Vajpayee Poornima, Dhawan Alok, Shanker Rishi
Environmental Microbiology Division, Industrial Toxicology Research Centre, Lucknow-226001, Uttar Pradesh, India.
Environ Mol Mutagen. 2006 Aug;47(7):483-9. doi: 10.1002/em.20217.
Wetlands play a key role in maintaining environmental quality, and wetlands plants could serve as model organisms for determining the genotoxic effects of pollutants contaminating these areas. In the present study, DNA damage was evaluated in a wetlands plant, Bacopa monnieri L., as a potential tool for the assessment of ecogenotoxicity. The Comet assay was used for detecting DNA damage in B. monnieri exposed to two model mutagens, ethyl methanesulfonate (EMS) and methyl methanesulfonate (MMS). Significant (P < 0.05) dose-dependent increases in DNA damage were observed following treatments conducted by exposing both isolated nuclei (acellular or in vitro exposure) and whole plants (in vivo exposure) to 0.01-5 mM EMS and 0.05-100 microM MMS for 2 hr at (26 +/- 2) degrees C. The assay was then used to evaluate the genotoxic potential of cadmium (Cd), a wetlands contaminant. In vitro exposure of nuclei from untreated leaves to 0.001-200 microM Cd for 2 hr resulted in significant (P < 0.05) levels of DNA damage. Cd concentrations >or=0.01 microM induced DNA damage as evidenced by increases in the Olive tail moment. In vivo exposure of plants to 0.01-500 microM Cd for 2, 4, and 18 hr resulted in dose- and time-dependent increases in DNA damage in the nuclei isolated from roots and leaves. Cd-induced DNA damage was greater in roots than leaves. To our knowledge, this is the first report describing the use of a wetlands plant for genotoxicity assessment, using the Comet assay.
湿地在维持环境质量方面发挥着关键作用,湿地植物可作为模式生物,用于确定污染这些区域的污染物的遗传毒性效应。在本研究中,对湿地植物水薄荷(Bacopa monnieri L.)的DNA损伤进行了评估,将其作为评估生态遗传毒性的一种潜在工具。彗星试验用于检测暴露于两种模式诱变剂甲磺酸乙酯(EMS)和甲磺酸甲酯(MMS)的水薄荷的DNA损伤。在(26±2)℃下,将分离的细胞核(无细胞或体外暴露)和整株植物(体内暴露)暴露于0.01 - 5 mM EMS和0.05 - 100 μM MMS中2小时后,观察到DNA损伤随剂量显著(P < 0.05)增加。然后该试验用于评估湿地污染物镉(Cd)的遗传毒性潜力。将未处理叶片的细胞核在体外暴露于0.001 - 200 μM Cd中2小时,导致DNA损伤达到显著(P < 0.05)水平。Cd浓度≥0.01 μM时诱导了DNA损伤,如橄榄尾矩增加所示。将植物在体内暴露于0.01 - 500 μM Cd中2、4和18小时,导致从根和叶中分离的细胞核中的DNA损伤随剂量和时间增加。Cd诱导的DNA损伤在根中比在叶中更大。据我们所知,这是第一篇描述使用彗星试验,利用湿地植物进行遗传毒性评估的报告。