Genotoxicity testing of bovine lymphocytes exposed to epoxiconazole using alkaline and neutral comet assay

Epoxiconazole belongs in the class of azoles which have been developed to protect crops from fungal diseases. The mechanism of action of these fungicides is to inhibit the specific cytochrome P450 enzyme (CYP), CYP51 (lanosterol 14α-demethylase) which contributes to ergosterol biosynthesis. Since r...

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Main Authors: Simona Koleničová, Beáta Holečková, Martina Galdíková, Viera Schwarzbacherová, Monika Drážovská
Format: Article
Language:English
Published: Firenze University Press 2021-03-01
Series:Caryologia
Online Access:https://riviste.fupress.net/index.php/caryologia/article/view/984
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spelling doaj-331bdf0a457347c29748ed1af3f8a7982021-04-07T17:25:16ZengFirenze University PressCaryologia 0008-71142165-53912021-03-0110.13128/caryologia-984Genotoxicity testing of bovine lymphocytes exposed to epoxiconazole using alkaline and neutral comet assay Simona Koleničová0Beáta HolečkováMartina GaldíkováViera SchwarzbacherováMonika DrážovskáDepartment of genetics Epoxiconazole belongs in the class of azoles which have been developed to protect crops from fungal diseases. The mechanism of action of these fungicides is to inhibit the specific cytochrome P450 enzyme (CYP), CYP51 (lanosterol 14α-demethylase) which contributes to ergosterol biosynthesis. Since ruminants and cattle are exposed to contaminants during grazing, they are a suitable experimental model for genotoxicity testing. In our experiment, epoxiconazole (EPX) (active agent, 99% of purity) was tested in vitro for its potential genotoxic and cytotoxic effects on bovine lymphocytes, isolated from whole peripheral blood. We exposed the lymphocytes to EPX at concentrations of 2.5, 5, 10, 25, 50 and 100 μg/mL by two different ways: immediately after isolation of lymphocytes during 2 h in RPMI 1640 medium (without phytohaemagglutinin, PHA) as well as on the last 2 h of 48-h culture (with PHA). In a second case, we chose 48 h culture because the lymphocytes usually start DNA replication 24 h after the start of the cultures; therefore, we incubated the cells longer to obtain dividing (proliferating) cells. The levels of DNA damage were measured using alkaline and neutral comet assays. The results of alkaline comet assay showed the significantly increased percentage of DNA breaks in both lymphocytes in medium without PHA (2 h of exposure; non-proliferating cells) and lymphocytes cultured during 48 h in medium with PHA (exposure for the last 2 h of cultivation; proliferating cells). Similarly, neutral comet assay showed dose-dependent elevation of the DNA migration induced in both non-proliferating and proliferating lymphocytes treated with EPX when compared with negative controls. Our results suggest that epoxiconazole fungicide is capable of causing damage to the genetic material of the bovine cells. https://riviste.fupress.net/index.php/caryologia/article/view/984
collection DOAJ
language English
format Article
sources DOAJ
author Simona Koleničová
Beáta Holečková
Martina Galdíková
Viera Schwarzbacherová
Monika Drážovská
spellingShingle Simona Koleničová
Beáta Holečková
Martina Galdíková
Viera Schwarzbacherová
Monika Drážovská
Genotoxicity testing of bovine lymphocytes exposed to epoxiconazole using alkaline and neutral comet assay
Caryologia
author_facet Simona Koleničová
Beáta Holečková
Martina Galdíková
Viera Schwarzbacherová
Monika Drážovská
author_sort Simona Koleničová
title Genotoxicity testing of bovine lymphocytes exposed to epoxiconazole using alkaline and neutral comet assay
title_short Genotoxicity testing of bovine lymphocytes exposed to epoxiconazole using alkaline and neutral comet assay
title_full Genotoxicity testing of bovine lymphocytes exposed to epoxiconazole using alkaline and neutral comet assay
title_fullStr Genotoxicity testing of bovine lymphocytes exposed to epoxiconazole using alkaline and neutral comet assay
title_full_unstemmed Genotoxicity testing of bovine lymphocytes exposed to epoxiconazole using alkaline and neutral comet assay
title_sort genotoxicity testing of bovine lymphocytes exposed to epoxiconazole using alkaline and neutral comet assay
publisher Firenze University Press
series Caryologia
issn 0008-7114
2165-5391
publishDate 2021-03-01
description Epoxiconazole belongs in the class of azoles which have been developed to protect crops from fungal diseases. The mechanism of action of these fungicides is to inhibit the specific cytochrome P450 enzyme (CYP), CYP51 (lanosterol 14α-demethylase) which contributes to ergosterol biosynthesis. Since ruminants and cattle are exposed to contaminants during grazing, they are a suitable experimental model for genotoxicity testing. In our experiment, epoxiconazole (EPX) (active agent, 99% of purity) was tested in vitro for its potential genotoxic and cytotoxic effects on bovine lymphocytes, isolated from whole peripheral blood. We exposed the lymphocytes to EPX at concentrations of 2.5, 5, 10, 25, 50 and 100 μg/mL by two different ways: immediately after isolation of lymphocytes during 2 h in RPMI 1640 medium (without phytohaemagglutinin, PHA) as well as on the last 2 h of 48-h culture (with PHA). In a second case, we chose 48 h culture because the lymphocytes usually start DNA replication 24 h after the start of the cultures; therefore, we incubated the cells longer to obtain dividing (proliferating) cells. The levels of DNA damage were measured using alkaline and neutral comet assays. The results of alkaline comet assay showed the significantly increased percentage of DNA breaks in both lymphocytes in medium without PHA (2 h of exposure; non-proliferating cells) and lymphocytes cultured during 48 h in medium with PHA (exposure for the last 2 h of cultivation; proliferating cells). Similarly, neutral comet assay showed dose-dependent elevation of the DNA migration induced in both non-proliferating and proliferating lymphocytes treated with EPX when compared with negative controls. Our results suggest that epoxiconazole fungicide is capable of causing damage to the genetic material of the bovine cells.
url https://riviste.fupress.net/index.php/caryologia/article/view/984
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AT martinagaldikova genotoxicitytestingofbovinelymphocytesexposedtoepoxiconazoleusingalkalineandneutralcometassay
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