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Diss Factsheets

Administrative data

Endpoint:
in vitro gene mutation study in bacteria
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2019-11-29 to 2020-02-24
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2020
Report date:
2020

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
Version / remarks:
adopted 21 July, 1997
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
Manganate(1-), glycinato-N,O)[sulfato(2-)-O]-, hydrogen
EC Number:
838-538-0
Cas Number:
52139-31-8
Molecular formula:
C2H5MnNO6S
IUPAC Name:
Manganate(1-), glycinato-N,O)[sulfato(2-)-O]-, hydrogen

Method

Target gene:
his locus
Species / strainopen allclose all
Species / strain / cell type:
S. typhimurium TA 1537
Additional strain / cell type characteristics:
not applicable
Species / strain / cell type:
S. typhimurium TA 1535
Additional strain / cell type characteristics:
not applicable
Species / strain / cell type:
S. typhimurium TA 102
Additional strain / cell type characteristics:
not applicable
Species / strain / cell type:
S. typhimurium TA 100
Additional strain / cell type characteristics:
not applicable
Species / strain / cell type:
S. typhimurium TA 98
Additional strain / cell type characteristics:
not applicable
Metabolic activation:
with and without
Metabolic activation system:
Type and composition of metabolic activation system: S9 liver Mix
- source of S9 : S9 was obtained by Trinova Biochem GmbH, Gießen.
- method of preparation of S9 mix: produced from the livers of male Sprague-Dawley rats which were treated with 500 mg Aroclor 1254/kg body weight intra-peritoneally.
- concentration or volume of S9 mix and S9 in the final culture medium: 500µL
Test concentrations with justification for top dose:
nominal concentrations: 0, 50, 150, 500, 1500, 5000 µg/plate Experiment 1 and 0, 78, 156, 313, 625, 1250, 2500, 5000 /plate Experiment 2
Vehicle / solvent:
- Vehicle(s)/solvent(s) used: DMSO; demineralized water
- Justification for choice of solvent/vehicle: DMSO was chosen due to the solubility of the positive controls 4-Nitro-1,2-phenylene diamine, benzo-a-pyrene and 2-amino anthracene
Controls
Untreated negative controls:
no
Negative solvent / vehicle controls:
yes
True negative controls:
no
Positive controls:
yes
Positive control substance:
sodium azide
benzo(a)pyrene
other: 4-Nitro-1,2-phenylene diamine: without metabolic activation, TA98, TA102, TA1537, 20 µg (TA98) and 30 µg (TA102 and TA1537) 2-Amino-anthracene: with metabolic activation, TA 100, TA102, TA1535, TA1537, 1µg (TA100, TA1535) and 2.4 µg (TA102, TA1537)
Details on test system and experimental conditions:
NUMBER OF REPLICATIONS:
- Number of cultures per concentration: triplicate for each with and without metabolic acitvation
- Number of independent experiments : 2

METHOD OF TREATMENT/ EXPOSURE:
- Cell density at seeding (if applicable): > E+09 cells/mL
- Test substance added in agar (plate incorporation)and in the second experiment with preincubation


METHODS FOR MEASUREMENT OF CYTOTOXICITY
- Method: background growth inhibition
- Any supplementary information relevant to cytotoxicity: No cytotoxicity nor precipitation occurred with the test item during the experimental time.

Rationale for test conditions:
as recommended by OECD Testguideline 471
Evaluation criteria:
The colonies were counted visually and the numbers were recorded. A substance is considered to be mutagenic, if a reproducible increase with or without metabolic activation of revertant colonies per plate exceeding an increase factor of 2 for the bacteria strains TA98, TA100, TA102, TA1535 and TA1537 compared to vehicle controls in at least one strain can be observed. A concentration-related increase over the range tested is also taken as a sign of mutagenic activity. A substance is not mutagenic if it does not meet these criteria. If the criteria listed above are not clearly met, the results will be assessed as equivocal and will be discussed.
Statistics:
The colonies were counted visually and the numbers were recorded. A validated spread-sheet software (Microsoft Excel®) was used to calculate mean values and standard deviations of each treatment, solvent control and positive control.

Results and discussion

Test resultsopen allclose all
Key result
Species / strain:
S. typhimurium TA 1537
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
Vehicle controls validity:
valid
Untreated negative controls validity:
not examined
True negative controls validity:
not examined
Positive controls validity:
valid
Remarks:
The positive control of strain TA 1537 was slightly outside the historical data. However, since the number of revetants was increased this was not considered to reduce the validity of the test result.
Key result
Species / strain:
S. typhimurium TA 1535
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
Vehicle controls validity:
valid
Untreated negative controls validity:
not examined
True negative controls validity:
not examined
Positive controls validity:
valid
Key result
Species / strain:
S. typhimurium TA 102
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
Vehicle controls validity:
valid
Untreated negative controls validity:
not examined
True negative controls validity:
not examined
Positive controls validity:
valid
Key result
Species / strain:
S. typhimurium TA 100
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
Vehicle controls validity:
valid
Untreated negative controls validity:
not examined
True negative controls validity:
not examined
Positive controls validity:
valid
Key result
Species / strain:
S. typhimurium TA 98
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
Vehicle controls validity:
valid
Untreated negative controls validity:
not examined
True negative controls validity:
not examined
Positive controls validity:
valid
Additional information on results:
TEST-SPECIFIC CONFOUNDING FACTORS
- Data on pH: not reported
- Water solubility: The test item is not completely soluble in a concentration of 50 g/L in any of the solvents directly after preparation. But after a storage of 24 hours at room temperature (20 ± 5 °C)
and vortexing, the test item in demin. water appeared soluble.

RANGE-FINDING/SCREENING STUDIES (if applicable):
In a non-GLP pre-test, the solubility of the test item was tested in a concentration of 50 g/L in demineralised (demin.) water, dimethyl sulfoxide (DMSO), acetone, ethanol and tetrahydrofuran (THF). The test item is not completely soluble in a concentration of 50 g/L in any of the solvents directly after preparation. But after a storage of 24 hours at room temperature (20 ± 5 °C)
and vortexing, the test item in demin. water appeared soluble. Based on these results of the non-GLP pre-test, a test item suspension containing 50 ± 5 g/L in demin. water was prepared

STUDY RESULTS
- Concurrent vehicle negative and positive control data Please refer to 'Any other infomation on results incl. tables'


Ames test:
- Signs of toxicity : No
- Individual plate counts : Please refer to 'Any other information on results incl. tables'.
- Mean number of revertant colonies per plate and standard deviation: Please refer to 'Any other information on results incl. tables'.


HISTORICAL CONTROL DATA (with ranges, means and standard deviation, and 95% control limits for the distribution as well as the number of data)
- Positive historical control data: Please refer to 'Any other information on results incl. tables'.
- Negative (solvent/vehicle) historical control data: Please refer to 'Any other information on results incl. tables'.

Any other information on results incl. tables

Table 1: Number of revertants per plate (mean of 3 plates), first experiment

 

 

TA98

 

TA100

TA102

 

TA1535

 

TA1537

Conc.
[µg] per plate

— MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

+ MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

— MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

+ MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

— MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

+ MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

— MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

+ MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

— MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

+ MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

DMSO

13

no

16

no

60

no

69

no

259

no

277

no

17

no

13

no

9

no

8

no

0*

 15

 no

15

 no

71

 no

73

 no

264

no

275

no

10

no

18

no

7

 no

9

 no

50

 12

 no

16

 no

63

 no

67

 no

309

no

293

no

8

no

11

no

7

 no

8

 no

150

 13

 no

15

 no

67

 no

61

 no

317

no

320

no

14

no

12

no

7

 no

8

 no

500

 9

 no

12

 no

72

 no

77

 no

299

no

291

no

14

no

15

no

8

 no

10

 no

1500

 10

 no

14

 no

71

 no

86

 no

285

no

317

no

13

no

10

no

7

 no

8

 no

5000

 11

 no

10

 no

103

 no

87

 no

296

no

285

no

8

no

13

no

8

 no

8

 no

Positive control

 sg

 no

98

 no

sg

 no

sg

 no

605

no

sg

no

221

no

175

no

232

 no

168

 no

*solvent/vehicle control with water

Table 2: Number of revertants per plate (mean of 3 plates), second experiment

 

 

TA98

 

TA100

TA102

 

TA1535

 

TA1537

Conc.
[µg] per plate

— MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

+ MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

— MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

+ MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

— MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

+ MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

— MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

+ MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

— MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

+ MA

Cytotoxic
(yes/no)

Precipitates

(yes/no)

DMSO

18

no

20

no

81

no

83

no

355

no

365

no

9

no

12

no

6

no

8

no

0*

20

no

19

no

91

no

89

no

371

no

376

no

10

no

10

no

5

no

8

no

78

13

 no

16

 no

71

 no

75

 no

341

no

328

no

9

no

8

no

5

 no

5

 no

156

11

 no

12

 no

68

 no

72

 no

333

no

325

no

10

no

9

no

5

 no

5

 no

313

12

 no

12

 no

72

 no

71

 no

349

no

355

no

9

no

9

no

5

 no

5

 no

625

19

 no

16

 no

75

 no

71

 no

360

no

339

no

6

no

9

no

5

 no

5

 no

1250

15

 no

18

 no

79

 no

85

 no

347

no

336

no

8

no

5

no

4

 no

5

 no

2500

13

no

20

no

83

no

81

no

355

no

325

no

7

no

9

no

4

no

5

no

5000

19

no

18

no

91

no

87

no

339

no

325

no

6

no

7

no

5

no

4

no

Positive control

sg

 no

111

 no

sg

 no

sg

 no

765

no

872

no

248

no

167

no

152

 no

160

 no

*solvent/vehicle control with water

Concurrent conttrols

DMSO Experiment 1/Vehicle control

Strain

TA98

TA100

TA102

TA1535

TA1537

Induction

-S9

+S9

-S9

+S9

-S9

+S9

-S9

+S9

-S9

+S9

Repl.1

11

15

60

62

256

288

15

15

11

8

Repl.2

14

13

62

80

272

264

17

10

8

9

Repl.3

14

19

58

66

248

280

18

14

8

8

Mean

13

16

60

69

259

277

17

13

9

8

sd

1.7

3.1

2.0

9.5

12.2

12.2

1.5

2.6

1.7

0.6

Demin Water Experiment 1/Vehicle control

Strain

TA98

TA100

TA102

TA1535

TA1537

Induction

-S9

+S9

-S9

+S9

-S9

+S9

-S9

+S9

-S9

+S9

Repl.1

15

18

62

70

280

9

17

8

9

 

Repl.2

13

10

78

72

248

272

9

17

8

10

Repl.3

16

17

72

76

264

272

12

19

6

8

Mean

15

15

71

73

264

275

10

18

7

9

sd

1.5

4.4

8.1

3.1

16.0

4.6

1.7

1.2

1.2

1.0

Positive control Experiment 1

Strain

TA98

TA100

TA102

TA1535

TA1537

Induction

-S9

+S9

-S9

+S9

-S9

+S9

-S9

+S9

-S9

+S9

Substance

NPD

BaP

Na-azide

2-AA

NPD

2-AA

Na-azide

2-AA

NPD

2-AA

Repl.1

s.g.

100

s.g.

s.g.

576

s.g.

220

180

232

160

Repl.2

s.g.

80

s.g.

s.g.

608

s.g.

228

172

240

192

Repl.3

s.g.

114

s.g.

s.g.

632

s.g.

216

172

224

152

Mean

--

98

--

--

605

--

221

175

232

168

sd

--

17.1

--

--

28.1

--

6.1

4.6

8.0

21.2

f(l)

>2

6.13

>2

>2

2.34

>2

22.10

13.46

25.78

21.00

Rev. abs.

--

82

--

--

346

--

211

162

223

160

s.g.= strong growth, too strong for counting of revertants

f(l) = increase factor

Rev.abs. = absolute revertants

Demin. Water Experiment 2/Vehicle control

Strain

TA98

TA100

TA102

TA1535

TA1537

Induction

-S9

+S9

-S9

+S9

-S9

+S9

-S9

+S9

-S9

+S9

Repl.1

19

20

96

96

352

368

9

10

6

9

Repl.2

20

19

92

92

384

384

12

10

5

7

Repl.3

20

19

84

80

376

376

10

11

4

7

Mean

20

19

91

89

371

376

10

10

5

8

sd

0.6

0.6

6.1

8.3

16.7

8.0

1.5

0.6

1.0

1.2

DMSO Experiment 2/Vehicle control

Strain

TA98

TA100

TA102

TA1535

TA1537

Induction

-S9

+S9

-S9

+S9

-S9

+S9

-S9

+S9

-S9

+S9

Repl.1

18

19

76

80

352

360

9

11

6

9

Repl.2

18

20

80

84

360

368

8

15

6

6

Repl.3

18

21

88

84

352

368

10

10

6

8

Mean

18

20

81

83

355

365

9

12

6

8

sd

0.0

1.0

6.1

2.3

4.6

4.6

1.0

2.6

0.0

1.5

Positive control Experiment 2

Strain

TA98

TA100

TA102

TA1535

TA1537

Induction

-S9

+S9

-S9

+S9

-S9

+S9

-S9

+S9

-S9

+S9

Substance

NPD

BaP

Na-azide

2-AA

NPD

2-AA

Na-azide

2-AA

NPD

2-AA

Repl.1

s.g.

112

s.g.

s.g.

752

856

240

164

156

168

Repl.2

s.g.

112

s.g.

s.g.

768

864

264

168

132

168

Repl.3

s.g.

108

s.g.

s.g.

776

896

240

168

168

144

Mean

--

111

--

--

765

872

248

167

152

160

sd

--

2.3

--

--

12.2

21.2

13.9

2.3

18.3

13.9

f(l)

>2

5.55

>2

>2

2.15

2.39

24.80

13.92

25.33

20.00

Rev. abs.

--

91

--

--

410

507

238

155

146

152

s.g.= strong growth, too strong for counting of revertants

f(l) = increase factor

Rev.abs. = absolute revertants

Applicant's summary and conclusion

Conclusions:
There was no evidence of induced mutant colonies over background, when manganese monoglycinate sulfate was tested with and without metabolic activation up to the recommended limit concentration (5000 µg/plate).
Executive summary:

In a reverse gene mutation assay in bacteria according to EU Method B.14 (Version Commission Directive 92/69/EEC), strains TA1535, TA 1537, TA 102, TA 100 and TA 98of S. typhimurium were exposed to manganese monoglycinate sulfate. Test was performed with concentrations up to the recommended limit concentration of 5000 µg/plate in the absence and the presence of mammalian metabolic activation

 

No evidence of biologically significant mutagenic activity of the test item was found in the presence and absence of metabolic activation, up to the limit concentration of 5000 µg/plate. The positive controls induced the appropriate responses in the corresponding strains and activity of metabolizing system was confirmed.

 

There was no evidence of induced mutant colonies over background.

 

The adopted OECD TG 471 (1997) requires at least 5 test strains and the use of E. coli WP2 strains or Salmonella typhimurium TA 102 to detect certain oxidizing mutagens, cross-linking agents and hydrazines. However, manganese glycinate sulfate is not a highly reactive agent and is therefore not expected to be a cross-linking agent, has no oxidizing properties and is no hydrazine. Thus, a test according to EU Method B.13/14 (Version Commission Directive 92/69/EEC without E. coli WP2 strains or Salmonella typhimurium TA 102 is considered as sufficient to evaluate the mutagenic activity of manganese glycinate sulfate in this bacterial test system.