Laboratoire de Biologie et de Pathologie Végétales EA 1157, SFR 4207 QUASAV, Nantes University, 44322 Nantes, France.
Plant Methods. 2013 Aug 6;9(1):32. doi: 10.1186/1746-4811-9-32.
Some root-parasitic plants belonging to the Orobanche, Phelipanche or Striga genus represent one of the most destructive and intractable weed problems to agricultural production in both developed and developing countries. Compared with most of the other weeds, parasitic weeds are difficult to control by conventional methods because of their life style. The main difficulties that currently limit the development of successful control methods are the ability of the parasite to produce a tremendous number of tiny seeds that may remain viable in the soil for more than 15 years. Seed germination requires induction by stimulants present in root exudates of host plants. Researches performed on these minute seeds are until now tedious and time-consuming because germination rate is usually evaluated in Petri-dish by counting germinated seeds under a binocular microscope.
We developed an easy and fast method for germination rate determination based on a standardized 96-well plate test coupled with spectrophotometric reading of tetrazolium salt (MTT) reduction. We adapted the Mosmann's protocol for cell cultures to germinating seeds and determined the conditions of seed stimulation and germination, MTT staining and formazan salt solubilization required to obtain a linear relationship between absorbance and germination rate. Dose-response analyses were presented as applications of interest for assessing half maximal effective or inhibitory concentrations of germination stimulants (strigolactones) or inhibitors (ABA), respectively, using four parameter logistic curves.
The developed MTT system is simple and accurate. It yields reproducible results for germination bioassays of parasitic plant seeds. This method is adapted to high-throughput screenings of allelochemicals (stimulants, inhibitors) or biological extracts on parasitic plant seed germination, and strengthens the investigations of distinctive features of parasitic plant germination.
列当属、独脚金属莲属或菟丝子属的一些根寄生植物是发达国家和发展中国家农业生产中最具破坏性和最难解决的杂草问题之一。与大多数其他杂草相比,寄生杂草由于其生活方式,很难通过常规方法控制。目前,限制成功控制方法发展的主要困难是寄生虫产生大量微小种子的能力,这些种子在土壤中可能存活超过 15 年。种子发芽需要由宿主植物根分泌物中存在的刺激物诱导。到目前为止,对这些微小种子的研究由于发芽率通常在双筒显微镜下通过计数发芽种子在培养皿中进行评估而繁琐且耗时。
我们开发了一种简单快速的发芽率测定方法,基于标准化的 96 孔板试验,结合四唑盐(MTT)还原的分光光度读数。我们适应了 Mosmann 的细胞培养物方案来发芽种子,并确定了种子刺激和发芽的条件、MTT 染色和甲臜盐溶解所需的条件,以获得吸光度与发芽率之间的线性关系。剂量反应分析分别作为评估发芽刺激剂(独脚金属莲内酯)或抑制剂(ABA)的半最大有效或抑制浓度的应用进行了介绍,使用四参数逻辑曲线。
开发的 MTT 系统简单准确。它为寄生植物种子的发芽生物测定提供了可重复的结果。该方法适用于寄生植物种子发芽的化感物质(刺激物、抑制剂)或生物提取物的高通量筛选,并加强了寄生植物发芽特征的研究。