M. De Méo , M. Laget , C. Di Giorgio , H. Guiraud , A. Botta , M. Castegnaro , G. Duménil
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The response was limited to the induction factor (IF, number of induced revertants/number of spontaneous revertants) with <em>Salmonella typhimurium</em> TA98. The optimal conditions for BaP were: a 60 min period of liquid incubation and a volume of 0.1 ml (approx. 10<sup>8</sup> cells/plate) of an overnight culture grown in 50 ml of Nutrient Broth No. 2 from a 250 ml flask. The S9 mix (0.1 ml, final volume) included 1.5% of S9, 1.0 mM NADP and 4.4 mM G6P. The maximal IF was 15.79. The optimal conditions for SU were: a 60 min period of liquid incubation and a volume of 0.1 ml (approx. 10<sup>8</sup> cells/plate) of an overnight culture grown in 7 ml of Nutrient Broth No. 2 from a 20 × 180 mm tube. The S9 mix (0.1 ml, final volume) included: 4% S9, 4.2 mM NADP and 5.2 mM G6P. The maximal I7F was 10.95. These optimal conditions did not modify the spontaneous frequencies of the tester strains: TA97a, TA98, TA100 and TA102. The dose-response curves of mutagenic urine samples were found to be non-linear. This micromethod required 8-fold less urine sample and 12.5-fold less liver homogenate as compared to the standard plate incorporation assay and was from 6.2- to 11.8-fold more sensitive to evaluate urine mutagenicity. The sensitivity of this technique was found to be limited to individuals smoking more than approx. 5 cigarettes/day by the standard extraction-concentration procedure.</p></div>","PeriodicalId":100940,"journal":{"name":"Mutation Research/Reviews in Genetic Toxicology","volume":"340 2","pages":"Pages 51-65"},"PeriodicalIF":0.0000,"publicationDate":"1996-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0165-1110(96)90039-1","citationCount":"43","resultStr":"{\"title\":\"Optimization of the Salmonella/mammalian microsome assay for urine mutagenesis by experimental designs\",\"authors\":\"M. De Méo , M. 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引用次数: 43
摘要
用沙门氏菌致突变性试验评估尿液的致突变性常常受到样本量的限制。采用析因设计和Doehlert设计对试验进行优化。采用2个分数因子设计23-1(3因素,4个试验)来评估S9在混合物中所占的百分比、孵育时间、接种量和生长条件的主要影响。采用Doehlert设计(3因素,13个试验)研究混合料中NADP、G6P和S9的主要作用及其相互作用。阳性标记物为苯并[a]芘(BaP, 0.3 μg/plate)和一池吸烟者尿液(SU, 1.25 ml当量/plate)。鼠伤寒沙门菌TA98的诱导因子(IF,诱导复归物数/自发复归物数)限制了应答。BaP的最佳条件为:液体孵育60 min,体积为0.1 ml(约为10ml)。108个细胞/板)在250ml烧瓶中的50ml 2号营养液中培养过夜。S9混合物(0.1 ml,终体积)含有1.5%的S9, 1.0 mM NADP和4.4 mM G6P。最大IF为15.79。SU的最佳条件为:液体孵育60分钟,体积为0.1 ml(约1 ml)。从一个20 × 180 mm的管中培养7 ml 2号营养液,培养108个细胞/板。S9混合物(0.1 ml,终体积)包括:4% S9, 4.2 mM NADP和5.2 mM G6P。最大I7F为10.95。这些优化条件对TA97a、TA98、TA100和TA102的自发频率没有影响。结果表明,致突变尿样的剂量-反应曲线呈非线性。与标准平板掺入法相比,该方法所需尿液样品减少了8倍,肝脏匀浆减少了12.5倍,评估尿液致突变性的敏感性提高了6.2- 11.8倍。研究发现,这种技术的敏感性仅限于吸烟人数超过大约的个人。5支/天,按标准提取-浓缩程序。
Optimization of the Salmonella/mammalian microsome assay for urine mutagenesis by experimental designs
Assessing urine mutagenicity with the Salmonella mutagenicity test is often limited by the volumes of the samples. Optimization of the assay was performed with factorial and Doehlert designs. Two fractional factorial designs 23-1 (3 factors, 4 experiments) were used to estimate the main effects of the percent S9 in the mix, the time of liquid incubation, the inoculum size and the growth conditions. A Doehlert design (3 factors, 13 experiments) was used to study the main effects and the interactions of the NADP, G6P and S9 in the mix. The positive markers were benzo[a]pyrene (BaP, 0.3 μg/plate) and a pool of smokers' urine (SU, 1.25 ml equivalent/plate). The response was limited to the induction factor (IF, number of induced revertants/number of spontaneous revertants) with Salmonella typhimurium TA98. The optimal conditions for BaP were: a 60 min period of liquid incubation and a volume of 0.1 ml (approx. 108 cells/plate) of an overnight culture grown in 50 ml of Nutrient Broth No. 2 from a 250 ml flask. The S9 mix (0.1 ml, final volume) included 1.5% of S9, 1.0 mM NADP and 4.4 mM G6P. The maximal IF was 15.79. The optimal conditions for SU were: a 60 min period of liquid incubation and a volume of 0.1 ml (approx. 108 cells/plate) of an overnight culture grown in 7 ml of Nutrient Broth No. 2 from a 20 × 180 mm tube. The S9 mix (0.1 ml, final volume) included: 4% S9, 4.2 mM NADP and 5.2 mM G6P. The maximal I7F was 10.95. These optimal conditions did not modify the spontaneous frequencies of the tester strains: TA97a, TA98, TA100 and TA102. The dose-response curves of mutagenic urine samples were found to be non-linear. This micromethod required 8-fold less urine sample and 12.5-fold less liver homogenate as compared to the standard plate incorporation assay and was from 6.2- to 11.8-fold more sensitive to evaluate urine mutagenicity. The sensitivity of this technique was found to be limited to individuals smoking more than approx. 5 cigarettes/day by the standard extraction-concentration procedure.