci.2010.05.006
47- Zhu, J.H., Dong, K., Yang, Z.X., & Dong, Y. (2017). Advances in the mechanism of crop disease control by intercropping. Chin Journal of Ecology, 36, 1117-1126. https://doi.org/10.13292/j.1000-4890.201704.016
 
CAPTCHA Image