Inhibitory Effect of Endophytic Bacteria with Auxin Production Ability on Diplodia bulgarica, the Causative Agent of Apple Canker in East Azerbaijan Province

Document Type : Research Article

Authors

1 Department of Plant Protection, Faculty of Agriculture, University of Tabriz, Tabriz, Iran

2 Department of Soil Science, Faculty of Agriculture, University of Tabriz, Tabriz, Iran

Abstract

Introduction
 The apple (Malus domestica Borkh.), a cornerstone of Iran's agricultural exports, plays an important role in the nation's economy. The cultivation of this fruit, however, is frequently exposed to a multitude of pests and diseases, especially fungi from the Botryosphaeriaceae family emerging as a significant threat. Among these, Diplodia bulgarica is a particularly harmful fungus that causes a lot of damage to apple orchards. Traditional management strategies have predominantly relied on chemical fungicides; however, these methods have several problems, including environmental contamination, food safety concerns, and the potential for pathogen resistance. These issues highlight the critical need for alternative solutions. To deal with these problems, experts in plant diseases are looking more at using biological control agents as a viable and environmentally friendly option. Endophytic bacteria, a group of non-pathogenic microorganisms that inhabit plant tissues, are leading this change. By producing essential growth factors, these bacteria not only enhance the metabolic processes of their host plants but also protect them from many diseases and environmental stress. Their mode of action is not limited to direct antagonistic actions like nutrient competition and antibiotic production; they also take in a range of indirect strategies that effectively inhibit plant diseases. Using endophytic bacteria to control plant diseases is a new, exciting and promising direction toward sustainable agriculture. Their dual role as biocontrol agents and promoters of plant health offers a comprehensive strategy for enhancing crop resilience. Ongoing research is revealing how endophytic bacteria could transform the way we protect plants and increase farm yields, marking a new era in the management of apple and other fruit tree diseases.
Materials and Methods
 This study aimed to isolate auxin-producing endophytic bacteria from apple trees in the orchards of East Azerbaijan province and assess their capacity to inhibit the pathogenic fungus Diplodia bulgarica the major causal agent of apple tree decline in Northwest Iran. To do this, healthy branches from apple trees in East Azerbaijan province in northwest Iran were sampled, resulting in 110 isolates of endophytic bacteria being isolated and subsequently analyzed. Employing the dual-culture method, researchers identified the most effective isolate exhibiting the strongest antagonistic effect. Subsequently, fifty isolates out of the initial 110 were chosen for further investigation based on their promising antifungal properties. To statistically analyze the auxin production data, researchers conducted a variance analysis (ANOVA). Finally, Duncan's multiple range test (DMRT) at a 1% significance level was used to compare the mean auxin production values among these selected isolates. Identification was carried out based on polymerase chain reaction (PCR) and sequencing of the 16S rDNA region, along with biochemical assays including gram staining, catalase, oxidase, arginine hydrolase, and others.
 Results and Discussion
 The dual-culture assay results led to the selection and preservation of 50 isolates demonstrating varying degrees of antagonistic potential. Of these, 37 isolates (74%) were identified as gram-positive, while the remaining 13 isolates were gram-negative. The inhibition percentage of these isolates ranged from 10% to 79%. Notably, five endophytes exhibited high inhibition rates (74-79%), were also effective in auxin production. The auxin production assay revealed that, on average, bacterial isolates produced 5.5 mg/ml of auxin in the absence of tryptophan and 8.58 mg/ml in its presence. Based on biochemical and molecular identification, all five isolates belonged to the Bacillus genus, with more than 99% similarity. These included Bacillus xiamenensis, Bacillus sonorensis, Bacillus tequilensis, Bacillus mojavensis, and Bacillus subtilis. Bacillus mojavensis demonstrated the highest auxin production, yielding up to tenfold more auxin without tryptophan and fivefold more with tryptophan compared to other isolates. The study also found that adding L-tryptophan to the bacterial growth medium generally increased auxin production. In the qualitative evaluation, a pink color change was observed exclusively in the B. mojavensis isolate.
 Conclusion
 While fungicides are highly effective, their escalating use has led to serious repercussions, including environmental pollution, toxic residues in food, pathogen resistance, and socio-economic issues. The substantial costs and consumer demand for chemical-free produce have spurred researchers to seek viable alternatives to these agents. In this study, five Bacillus bacterial isolates were identified from apple trees in Iran's northwestern regions. These isolates not only exhibit strong inhibitory effects against the fungus Diplodia bulgarica but also possess the capability to produce significant amounts of the phytohormone auxin (IAA). Consequently, they can be recommended to farmers as both an alternative to fungicides and as biofertilizers. The deployment of these bacteria promises not only the effective and safe mitigation of pathogens but also supports plant growth and development through hormone production.

Keywords

Main Subjects


©2024 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. Abdollahzadeh, J. (2015). Diplodia bulgarica, as a new pathogen and potential threat to the apple industry in Iran. Phytopathologia Mediterranea, 54, 128–132. https://doi.org/10.14601/Phytopathol_Mediterr-14686
  2. Ahmad, F., Ahmad, I., & Khan, M.S. (2008). Screening of free-living rhizospheric bacteria for their multiple plant growth promoting activities. Microbiology Research, 163, 173–181. https://doi.org/10.1016/j.micres.2006.04.001
  3. Ahmadzadeh, M., & Sharifi-Tehrani, A. (2021). Plant probiotic bacteria. University of Tehran Press, 629 pp. (In Persian)
  4. Ali, B., Sabri, N., Ljung, K., & Hasnain, S. (2009). Quantification of indole-3-acetic from plant associated Bacillus and their phytostimulatory effect on Vigna radiata (L.). World Journal of Microbiology and Biotechnology, 25, 519-526. https://doi.org/10.1007/s11274-008-9918-9
  5. Alijani, N., Manafi Shabestari, M., & Ghosta, Y. (2016). Biocontrol effects of endophytic fungi isolated from apple trees against Diplodia bulgarica the causal agent of apple canker disease. In 22th Iranian Plant Protection Congress (p. 339). (In Persian)
  6. Alizadeh, M., Khakvar, R., & Babai-Ahari, A. (2017). Isolation and characterization of bacterial agents associated of wetwood disease on elm trees in Iran. Acta Phytopathologica et Entomologica Hungarica52, 157-168. https://doi.org/10.1556/038.52.2017.028
  7. Amaresan, N., Jayakumar, V., & Thajuddin, N. (2012). Isolation and characterization of endophytic bacteria associated with chili (Capsicum annuum) grown in coastal agricultural ecosystem. Indian Journal of Biotechnology, 13, 247-255.
  8. Arzanlou, M., Mousavi, S., Bakhshi, M., Khakvar, R., & Bandehagh, A. (2016). Inhibitory effects of antagonistic bacteria inhabiting the rhizosphere of the Sugar beet plants, on Cercospora beticola, the causal agent of Cercospora leaf spot disease on Sugar beet. Journal of Plant Protection Research56, 6-14. https://doi.org/10.1515/jppr-2016-0002
  9. Binandeh, N. (2016). biological control of white rot of root in some cultivars of apples and pears using antagonistic bacteria. Master thesis. Tarbiat Modarres University. 125Pp. (In Persian)
  10. Bric, J.M., Bosrock, R.M., & Silversone, S.E. (1991). Rapid in situ assay for indole acetic acid production by bacteria immobilization on a nitrocellulose membrane. Applied and Environmental Microbiology, 57, 535-538. https://doi.org/10.1128%2Faem.57.2.535-538.1991
  11. Cawoy, H., Mariutto, M., Henry, G., Fisher, C., & Vasilyeva, N. (2014). Plant defense stimulation by natural isolates of Bacillus depends on efficient surfactin production. Molecular Plant-Microbe Interactions, 27, 87–100. https://doi.org/10.1094/mpmi-09-13-0262-r
  12. Deaker, R., László Kecskés, M., Timothy Rose, M., Amprayn, K., & Krishnen, G. (2011). Practical methods for the quality control of inoculant biofertilizers. Australian Center for International Agriculture Research,
  13. Duca, D., Lorv, J., Chery, L., Rose, D., & Bernard, R. (2014). Indol-3- acetic acid in plant- microbe interactions. Antonie van Leeuwenhoek, 106, 85-125. https://doi.org/10.1007/s10482-013-0095-y
  14. Eken, C. (2022). Diplodia bulgarica, cause of postharvest rot on apples in Turkey. Australasian Plant Disease Notes17, 15. https://doi.org/10.1007/s13314-022-00460-4
  15. Geetha, T., Vishwaprakash, N., Sycheva, M., & Babu, J.R. (2012). Sequestosome 1/p62: across diseases. Biomarkers, 17, 99–103. https://doi.org/10.3109/1354750x.2011.653986
  16. Gholami, M., Khakvar, R., & Aliasgarzad, N. (2013). Application of endophytic bacteria for controlling anthracnose disease (Colletotrichum lindemuthianum) on bean plants. Archives of Phytopathology and Plant Protection46, 1831-1838. https://doi.org/10.1080/03235408.2013.778477
  17. Gholami, M., Khakvar, R., & Niknam, G. (2014). Introduction of some new endophytic bacteria from Bacillus and Streptomyces genera as successful biocontrol agents against Sclerotium rolfsiiArchives of Phytopathology and Plant Protection47, 122-130. https://doi.org/10.1080/03235408.2013.805043
  18. Hanifeh, S., Zafari, D., & Soleimani, M.J. (2017) Reaction of some apple cultivars to Diplodia bulgarica in Iran. Mycosphere, 8, 1253–1260. https://doi.org/10.5943/mycosphere/8/2/9
  19. Jacob, J., Krishnan, G.V., Thankappan, D., & Amma, D.K.B. (2020). Endophytic bacterial strains induced systemic resistance in agriculturally important crop plants. In Microbial Endophytes(pp. 75-105). Woodhead Publishing. https://doi.org/10.1016/B978-0-12-819654-0.00004-1
  20. Jahanbakhsh, V., Mahdikhani Moghadam, E., Baghaee Ravari, S., & Rouhani, H. (2014). Study plant growth promoting Bacillus isolates in tomato root colonization and Meloidogyne javanica population reduction. Journal of Iranian Plant Protection Research,28, 79-86. https://doi.org/10.22067/jpp.v28i1.36035
  21. Javadi-Dodaran, N., Khakvar, R., & Aliasgarzad, N. (2022). Isolation and characterization of bacterial endophytes from weeds against Pseudomonas syringae syringae causing bacterial canker of stone fruit trees. Fundamental and Applied Agriculture7, 104-111. https://doi.org/10.5455/faa.26526
  22. Kumar, A., Prakash, A., & Johri, B.N. (2011). Bacillus as PGPR in crop ecosystem. Bacteria in Agrobiology. Crop Ecosystems, 1, 37-59. https://doi.org/10.1007/978-3-642-18357-7_2
  23. Luna, C.L., Mariano, R.L.R., & Souto-Maior, A.M. (2002). Production of a biocontrol agent for crucifers black rot disease. Brazilian Journal of Chemical Engineering, 19, 133-140. https://doi.org/10.1590/S0104-66322002000200007
  24. Majeed, A., Abbasi, M.K., Hameed, S., Imran, A., & Rahim, N. (2015). Isolation and characterization of plant growth-promoting rhizobacteria from wheat rhizosphere and their effect on plant growth promotion. Frontiers in Microbiology, 6, 198. https://doi.org/10.3389%2Ffmicb.2015.00198
  25. Mantelin, S., & Touraine, B. (2004). Plant growth-promoting bacteria and nitrate availability: impacts on root development and nitrate uptake. Journal of Experimental Botany, 55, 27-34. https://doi.org/10.1093/jxb/erh010
  26. Moslehi, S., Pourmehr, S., Shirzad, A., & Khakvar, R. (2021). Potential of some endophytic bacteria in biological control of root-knot nematode Meloidogyne incognitaEgyptian Journal of Biological Pest Control31, 1-11. https://doi.org/10.1186/s41938-021-00396-4
  27. Najari, H.H. (2020). Guide to planting and growing apples. Jahad Daneshgahi Press. 430 Pp. (In Persian)
  28. Norozi, H., Baghaee-Ravari, S., & Mojerlou, S. (2023). Biocontrol potential of Bacillus strains in interaction with Rhizoctonia solani pathogen of potato. Iranian Journal of Plant Protection Science54, 187-205. https://doi.org/10.22059/ijpps.2023.357079.1007026
  29. Parent, P.Z., Basime, G.C., Nachigera, G.M., Thonart, P., & Ongena, M. (2018). Efficacy of Bacillus amyloliquefaciens as biocontrol agent to fight fungal diseases of maize under tropical climates: from lab to field assays in south Kivu. Environmental Science and Pollution Research International25(30), 29808–29821. https://doi.org/10.1007/s11356-017-9314-9.
  30. Sadfi, N., Cherif, M., Hajlaoui, M.R., Boudabbous, A., & Belanger, R. (2002). Isolation and partial purification of antifungal metabolites produced by Bacillus cereus. Annals of Microbiology, 52, 323-338.
  31. Sambrook, J., Russell, D.W., & Russell, D.W. (2001). Molecular cloning a laboratory manual (3-volume set) . New York: Cold spring harbor laboratory press, 999, 502-510.
  32. Schaad, N.W., Jones, J.B., & Chun, W. (2001). Laboratory guide for the identification of plant pathogenic bacteria(No. Ed. 3). American Phytopathological Society (APS Press).
  33. Shrivastava, U.P., & Kumar, A. (2011). A simple and rapid plate assay for the screening of indole-3- acetic acid (IAA) producing microorganisms. International Journal of Applied Biology and Pharmaceutical Technology, 2, 120-124.
  34. Souto, G.I., Correa, O.S., Montecchia, M.S., Kerber, N.L., Pucheu, N.L., Bachur, M., & García, A.F. (2004). Genetic and functional characterization of a Bacillus strain excreting surfactin and antifungal metabolites partially identified as iturin-like compounds. Journal of Applied Microbiology, 97, 1247-1256. https://doi.org/10.1111/j.1365-2672.2004.02408.x
  35. Szilagyi-Zecchin, V.J., Ikeda, A.C., Hungria, M., Adamoski, D., Kava-Cordeiro, V., Glienke, C., & Galli-Terasawa, L.V. (2014). Identification and characterization of endophytic bacteria from corn (Zea mays) roots with biotechnological potential in agriculture. AMB Express, 4, 2-9. https://doi.org/10.1186%2Fs13568-014-0026-y
  36. Thoa, N.T.K., Mai, D.T.H., Hiu, B.L., Duong, C.A., Chau, N.N.B., Nghiep, N.M., & Quoc, N.B. (2022). Roles of β-Indole acetic acid (IAA) producing endophytic bacteria on the recovery of plant growth and survival ability of sugarcane infected white leaf disease (SWLD). Current Microbiology79, 389. https://doi.org/10.1007/s00284-022-03091-1
  37. Vasebi, Y., Khakvar, R., & Vinatzer, B.A. (2023). Characterization of culturable epiphytic and endophytic bacteria of Prunus and their potential for plant growth promotion and antagonistic activity against bacterial canker disease. Journal of Plant Pathology105(3), 749-766. https://doi.org/10.1007/s42161-023-01342-z
  38. Wahyudi, A.T., Astuti, R.P., Widyawati, A., Meryandini, A., & Nawangsih, AA. (2011). Characterization of Bacillus strains isolated from rhizosphere of soybean plants for their use as potential plant growth for promoting Rhizobacteria. Journal of Microbiology and Antimicrobials, 3, 34-40.
  39. Zeynali Bari, R., Abrinbana, M., & Ghosta, Y. (2021). Genetic variation, vegetative compatibility, and aggressiveness diversity of Diplodia bulgarica isolates from apple orchards in West Azarbaijan province of Iran. Plant Pathology70, 1326-1341. https://doi.org/10.1111/ppa.13374
CAPTCHA Image