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Role of Plant-Microorganism Interactions in Plant Tolerance to Arsenic

  • Anna Kowalczyk
  • Dariusz Latowski
Chapter

Abstract

In this chapter, the review of the newest reports on plant-microbe interactions in plant tolerance to arsenic (As) is presented in two aspects. One is the bacteria effect on regulation of As availability in growth environment of the plant, and the second is direct influence of them on plant organism tolerance to As. The role of As oxidization or reduction mechanisms which were developed by microbes colonizing soil or water in plant tolerance to As is discussed. The meaning of rhizospheric bacteria contribution to bioavailability of elements such as phosphorus, iron, silicon or As, by mineral solubilization, as well as the significance of the bacteria siderophores in plant As tolerance is also explained. As and Fe released from iron(III) arsenate by symbiotic bacteria of As-hyperaccumulator fern, Pteris vittata, are not omitted. The role of As-resistant representatives of plant growth-promoting bacteria (PGPB) group in the reduction of As uptake by plants from contaminated soil is also described. Considering novel aspects of plant-microbe interactions under As stress, the content of this chapter refines previous knowledge about plant physiology in terms of As tolerance and in the field of As-resistant plant-microbe model application in environment remediation.

Keywords

Metalloids Phytoremediation Plant-microbe interaction Pteris vittata Soil pollution 

References

  1. Ahmed E, Holmström SJM (2014) Siderophores in environmental research: roles and applications. Microb Biotechnol 7:196–208.  https://doi.org/10.1111/1751-7915.12117 CrossRefPubMedPubMedCentralGoogle Scholar
  2. Awasthi S, Chauhan R, Srivastava S et al (2017) The journey of arsenic from soil to grain in rice. Front Plant Sci 8:1007.  https://doi.org/10.3389/fpls.2017.01007 CrossRefPubMedPubMedCentralGoogle Scholar
  3. Azeem M, Riaz A, Chaudhary AN et al (2014) Microbial phytase activity and their role in organic P mineralization. Arch Agron Soil Sci 61:751–766.  https://doi.org/10.1080/03650340.2014.963796 CrossRefGoogle Scholar
  4. Bais HP, Weir TL, Perry LG et al (2006) The role of root exudates in rhizosphere interactions with plants and other organisms. Annu Rev Plant Biol 57:233–266.  https://doi.org/10.1146/annurev.arplant.57.032905.105159 CrossRefPubMedGoogle Scholar
  5. Batool K, Zahra tuz F, Rehman Y (2017) Arsenic-redox transformation and plant growth promotion by purple nonsulfur bacteria Rhodopseudomonas palustris CS2 and Rhodopseudomonas faecalis SS5. Bio Med Res Int 2017:1–8.  https://doi.org/10.1155/2017/6250327 CrossRefGoogle Scholar
  6. Blute NK, Brabander DJ, Hemond HF et al (2004) Arsenic sequestration by ferric iron plaque on cattail roots. Environ Sci Technol 38:6074–6077.  https://doi.org/10.1021/es049448g CrossRefPubMedGoogle Scholar
  7. Bulgarelli D, Schlaeppi K, Spaepen S et al (2013) Structure and functions of the bacterial microbiota of plants. Annu Rev Plant Biol 64:807–838.  https://doi.org/10.1146/annurev-arplant-050312-120106 CrossRefPubMedGoogle Scholar
  8. Busby PE, Soman C, Wagner M et al (2017) Research priorities for harnessing plant microbiomes in sustainable agriculture. PLoS Biol 15(3):e2001793.  https://doi.org/10.1371/journal.pbio.2001793 CrossRefPubMedPubMedCentralGoogle Scholar
  9. Chen Y, Fu JW, Han YH et al (2016) High As exposure induced substantial arsenite efflux in As-hyperaccumulator Pteris vittata. Chemosphere 144:2189–2194.  https://doi.org/10.1016/j.chemosphere.2015.11.001 CrossRefPubMedGoogle Scholar
  10. Coats VC, Rumpho ME (2014) The rhizosphere microbiota of plant invaders: an overview of recent advances in the microbiomics of invasive plants. Front Microbiol 5:368.  https://doi.org/10.3389/fmicb.2014.00368 CrossRefPubMedPubMedCentralGoogle Scholar
  11. Das J, Sarkar P (2018) Remediation of arsenic in mung bean (Vigna radiata) with growth enhancement by unique arsenic-resistant bacterium Acinetobacter lwoffii. Sci Total Environ 624:1106–1118.  https://doi.org/10.1016/j.scitotenv.2017.12.157 CrossRefPubMedGoogle Scholar
  12. Garg N, Aggarwal N (2012) Effect of mycorrhizal inoculations on heavy metal uptake and stress alleviation of Cajanus cajan (L.) Millsp. Genotypes grown in cadmium and lead contaminated soil. Plant Growth Regul 66:9–26.  https://doi.org/10.1007/s10725-011-9624-8 CrossRefGoogle Scholar
  13. Garg N, Bhandari P (2012) Influence of cadmium stress and arbuscular mycorrhizal fungi on nodule senescence in Cajanus cajan (L.) Millsp. Int J Phytoremediation 14:62–74.  https://doi.org/10.1080/15226514.2011.573822 CrossRefPubMedGoogle Scholar
  14. Garg N, Singla P, Bhandari P (2015) Metal uptake, oxidative metabolism, and mycorrhization in pigeonpea and pea under arsenic and cadmium stress. Turk J Agric For 39:234–250.  https://doi.org/10.3906/tar-1406-121 CrossRefGoogle Scholar
  15. Ghosh P, Rathinasabapathi B, Ma LQ (2011) Arsenic-resistant bacteria solubilized arsenic in the growth media and increased growth of arsenic hyperaccumulator Pteris vittata L. Bioresour Technol 102:8756–8761.  https://doi.org/10.1016/j.biortech.2011.07.064 CrossRefPubMedGoogle Scholar
  16. Ghosh P, Rathinasabapathi B, Ma LQ (2015) Phosphorus solubilization and plant growth enhancement by arsenic-resistant bacteria. Chemosphere 134:1–6.  https://doi.org/10.1016/j.chemosphere.2015.03.048 CrossRefPubMedGoogle Scholar
  17. Gupta M, Khan E (2015) Mechanism of arsenic toxicity and tolerance in plants: role of silicon and signalling molecules. In: Tripathi B, Müller M (eds) Stress responses in plants. Springer, Cham, pp 143–157.  https://doi.org/10.1007/978-3-319-13368-3_6 CrossRefGoogle Scholar
  18. Han YH, Fu JW, Chen Y (2016a) Arsenic uptake, arsenite efflux and plant growth in hyperaccumulator Pteris vittata: role of arsenic-resistant bacteria. Chemosphere 144:1937–1942.  https://doi.org/10.1016/j.chemosphere.2015.10.096 CrossRefPubMedGoogle Scholar
  19. Han YH, Yang GM, Fu JW et al (2016b) Arsenic-induced plant growth of arsenic-hyperaccumulator Pteris vittata: impact of arsenic and phosphate rock. Chemosphere 149:366–372.  https://doi.org/10.1016/j.chemosphere.2016.01.118 CrossRefPubMedGoogle Scholar
  20. Han YH, Jia MR, Liu X et al (2017a) Bacteria from the rhizosphere and tissues of As-hyperaccumulator Pteris vittata and their role in arsenic transformation. Chemosphere 186:599–606.  https://doi.org/10.1016/j.chemosphere.2017.08.031 CrossRefPubMedGoogle Scholar
  21. Han YH, Liu X, Rathinasabapathi B (2017b) Mechanisms of efficient As solubilization in soils and As accumulation by As-hyperaccumulator Pteris vittata. Environ Pollut 227:569–597.  https://doi.org/10.1016/j.envpol.2017.05.001 CrossRefPubMedGoogle Scholar
  22. Hu H, Zhang J, Wang H et al (2013) Effect of silicate supplementation on the alleviation of arsenite toxicity in 93–11 (Oryza sativa L.). Environ Sci Pollut Res 20:8579–8589.  https://doi.org/10.1007/s11356-013-1811-x CrossRefGoogle Scholar
  23. Hu M, Li F, Liu C et al (2015) The diversity and abundance of As(III)-oxidizers on root iron plaque is critical for arsenic bioavailability to rice. Sci Rep 5:13611.  https://doi.org/10.1038/srep13611 CrossRefPubMedPubMedCentralGoogle Scholar
  24. Jia Y, Huang H, Hen Z et al (2014) Arsenic uptake by rice is influenced by microbe-mediated arsenic redox changes in the rhizosphere. Environ Sci Technol 48:1001–1007.  https://doi.org/10.1021/es403877s CrossRefPubMedGoogle Scholar
  25. Kong W, Liu F, Zhang C et al (2016) Non-destructive determination of malondialdehyde (MDA) distribution in oilseed rape leaves by laboratory scale NIR hyperspectral imaging. Sci Rep 14:35393.  https://doi.org/10.1038/srep35393 CrossRefGoogle Scholar
  26. Latowski D, Kowalczyk A (2016) Biochemical pathways of arsenic uptake from the environment to human cells. Mol Biophys Biochem 1:9–16.  https://doi.org/10.15761/MBB.1000103 CrossRefGoogle Scholar
  27. Lehmann T, Hoffmann M, Hentrich M et al (2010) Indole-3-acetamide-dependent auxin biosynthesis: a widely distributed way of indole-3-acetic acid production? Eur J Cell Biol 89:895–905.  https://doi.org/10.1016/j.ejcb.2010.06.021 CrossRefPubMedGoogle Scholar
  28. Liu X, Yang GM, Guan DX et al (2015) Catecholate-siderophore produced by as-resistant bacterium effectively dissolved FeAsO4 and promoted Pteris vittata growth. Environ Pollut 206:376–381.  https://doi.org/10.1016/j.envpol.2015.07.034 CrossRefPubMedGoogle Scholar
  29. Liu X, Fu JW, Guan DX et al (2016) Arsenic induced phytate exudation, and promoted FeAsO4 dissolution and plant growth in As-hyperaccumulator Pteris vittata. Environ Sci Technol 50:9070–9077.  https://doi.org/10.1021/acs.est.6b0066 CrossRefPubMedGoogle Scholar
  30. Liu X, Fu JW, Da Silva E et al (2017a) Microbial siderophores and root exudates enhanced goethite dissolution and Fe/As uptake by As-hyperaccumulator Pteris vittata. Environ Pollut 223:230–237.  https://doi.org/10.1016/j.envpol.2017.01.016 CrossRefPubMedGoogle Scholar
  31. Liu X, Fu JW, Tang N et al (2017b) Phytate induced arsenic uptake and plant growth in arsenic-hyperaccumulator Pteris vittata. Environ Pollut 226:212–218.  https://doi.org/10.1016/j.envpol.2017.04.021 CrossRefPubMedGoogle Scholar
  32. Mallick I, Bhattacharyya C, Mukherji S et al (2018) Effective rhizoinoculation and biofilm formation by arsenic immobilizing halophilic plant growth promoting bacteria (PGPB) isolated from mangrove rhizosphere: a step towards arsenic rhizoremediation. Sci Total Environ 610:1239–1250.  https://doi.org/10.1016/j.scitotenv.2017.07.234 CrossRefPubMedGoogle Scholar
  33. Martin F, Kohler A, Murat C et al (2016) Unearthing the roots of ectomycorrhizal symbioses. Nat Rev Microbiol 14(12):760–773.  https://doi.org/10.1038/nrmicro.2016.149 CrossRefPubMedGoogle Scholar
  34. Martin FM, Uroz S, Barker DG (2017) Ancestral alliances: plant mutualistic symbioses with fungi and bacteria. Science 356:eaad4501.  https://doi.org/10.1126/science.aad4501 CrossRefPubMedGoogle Scholar
  35. Mathews S, Ma LQ, Rathinasabapathi B et al (2010) Arsenic transformation in the growth media and biomass of hyperaccumulator Pteris vittata L. Bioresour Technol 101:8024–8030.  https://doi.org/10.1016/j.biortech.2010.05.042 CrossRefPubMedGoogle Scholar
  36. Mora Y, Díaz R, Vargas-Lagunas C (2014) Nitrogen-fixing rhizobial strains isolated from common bean seeds: phylogeny, physiology, and genome analysis. Appl Environ Microbiol 80:5644–5654.  https://doi.org/10.1128/AEM.01491-14 CrossRefPubMedPubMedCentralGoogle Scholar
  37. Müller B, Vogel C, Bai Y et al (2016) The plant microbiota: systems-level insights and perspectives. Annu Rev Genet 50:211–234.  https://doi.org/10.1146/annurev-genet-120215-034952 CrossRefPubMedGoogle Scholar
  38. Pandey S, Ghosh PK, Ghosh S et al (2013) Role of heavy metal resistant Ochrobactrum sp. and Bacillus spp. strains in bioremediation of a rice cultivar and their PGPR like activities. J Microbiol 51:11–17.  https://doi.org/10.1007/s12275-013-2330-7 CrossRefPubMedGoogle Scholar
  39. Ramos-Garza J, Bustamante-Brito R, Ángeles de Paz G et al (2015) Isolation and characterization of yeasts associated with plants growing in heavy-metal- and arsenic-contaminated soils. Canadian J Microbiol 62:307–319.  https://doi.org/10.1139/cjm-2015-0226 CrossRefGoogle Scholar
  40. Schneider J, Stürmer SL, Guilherme LR et al (2013) Arbuscular mycorrhizal fungi in arsenic-contaminated areas in Brazil. J Hazard Mater 262:1105–1115.  https://doi.org/10.1016/j.jhazmat.2012.09.063 CrossRefPubMedGoogle Scholar
  41. Sharma VK, Sohn M (2009) Aquatic arsenic: toxicity, speciation, transformations, and remediation. Environ Int 35:743–759.  https://doi.org/10.1016/j.envint.2009.01.005 CrossRefPubMedGoogle Scholar
  42. Singh N, Marwa N, Mishra SK et al (2016) Brevundimonas diminuta mediated alleviation of arsenic toxicity and plant growth promotion in Oryza sativa L. Ecotoxicol Environ Saf 125:25–34.  https://doi.org/10.1016/j.ecoenv.2015.11.020 CrossRefPubMedGoogle Scholar
  43. Srivastava S, Singh N (2014) Mitigation approach of arsenic toxicity in chickpea grown in arsenic amended soil with arsenic tolerant plant growth promoting Acinetobacter sp. Ecol Eng 60:146–153.  https://doi.org/10.1016/j.ecoleng.2014.05.008 CrossRefGoogle Scholar
  44. Wang X, Ma LQ, Rathinasabapathi B et al (2011a) Mechanisms of efficient arsenite uptake by arsenic hyperaccumulator Pteris vittata. Environ Sci Technol 45:9719–9725.  https://doi.org/10.1021/es2018048 CrossRefPubMedGoogle Scholar
  45. Wang Q, Xiong D, Zhao P et al (2011b) Effect of applying an arsenic-resistant and plant growth-promoting rhizobacterium to enhance soil arsenic phytoremediation by Populus deltoides LH05-17. J Appl Microbiol 111:1065–1074.  https://doi.org/10.1111/j.1365-2672.2011.05142.x CrossRefPubMedGoogle Scholar
  46. Xu XY, McGrath SP, Zhao FJ (2007) Rapid reduction of arsenate in the medium mediated by plant roots. New Phytol 176:590–599.  https://doi.org/10.1111/j.1469-8137.2007.02195.x CrossRefPubMedGoogle Scholar
  47. Zgadzaj R, Garrido-Oter R, Jensen D et al (2016) Root nodule symbiosis in Lotus japonicus drives the establishment of distinctive rhizosphere, root, and nodule bacterial communities. Proc Natl Acad Sci U S A 113:7996–8005.  https://doi.org/10.1073/pnas.1616564113pmid:27864511 CrossRefGoogle Scholar
  48. Zhao FJ, Ma JF, Meharg AA et al (2009) Arsenic uptake and metabolism in plants. New Phytol 181:777–794.  https://doi.org/10.1111/j.1469-8137.2008.02716.x CrossRefPubMedGoogle Scholar
  49. Zhu LJ, Guan DX, Luo J et al (2014) Characterization of arsenic-resistant endophytic bacteria from hyperaccumulators Pteris vittata and Pteris multifida. Chemosphere 113:9–16.  https://doi.org/10.1016/j.chemosphere.2014.03.081 CrossRefPubMedGoogle Scholar

Copyright information

© Springer Nature Singapore Pte Ltd. 2018

Authors and Affiliations

  • Anna Kowalczyk
    • 1
  • Dariusz Latowski
    • 1
  1. 1.Faculty of Biochemistry, Biophysics and Biotechnology, Department of Plant Physiology and BiochemistryJagiellonian University in KrakowKrakowPoland

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