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Phanerochaete chrysosporium as a model organism to assess the toxicity of municipal landfill leachate from Elazığ, Turkey

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Abstract

In order to evaluate the potential ecological risk and the toxic effect of landfill leachate (LL), Phanerochaete chrysosporium was exposed to LL and their biochemical response was observed by using antioxidant parameters. Phanerochaete chrysosporium, ME 446, was kept at 4 °C after being sub-cultured at 28 °C on Sabouraud Dextrose Agar (SDA). Superoxide dismutase (SOD), catalase (CAT) activities, and malaondialdehyde (MDA) and glutathione (GSH) levels of P. chrysosporium exposed to different dilution rates of leachate (1/10 and 1/20) for 24 and 96 h were analyzed by using the ELISA method. The physiochemical parameters such as pH, conductivity, total dissolved solids (TDS), dissolved oxygen (DO), chemical oxygen demand (COD) of leachate, and reference water were analyzed by using the YSI Professional Plus handheld multiparameter meter. In this study, SOD activities were decreased in the application groups compared with the Control Group at the 24th and 96th hours. CAT activities and GSH levels increased in the application groups compared with the Control Group at the 24th hour but decreased at the 96th hours. MDA levels increased in all of the application groups when compared with the Control Group for both 24 and 96 h. Different concentration of LL induces oxidative stress in P. chrysosporium, increased CAT activity and MDA levels, and decreased SOD activity and GSH levels.

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References

  • Adeyemi O, Oleyede O, Oladiji A (2007) Biochemical evaluation of oxidative damage induced by leachate contaminated groundwater on selected tissues of rats. The Int J Toxicol 4(2):1–5

    Google Scholar 

  • Al-Daihan S, Kaggwa J, El-Ansary A (2010) The effect of a sublethal concentration of Solanum nigrum on some antioxidants in Biomphalaria arabica. J Egypt Soc Parasitol 40:205–214

    Google Scholar 

  • APHA (1998) Standard methods for the examination of water and wastewater, 20th edn. American Public Health Association, American Water Works Association and Water Environmental Federation, Washington DC

    Google Scholar 

  • Apha AWWA, WPCF (2005) American public health association. American Water Works Association, Water Pollution Control Federation, Washington

    Google Scholar 

  • Arunbabu V, Indu KS, Ramasamy EV (2017) Leachate pollution index as an effective tool in determining the phytotoxicity of municipal solid waste leachate. Waste Manag 68:329–336

    CAS  Google Scholar 

  • Barata C, Varo I, Navarro JC, Arun S, Porte C (2005) Antioxidantenzyme activities and lipid peroxidation in the freshwater cladoceran Daphnia magna exposed to redoxcycling compounds. Comp Biochem Physiol 140C:175–186

    CAS  Google Scholar 

  • Baun A, Kloft L, Bjerg PL, Nyholm N (1999) Toxicity testing of organic chemicals in groundwater polluted with landfill leachate. Environ Toxicol Chem 18:2046–2053

    CAS  Google Scholar 

  • Baun A, Jensen SD, Bjerg PL, Christensen TH, Nyholm N (2000) Toxicity of organic chemical pollution in groundwater downgradient of a landfill (Grindsted, Denmark). Environ Sci Technol 34:1647–1652

    CAS  Google Scholar 

  • Cadenas E (1995) Antioxidant and prooxidant functions of DT-diaphorase in quinone metabolism. Biochemical Pharm 49:127–140

    CAS  Google Scholar 

  • Chen A, Zeng G, Chen G, Fan J, Zou Z, Li H, Hu X, Long F (2011) Simultaneous cadmium removal and 2,4-dichlorophenol degradation from aqueous solutions by Phanerochaete chrysosporium. Appl Microbiol Biotechnol 91:811–821

    CAS  Google Scholar 

  • Choudhary M, Jetley UK, Khan MA, Zutshi S, Fatma T (2007) Effect of heavy metal stress on proline, malondialdehyde, and superoxide dismutase activity in the cyanobacterium Spirulina platensis-S5. Ecotoxicol Environ Saf 66(2):204–209

    CAS  Google Scholar 

  • Christensen TH, Kjeldsen P, Albrechtsen HJ, Heron HJ, Nielsen PH, Bjerg PL, Holm PE (1994) Attenuation of landfill leachate pollutants in aquifers. Crit Rev Environ Sci Technol 24:119–202

    CAS  Google Scholar 

  • Demirci O, Hamamcı DA (2013) Antioxidant responses in Phanerochaete chrysosporium exposed to Astrazone Red FBL textile dye. Cell Biochem Funct 31:86–90

    CAS  Google Scholar 

  • Ercal N, Gurer-Orhan H, Aykin-Burns N (2001) Toxic metals and oxidative stress part I: mechanisms involved in metal induced oxidative damage. Curr Top Med Chem 1:529–539

    CAS  Google Scholar 

  • Espinosa-Ortiz EJ, Rene ER, Hullebusch EDv Lens PNL (2015) Removal of selenite from wastewater in a Phanerochaete chrysosporium pellet based fungal bioreactor. Int Biodeterior Biodegrad 102:361–369

    CAS  Google Scholar 

  • Farber JL (1994) Mechanisms of cell injury by activated oxygen species. Environ Health Perspect 102(10):17–24

    CAS  Google Scholar 

  • Farombi EO, Akintunde JK, Nzute N, Adedara IA, Arojojoye O (2011) Municipal landfill leachate induces hepatotoxicity and oxidative stress in rats. Toxicol Ind Health 28(6):532–541

    Google Scholar 

  • Giustarini D, Rossi R, Milzani A, Colombo R, Dalle-Donne I (2004) S-glutathionylation: from redox regulation of protein functions to human diseases. J Cell Mol Med 8(2):201–212

    CAS  Google Scholar 

  • Guangke LI, Sang N, Li GK (2005) Chromosomal aberrations induced in mouse bone marrow cells by municipal landfill leachate. EnvironToxicol Pharmacol 20:219–224

    Google Scholar 

  • Guoyao W, Yun-Zhong F, Sheng Y, Joanne R, Nancy D (2004) Glutathione metabolism and its implications for health. J Nutr 134(3):489–492

    Google Scholar 

  • Gupta A, Rajamani P (2015) Toxicity assessment of municipal solid waste landfill leachate collected in different seasons from Okhala landfill site of Delhi. J Biomed Sci Eng 8:357–369

    CAS  Google Scholar 

  • Halliwell B, Gutteridge JMC (eds) (1999) Free radicals in biology and medicine, 3rd edn. Oxford University Press, Oxford

    Google Scholar 

  • Hermes-Lima M (2004) Oxygen in biology and biochemistry: role of free radicals. In: Storey KB (ed) Functional metabolism: regulation and adaptation. John Wiley & Sons, Inc., USA

    Google Scholar 

  • Hu L, Liu Y, Zeng G, Chen G, Wan J, Zeng Y, Wang L, Wu H, Xu P, Zhang C, Cheng M, Hu T (2017) Organic matters removal from landfill leachate by İmmobilized Phanerochaete chrysosporium loaded with graphitic carbon nitride under visible light irradiation. Chemosphere. 184:1071–1079

    CAS  Google Scholar 

  • Huang C, Cui Lai, Piao X, Guangming Z, Danlian H, Jiachao Z , Chen Z, Min C , Jia W, Rongzhong W (2017a) Lead-induced oxidative stress and antioxidant response provide insight into the tolerance of Phanerochaete chrysosporium to lead exposure Chemosphere 187: 70–77

  • Huang Z, Chen G, Zeng G, Guo Z, He K, Hu L, Wu J, Zhang L, Zhu Y, Song Z (2017b) Toxicity mechanisms and synergies of silver nanoparticles in 2,4-dichlorophenol degradation by Phanerochaete chrysosporium. J Hazard Mater 321:37–46

    CAS  Google Scholar 

  • Huang Z, He K, Song Z, Zeng G, Chen A, Yuan L, Li H, Hu L, Guo Z, Chen G (2018a) Antioxidative response of Phanerochaete chrysosporium against silver nanoparticle-induced toxicity and its potential mechanism. Chemosphere 211:573–583

    CAS  Google Scholar 

  • Huang Z, Xu P, Chen G, Zeng G, Chen A, Song Z, He K, Yuan L, Li H, Hu L (2018b) Silver ion-enhanced particle-specific cytotoxicity of silver nanoparticles and effect on the production of extracellular secretions of Phanerochaete chrysosporium. Chemosphere. 196:575–584

    CAS  Google Scholar 

  • Huang Z, Zeng Z, Chen A, Zeng G, Xiao R, Xu P, He K, Song Z, Hu L, Peng M, Huang T, Chen G (2018c) Differential behaviors of silver nanoparticles and silver ions towards cysteine: bioremediation and toxicity to Phanerochaete chrysosporium. Chemosphere. 203:199–208

    CAS  Google Scholar 

  • Kurniawan F (2011) Analisis Ketepatan Pengukur Nilai Tegangan dan Arus RMS Jala-Jala Listrik Berbasis Mikrokontroler ATmega8535. Jurnal Angkasa 3:2

    Google Scholar 

  • Li G, Sang N, Guo D (2006) Oxidative damage induced in hearts, kidneys and spleens of mice by landfill leachate. Chemosphere 65:1058–1063

    CAS  Google Scholar 

  • Li X, Xu J, Toledo R, Ad Shim H (2016) Enhanced carbamazepine removal by immobilized Phanerochaete chrysosporium in a novel rotating suspension cartridge reactor under non-sterile condition. Int Biodeterior Biodegrad 115:102–109

    CAS  Google Scholar 

  • Noaksson E, Tjarnlund U, Bosveld ATC, Balk L (2001) Evidence for endocrine disruption in Perch (Perca fluviatilis) and Roach (Rutilus rutilus) in a remote Swedish lake in the vicinity of a public refuse dump. Toxicol Appl Pharmacol 174:160–176

    CAS  Google Scholar 

  • Placer ZA, Cushmann LL, Johnson BC (1966) Estimation of products of lipid peroxidation (as malondialdehyde) in biochemical systems. Anal Biochem 16:359–364

    CAS  Google Scholar 

  • Pouls M (1999) Heavy metal toxicity and cardiovascular diseases. Extreme Health’s Director of Research, Townsend Letter, USA

    Google Scholar 

  • Qi X, Hauswirth WW, Guy J (2007) Dual gene therapy with extracellular superoxide dismutase and catalase attenuates experimental optic neuritis. Mol Vis 13:1–11

    CAS  Google Scholar 

  • Ryter SW, Kim HP, Hoetzel A, Park JW, Nakahira K, Wang X, Choi AM (2007) Mechanism of cell death in oxidative stress. Antioxid Redox Signal 9:49–89

    CAS  Google Scholar 

  • Sahu B, Sahu AK, Chennareddy SR, Soni A, Naithani SC (2017) Insights on germinability and desiccation tolerance in developing neem seeds (Azadirachta indica): role of AOS, antioxidative enzymes and dehydrin-like protein. Plant Physiol Biochem 112:64–73

    CAS  Google Scholar 

  • Sang N, Han M, Li GK, Huang MZ (2010) Landfill leachate affects metabolic responses of Zea mays seedlings. Waste Manag 30:856–862

    CAS  Google Scholar 

  • Schrab GE, Brown KW, Donnelly KC (1993) Acute and genetic toxicity of municipal landfill leachate. Water Air Soil Pollut 69:99–112

    CAS  Google Scholar 

  • Sedighi M, Karimi A, Vahabzadeh F (2009) Involvement of ligninolytic enzymes of Phanerochaete chrysosporium in treating the textile effluent containing Astrazon Red FBL in a packed-bed bioreactor. J Hazard Mater 169:88–93

    CAS  Google Scholar 

  • Serdar O, Yildirim NC, Tatar Ş, Yildirim N, Ogedey A (2018) Antioxidant biomarkers in Gammarus pulex to evaluate the efficiency of electrocoagulation process in landfill leachate treatment. Environ Sci Pollut Res 25(13):12538–12544

    CAS  Google Scholar 

  • Siddique HR, Gupta SC, Mitra K, Urthy RC, Saxena DK, Debapratim K (2007) Chowdhuri induction of biochemical stress markers and apoptosis in transgenic Drosophila melanogaster against complex chemical mixtures: role of reactive oxygen species. Chem Biol Interact 169:171–188

    CAS  Google Scholar 

  • Valko M, Rhodes CJ, Moncol J, Izakovic M, Mazur M (2006) Chem Biol Interact 160:1–40

    CAS  Google Scholar 

  • Videla LA (2009) Oxidative stress signaling underlying liver disease and hepatoprotective mechanisms. World J Hepatol 1(1):72–78

    Google Scholar 

  • Wan J, Zeng G, Huang D, Huang C, Lai C, Li N, Wei Z, Xu P, He X, Lai M, He Y (2015) The oxidative stress of Phanerochaete chrysosporium against lead toxicity. Appl Biochem Biotechnol 175:1981–1991

    CAS  Google Scholar 

  • Weydert CJ, Cullen JJ (2010) Measurement of superoxide dismutase, catalase, and glutathione peroxidase in cultured cells and tissue. Nat Protoc 5:51–66

    CAS  Google Scholar 

  • Yildirim N, Asma D (2010) Response of antioxidant defence system to cadmium-induced toxicity in white rot fungus Phanerochaete Chrysosporium. Fresenius Environ Bull 19(12):3059–3065

  • Yildirim NC, Tanyol M, Serdar O, Tatar S (2018) Biochemical responses of Gammarus pulex to malachite green solutions decolorized by Coriolus versicolor as a biosorbent under batch adsorption conditions optimized with response surface methodology. Ecotoxicol Environ Saf 156:41–47

    CAS  Google Scholar 

  • Zeng GM, Chen AW, Chen GQ, Hu XJ, Guan S, Shang C, Lu LH, Zou ZJ (2012) Responses of Phanerochaete chrysosporium to toxic pollutants: physiological flux, oxidative stress, and detoxification. Environ Sci Technol 46(14):7818–7825

    CAS  Google Scholar 

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Correspondence to Numan Yildirim.

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Yildirim, N., Yildirim, N.C., Tatar, S. et al. Phanerochaete chrysosporium as a model organism to assess the toxicity of municipal landfill leachate from Elazığ, Turkey. Environ Sci Pollut Res 26, 12807–12812 (2019). https://doi.org/10.1007/s11356-019-04813-y

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