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Ochrobactrum sp. NBRISH6 Inoculation Enhances Zea mays Productivity, Mitigating Soil Alkalinity and Plant Immune Response

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Abstract

Intensifying sodic land characterized by high alkaline pH is an incipient environmental hazard-limiting agricultural potential. In this study, we investigated the effects of plant growth-promoting bacteria Ochrobactrum sp. strain NBRISH6 on the growth and physiology of maize (Zea mays L.) grown under alkaline stress at two soil pH levels. Additionally, we also studied the effects of NBRISH6 on soil fertility parameters. A greenhouse experiment was designed using two live soils (pH 8.2 and 10.2) in earthen pots using maize as a host. Results revealed a significant increase in plant growth and a decrease in defense enzymes in both soil types due to NBRISH6 inoculation as compared to non-treated control. Furthermore, activities of all soil enzymes along with bacterial diversity increased in NBRISH6 treatment under normal as well as stressed conditions. In addition, field evaluation of NBRISH6 inoculation using maize was carried out under normal and alkaline conditions, which resulted in significant enhancement of all vegetative parameters as compared to respective controls. Therefore, the study suggested that Ochrobactrum sp. NBRISH6 can be used to develop a bioinoculant formulation to ameliorate abiotic stresses and enhanced crop productivity.

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References

  1. Rengasamy P (2010) Soil processes affecting crop production in salt-affected soils. Fun Plant Biol 37:13–620

    Google Scholar 

  2. Liu J, Tang L, Gao H et al (2019) Enhancement of alfalfa yield and quality by plant growth promoting rhizobacteria under saline-alkali conditions. J Sci Food Agric 99:281–289

    Article  CAS  Google Scholar 

  3. Damodaran T, Rai RB, Jha SK et al (2014) Rhizosphere and endophytic bacteria for induction of salt tolerance in gladiolus grown in sodic soils. J Plant Interact 9:577–584

    Article  CAS  Google Scholar 

  4. Sapre S, Gontia-Mishra I, Tiwari S (2018) Klebsiella sp. confers enhanced tolerance to salinity and plant growth promotion in oat seedlings (Avena sativa). Microbiol Res 206:25–32

    Article  CAS  PubMed  Google Scholar 

  5. Khoshoo TN (1987) Ecodevelopment of alkaline land Banthara—a case study. NBRI, CSIR PID, New Delhi

  6. Garg VK (2000) Bio-reclamation of sodic wasteland—a case study. Land Degrad Dev 11:163–172

    Article  Google Scholar 

  7. Garg VK (2002) Sustainable rehabilitation of sodic soils through biological means—a case study. In: 12th ISCO Conference, Beijing, pp 149–155. http://www.tucson.ars.ag.gov/isco/isco12/VolumeIII/Sustainable.Rehabilitation.pdf

  8. Singh PK, Kumar P, Tandon PK (2014) Soil sodicity alters antioxidative enzymes, photosynthestic pigments water content and essential oil quality of fennel (Foeniculum vulgare Mill). Res J Soil Biol 6:1–16

    Article  Google Scholar 

  9. Fa-Hu LI, Keren R (2009) Calcareous sodic soil reclamation as affected by corn stalk application and incubation: a laboratory study. Pedosphere 19:465–475

    Article  Google Scholar 

  10. Singh K, Pandey VC, Singh B, Singh RR (2012) Ecological restoration of degraded sodic lands through afforestation and cropping. Ecol Eng 43:70–80

    Article  Google Scholar 

  11. Singh K (2016) Microbial and enzyme activities of saline and sodic soils. Land Degrad Dev 27:706–718

    Article  Google Scholar 

  12. Khatri-Chhetri A, Aggarwal PK, Joshi PK, Vyas S (2017) Farmers’ prioritization of climate-smart agriculture (CSA) technologies. Agri system 151:184–191

    Article  Google Scholar 

  13. FAO (2014) Save and grow in practices: maize rice and wheat. http://www.fao.org/ag/save-and-grow/MRW/en/1/index.html

  14. Latef AA, Tran LP (2016) Impacts of priming with silicon on the growth and tolerance of maize plants to alkaline stress. Front Plant Sci 7:243

    PubMed  PubMed Central  Google Scholar 

  15. Salazar S, Sánchez LE, Alvarez J et al (2011) Correlation among soil enzyme activities under different forest system management practices. Ecol Eng 37:1123–1131

    Article  Google Scholar 

  16. Islam F, Yasmeen T, Ari MS et al (2016) Plant growth promoting bacteria confer salt tolerance in Vigna radiata by up-regulating antioxidant defense and biological soil fertility. Plant Growth Regul 80:23–36

    Article  CAS  Google Scholar 

  17. Dixit VK, Misra S, Mishra SK et al (2020) Characterization of plant growth-promoting alkalotolerant Alcaligenes and Bacillus strains for mitigating the alkaline stress in Zea mays. Antonie Van Leeuwenhoek 9:1–7

    Google Scholar 

  18. Mbarki S, Cerdà A, Brestic A et al (2017) Vineyard compost supplemented with Trichoderma Harzianum T78 improve saline soil quality. Land Degrad Dev 28:1028–1037

    Article  Google Scholar 

  19. Mishra SK, Khan MH, Misra S et al (2017) Characterization of Pseudomonas spp. and Ochrobactrum sp. isolated from volcanic soil. Antonie Van Leeuwenhoek 10:253–270

    Article  Google Scholar 

  20. Mishra SK, Khan MH, Misra S et al (2020) Drought tolerant Ochrobactrum sp. inoculation performs multiple roles in maintaining the homeostasis in Zea mays L. subjected to deficit water stress. Plant Physiol Biochem 150:1–4

    Article  CAS  PubMed  Google Scholar 

  21. Nautiyal CS (1997) A method for selection and characterization of rhizosphere-competent bacteria of chickpea. Current Microbiol 34:12–17

    Article  CAS  PubMed  Google Scholar 

  22. Khan N, Mishra A, Chauhan PS et al (2012) Paenibacillus lentimorbus enhances growth of chickpea (Cicer arietinum L.) in chromium-amended soil. Antonie Van Leeuwenhoek 1:453–459

    Article  Google Scholar 

  23. Srivastava S, Chaudhry V, Mishra A et al (2012) Gene expression profiling through microarray analysis in Arabidopsis thaliana colonized by Pseudomonas putida MTCC5279, a plant growth promoting rhizobacterium. Plant Signal Behav 7:235–245

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Nautiyal CS, Srivastava S, Chauhan PS et al (2013) Plant growth-promoting bacteria Bacillus amyloliquefaciens NBRISN13 modulates gene expression profile of leaf and rhizosphere community in rice during salt stress. Plant Physiol Biochem 66:1–9

    Article  CAS  PubMed  Google Scholar 

  25. Singh A, Chauhan PS (2022) N-acyl homoserine lactone mediated quorum sensing exhibiting plant growth-promoting and abiotic stress tolerant bacteria demonstrates drought stress amelioration. J Pure App Microbiol 16(1):669–684

    Article  CAS  Google Scholar 

  26. Dubois M, Gilles KA, Hamilton JK et al (1956) Colorimetric method for determination of sugars and related substances. Anal Chem 28:350–356

    Article  CAS  Google Scholar 

  27. Joshi H, Mishra SK, Prasad V, Chauhan PS (2023) Bacillus amyloliquefaciens modulate sugar metabolism to mitigate arsenic toxicity in Oryza sativa L. var Saryu-52. Chemosphere 137070

  28. Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Annal Biochem 72:248–254

    Article  CAS  Google Scholar 

  29. Nakano Y, Asada K (1981) Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol 22:867–880

    CAS  Google Scholar 

  30. Hemeda HK, Klein BP (1990) Effects of naturally occurring antioxidants on peroxidase activity of vegetable extracts. J Food Sci 55:184–185

    Article  CAS  Google Scholar 

  31. Aebi H (1984) Catalase in vitro. Methods Enzymol 105:121–126

    Article  CAS  PubMed  Google Scholar 

  32. Beauchamp C, Fridovich I (1971) Superoxide dismutase: Improved assays and an assay applicable to acrylamide gels. Anal Biochem 44:276–287

    Article  CAS  PubMed  Google Scholar 

  33. Alef K, Nannipieri P (1995) Methods in applied soil microbiology and biochemistry. Academic Press, London

  34. Tabatabai TA (1982) Soil enzymes. In: Page AL, Miller RH, Keeney DR (eds) Methods of soil analysis: II. Chemical and microbiological properties, 2nd edn. Am Soc Agron, Agronomy 10, Madison, Wisconsin, pp 903–947

  35. Kandeler E, Gerber H (1988) Short-term assay of soil urease activity using colorimetric determination of ammonium. Biol Fertil Soils 6:68–72

    Article  CAS  Google Scholar 

  36. Ladd JN, Butler JHA (1972) Short-term assays of soil proteolytic enzyme activities using proteins and dipeptide derivatives as substrates. Soil Biol Biochem 4:19–30

    Article  CAS  Google Scholar 

  37. Tabatabai MA (1994) Soil enzymes. In: Weaver RW, et al. (eds) Methods of soil analysis: microbiological and biochemical properties. Part 2. SSSA book series no. 5. SSSA, Madison, pp 775–883

  38. Muyzer G, De Waal EC, Uitterlinden A (1993) Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction-amplified genes coding for 16S rRNA. Appl Environ Microbiol 59:695–700

    Article  CAS  PubMed Central  Google Scholar 

  39. Tamura K, Dudley J, Nei M, Kumar S (2007) MEGA4: molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol Biol Evol 24:1596–1599

    Article  CAS  PubMed  Google Scholar 

  40. Paul D, Lade H (2014) Plant-growth-promoting rhizobacteria to improve crop growth in saline soils: A review. Agron Sustain Dev 34:737–752

    Article  Google Scholar 

  41. Vivekanandan M, Karthik R, Leela, (2015) Improvement of crop productivity in saline soils through application of saline-tolerant rhizosphere bacteria-Current perspective. Int J Curr Adv Res 3:1273–1283

    CAS  Google Scholar 

  42. İpek M, Eşitken A (2017) The actions of PGPR on micronutrient availability in soil and plant under calcareous soil conditions: an evaluation over Fe nutrition. In: Plant-microbe interactions in agro-ecological perspectives. Springer, Berlin, pp 81–100

  43. Misra S, Dixit VK, Khan MH et al (2017) Exploitation of agro-climatic environment for selection of 1- aminocyclopropane-1-carboxylic acid (ACC) deaminase producing salt tolerant indigenous plant growth promoting rhizobacteria. Microbiol Res 205:25–34

    Article  CAS  PubMed  Google Scholar 

  44. Souza RD, Ambrosini A, Passaglia LMP (2015) Plant growth-promoting bacteria as inoculants in agricultural soils. Genet Mol Biol 38:401–419

    Article  PubMed  PubMed Central  Google Scholar 

  45. Heydarian Z, Yu M, Gruber M, Glick BR et al (2016) Inoculation of soil with plant growth promoting bacteria producing 1-aminocyclopropane-1-carboxylate deaminase or expression of the corresponding acdS gene in transgenic plants increases salinity tolerance in Camelina sativa. Front Microbiol 7:1966

    Article  PubMed  PubMed Central  Google Scholar 

  46. Compant S, Clément C, Sessitsch A (2010) Plant growth-promoting bacteria in the rhizo-and endosphere of plants: their role, colonization, mechanisms involved and prospects for utilization. Soil Biol Biochem 42:669–678

    Article  CAS  Google Scholar 

  47. Glick BR (2012) Plant growth-promoting bacteria: mechanisms and applications. Scientifica. https://doi.org/10.6064/2012/963401

    Article  PubMed  PubMed Central  Google Scholar 

  48. Paganin P, Isca C, Tasso F et al (2023) A bacterial formula with native strains as alternative to chemical fertiliser for tomato crop. Plant Growth Regul. https://doi.org/10.1007/s10725-023-00993-3

    Article  Google Scholar 

  49. Damodaran T, Mishra VK, Jha SK et al (2019) Identification of Rhizosphere bacterial diversity with promising salt tolerance, PGP traits and their exploitation for seed germination enhancement in sodic soil. Agric Res 8:36–43

    Article  CAS  Google Scholar 

  50. Singh RP, Jha PN (2016) The multifarious PGPR Serratia marcescens CDP-13 augments induced systemic resistance and enhanced salinity tolerance of wheat (Triticum aestivum L.). PLoS One 11:e0155026

  51. Tiwari S, Lata C, Chauhan PS, Nautiyal CS (2016) Pseudomonas putida attunes morphophysiological, biochemical and molecular responses in Cicer arietinum L. during drought stress and recovery. Plant Physiol Biochem 99:108–117

    Article  CAS  PubMed  Google Scholar 

  52. Housh AB, Noel R, Powell A et al (2023) Studies using mutant strains of Azospirillum brasilense reveal that atmospheric nitrogen fixation and auxin production are light dependent processes. Microorganisms 11(7):1727

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  53. Choudhary DK, Kasotia A, Jain S, Vaishnav A et al (2016) Bacterial-mediated tolerance and resistance to plants under abiotic and biotic stresses. J Plant Growth Regul 35:276–300

    Article  CAS  Google Scholar 

  54. Habib SH, Kausar H, Saud HM (2016) Plant growth-promoting rhizobacteria enhance salinity stress tolerance in okra through ROS-scavenging enzymes. Biomed Res Int 2016:6284547

    Article  PubMed  PubMed Central  Google Scholar 

  55. Ravi B, Foyer CH, Pandey GK (2023) The integration of reactive oxygen species (ROS) and calcium signalling in abiotic stress responses. Plant, Cell Environ 46:1985–2006

    Article  CAS  PubMed  Google Scholar 

  56. Kumar M, Mishra S, Dixit V et al (2016) Synergistic effect of Pseudomonas putida and Bacillus amyloliquefaciens ameliorates drought stress in chickpea (Cicer arietinum L.). Plant Signal Behav 11:e1071004

  57. Naveed M, Mitter B, Reichenauer TG et al (2014) Increased drought stress resilience of maize through endophytic colonization by Burkholderia phytofirmans PsJN and Enterobacter sp. FD17. Environ Exp Bot 1:30–39

    Article  Google Scholar 

  58. Xiu-Mei LIU, Qi LI, Wen-Ju L, Yong J (2008) Distribution of soil enzyme activities and microbial biomass along a latitudinal gradient in farmlands of Songliao Plain, Northeast China. Pedosphere 18:431–440

    Article  Google Scholar 

  59. Nayak T (2017) Effect of long-term fertilization and manuring on soil quality index and carbon stock under rice-wheat cropping system in vertisols. PhD diss., Indira Gandhi Krishi Vishwavidhyalaya, Raipur http://krishikosh.egranth.ac.in/handle/1/5810025198

  60. Ahemad M, Kibret M (2014) Mechanisms and applications of plant growth promoting rhizobacteria: current perspective. J King Saud Univ Sci 26:1–20

    Article  Google Scholar 

  61. Çam S, Küçük Ç, Almaca A (2023) Bacillus strains exhibit various plant growth promoting traits and their biofilm-forming capability correlates to their salt stress alleviation effect on maize seedlings. J Biotechnol 369:35–42

    Article  PubMed  Google Scholar 

  62. Bhat MA, Mishra AK, Jan S et al (2023) Plant growth promoting rhizobacteria in plant health: a perspective study of the underground interaction. Plants 12(3):629

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  63. Oburger E, Gruber B, Schindlegger Y et al (2014) Root exudation of Phyto siderophores from soil grown wheat. New Phytol 203:1161–1174

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  64. Keiluweit M, Bougoure JJ, Nico PS et al (2015) Mineral protection of soil carbon counteracted by root exudates. Nat Clim Chang 5:588–595

    Article  CAS  Google Scholar 

  65. Shanmugam SG, Kingery WL (2018) Changes in soil microbial community structure in relation to plant succession and soil properties during 4000 years of pedogenesis. Eur J Soil Biol 88:80–88

    Article  Google Scholar 

  66. Chandra LR, Gupta S, Pande V, Singh N (2016) Impact of forest vegetation on soil characteristics: a correlation between soil biological and physico-chemical properties. 3 Biotech 6:188

  67. Valarini PJ, Alvarez MCD, Gasco JM et al (2003) Assessment of soil properties by organic matter and EM-microorganism incorporation. Revista Brasileira De Ciencia Do Solo 27:519–525

    Article  Google Scholar 

  68. Wu J, Yang YS, Lin J (2005) Advanced tertiary treatment of municipal wastewater using raw and modified diatomite. J Hazard Mater 127:196–203

    Article  CAS  PubMed  Google Scholar 

  69. Schmidt MWI, Torn MS, Abiven S et al (2011) Persistence of soil organic matter as an ecosystem property. Nature 478:49–56

    Article  CAS  PubMed  Google Scholar 

  70. Sinsabaugh RL, Lauber CL, Weintraub MN et al (2008) Stoichiometry of soil enzyme activity at global scale. Ecol Lett 11:1252–1264

    Article  PubMed  Google Scholar 

  71. Nannipieri P, Ceccanti B, Cervelli S, Matarese E (1980) Extraction of phosphatase, urease, proteases, organic carbon, and nitrogen from soil. Soil Sci Society America J 44:1011–1016

    Article  CAS  Google Scholar 

  72. Nannipieri P, Ascher J, Ceccherini M et al (2003) Microbial diversity and soil functions. Eur J Soil Sci 54:655–670

    Article  Google Scholar 

  73. Ellis RJ, Morgan P, Weightman AJ, Fry JC (2003) Cultivation-dependent and-independent approaches for determining bacterial diversity in heavy-metal-contaminated soil. Appl Environ Microbiol 69:3223–3230

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  74. Chaudhry V, Rehman A, Mishra A et al (2012) Changes in bacterial community structure of agricultural land due to long-term organic and chemical amendments. Microb Ecol 64:450–460

    Article  PubMed  Google Scholar 

  75. Misra S, Dixit VK, Mishra SK, Chauhan PS (2019) Demonstrating the potential of abiotic stress-tolerant Jeotgalicoccus huakuii NBRI 13E for plant growth promotion and salt stress amelioration. Ann Microbiol 69:419–434

    Article  CAS  Google Scholar 

  76. Gupta S, Kaushal R, Spehia RS et al (2017) Productivity of capsicum influenced by conjoint application of isolated indigenous PGPR and chemical fertilizers. J Plant Nutr 40:921–927

    Article  CAS  Google Scholar 

  77. Sood G, Kaushal R, Chauhan A, Gupta S (2018) Effect of conjoint application of indigenous PGPR and chemical fertilizers on productivity of maize (Zea mays L.) under mid hills of Himachal Pradesh. J Plant Nutr 41:297–303

    Article  CAS  Google Scholar 

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Acknowledgements

The authors acknowledge the Director, CSIR-National Botanical Research Institute, for providing facilities and support during the study.

Funding

The authors acknowledge the Director, CSIR-National Botanical Research Institute for providing facilities and support during the study. This work is supported by in-house project (OLP116) funded by the Council of Scientific and Industrial Research, New Delhi, India.

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PSC conceived and coordinated the research. SKM, SM, VKD, and SK conducted the experiments and analyzed the data. PSC, SKM, and SM wrote the manuscript. All authors read and approved the manuscript.

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Correspondence to Puneet Singh Chauhan.

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Mishra, S.K., Misra, S., Dixit, V.K. et al. Ochrobactrum sp. NBRISH6 Inoculation Enhances Zea mays Productivity, Mitigating Soil Alkalinity and Plant Immune Response. Curr Microbiol 80, 328 (2023). https://doi.org/10.1007/s00284-023-03441-7

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