Use of the single cell gel electrophoresis/comet assay for detecting DNA damage in aquatic (marine and freshwater) animals

被引:466
作者
Lee, RF
Steinert, S
机构
[1] Skidaway Inst Oceanog, Savannah, GA 31411 USA
[2] Comp Sci Corp, CSC Biomarker Lab, San Diego, CA 92110 USA
关键词
single cell gel electrophoresis; comet assays; DNA damage; aquatic; marine; fish;
D O I
10.1016/S1383-5742(03)00017-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The comet assay is a rapid, sensitive and inexpensive method for measuring DNA strand breaks. The comet assay has advantages over other DNA damage methods, such as sister chromatid exchange, alkali elution and micronucleus assay, because of its high sensitivity and that DNA strand breaks are determined in individual cells. This review describes a number of studies that used the comet assay to determine DNA strand breaks in aquatic animals exposed to genotoxicants both in vitro and in vivo, including assessment of DNA damage in aquatic animals collected from contaminated sites. One difficulty of using the comet assay in environmental work is that of comparing results from studies that used different methods, such as empirical scoring or comet tail lengths. There seems to be a consensus in more recent studies to use both the intensity of the tail and the length of the tail, i.e. DNA tail moment, percentage of DNA in the tail. The comet assay has been used to assess DNA repair and apoptosis in aquatic animals and modifications of the comet assay have allowed the detection of specific DNA lesions. There have been some recent studies to link DNA strand breaks in aquatic animals to effects on the immune system, reproduction, growth, and population dynamics. Further work is required before the comet assay can be used as a standard bio-indicator in aquatic environments, including standardization of methods (such as ASTM method E2186-02a) and measurements. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:43 / 64
页数:22
相关论文
共 155 条
[51]  
Heflich R.H., 1991, GENETIC TOXICOLOGY, P143
[52]   Two- and one-electron dependent in vitro reductive metabolism of nitroaromatics by Mytilus edulis, Carcinus maenas and Asterias rubens [J].
Hetherington, LH ;
Livingstone, DR ;
Walker, CH .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY, 1996, 113 (02) :231-239
[53]   Cytochromes P450 in crustacea [J].
James, MO ;
Boyle, SM .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY, 1998, 121 (1-3) :157-172
[54]   MICRONUCLEUS TEST AS PART OF A SHORT-TERM MUTAGENICITY TEST PROGRAM FOR THE PREDICTION OF CARCINOGENICITY EVALUATED BY 143 AGENTS TESTED [J].
JENSSEN, D ;
RAMEL, C .
MUTATION RESEARCH, 1980, 75 (02) :191-202
[55]   THE PHOTOTOXICITY OF NITRO POLYCYCLIC AROMATIC-HYDROCARBONS OF ENVIRONMENTAL IMPORTANCE [J].
KAGAN, J ;
WANG, TP ;
BENIGHT, AS ;
TUVESON, RW ;
WANG, GR ;
FU, PP .
CHEMOSPHERE, 1990, 20 (05) :453-466
[56]   THE PHOTOTOXICITY OF NONCARCINOGENIC POLYCYCLIC AROMATIC-HYDROCARBONS IN AQUATIC ORGANISMS [J].
KAGAN, J ;
KAGAN, ED ;
KAGAN, IA ;
QUIGLEY, S .
CHEMOSPHERE, 1985, 14 (11-12) :1829-1834
[57]   Genotoxic potential of marine sediments from the North Sea [J].
Kammann, U ;
Riggers, JC ;
Theobald, N ;
Steinhart, H .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2000, 467 (02) :161-168
[59]   A CRITICAL-REVIEW OF PERMEABILIZED CELL SYSTEMS FOR STUDYING MAMMALIAN DNA-REPAIR [J].
KEENEY, S ;
LINN, S .
MUTATION RESEARCH, 1990, 236 (2-3) :239-252
[60]   Damage to grass shrimp (Palaemonetes pugio) embryo DNA by summer sunlight followed by DNA repair in the dark [J].
Kim, GB ;
Lee, RF ;
Mitchell, DL .
MARINE BIOLOGY, 2000, 137 (04) :675-682