Environmentally Relevant Concentrations of Lead Induce Toxic Stress in Nile Tilapia (Oreochromis niloticus)

Authors

  • Musa A. Ibrahim Department of Biology, Faculty of Life Sciences, University of Maiduguri, P.M.B. 1069, Maiduguri 600230, Borno State, Nigeria.
  • Musa Ibrahim Department of Biology, Faculty of Life Sciences, University of Maiduguri, P.M.B. 1069, Maiduguri 600230, Borno State, Nigeria.
  • Philip W. Edward Department of Biology, Faculty of Life Sciences, University of Maiduguri, P.M.B. 1069, Maiduguri 600230, Borno State, Nigeria.
  • Mayelmi H. Markus Department of Biology, Faculty of Life Sciences, University of Maiduguri, P.M.B. 1069, Maiduguri 600230, Borno State, Nigeria.
  • Hauwa I. Dibal Department of Biology, Faculty of Life Sciences, University of Maiduguri, P.M.B. 1069, Maiduguri 600230, Borno State, Nigeria.
  • Mathias N. Bwala Borno State Field Office, National Environmental Standards and Regulations Enforcement Agency (NESREA), C/O Borno State Afforestation Office Complex, Angwan Doki, Behind Dujima Hotel, Maiduguri, Borno State, Nigeria.
  • Usman A. Ibrahim Department of Civil and Water Resources Engineering, Faculty of Engineering, University of Maiduguri, P.M.B. 1069, Maiduguri 600230, Borno State, Nigeria.

DOI:

https://doi.org/10.54987/jemat.v14i1.213

Keywords:

Lead, Biomarkers, Aquatic ecosystems, Oxidative stress, Toxicity

Abstract

Lead (Pb) is a common toxic metal and can be harmful to fish health even at low concentrations. The toxicity of environmentally relevant nominal concentrations of Pb (0.125-1.000 mg/L) to juvenile tilapia (Oreochromis niloticus; initial total length 9.1 +/- 0.5 cm; body weight 10.6 +/- 2.3 g) was studied for 28 days with continuous aeration (dissolved oxygen 5.2-5.4 mg/L). Measured and nominal Pb concentrations were highly correlated (R2 = 0.9995, p = 0.0002). Tissue Pb concentration increased with waterborne Pb concentration (p = 0.0004) and the average bioconcentration factor was 0.33 L/kg. Viscerosomatic and hepatosomatic indices were lower in Pb-exposed fish than in controls while gonadosomatic index was not significantly different among groups. Water temperature and pH were relatively stable and electrical conductivity and total dissolved solids varied among treatments. Reduced glutathione, malondialdehyde and superoxide dismutase differed significantly among groups, while catalase activity did not. Electrical conductivity was positively correlated with total dissolved solids (r = 0.97) and negatively correlated with pH (r = -0.90). These results show that environmentally relevant Pb exposure can modify organ condition, tissue metal burden, and oxidative-stress responses in juvenile Nile tilapia, supporting the need for routine monitoring of Pb in freshwater and aquaculture systems.

References

1 Lee JW, Choi H, Hwang UK, Kang JC, Kang YJ, Kim KI, et al. Toxic effects of lead exposure on bioaccumulation, oxidative stress, neurotoxicity, and immune responses in fish: a review. Environ Toxicol Pharmacol. 2019;68:101-108. https://doi.org/10.1016/j.etap.2019.03.010

2 Cheng H, Hu Y. Lead (Pb) isotopic fingerprinting and its applications in lead pollution studies in China: a review. Environ Pollut. 2010;158:1134-1146. https://doi.org/10.1016/j.envpol.2009.12.028

3 Wang Z, Bao J, Wang T, Moryani HT, Kang W, Zheng J, et al. Hazardous heavy metals accumulation and health risk assessment of different vegetable species in contaminated soils from a typical mining city, Central China. Int J Environ Res Public Health. 2021;18:2617. https://doi.org/10.3390/ijerph18052617

4 Kim JH, Kang JC. The immune responses in juvenile rockfish, Sebastes schlegelii, exposed to dietary lead(II). Environ Toxicol Pharmacol. 2016;46:211-216.

5 Olaifa FE, Olaifa AK, Lewis OO. Toxic stress of lead on Clarias gariepinus (African catfish) fingerlings. Afr J Biomed Res. 2003;6:101-104.

6 Emenike EC, Iwuozor KO, Anidiobi SU. Heavy metal pollution in aquaculture: sources, impacts and mitigation techniques. Biol Trace Elem Res. 2022;200:4476-4492. https://doi.org/10.1007/s12011-021-03037-x

7 Reda RM, Zaki EM, Aioub AAA, Metwally MMM, Yassin AM, Mahsoub F. Behavioral, biochemical, immune, and histological responses of Nile tilapia (Oreochromis niloticus) to lead, mercury, and pendimethalin exposure: individual and combined effects. Environ Sci Eur. 2025;37:11. https://doi.org/10.1186/s12302-024-01047-9

8 Dixit R, Wasiullah, Malaviya D, Pandiyan K, Singh UB, Sahu A, et al. Bioremediation of heavy metals from soil and aquatic environment: an overview of principles and criteria of fundamental processes. Sustainability. 2015;7:2189-2212. https://doi.org/10.3390/su7022189

9 Alsaleh M. The role of the fishery industry in the shift towards sustainable food security: a critical study of blue food. Environ Sci Pollut Res Int. 2023;30:105575-105594. https://doi.org/10.1007/s11356-023-29747-4

10 Wang J, Zhang R, He T, Belgrano A. Editorial: blue foods security and sustainability. Front Mar Sci. 2024;11:1487645. https://doi.org/10.3389/fmars.2024.1487645

11 Bwala MN. Assessment of heavy metals in sediments, water and Clarias gariepinus from Alau Dam, Borno State, Nigeria. Sahel J Life Sci FUDMA. 2023;1:155-162.

12 Opaluwa OD, Aremu MO, Ogbo LO, Magaji JI, Odiba IE, Ekpo ER. Assessment of heavy metals in water, fish and sediments from Uke Stream, Nasarawa State, Nigeria. Curr World Environ. 2012;7:213-230.

13 Edward M, Muhib A. Heavy metals concentration in water, sediment, and fish around Escravos River, Nigeria. World J Res Rev. 2020;10:28-37.

14 Akubuo FC, Osuji LC, Hart AI. Temporal variations of heavy metal concentrations in selected fishes, sediments and surface water along an artisanal refinery site, Rivers State, Nigeria. J Environ Sci Health B. 2023;58:235-245.

15 Davies IC, Ekperusi AO. Evaluation of heavy metal concentrations in water, sediment and fishes of New Calabar River in southern Nigeria. J Aquat Sci Mar Biol. 2021;4:12-20.

16 Verstraeten SV, Aimo L, Oteiza PI. Aluminium and lead: molecular mechanisms of brain toxicity. Arch Toxicol. 2008;82:789-802. https://doi.org/10.1007/s00204-008-0345-3

17 Rogers JT, Richards JG, Wood CM. Ionoregulatory disruption as the acute toxic mechanism for lead in the rainbow trout (Oncorhynchus mykiss). Aquat Toxicol. 2003;64:215-234. https://doi.org/10.1016/S0166-445X(03)00053-5

18 Abdelzaher MF, Azab AM, Authman MMN, Shaban WM. Impact of lead and cadmium chronic exposure on some physiological parameters of Nile tilapia (Oreochromis niloticus). Egypt J Aquat Biol Fish. 2022;26:421-432.

19 Çiftçi N, Karayakar F, Ay Ö, Cicik B, Erdem C. Effects of copper and lead on some haematological parameters of Oreochromis niloticus. Fresenius Environ Bull. 2015;24:2771-2775.

20 El-Sayed EE. Accumulation of some heavy metals and its effect on hematological indices of freshwater fish, Oreochromis niloticus. Egypt J Aquat Biol Fish. 2015;19:89-100.

21 Dos Santos CR, Cavalcante ALM, Hauser-Davis RA, Lopes RM, Da Costa Mattos RCO. Effects of sub-lethal and chronic lead concentrations on blood and liver ALA-D activity and hematological parameters in Nile tilapia. Ecotoxicol Environ Saf. 2016;129:250-256.

22 Khalesi MK, Abedi Z, Behrouzi S, Kohestan Eskandari S. Haematological, blood biochemical and histopathological effects of sublethal cadmium and lead concentrations in common carp. Bulg J Vet Med. 2017;20:141-150.

23 Kumar M, Kumar D, Kumar R. Effect of heavy metals cadmium, lead and copper on the blood characteristics of freshwater catfish Clarias batrachus. Int J Adv Res Biol Sci. 2017;4:129-134.

24 Abdel-Warith AA, Younis EMI, Al-Asgah NA, Rady AM, Allam HY. Bioaccumulation of lead nitrate in tissues and its effects on haematological and biochemical parameters of Clarias gariepinus. Saudi J Biol Sci. 2020;27:840-845.

25 Azua ET, Akaahan TJ. Toxic stress exhibited by juveniles of Clarias gariepinus exposed to different concentrations of lead. J Res Environ Sci Toxicol. 2017;6:8-11.

26 Gurer H, Ercal N. Can antioxidants be beneficial in the treatment of lead poisoning? Free Radic Biol Med. 2000;29:927-945. https://doi.org/10.1016/S0891-5849(00)00413-5

27 Maiti AK, Saha NC, Paul G. Effect of lead on oxidative stress, Na+/K+-ATPase activity and mitochondrial electron transport chain activity of the brain of Clarias batrachus L. Bull Environ Contam Toxicol. 2010;84:672-676.

28 Musa AM, Oyedeji DE, Mada SB. Bioaccumulation of heavy metals in some tissues of croaker fish from oil-spilled rivers of Niger Delta region, Nigeria. Asian Pac J Trop Biomed. 2017;7:563-568. https://doi.org/10.1016/j.apjtb.2017.05.008

29 Olabemiwo OM, Alade AO, Tella AC, Adediran GO. Assessment of polycyclic aromatic hydrocarbons content in smoked Clarias gariepinus and Tilapia guineensis fish species available in western Nigeria. Int J Basic Appl Sci. 2011;11:135-150.

30 Misra HP, Fridovich I. The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem. 1972;247:3170-3175. https://doi.org/10.1016/S0021-9258(19)45228-9

31 Aebi H. Catalase in vitro. Methods Enzymol. 1984;105:121-126. https://doi.org/10.1016/S0076-6879(84)05016-3

32 Ellman GL. Tissue sulfhydryl groups. Arch Biochem Biophys. 1959;82:70-77. https://doi.org/10.1016/0003-9861(59)90090-6

33 Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979;95:351-358. https://doi.org/10.1016/0003-2697(79)90738-3

34 Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976;72:248-254. https://doi.org/10.1016/0003-2697(76)90527-3

35 Arnot JA, Gobas FAPC. A review of bioconcentration factor (BCF) and bioaccumulation factor (BAF) assessments for organic chemicals in aquatic organisms. Environ Rev. 2006;14:257-297. https://doi.org/10.1139/a06-005

Downloads

Published

31.07.2026

Issue

Section

Articles

How to Cite

Environmentally Relevant Concentrations of Lead Induce Toxic Stress in Nile Tilapia (Oreochromis niloticus). (2026). Journal of Environmental Microbiology and Toxicology, 14(1), 18-24. https://doi.org/10.54987/jemat.v14i1.213