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Detecting ingested plant DNA in soil-living insect larvae

机译:检测生活在土壤中的昆虫幼虫中的植物DNA

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摘要

Although a significant proportion of plant tissue is located in roots and other below-ground parts of plants, little is known on the dietary choices of root-feeding insects. This is caused by a lack of adequate methodology which would allow tracking below-ground trophic interactions between insects and plants. Here, we present a DNA-based approach to examine this relationship. Feeding experiments were established where either wheat (Triticum aestivum) or maize (Zea mays) was fed to Agriotes larvae (Coleoptera: Elateridae), allowing them to digest for up to 72 h. Due to the very small amount of plant tissue ingested (max = 6.76 mg), DNA extraction procedures and the sensitivity of polymerase chain reaction (PCR) had to be optimized. Whole-body DNA extracts of larvae were tested for the presence of both rbcL and trnL plastid DNA using universal primers. Moreover, based on cpDNA sequences encoding chloroplast tRNA for leucine (trnL), specific primers for maize and wheat were developed. With both, general and specific primers, plant DNA was detectable in the guts of Agriotes larvae for up to 72 h post-feeding, the maximum time of digestion in these experiments. No significant effect of time since feeding on plant DNA detection success was observed, except for the specific primers in maize-fed larvae. Here, plant DNA detection was negatively correlated with the duration of digestion. Both, meal size and initial mass of the individual larvae did not affect the rate of larvae testing positive for plant DNA. The outcomes of this study represent a first step towards a specific analysis of the dietary choices of soil-living herbivores to further increase our understanding of animal–plant feeding interactions in the soil.
机译:尽管很大一部分植物组织都位于植物的根部和其他地下部分,但在以根为食的昆虫的饮食选择上知之甚少。这是由于缺乏足够的方法来跟踪昆虫与植物之间的地下营养相互作用所致。在这里,我们提出了一种基于DNA的方法来检查这种关系。建立了将小麦(Triticum aestivum)或玉米(Zea mays)喂入Agriotes幼虫(Coleoptera:Elateridae)的饲喂实验,使它们消化长达72小时。由于摄入的植物组织非常少(最大= 6.76 mg),因此必须优化DNA提取程序和聚合酶链反应(PCR)的敏感性。使用通用引物测试幼虫的全身DNA提取物是否存在rbcL和trnL质体DNA。此外,基于亮氨酸(trnL)编码叶绿体tRNA的cpDNA序列,开发了玉米和小麦的特异性引物。使用普通引物和特异性引物,在喂食后长达72小时(这是这些实验中的最大消化时间)后,在Agriotes幼虫的肠道中可检测到植物DNA。除了饲喂玉米幼虫的特异性引物外,自喂食以来对植物DNA检测成功的时间没有显着影响。在这里,植物DNA检测与消化时间负相关。幼虫的进食量和初始质量均不影响幼虫对植物DNA呈阳性反应的速率。这项研究的结果代表着对生活在土壤中的食草动物的饮食选择进行具体分析的第一步,以进一步增进我们对土壤中植物与植物之间的进食相互作用的理解。

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