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Silicate solubilizing bacteria UPMSSB7, a potential biocontrol agent against white root rot disease pathogen of rubber tree

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Abstract

Rigidoporus microporus is a causal agent of white root rot disease of rubber trees. Chemical control is commonly used against this disease but it is expensive, causes environmental pollution and fungal resistance. Silicon is a beneficial element which enhances plant growth and disease resistance but mostly present in insoluble forms. Silicate solubilizing bacteria (SSB) can solubilize the insoluble forms of silicates. This study aimed to screen and evaluate potential SSB with solubilizing activity, plant growth promoting traits and antagonistic activity against R. microporus. Bacteria were isolated from healthy rubber plantation area. Five out of 26 bacterial isolates which showed the ability to solubilize silicate on magnesium trisilicate media were screened in vitro for growth promoting traits and production of indole-3-acetic acid (IAA), siderophores and hydrolytic enzymes. The investigation of antagonistic activity against R. microporus was conducted using dual culture test. The potential SSB isolates were identified by 16S rRNA gene sequencing. The isolate UPMSSB7 showed the highest solubilization of silicate, phosphate (P) and potassium (K) (solubilizing index 4.67, 2.52 and 2.61, respectively). It also showed highest silicate solubilization at 5 and 10 days (9.76 and 11.55 mg L−1, respectively) in liquid assay. It strongly inhibited the growth of R. microporus with percent inhibition of radial growth of 57.24% and produced highest IAA (19.96 µg mL−1). All the isolates produced siderophores. Two isolates, UPMSSB7 and UPMSSB10, were able to secrete cellulase enzyme, but pectinase was produced by UPMSSB7 only. The isolate UPMSSB7 was identified as Enterobacter sp. This isolate was found to be the most potent antagonistic isolate against R. microporus and simultaneously the most efficient one in solubilizing insoluble silicates, as well as P and K.

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Abbreviations

IAA:

Indole-3-acetic acid

CAS:

Chrome Azurol S

CFU:

Colony forming units

CMC:

Carboxymethyl cellulose

LB:

Luria Bertani

NCBI:

National Center for Biotechnology Information

Nfb:

Nitrogen free bromothymol

PDA:

Potato dextrose agar

PGPR:

Plant growth-promoting rhizobacteria

PIRG:

Percent inhibition of radial growth

PVK:

Pikovskaya

rpm:

Rotation per minute

rRNA:

Ribosomal ribonucleic acid

SAS:

Statistical Analysis Software

SSB:

Silicate solubilizing bacteria

TSB:

Tryptic Soy Broth

References

  1. Francois F, Wilfried RB, James GM, Richard RB (2005) Silicon and plant disease resistance against pathogenic fungi. FEMS Microbiol Lett 249:1–6

    Google Scholar 

  2. Bélanger RR, Benhamou N, Menzies JG (2003) Cytological evidence of an active role of silicon in wheat resistance to powdery mildew (Blumeria graminis f. sp. tritici). Phytopathology 93:402–412

    Google Scholar 

  3. Ma JF, Yamaji N (2006) Silicon uptake and accumulation in lower plants. Trends Plant Sci 11:392–397

    CAS  Google Scholar 

  4. Rodrigues FA, Datnoff LE (2005) Silicon and rice disease management. Fitopatol Bras 30:457–469

    Google Scholar 

  5. Vasanthi N, Saleena LM, Raj SA (2012) Silicon in day today life. World Appl Sci J 17:1425–1440

    CAS  Google Scholar 

  6. Goh YK, Marzuki NF, Liew YA, Goh YK, Goh KJ (2018) Antagonistic effects of fungicolous ascomycetous Cladobotryum semicirculare on Rigidoporus microporus white root disease in rubber trees (Hevea brasiliensis) under in vitro and nursery experiments. J Rubber Res 21:62–72

    Google Scholar 

  7. Kaewchai S, Wang HK, Lin FC, Hyde KD, Soytong K (2009) Genetic variation among isolates of Rigidoporus microporus causing white root disease of rubber trees in Southern Thailand revealed by ISSR markers and pathogenicity. Afr J Microbiol Res 3:641–648

    CAS  Google Scholar 

  8. Evueh GA, Ogbebor NO (2008) Use of phylloplane fungi as biocontrol agent against Colletotrichum leaf disease of rubber (Hevea brasiliensis Muell. Arg.). Afr J Biotechnol 7:2569–2572

    Google Scholar 

  9. Mohammed CL, Rimbawanto A, Page DE (2014) Management of basidiomycete root- and stem-rot diseases in oil palm, rubber and tropical hardwood plantation crops. For Pathol 44:428–446

    Google Scholar 

  10. Soytong K, Srinon W, Ratanacherdchai K, Kanokmedhakul S, Kanokmedhakul K (2005) Application of antagonistic fungi to control anthracnose disease of grape. Agric Technol 1:33–42

    Google Scholar 

  11. Haggag WM, Mohamed HAA (2007) Biotechnological aspects of microorganisms used in plant biological control. Am-Eurasian J Sustain Agric 1:7–12

    Google Scholar 

  12. Jayasinghe CK (2010) White root disease of rubber tree: an overview. In: Proceedings of international workshop on white root disease of Hevea rubber. 14–16th Dec. 2010, Hotel Janaki, Colombo, Sri-Lanka, pp 1–8

  13. Ng LC, Anuar SNA, Jong JW, Elham MSH (2016) Phytobeneficial and plant growth promotion properties of silicon-solubilising rhizobacteria on the growth and control of rice sheath blight disease. Asian J Plant Sci 15:92–100

    CAS  Google Scholar 

  14. Vijayapriya M, Muthukkaruppan SM (2010) Isolation and screening of silicate solubilizing bacteria and its biocontrol nature against Pyricularia oryzae. Int J Recent Sci Res 4:87–91

    Google Scholar 

  15. Lee KE, Adhikari A, Kang SM, You YH, Joo GJ, Kim JH, Kim SJ, Lee IJ (2019) Isolation and characterization of the high silicate and phosphate solubilizing novel strain Enterobacter ludwigii GAK2 that promotes growth in rice plants. Agronomy 9:144

    Google Scholar 

  16. Farina R, Beneduzi A, Ambrosini A, de Campos SB, Lisboa BB, Wendisch VF, Vargas LK, Passaglia LMP (2012) Diversity of plant growth promoting rhizobacteria communities associated with the stages of canola growth. App Soil Ecol 55:44–52

    Google Scholar 

  17. Chi Q, Tang W, Liu L, Meng J, Dong X, Chen W, Li X (2018) Isolation, properties of Enterobacter sp. LX3 capable of producing indoleacetic acid. Appl Sci 8:2108

    CAS  Google Scholar 

  18. Velusamy P, Kim KY (2011) Chitinolytic activity of Enterobacter sp. KB3 antagonistic to Rhizoctonia solani and its role in the degradation of living fungal hyphae. Int Res J Microbiol 2:206–214

    Google Scholar 

  19. Vasanthi N, Saleena LM, Raj SA (2018) Silica solubilization potential of certain bacterial species in the presence of different silicate minerals. Silicon 10:267–275

    CAS  Google Scholar 

  20. Senthilkumar M, Swarnlakshmi K, Govindasamy V, Lee YK, Annapurna K (2009) Biocontrol potential of soybean bacterial endophytes against charcoal rot fungus Rhizoctonia bataticola. Curr Microbiol 58:288–293

    CAS  Google Scholar 

  21. Mandal S, Dutta P, Majumdar S (2017) Plant growth promoting and antagonistic activity of Bacillus strains isolated from rice rhizosphere. Int J Pharm Bio Sci 8:408–415

    CAS  Google Scholar 

  22. Radhakrishnan R, Hashem A, Abd-Allah EF (2017) Bacillus: a biological tool for crop improvement through bio-molecular changes in adverse environments. Front Physiol 8:667

    Google Scholar 

  23. Vasanthi N, Saleena LM, Raj SA (2013) Evaluation of media for isolation and screening of silicate solubilising bacteria. Int J Curr Res 5:406–408

    Google Scholar 

  24. Edi-Premono M, Moawad AM, Vlek PLG (1996) Effect of phosphate solubilizing Pseudmonas putida on the growth of maize and its survival in the rhizosphere. Indo J Crop Sci 11:13–23

    Google Scholar 

  25. Naureen Z, Hameed S, Yasmin S, Malik KA, Hafeez FY (2005) Characterization and screening of bacteria from maize grown in Indonesian and Pakistani soils. J Basic Microbiol 45:447–459

    CAS  Google Scholar 

  26. Hassan MN, Afghan S, Hafeez FY (2010) Suppression of red rot caused by Colletotrichum falcatum on Sugarcane plants using plant growth-promoting rhizobacteria. Biocontrol 55:531–542

    Google Scholar 

  27. Lü C, Huang B (2010) Isolation and characterization of azotobacteria from pine rhizosphere. Afr J Microbiol Res 4:1299–1306

    Google Scholar 

  28. Dobereiner J, Day JM (1976) Associative symbioses in tropical grasses: Characterization of microorganisms, dinitrogen-fixing sites. In: Newton WE, Nyman CJ (eds) Proceedings of the 1st international symposium on nitrogen fixation. Washington State University Press, Pullman, pp 518–538

    Google Scholar 

  29. Gordon SA, Weber RP (1951) Colorimetric estimation of indoleacetic acid. Plant Physiol 26:192–195

    CAS  Google Scholar 

  30. Schwyn B, Neilands JB (1987) Universal chemical assay for the detection and determination of siderophores. Anal Biochem 160:47–56

    CAS  Google Scholar 

  31. Kasana RC, Salwan R, Dhar H, Dutt S, Gulati A (2008) A rapid and easy method for the detection of microbial cellulases on agar plates using Gram’s iodine. Curr Microbiol 57:503–507

    CAS  Google Scholar 

  32. Yogesh K, Vamsi KK, Amol B, Nikhil G, Soham T, Prasad P, Girish G, Mayank G, Amol J, Adarsh M, Joshi B, Mishra D (2009) Study of pectinase production in submerged fermentation using different strains of Aspergillus niger. Int J Microbiol Res 1:13–17

    Google Scholar 

  33. Jinantana J, Sariah M (1998) Potential for biological control of Slerotium foot rot of chilli by Trichoderma spp. Pertanika J Trop Agric Sci 21:1–10

    Google Scholar 

  34. Joseph MH, Dhargave TS, Deshpande CP, Srivastava AK (2015) Microbial solubilisation of phosphate: Pseudomonas versus Trichoderma. Ann Plant Soil Res 17:227–232

    Google Scholar 

  35. Naureen Z, Aqeel M, Hassan MN, Gilani SA, Bouqellah N, Mabood F, Hussain J, Hafeez FY (2015) Isolation and screening of silicate bacteria from various habitats for biological control of phytopathogenic fungi. Am J Plant Sci 6:2850–2859

    CAS  Google Scholar 

  36. Muralikannan N, Anthomiraj S (1998) Occurrence of silicate solubilizing bacteria in rice ecosystem. Madras Agric J 85:47–50

    Google Scholar 

  37. Sahebi M, Hanafi M, Siti A, Akmar N, Rafii MY, Azizi P, Tengoua FF, Azwa JNM, Shabanimofrad M (2015) Importance of silicon and mechanisms of biosilica formation in plants. Biomed Res Int 2015:1–16

    Google Scholar 

  38. Mathesius U (2008) Auxin: at the root of nodule development? Funct Plant Biol 35:651–668

    CAS  Google Scholar 

  39. Shoebitz M, Ribaudo CM, Pardo MA, Cantore ML, Ciampi L, Curá JA (2009) Plant growth promoting properties of a strain of Enterobacter ludwigii isolated from Lolium perenne rhizosphere. Soil Biol Biochem 41:1768–1774

    CAS  Google Scholar 

  40. Park YG, Mun BG, Kang SM, Hussain A, Shahzad R, Seo CW, Kim AY, Lee SU, Oh KY, Lee DY, Lee IJ, Yun BW (2017) Bacillus aryabhattai SRB02 tolerates oxidative and nitrosative stress and promotes the growth of soybean by modulating the production of phytohormones. PLoS One 12:e0173203

    Google Scholar 

  41. Kämpfer P, Ruppel S, Remus R (2005) Enterobacter radicincitans sp. nov., a plant growth promoting species of the family Enterobacteriaceae. Syst Appl Microbiol 28:213–221

    Google Scholar 

  42. Khalifa AY, Alsyeeh AM, Almalki MA, Saleh FA (2016) Characterization of the plant growth promoting bacterium, Enterobacter cloacae MSR1, isolated from roots of non-nodulating Medicago sativa. Saudi J Biol Sci 23:79–86

    CAS  Google Scholar 

  43. Bowen P, Menzies J, Ehret D (1992) Soluble silicon sprays inhibit powdery mildew development on grape leaves. J Amer Soc Hortic Sci 117:906–912

    CAS  Google Scholar 

  44. Simonsson M, Andersson S, Andrist-Rangel Y, Hillier S, Mattsson L, Oborn I (2007) Potassium release and fixation as a function of fertilizer application rate and soil parent material. Geoderma 140:188–198

    CAS  Google Scholar 

  45. Sugumaran P, Janarthanam B (2007) Solubilization of potassium containing minerals by bacteria and their effect on plant growth. World J Agric Sci 3:350–355

    Google Scholar 

  46. Khleekorn S, Wongrueng S (2014) Evaluation of antagonistic bacteria inhibitory to Colletotrichum musae on banana. J Agric Technol 10:383–390

    Google Scholar 

  47. Naureen Z, Price AH, Wilson MJ, Hafeez FY, Roberts MR (2009) Suppression of rice blast disease by siderophore-producing bioantagonistic bacterial isolates isolated from the rhizosphere of rice grown in Pakistan. Crop Prot 28:1052–1060

    Google Scholar 

  48. Naureen Z, Hafeez FY, Hussain J, Al-Harrasi A, Bouqellah N, Roberts MR (2015) Suppression of incidence of Rhizoctonia solani in rice by siderophore producing rhizobacterial strains based on competition for iron. Eur Sci J 11:186–207

    Google Scholar 

  49. Sheng XF, Zhao F, He LY, Qiu G, Chen L (2008) Isolation and characterization of silicate mineral-solubilising Bacillus globisporus Q12 from the surface of weathered feldspar. Can J Microbiol 54:1064–1068

    CAS  Google Scholar 

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Acknowledgements

The authors wish to express their sincere thanks to Institute of Plantation Studies, Universiti Putra Malaysia (UPM) for the Geran Putra IPB (Sub-Project) research Grant (GP-IPB/2017/9523502) and also to Bahauddin Zakariya University (BZU), Multan, Pakistan for granting foreign Ph.D. scholarship to Mr. Imran Shabbir.

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Correspondence to Mohd Yusoff Abd Samad.

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Shabbir, I., Samad, M.Y.A., Othman, R. et al. Silicate solubilizing bacteria UPMSSB7, a potential biocontrol agent against white root rot disease pathogen of rubber tree. J Rubber Res 23, 227–235 (2020). https://doi.org/10.1007/s42464-020-00052-w

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