1,2-dibromoethane

Genetic toxicity: in vitro

Administrative data

Endpoint:

in vitro gene mutation study in bacteria

Remarks:

Type of genotoxicity: gene mutation

Type of information:

experimental study

Adequacy of study:

key study

Study period:

not reported.

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

other: Study conducted in accordance with generally accepted scientific principles, possibly with incomplete reporting or methodological deficiencies, which do not affect the quality of the relevant results.

Data source

Reference

Reference Type:

publication

Title:

Further mutagenicity studies on pesticides in bacterial reversion assay systems.

Author:

Moriya, M., Ohta, T., Watanabe, K., Miyazawa, T., Kato, K. & Shirasu, Y.

Year:

1983

Bibliographic source:

Mutation Reseach., 1983, Vol. 116, p.185-216, ©Elsevier Biomedical Press.

Materials and methods

Test guideline

Qualifier:

equivalent or similar to guideline

Guideline:

OECD Guideline 471 (Bacterial Reverse Mutation Assay)

Deviations:

not specified

GLP compliance:

not specified

Type of assay:

bacterial reverse mutation assay

Test material

Test material information

Constituent 1

Reference substance name:

1,2-dibromoethane

EC Number:

203-444-5

EC Name:

1,2-dibromoethane

Cas Number:

106-93-4

Molecular formula:

C2H4Br2

IUPAC Name:

1,2-dibromoethane

Details on test material:

Most of the pesticide samples were obtained from the Agricultural Chemicals Inspection Station of the Ministry of Agriculture, Forestry and Fisheries (Kodaira). They were standard materials obtainable in Japan. Pesticides soluble in water were dissolved in sterile distilled water, and all the other pesticides were dissolved in dimethyl sulfoxide (DMSO).

Method

Target gene:

Salmonella typhimurium: Histidine locus.
Escherichia coli: Tryptophan locus

Species / strain

Species / strain 1

Species / strain / cell type:

S. typhimurium TA 1535, TA 1537, TA 98 and TA 100

Additional strain / cell type characteristics:

other: TA1537 & TA98 frameshift mutation,

Species / strain 2

Species / strain / cell type:

S. typhimurium TA 1538

Additional strain / cell type characteristics:

other: frameshift

Species / strain 3

Species / strain / cell type:

E. coli WP2

Additional strain / cell type characteristics:

not specified

Metabolic activation:

with and without

Metabolic activation system:

S9

Test concentrations with justification for top dose:

Pesticides were tested up to a dose of 5000 µg/plate, unless the compounds showed toxicity to bacteria at the dose. When a pesticide showed mutagenicity only at higher doses such as 1000-5000 µg/plate, the compound was tested at doses of more than 5000 µg/plate to obtain a dose-response relationship.

Vehicle / solvent:

Pesticides soluble in water were dissolved in sterile distilled water, and all the other pesticides were dissolved in dimethyl sulfoxide (DMSO).

Controls

Untreated negative controls:

not specified

Negative solvent / vehicle controls:

not specified

True negative controls:

not specified

Positive controls:

not specified

Positive control substance:

not specified

Details on test system and experimental conditions:

Most procedures were performed according to the methods described by Ames et al. (1975). When the E. coil strain was used, histidine and biotin in top agar were replaced by tryptophan at the same concentration. To 2 ml of the top agar were added 0.1 ml of one of bacterial suspensions in phosphate buffer (1/15 M), 0.1 ml of a solution of a pesticide and, when required, 0.5 ml of the S9 mix (0.3 ml of S9 fraction/ml S9 mix). The contents were poured onto the surface of a minimal agar plate with modified Vogel-Bonnet E medium (Moriya et al., 1978). Plates were incubated at 37°C for 2 days, after which the number of revertant colonies on each plate was counted.
For the gaseous pesticide, methyl bromide, a plate overlaid with the top agar containing one of the strains with or without the S9 mix was placed upside down without a lid in a glass container. Gaseous methyl bromide was injected into the container from a syringe. The container was incubated at 37°C for 2 days with stirring of the inside air by a small electric fan.
Pesticides were tested up to a dose of 5000 /µg/plate, unless the compounds showed toxicity to bacteria at the dose. When a pesticide showed mutagenicity only at higher doses such as 1000-5000/µg/plate, the compound was tested at doses of more than 5000 µg/plate to obtain a dose-response relationship.

Ames, B.N., McCann, J. & Yamasaki, E. (1975) Methods for detecting carcinogens and mutagens with the Salmonella/mammalian-microsome mutagenicity test, Mutation Res., Vol. 31, pp. 347-364.

Moriya, M., Kato, K. & Shirasu, Y. (1978) Effects of cysteine and a liver metabolic activation system on the activities of mutagenic pesticides, Mutation Res., Vol. 57, pp. 259-263.

Evaluation criteria:

not reported.

Statistics:

not reported.

Results and discussion

Test results

Test results 1

Species / strain:

S. typhimurium, other: TA1535, TA100, TA98

Metabolic activation:

without

Genotoxicity:

positive

Cytotoxicity / choice of top concentrations:

not specified

Vehicle controls validity:

not specified

Untreated negative controls validity:

not specified

Positive controls validity:

not specified

Test results 2

Species / strain:

S. typhimurium, other: TA1537, TA1538

Metabolic activation:

without

Genotoxicity:

negative

Cytotoxicity / choice of top concentrations:

not specified

Vehicle controls validity:

not specified

Untreated negative controls validity:

not specified

Positive controls validity:

not specified

Test results 3

Species / strain:

E. coli WP2

Metabolic activation:

without

Genotoxicity:

positive

Cytotoxicity / choice of top concentrations:

not specified

Vehicle controls validity:

not specified

Untreated negative controls validity:

not specified

Positive controls validity:

not specified

Additional information on results:

The mutagenic action of EDB was not greatly affected by the addition of S9 mix.

Remarks on result:

other: strain/cell type:

Remarks:

Migrated from field 'Test system'.

Applicant's summary and conclusion

Conclusions:

Interpretation of results (migrated information):
positive

The test material was found to be mutagenic to S. typhimurium and E. coli both with and without metabolic activation under the conditions of the test.

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