Contrasting fish biomarker responses between streams with different environmental conditions
DOI:
https://doi.org/10.21664/2238-8869.2021v10i1.p427-443Keywords:
Ecotoxicology; Antioxidant enzymes; Genotoxicity.Abstract
Streams are environments susceptible to anthropic impacts that harm aquatic organisms by affecting their homeostasis. This study aimed to determine variations in the response of biochemical and genetic biomarkers of fish under the influence of anthropogenic impacts. For this, individuals of the tetra fish Astyanax lacustris were exposed in an impacted stream and one of its non-impacted tributaries (reference) during the dry and rainy seasons. For biochemical analyzes, we evaluated the antioxidant enzymes catalase and glutathione peroxidase and lipid peroxidation in tissue samples of gills and liver. For the genotoxicity test, we evaluated micronuclei and nuclear anomalies in blood samples. The antioxidant enzymes showed seasonal variation, regardless of the stream; lipid peroxidation didn’t differ between seasons or between streams. The frequency of micronuclei and nuclear abnormalities were more frequent in the impacted stream during the rainy season, probably in response to the leaching of toxic compounds that tends to be increased in that season. These results support the use of nuclear biomarkers in biomonitoring programs.
References
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Beutler E 1975. Red cell metabolism: a manual of biochemical methods 2º edition. New York, Grune e Stratton, 160 pp.
Bradford MM 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254. https://doi.org/10.1016/0003-2697(76)90527-3
Buss DF, Oliveira RB, Baptista DF 2008. Monitoramento Biológico de Ecossistemas Aquáticos Continentais. Oecol Bras 12(3):339-345. https://doi.org/10.4257/oeco.2008.1203.01
Carrasco KR, Tilbury KL, Myers MS 1990. Assessment of the Piscine Micronucleus Test as an in situ Biological indicator of Chemical Contaminant Effects. Can J Fish Aquat Sci 47(11):2123–2136. https://doi.org/10.1139/f90-237
Conselho Nacional do Meio Ambiente - CONAMA. Resolução nº 357, de 17 de março de 2005: dispõe sobre a classificação dos corpos de água e diretrizes ambientais para o seu enquadramento, bem como estabelece as condições e padrões de lançamento de efluentes, e dá outras providências. Diário Oficial da União, Brasília, n. 53, 18 mar. 2005, p. 58-63. Disponível em: <http://www.mma.gov.br/port/conama/res/res05/res35705.pdf>. Acesso em: 20 novembro 2017.
Dalzochio T, Gehlen G 2016. Confounding factors in biomonitoring using fish. Ecotoxicol Environ Contam 11(1):53–61. https://doi.org/10.5132/eec.2016.01.08
Dalzochio T, Rodrigues GZP, Simões LAR, de Souza MS, Petry IE, Andriguetti NB, Silva GJH, da Silva LB, Gehlen G 2018. In situ monitoring of the Sinos River, southern Brazil: water quality parameters, biomarkers, and metal bioaccumulation in fish. Environ Sci Pollut Res 25:9485–9500. https://doi.org/10.1007/s11356-018-1244-7
Dalzochio T, Souza MS de, Simões LAR, Silva GJH, Rodrigues GZP, Andriguetti NB, Silva LB da, Gehlen G 2019. Impact of Anthropogenic Activities on Water Quality of The Paranhana River, Southern Brazil. Braz Arch Biol Technol 62:e19180523. https://doi.org/10.1590/1678-4324-2019180523
de Lima Cardoso R, Carvalho-Neta RNF, de Castro ACL, Ferreira CFC, Silva MHL, de Jesus Azevedo JW, Sobrinho JRSC, Santos DMS 2018. Histological and Genotoxic Biomarkers in Prochilodus lacustris (Pisces, Prochilodontidae) for Environmental Assessment in a Protected Area in the Northeast of Brazil. Bull Environ Contam Toxicol 101:570–579. https://doi.org/10.1007/s00128-018-2464-8
Disner GR, Calado SLM, Silva Assis HC, Cestari MM 2017. Toxicity of naphthalene in the Neotropical Fish Astyanax Lacustris (Characiformes: Characidae) and Geophagus Brasiliensis (Perciformes: Cichlidae). Evidência 17(1):7–22. https://doi.org/10.18593/eba.v17i1.12976
Feidantsis K, Pörtner HO, Vlachonikola E, Antonopoulou E, Michaelidis B 2018. Seasonal Changes in Metabolism and Cellular Stress Phenomena in the Gilthead Sea Bream (Sparus aurata). Physiol Biochem Zool 91(3):878–895. https://doi.org/10.1086/697170
Fenech M 2000. The in vitro micronucleus technique. Mutat Res 455(1–2):81–95. https://doi.org/10.1016/S0027-5107(00)00065-8
Ghisi NC, Oliveira EC, Guiloski IC, de Lima SB, Silva de Assis HC, Longhi SJ, Prioli AJ, 2017. Multivariate and integrative approach to analyze multiple biomarkers in ecotoxicology: A field study in Neotropical region. Sci Total Environ 609:1208–1218. https://doi.org/10.1016/j.scitotenv.2017.07.266
Girardi R, Pinheiro A, Garbossa LHP, Torres É., 2016. Water quality change of rivers during rainy events in a watershed with different land uses in Southern Brazil. RBRH 21(3):514–524. https://doi.org/10.1590/2318-0331.011615179
Girotti AW 2002. Introduction to serial reviews on regulatory and cytoprotective aspects of lipid hydroperoxide metabolism. Free Radic Biol Med 33(2):153. https://doi.org/10.1016/S0891-5849(02)00854-7
Gomes JB, Pereira NJ, Sousa EL de, Sousa D da S, Lenz T de M, Santos DMS 2019. Evaluation of aquatic contamination in an urban lagoon environment in a coastal region in the north of Brazil. Biosci J 35(3):920–932. https://doi.org/10.14393/BJ-v35n3a2019-39858
Halliwell B, Gutteridge JMC 2015. Free Radicals in Biology and Medicine 5º edition. New York, Oxford University Press, 961 pp. https://doi.org/10.1093/acprof:oso/9780198717478.001.0001
Heath RL, Packer L 1968. Photoperoxidation in isolated chloroplasts. Arch Biochem Biophys 125(3):850–857. https://doi.org/10.1016/0003-9861(68)90654-1
Ighodaro OM, Akinloye OA 2018. First line defence antioxidants-superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPX): Their fundamental role in the entire antioxidant defence grid. Alex J Med 54(4):287–293. https://doi.org/10.1016/j.ajme.2017.09.001
Karr JR 1981. Assessment of Biotic Integrity Using Fish Communities. Fisheries 6(6):21–27. https://doi.org/10.1577/1548-8446(1981)006<0021:AOBIUF>2.0.CO;2
Lima LBD de, Morais PB de, Andrade RLT de, Mattos LV, Moron SE 2018. Use of biomarkers to evaluate the ecological risk of xenobiotics associated with agriculture. Environ Pollut 237:611–624. https://doi.org/10.1016/j.envpol.2018.02.011
Louiz I, Ben Hassine OK, Palluel O, Ben-Attia M, Aït-Aïssa S 2016. Spatial and temporal variation of biochemical biomarkers in Gobius niger (Gobiidae) from a southern Mediterranean lagoon (Bizerta lagoon, Tunisia): Influence of biotic and abiotic factors. Mar Pollut Bull 107(1):305–314. https://doi.org/10.1016/j.marpolbul.2016.03.045
Lushchak VI 2011. Environmentally induced oxidative stress in aquatic animals. Aquatic Toxicol 101(1):13–30. https://doi.org/10.1016/j.aquatox.2010.10.006
Madeira D, Narciso L, Cabral HN, Vinagre C, Diniz MS 2013. Influence of temperature in thermal and oxidative stress responses in estuarine fish. Comp Biochem Physiol A Mol Integr Physiol 166(2):237–243. https://doi.org/10.1016/j.cbpa.2013.06.008
Mansouri B, Ebrahimpour M, Babaei H 2012. Bioaccumulation and elimination of nickel in the organs of black fish (Capoeta fusca). Toxicol Ind Health 28(4):361–368. https://doi.org/10.1177/0748233711412425
Marques JA, Marangoni LFB, Bianchini A 2016. Bioindicadores e biomarcadores para avaliação de impactos em recifes de coral. In Zilberberg C, Abrantes, DP, Marques JA, Machado LF, Marangoni LF de B (Eds.). Conhecendo Os Recifes Brasileiros: Rede de Pesquisas Coral Vivo. Museu Nacional, UFRJ, Rio de Janeiro, p. 221–232.
Martínez-Álvarez RM, Morales AE, Sanz A 2005. Antioxidant Defenses in Fish: Biotic and Abiotic Factors. Rev Fish Biol Fish 15:75–88. https://doi.org/10.1007/s11160-005-7846-4
Mieiro CL, Dolbeth M, Marques TA, Duarte AC, Pereira ME, Pacheco M 2014. Mercury accumulation and tissue-specific antioxidant efficiency in the wild European sea bass (Dicentrarchus labrax) with emphasis on seasonality. Environ Sci Pollut Res Int 21(18): 10638–10651. https://doi.org/10.1007/s11356-014-3053-y
Mieiro CL, Pereira ME, Duarte AC, Pacheco M 2011. Brain as a critical target of mercury in environmentally exposed fish (Dicentrarchus labrax) - Bioaccumulation and oxidative stress profiles. Aquatic Toxicol 103(3–4):233–240. https://doi.org/10.1016/j.aquatox.2011.03.006
Mininni AN, Milan M, Ferraresso S, Petochi T, Di Marco P, Marino G, Livi S, Romualdi C, Bargelloni L, Patarnello T 2014. Liver transcriptome analysis in gilthead sea bream upon exposure to low temperature. BMC Genomics 15:765. https://doi.org/10.1186/1471-2164-15-765
Morozov AA, Yurchenko VV 2018. Seasonal changes in hepatic antioxidant enzyme activities of the perch Perca fluviatilis in the Upper Volga basin, Russia. Ichthyol Res 65: 265–269. https://doi.org/10.1007/s10228-017-0608-1
Oliveira M, Ahmad I, Maria VL, Ferreira CSS, Serafim A, Bebianno MJ, Pacheco M, Santos MA 2010. Evaluation of oxidative DNA lesions in plasma and nuclear abnormalities in erythrocytes of wild fish (Liza aurata) as an integrated approach to genotoxicity assessment. Mutat Res 703:83–89. https://doi.org/10.1016/j.mrgentox.2010.08.003
Ondei L de S, Teresa FB, Garcia DP, Felício AA, da Silva DGH, de Almeida EA 2020. Fish biomarker responses to perturbation by drought in streams. Neotrop Ichthyol 18(2):e190130. https://doi.org/10.1590/1982-0224-2019-0130
Petitjean Q, Jean S, Gandar A, Côte J, Laffaille P, Jacquin L 2019. Stress responses in fish: From molecular to evolutionary processes. Sci Total Environ 684:371–380. https://doi.org/10.1016/j.scitotenv.2019.05.357
Petrovic M, Ginebreda A, Acuña V, Batalla RJ, Elosegi A, Guasch H, de Alda ML, Marcé R, Muñoz I, Navarro-Ortega A, Navarro E, Vericat D, Sabater S, Barceló D 2011. Combined scenarios of chemical and ecological quality under water scarcity in Mediterranean rivers. TrAC Trends Anal Chem 30(8):1269–1278. https://doi.org/10.1016/j.trac.2011.04.012
Rocha MP da, Vaini JO, Crispim BDA, Seno LDO, Olivera KMP de, Grisolia AB 2018. Identification of microbiological contamination and mutagenic potential of surface waters of the municipality of Dourados, MS. Ciência e Natura 40:e38. https://doi.org/10.5902/2179460X29423
Santana MS, Yamamoto FY, Sandrini-Neto L, Filipak Neto F, Ortolani-Machado CF, Oliveira Ribeiro CA, Prodocimo MM 2018. Diffuse sources of contamination in freshwater fish: Detecting effects through active biomonitoring and multi-biomarker approaches. Ecotoxicol Environ Saf 149:173–181. https://doi.org/10.1016/j.ecoenv.2017.11.036
Scalon M, Rechenmacher C, Siebel A, Kayser M, Rodrigues MT, Maluf S, Rodrigues MAS, Silva L 2010. Evaluation of Sinos River water genotoxicity using the comet assay in fish. Braz J Biol 70(4 Suppl):1217–1222. https://doi.org/10.1590/S1519-69842010000600011
Sies H 1986. Biochemistry of Oxidative Stress. Angew Chem Int Ed Eng 25(12):1058–1071. https://doi.org/10.1002/anie.198610581
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2021-03-03
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CAMILO-COTRIM, Carlos Filipe; REIS, Max Miller Bicudo dos; TERESA, Fabrício Barreto; ONDEI, Luciana de Souza. Contrasting fish biomarker responses between streams with different environmental conditions. Fronteiras - Journal of Social, Technological and Environmental Science, [S. l.], v. 10, n. 1, p. 427–443, 2021. DOI: 10.21664/2238-8869.2021v10i1.p427-443. Disponível em: https://revistas2.unievangelica.edu.br/index.php/fronteiras/article/view/4716. Acesso em: 21 nov. 2024.
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