| تعداد نشریات | 282 |
| تعداد نشریات سازمان | 80 |
| تعداد شمارهها | 3,208 |
| تعداد مقالات | 35,560 |
| تعداد مشاهده مقاله | 53,001,252 |
| تعداد دریافت فایل اصل مقاله | 92,287,482 |
ارزیابی قابلیت همزیستی ارقام کلزا (Brassica napus L.) با قارچ اندوفیت Pseudogymnoascus pannorum | ||
| پژوهش های کاربردی زراعی | ||
| دوره 34، شماره 3 - شماره پیاپی 132، آبان 1400، صفحه 30-42 اصل مقاله (569.88 K) | ||
| نوع مقاله: مقاله پژوهشی | ||
| شناسه دیجیتال (DOI): 10.22092/aj.2021.354765.1550 | ||
| نویسندگان | ||
| داود رودی* 1؛ جیمز میلنر2؛ کرگ مک گیل3؛ ریچارد جانسون4؛ استوارت کارد5 | ||
| 1مرکز تحقیقات کشاورزی و منابع طبیعی خراسان رضوی، ایستگاه تحقیقات کشاورزی نیشابور | ||
| 2دانشگاه مسی ، دانشکده کشاورزی و محیط زیست، پالمرستون نورث، نیوزیلند | ||
| 3دانشگاه مسی نیوزیلند، دانشکده کشاورزی و محیط زیست، پالمرستون نورث، نیوزیلند | ||
| 4مرکز تحقیقات اگری سرچ، پالمرستون نورث، نیوزیلند | ||
| 5مرکزتحقیقاات اگری سرج، پالمرستون نورث، نیوزیلند | ||
| چکیده | ||
| استفاده از میکروارگانیسم های همزیست اندوفیتی می تواند باعث افزایش عملکرد و نیزمقاومت گیاهان به تنش های محیطی شود. در این مطالعه امکان همزیستی سویه ای از قارچ اندوفیتی Pseudogymnoascus pannorum با گیاه کلزا مطالعه شد. برای انجام این آزمایش، بذور کلزا پس از ضدعفونی با سوسپانسیونی از اسپور قارچ آغشته گردید و بذر هر رقم در داخل گلدان کشت شد و آزمایش در قالب طرح بلوکهای کامل تصادفی با سه تکرار در گلخانه مورد مطالعه قرار گرفت. درصد کلونیزاسیون قارچ در دو مرحله یک برگی و سه برگی رشد به روش ایزوله کردن قارچ از ساقه کلزا اندازه گیری شد. نتایج تجزیه واریانس آماری درصد کلونیزاسیون نشان دادکه ارقام مورد مطالعه با یکدیگر تفاوت معنی داری ندارند. بیشترین و کمترین میانگین درصد کلونیزاسیون قارچ در هر دو مرحله رشد به ترتیب مربوط به هیبرید Turan با 19.96 درصد و هیبریدLadoga 18.81با درصد بود. مقایسه میانگین درصد کلونیزاسیون ارقام مورد مطالعه در مرحله رشد یک و سه برگی با آزمون T-student جفت نشده نشان داد که اختلاف معنی دار در سطح 99 درصد است. درصد کلونیزاسیون قارچ در بافت های ساقه گیاه در مرحله یک برگی 17.77 درصد و در سه برگی 20.48 درصد بود. با توجه به نتایج این آزمایش که حاکی از توانایی ایجاد همزیستی گونه قارچ مورد مطالعه با کلزا می باشد، توصیه می شود اثرات این همزیستی بر افزایش مقاومت کلزا به تنش های محیطی مانند تنش سرما و نیز افزایش عملکرد ناشی از این همزیستی در تحقیقات آینده مورد مطالعه قرار گیرد. | ||
| کلیدواژهها | ||
| کانولا؛ مایه زنی بذر؛ همزیستی اندوفیتی؛ دامنه میزبانی | ||
| عنوان مقاله [English] | ||
| Association of oilseed rape cultivars (Brassica napus L.) with fungal endophyte of Pseudogymnoascus pannorum | ||
| نویسندگان [English] | ||
| Davood Roodi1؛ James Millner2؛ Craig McGill3؛ Richard Johnson4؛ Stuart Card5 | ||
| 1Agricultural Research, Education and Natural Resources of Khorasan Razavi,, Neyshabour Station, Neyshabour, Iran | ||
| 2Massey University, Institute of Agriculture and Environment, Palmerston North, New Zealand | ||
| 3Massey University.Institute of agriculture and environment, Palmerston North, New Zealand, | ||
| 4Agreserach Ltd., Palmerston North, New Zealand | ||
| 5Agreserach Ltd., Palmerston North, New Zealand | ||
| چکیده [English] | ||
| Introduction: Microorganisms that live inside plant tissues, termed endophytes, may offer benefits to their host affected to biotic and abiotic stress conditions including extreme temperatures (Card et al., 2016). Characterized endophytic strains which show no host specificity could be transferred from their original wild plant hosts into elite cultivars through different method of inoculation. Fungal endophyte of Pseudogymnoascus pannorum. is a psychotolerant fungus resistance to frosting temperature and associated with plants grown in the arctic regions. The association of a strain of Pseudogymnoascus pannorum which has been previously isolated from a wild turnip was investigated with five oilseed rape hybrids in this study (Roodi, 2019). Material and methods: Seeds of five oilseed rape hybrids were surface-disinfected and inoculated by immersing in spore suspension of the fungus. Seeds were then transferred to pots and placed in a glasshouse in a completely randomized block design with three replications. The colonization frequencies of brassica seedlings inoculated with fungal endophyte was assessed at two vegetative plant growth stages. This was done by plating the 15 small piece of disinfected tissue of stem of each hybrids in a Perti dish with Potato Dextrose Agar medium. Petri plates were incubated at 22˚C and checked regularly for microbial growth. The colonization tissue frequency of each hybrid calculated and data statically analysed. The penetration of fungal hyphae was also studied by a light microscope. Results and discussion: The results from re-isolation of fungal endophyte from inoculated oilseed rape hybrids demonstrated that the fungal endophyte of Pseudogymnoascus pannorum colonized shoot tissues of all five hybrids studied and establish a close association with all oilseed rape hybrids. The analysis of variance of colonization tissue frequency showed that there is no significant difference between hybrids. The highest and lowest colonization rate was belonging to hybrid Turan and Ladoga with 19.96 and 18.81 percent respectively. The visual observation of inoculated plants showed that the endophytes does not induce any disease symptoms or change in plant growth and development of brassica plants. Control plants were not infected with the fungal endophyte. Although the origin host of the fungal endophyte was a wild turnip of Brassica rapa species, the result from inoculation indicates that this strain shows no host specificity. This is consistence with the result of another study that showed a strain of Beauveria bassiana isolated from another host can colonize other species such as oilseed rape (Vidal & Jaber, 2015). However, there was a significant difference between rates of colonization at two different growth stages. The mean colonization frequency at one and three-leaf stage was statically compared with t-student (unpaired group) witch was significantly different (99%). The mean colonization rate of hybrids was 17.77 and 20.48 percent at one and three-leaf stage respectively. Microscopic study of stem tissues also illustrated that the hyphae of fungus penetrate inside the epidermal layer of stem tissue. Conclusion: In this study we demonstrated that a specific strain of Pseudogymnoascus pannorum is able to colonize the areal parts of oilseed rape hybrids and establish a close association. This genus of fungus is an endophyte with psychotolerant properties that occupies plant grown in arctic regions. The results from this study can be used for further investigations on symbiosis benefits of this association especially to study the induction of resistance of oilseed rape to environmental stresses such as frosting and plant growth enhancement. Acknowledgment: This study was supported by Agricultural Research, Education and Extension Organization of Iran, Massey University and AgResearch Ltd. (Grasslands campus), Grasslanz Technology and Ellet Trust foundation, New Zealand. Keywords: Key words: Canola, seed inoculation, endophytic association, host specificity References: 1- Card SD, Hume DE, Roodi D, McGill CR, Millner JP & Johnson RD (2015) Beneficial endophytic microorganisms of Brassica – A review. Biol Control 90: 102-112. 2- Roodi D, Millner JP, McGill CR, Johnson RD & Card SD (2019) Bio-prospecting of endophytes of Brassica. PhD dessertation. Faculty of plant science, Massey University. Palmerston North. New Zealand. Pp.161. 3- Vidal S & Jaber LR (2015) Entomopathogenic fungi as endophytes: plant-endophyte-herbivore interactions and prospects for use in biological control. Curr Sci 45-54. | ||
| کلیدواژهها [English] | ||
| Canola, seed inoculation, endophytic association, host specificity | ||
| مراجع | ||
|
Azevedo, J. L., Maccheroni, J.R.W., Pereira, J.O.,and de Araújo, W.L. 2000. Endophytic microorganisms: a review on insect control and recent advances on tropical plants. Electronic Journal of Biotechnology,3: 15-16. Bressan, W.,and Borges, M.T. 2004. Delivery methods for introducing endophytic bacteria into maize. BioControl,49: 315-322. Card, S., Johnson, L., Teasdale, S.,and Caradus, J. 2016. Deciphering endophyte behaviour: the link between endophyte biology and efficacious biological control agents. FEMS Microbiolgy Ecology,92(8). Card, S.D., Hume, D.E., Roodi, D., McGill, C.R., Millner, J.P.,and Johnson, R.D. 2015. Beneficial endophytic microorganisms of Brassica – A review. Biological Control90: 102-112. Finotti, E., Paolino, C., Lancia, B., and Mercantini, R. 1996. Metabolic differences between two Antarctic strains of Geomyces pannorum. Current Microbiology, 32(1), 7-10. Gautam, S., Mohankumar, S.,and Kennedy, J. 2016. Induced host plant resistance in cauliflower by Beauveria bassiana. Journal of Entomology and Zoology Studies4: 476-482. Hayes, M.A. 2012. The Geomyces Fungi: Ecology and Distribution. Bioscience62: 819-823. Johnson, J.M., Alex, T.,and Oelmüller, R. 2014.Piriformospora indica: The versatile and multifunctional root endophytic fungus for enhanced yield and tolerance to biotic and abiotic stress in crop plants. Journal of Tropical Agriculture,52: 103-122. Johnson, L.J., de Bonth, A.C.M., Briggs, L.R., et al.,.2013. The exploitation of epichloae endophytes for agricultural benefit. Fungal Diversity,60: 171-188. Kochkina, G. A., Ivanushkina, N. E., Akimov, V. N., Gilichinskii, D. A., and Ozerskaya, S. M. 2007. Halo-and psychrotolerant Geomyces fungi from Arctic cryopegs and marine deposits. Microbiology, 76(1), 31-38. Latch, G.and Christensen, M. 1985. Artificial infection of grasses with endophytes. Annals of Appiedl Biology,107: 17-24. Le Cocq, K., Gurr, S.J., Hirsch, P.R.,and Mauchline, T.H. 2017. Exploitation of endophytes for sustainable agricultural intensification. Molecular Plant Pathology,18: 469-473. Lohse, R., Jakobs-Schönwandt, D., Vidal, S.,and Patel, A.V. 2015. Evaluation of new fermentation and formulation strategies for a high endophytic establishment of Beauveria bassiana in oilseed rape plants. Biological Control,88: 26-36. Murphy, B.R., Doohan, F.M.,and Hodkinson, T.R. 2015. Fungal root endophytes of a wild barley species increase yield in a nutrient-stressed barley cultivar. Symbiosis, 65: 1-7. Murphy, B.R., Hodkinson, T.R., and Doohan, F.M. 2018. Endophytic Cladosporium strains from a crop wild relative increase grain yield in barley. In Biology and Environment.Proceedings of the Royal Irish Academy, 118(3): 147-156. Royal Irish Academy (2018, January). Nejad, P.,and Johnson, P.A. 2000. Endophytic bacteria induce growth promotion and wilt disease suppression in oilseed rape and tomato. Biological Control,18: 208-215. Petrini. O. 1996. Ecological and physiological aspects of host specificity in endophytic fungi. 87-100. St Louis, USA. Rice, A.V., and Currah, R.S. 2006. Two new species of Pseudogymnoascus with Geomyces anamorphs and their phylogenetic relationship with Gymnostellatospora. Mycologia, 98(2): 307-318. Rodriguez, R.J., White, J.Rr. J.F., Arnold, A.E.,and Redman, R.S. 2009. Fungal endophytes: diversity and functional roles. New Phytologist,182: 314-330. Roodi, D., Millner, J.P., McGill, C.R., Johnson, R.D., Jauregui, R.,and Card, S.D.2020. Methylobacterium, a major component of the culturable bacterial endophyte community of wild Brassica seed. PeerJ. 2020(7), doi: 10.7717/peerj.9514. Roodi, D., Millner, J.P., McGill, C.R., Johnson, R.D.,and Card, S.D. 2019.Bio-prospecting of endophytes of Brassica. PhD dessertation. Faculty of plant science, Massey University. Palmerston North. New Zealand. Rosa, L.H., Almeida, Vieira. Md.L., Santiago, I.F.,and Rosa, C.A. 2010. Endophytic fungi community associated with the dicotyledonous plant Colobanthus quitensis (Kunth) Bartl. (Caryophyllaceae) in Antarctica. FEMS Microbiology Ecology,73: 178-189. Tefera, T.,and Vidal, S. 2009. Effect of inoculation method and plant growth medium on endophytic colonisation of sorghum by the entomopathogenic fungus Beauveria bassiana. BioControl,54: 663-669. Truyens, S., Beckers, B., Thijs, S., Weyens, N., Cuypers, A.,and Vangronsveld, J. 2015. The effects of the growth substrate on cultivable and total endophytic assemblages of Arabidopsis thaliana. Plant and Soil,405: 325-336. Usuki, F., Narisawa, K., Yonezawa, M., Kakishima, M.,and Hashiba, T. 2002. An efficient inoculation method for colonisation of Chinese cabbage seedlings by the root endophytic fungus Heteroconium chaetospira. Journal of General Plant Pathology,68: 326-332. Vega, F.E. 2008. Insect pathology and fungal endophytes. Journal of Invertebrate Pathology,98: 277-279. Vega, F.E., Goettel, M.S., Blackwell, M., et al. 2009. Fungal entomopathogens: new insights on their ecology. Fungal Ecology,2: 149-159. Vidal, S.,and Jaber, L.R. 2015. Entomopathogenic fungi as endophytes: plant-endophyte-herbivore interactions and prospects for use in biological control. Current Science, 45-54. Vohník, M., Fendrych, M., Albrechtová, J.,and Vosátka, M. 2007. Intracellular colonisation of Rhododendron and Vaccinium roots by Cenococcum geophilum, Geomyces pannorum and Meliniomyces variabilis. Folia Microbiologica,52: 407-414. Zhang, Y.J., Huo, L.Q., Zhang, S., and Liu, X.Z. 2016. The complete mitochondrial genome of the cold-adapted fungus Pseudogymnoascus pannorum syn. Geomyces pannorum. Mitochondrial DNA Part A, 27(4): 2566-2567 | ||
|
آمار تعداد مشاهده مقاله: 1,252 تعداد دریافت فایل اصل مقاله: 649 |
||