Analysis of Chromosomal Damage Caused by Acetamiprid
Different chemicals can have genotoxic effects on the body, as confirmed by chromosome damage detection. Using conventional cytogenetic analysis and fluorescence in situ hybridization, we tested the extent of chromosome damage caused by the acetamiprid-based insecticide Mospilan 20SP on bovine perip...
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Online Access: | https://doi.org/10.2478/fv-2019-0015 |
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doaj-62154530d10146d7a8f01071c9a76c592021-09-05T21:01:06ZengSciendoFolia Veterinaria2453-78372019-06-01632252910.2478/fv-2019-0015fv-2019-0015Analysis of Chromosomal Damage Caused by AcetamipridStupáková K.0Galdíková M.1Schwarzbacherová V.2Holečková B.3Department of Biology and Genetics, Institute of Genetics, University of Veterinary Medicine and Pharmacy, Komenského 73, 041 81Košice, SlovakiaDepartment of Biology and Genetics, Institute of Genetics, University of Veterinary Medicine and Pharmacy, Komenského 73, 041 81Košice, SlovakiaDepartment of Biology and Genetics, Institute of Genetics, University of Veterinary Medicine and Pharmacy, Komenského 73, 041 81Košice, SlovakiaDepartment of Biology and Genetics, Institute of Genetics, University of Veterinary Medicine and Pharmacy, Komenského 73, 041 81Košice, SlovakiaDifferent chemicals can have genotoxic effects on the body, as confirmed by chromosome damage detection. Using conventional cytogenetic analysis and fluorescence in situ hybridization, we tested the extent of chromosome damage caused by the acetamiprid-based insecticide Mospilan 20SP on bovine peripheral blood lymphocytes at concentrations of, 2.5, 5, 25 and 50 µg.ml−1 after a 24 h incubation period. During the experiment, the presence of unstable aberrations—chromosomal and chromatid breaks and gaps—were detected by conventional cyto-genetic analysis. With increasing insecticide concentrations, we observed a statistically significant increase in chromosome damage frequency after 24 hours of exposure. Fluorescence in situ hybridization was used to detect stable structural aberrations; whole-chromosome painting probes for bovine chromosomes 1 and 7 (BTA 1 and BTA 7) were used for this purpose. As a result of exposure to the insecticide, neither BTA 1/BTA 7 translocations nor other types of translocations were observed.https://doi.org/10.2478/fv-2019-0015acetamipridconventional cytogenetic analysischromosomal aberrationsfluorescence in situ hybridization |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Stupáková K. Galdíková M. Schwarzbacherová V. Holečková B. |
spellingShingle |
Stupáková K. Galdíková M. Schwarzbacherová V. Holečková B. Analysis of Chromosomal Damage Caused by Acetamiprid Folia Veterinaria acetamiprid conventional cytogenetic analysis chromosomal aberrations fluorescence in situ hybridization |
author_facet |
Stupáková K. Galdíková M. Schwarzbacherová V. Holečková B. |
author_sort |
Stupáková K. |
title |
Analysis of Chromosomal Damage Caused by Acetamiprid |
title_short |
Analysis of Chromosomal Damage Caused by Acetamiprid |
title_full |
Analysis of Chromosomal Damage Caused by Acetamiprid |
title_fullStr |
Analysis of Chromosomal Damage Caused by Acetamiprid |
title_full_unstemmed |
Analysis of Chromosomal Damage Caused by Acetamiprid |
title_sort |
analysis of chromosomal damage caused by acetamiprid |
publisher |
Sciendo |
series |
Folia Veterinaria |
issn |
2453-7837 |
publishDate |
2019-06-01 |
description |
Different chemicals can have genotoxic effects on the body, as confirmed by chromosome damage detection. Using conventional cytogenetic analysis and fluorescence in situ hybridization, we tested the extent of chromosome damage caused by the acetamiprid-based insecticide Mospilan 20SP on bovine peripheral blood lymphocytes at concentrations of, 2.5, 5, 25 and 50 µg.ml−1 after a 24 h incubation period. During the experiment, the presence of unstable aberrations—chromosomal and chromatid breaks and gaps—were detected by conventional cyto-genetic analysis. With increasing insecticide concentrations, we observed a statistically significant increase in chromosome damage frequency after 24 hours of exposure. Fluorescence in situ hybridization was used to detect stable structural aberrations; whole-chromosome painting probes for bovine chromosomes 1 and 7 (BTA 1 and BTA 7) were used for this purpose. As a result of exposure to the insecticide, neither BTA 1/BTA 7 translocations nor other types of translocations were observed. |
topic |
acetamiprid conventional cytogenetic analysis chromosomal aberrations fluorescence in situ hybridization |
url |
https://doi.org/10.2478/fv-2019-0015 |
work_keys_str_mv |
AT stupakovak analysisofchromosomaldamagecausedbyacetamiprid AT galdikovam analysisofchromosomaldamagecausedbyacetamiprid AT schwarzbacherovav analysisofchromosomaldamagecausedbyacetamiprid AT holeckovab analysisofchromosomaldamagecausedbyacetamiprid |
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