The Ames Salmonella/microsome mutagenicity assay

被引:1571
作者
Mortelmans, K
Zeiger, E
机构
[1] SRI Int, Mol & Genet Toxicol Program, Menlo Park, CA 94025 USA
[2] NIEHS, Environm Toxicol Program, Res Triangle Pk, NC 27709 USA
关键词
Ames Salmonella/microsome mutagenicity assay; Salmonella strains; gene mutation;
D O I
10.1016/S0027-5107(00)00064-6
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 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
The Ames Salmonella/microsome mutagenicity assay (Salmonella test; Ames test) is a short-term bacterial reverse mutation assay specifically designed to detect a wide range of chemical substances that can produce genetic damage that leads to gene mutations. The test employs several histidine dependent Salmonella strains each carrying different mutations in various genes in the histidine operon. These mutations act as hot spots for mutagens that cause DNA damage via different mechanisms. When the Salmonella tester strains are grown on a minimal media agar plate containing a trace of histidine, only those bacteria that revert to histidine independence (his(+)) are able to form colonies. The number of spontaneously induced revertant colonies per plate is relatively constant. However, when a mutagen is added to the plate, the number of revertant colonies per plate is increased, usually in a dose-related manner. The Ames test is used world-wide as an initial screen to determine the mutagenic potential of new chemicals and drugs. The test is also used for submission of data to regulatory agencies for registration or acceptance of many chemicals, including drugs and biocides. International guidelines have been developed for use by corporations and testing laboratories to ensure uniformity of testing procedures. This review provides historical aspects of how the Ames was developed and detailed procedures for performing the test, including the design and interpretation of results. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:29 / 60
页数:32
相关论文
共 95 条
[1]
ACTIVATION OF THE FOOD MUTAGENS IQ AND MEIQ BY HEPATIC S9 FRACTIONS DERIVED FROM VARIOUS SPECIES [J].
ALLDRICK, AJ ;
ROWLAND, IR .
MUTATION RESEARCH, 1985, 144 (02) :59-62
[2]
Ames B.N., 1971, CHEMICAL MUTAGENS PR, P267
[3]
IMPROVED BACTERIAL TEST SYSTEM FOR DETECTION AND CLASSIFICATION OF MUTAGENS AND CARCINOGENS [J].
AMES, BN ;
LEE, FD ;
DURSTON, WE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (03) :782-786
[4]
CARCINOGENS ARE MUTAGENS - SIMPLE TEST SYSTEM COMBINING LIVER HOMOGENATES FOR ACTIVATION AND BACTERIA FOR DETECTION [J].
AMES, BN ;
DURSTON, WE ;
YAMASAKI, E ;
LEE, FD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (08) :2281-2285
[5]
METHODS FOR DETECTING CARCINOGENS AND MUTAGENS WITH SALMONELLA-MAMMALIAN-MICROSOME MUTAGENICITY TEST [J].
AMES, BN ;
MCCANN, J ;
YAMASAKI, E .
MUTATION RESEARCH, 1975, 31 (06) :347-363
[6]
FRAMESHIFT MUTAGENESIS IN SALMONELLA [J].
AMES, BN ;
WHITFIELD, HJ .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1966, 31 :221-+
[7]
THERMODYNAMIC PROPERTIES OF MO-C [J].
ANDERSSON, JO .
CALPHAD-COMPUTER COUPLING OF PHASE DIAGRAMS AND THERMOCHEMISTRY, 1988, 12 (01) :1-8
[8]
[Anonymous], 1976, FUNDAMENTALS CANC PR
[9]
[Anonymous], [No title captured]
[10]
IMPROVED METHOD FOR MUTAGENICITY TESTING OF GASEOUS COMPOUNDS BY USING A GAS SAMPLING BAG [J].
ARAKI, A ;
NOGUCHI, T ;
KATO, F ;
MATSUSHIMA, T .
MUTATION RESEARCH, 1994, 307 (01) :335-344