Silver nanoparticles induced genotoxicity and oxidative stress in tomato plants

Silver nanoparticles induced genotoxicity and oxidative stress in tomato plants

Among nanoparticles, silver nanoparticles (AgNPs) are intensively used in many materials owing to their antibacterial effects. In the present study different concentrations of AgNPs in Hoagland solution were applied to tomato seedlings. Total chlorophyll content, relative water content (RWC), antioxidant enzyme activities, and malondialdehyde content (MDA) as well as the genomic template stability (GTS) were analyzed. The intersimple sequence repeat polymerase chain reaction assay (ISSR-PCR) was used to determine the genotoxic effects of AgNPs on DNA. RWC did not change under AgNPs treatments; however, total chlorophyll content was significantly reduced by AgNPs applications. ISSR profiles demonstrated a consistent increase in polymorphic bands by the increase in the concentration of AgNPs. GTS value was also reduced depending on the concentration of AgNPs. SOD and APX activities were increased under low AgNPs treatments; however, these activities were decreased under high concentrations of AgNPs treatments. Tomato plants could be sensitive to AgNPs within the increase in MDA content in all of the AgNPs treatments. AgNPs nanotoxicity could be quite dose-dependent. AgNPs could also have negative effects on tomato plants by enhancing DNA damage and lipid peroxidation.

___

  • Arnon DI (1949). Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant Physiol 24: 1-15.
  • Allen RD, Gupta SA, Webb RP, Holaday AS (1994). Protection of plants from oxidative stress using SOD transgenes: interactions with endogenous enzymes. In: Asada K, Yoshikawa T, editors. Frontiers of Reactive Oxygen Species in Biology and Medicine. Amsterdam, Netherlands: Excerpta Medica, pp. 321-322.
  • Atienzar FA, Conradi M, Evenden AJ, Jha AN, Depledge MH (1999). Qualitative assessment of genotoxicity using random-amplified polymorphic DNA: comparison of genomic template stability with key fitness parameters in Daphnia magna exposed to benzo[a]pyrene. Environ Toxicol Chem 18: 2275-2282.
  • Bajpai R, Shukla V, Singh N, Rana TS, Upreti DK (2015). Physiological and genetic effects of chromium (+VI) on toxitolerant lichen species, Pyxine cocoes. Environ Sci Pollut Res 22: 3727-3738.
  • Barrs HD, Weatherley PE (1962). A re-examination of the relative turgidity technique for estimating water deficit in leaves. Aust J Biol Sci 15: 413-428. 
  • Bergmeyer N (1970). Methoden der Enzymatischen Analyse. Berlin, Germany: Akademie Verlag.
  • Beyer WF, Fridowich I (1987). Assaying for superoxide dismutase activity: some large consequences of minor changes in conditions. Anal Biochem 161: 559-566.
  • Bornet B, Branchard M (2001). Nonanchored Inter Simple Sequence Repeat (ISSR) markers: reproducible and specific tools for genome fingerprinting. Plant Mol Biol Report 19: 209-215.
  • Bowler C, Van Montagu M, Inzé D (1992). Superoxide dismutase and stress tolerance. Ann Rev Plant Physiol Plant Mol Biol 43: 83-116.
  • Bradford MM (1976). A rapid and sensitive method for the quantization of micro-gram quantities of protein utilizing the principle of the protein-dye binding. Anal Biochem 72: 248- 254.
  • Carlberg I, Mannervik B (1985). Glutathione reductase. Methods Enzymol 113: 484-490.
  • Correia S, Matos M, Ferreira V, Martins N, Gonçalves S, Romano A, Pinto-Carnide O (2014). Molecular instability induced by aluminum stress in Plantago species. Mutat Res - Genet Toxicol Environ Mutagen 770: 105-111.
  • Dimkpa CO, Mclean JE, Martineau N, Britt DW, Haverkamp R, Anderson AJ (2013). Silver nanoparticles disrupt wheat (Triticum aestivum L.) growth in a sand matrix. Environ Sci Technol 47: 1082-1090.
  • Fatima RA, Ahmad M (2005). Certain antioxidant enzymes of Allium cepa as biomarkers for the detection of toxic heavy metals in wastewater. Sci Total Environ 346: 256-273.
  • Fulton TM, Chunwongse J, Tanksley SD (1995). Microprep protocol for extraction of DNA from tomato and other herbaceous plants. Plant Mol Biol Report 13: 207-209.
  • Ghosh M, Manivannan J, Sinha S, Chakraborty A, Mallick SK, Bandyopadhyay M, Mukherjee A (2012). In vitro and in vivo genotoxicity of silver nanoparticles. Mutat Res 749: 60-69.
  • Hoagland DR, Arnon DI (1950). The water culture method for growing plants without soil. Calif Agric Exp Stn 347: 1-39.
  • Hatami M, Ghorbanpour M (2014). Defense enzyme activities and biochemical variations of Pelargonium zonale in response to nanosilver application and dark storage. Turk J Biol 38: 130-139.
  • Karabal E, Yücel M, Öktem HA (2003). Antioxidant responses of tolerant and sensitive barley cultivars to boron toxicity. Plant Sci 164: 925-933.
  • Kumari M, Khan SS, Pakrashi S, Mukherjee A, Chandrasekaran N (2011). Cytogenetic and genotoxic effects of zinc oxide nanoparticles on root cells of Allium cepa. J Hazard Mater 190: 613-621.
  • Kumari M, Mukherjee A, Chandrasekaran N (2009). Genotoxicity of silver nanoparticles in Allium cepa. Sci Total Environ 407: 5243- 5246.
  • Lee WM, Kwak JI, An YJ (2012). Effect of silver nanoparticles in crop plants Phaseolus radiatus and Sorghum bicolor: media effect on phytotoxicity. Chemosphere 86: 491-499.
  • Ma X, Geiser-Lee J, Deng Y, Kolmakov A (2010). Interactions between engineered nanoparticles (ENPs) and plants: phytotoxicity, uptake and accumulation. Sci Total Environ 408: 3053-3061.
  • McShan D, Ray PC, Yu H (2014). Molecular toxicity mechanism of nanosilver. J Food Drug Anal 22: 116-127.
  • Mittler R (2002). Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7: 405-410.
  • Nair PMG, Chung IM (2015). Physiological and molecular level studies on the toxicity of silver nanoparticles in germinating seedlings of mung bean (Vigna radiata L.). Acta Physiol Plant 37: 1719.
  • Nair PMG, Chung IM (2014a). Physiological and molecular level effects of silver nanoparticles exposure in rice (Oryza sativa L.) seedlings. Chemosphere 112: 105-113.
  • Nair PMG, Chung IM (2014b). Assessment of silver nanoparticleinduced physiological and molecular changes in Arabidopsis thaliana. Environ Sci Pollut Res 21: 8858-8869.
  • Nakano Y, Asada K (1981). Hydrogen peroxide is scavenged by ascorbate specific peroxidase in spinach chloroplasts. Plant Cell Physiol 22: 867-880.
  • Oukarroum A, Barhoumi L, Pirastru L, Dewez D (2013). Silver nanoparticle toxicity effect on growth and cellular viability of the aquatic plant Lemna gibba. Environ Toxicol Chem 32: 902- 907.
  • Panda KK, Achary VMM, Krishnaveni R, Padhi BK, Sachindra SN, Surendra SN, Brahma PB (2011). In vitro biosynthesis and genotoxicity bioassay of silver nanoparticles using plants. Toxicol In Vitro 25: 1097-1105.
  • Patlolla AK, Berry A, May L, Tchounwou PB (2012). Genotoxicity of silver nanoparticles in Vicia faba : a pilot study on the environmental monitoring of nanoparticles. Int J Environ Res Public Heal 9: 1649-1662.
  • Pokhrel LR, Dubey B (2013). Evaluation of developmental responses of two crop plants exposed to silver and zinc oxide nanoparticles. Sci Total Environ 452-453: 321-332.
  • Porra RJ (2002). The chequered history of the development and use of simultaneous equations for the accurate determination of chlorophylls a and b. Photosynth Res 73: 149-156. 
  • Qian H, Peng X, Han X, Ren J, Sun L, Zhengwei F (2013). Comparison of the toxicity of silver nanoparticles and silver ions on the growth of terrestrial plant model Arabidopsis thaliana. J Environ Sci 25: 1947-1956.
  • Ravindran A, Prathna TC, Verma VK (2012). Bovine serum albumin mediated decrease in silver nanoparticle phytotoxicity: root elongation and seed germination assay. Toxicol Environ Chem 94: 91-98.
  • Saed-Moucheshi A, Shekoofa A, Pessarakli M (2014). Reactive oxygen species (ROS) generation and detoxifying in plants. J Plant Nutr 37: 1573-1585.
  • Sharma P, Bhatt D, Zaidi MGH, Saradhi PP, Khanna PK, Arora S (2012). Silver nanoparticle-mediated enhancement in growth and antioxidant status of Brassica juncea. Appl Biochem Biotechnol 167: 2225-2233.
  • Song U, Jun H, Waldman B, Roh J, Kim Y, Yi J, Lee EJ (2013). Functional analyses of nanoparticle toxicity: a comparative study of the effects of TiO2 and Ag on tomatoes (Lycopersicon esculentum). Ecotoxicol Environ Saf 93: 60-67.
  • Sukumaran S, Grant A (2013). Effects of genotoxicity and its consequences at the population level in sexual and asexual Artemia assessed by analysis of inter-simple sequence repeats (ISSR). Mutat Res - Genet Toxicol Environ Mutagen 757: 8-14.
  • Thuesombat P, Hannongbua S, Akasit S, Chadchawan S (2014). Effect of silver nanoparticles on rice (Oryza sativa L. cv. KDML 105) seed germination and seedling growth. Ecotoxicol Environ Saf 104: 302-309.
  • Unal D, Silah H (2013). Genotoxicity effects of Flusilazole on the somatic cells of Allium cepa. Pestic Biochem Physiol 107: 38- 43.
  • Vannini C, Domingo G, Onelli E, Mattia FD, Bruni I, Marsoni M, Bracale M (2014). Phytotoxic and genotoxic effects of silver nanoparticles exposure on germinating wheat seedlings. J Plant Physiol 171: 1142-1148.
  • Yasur J, Rani PU (2013). Environmental effects of nanosilver: impact on castor seed germination, seedling growth, and plant physiology. Environ Sci Pollut Res Int 20: 8636-8648.
  • Zietkiewicz E, Rafalski A, Labuda D (1994). Genome fingerprinting by simple sequence repeat (SSR)-anchored polymerase chain reaction amplification. Genomics 15: 176-83.