环境 DNA 能否用于害虫农业生物安全?检测储藏稻米中的甲虫

Q1 Agricultural and Biological Sciences Environmental DNA Pub Date : 2024-07-09 DOI:10.1002/edn3.585
Anthony R. Vastano, Michael C. Allen, Cory J. Penca, Oliver C. Stringham, Michael J. Domingue, Julie L. Lockwood
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引用次数: 0

摘要

环境 DNA(eDNA)近来已成为入侵物种生物安全的有效工具。我们探索了利用 eDNA 检测卡普拉甲虫(Trogoderma granarium,Everts 1898)的方法,卡普拉甲虫是一种入侵谷物和其他食品的昆虫,对全球经济影响很大。我们开发了一种新方法来聚集沉积在储藏谷物中的卡布拉甲虫 eDNA,该方法需要清洗大米样品、过滤样品,并使用标准 qPCR 工作流程检测甲虫的痕量 DNA。为了探索这种方法的性能,我们在 500 克大米中饲养了 500 只卡帕甲虫幼虫,为期 14 天,然后将其取出。然后,我们用这种 "加标 "大米创建了一系列卡布拉甲虫幼虫的模拟密度。这种实验室方法模拟的条件与每 50 千克稻米中约 1.4 到 180 只甲虫的田间密度相当(每 100 克干净稻米样品中含 1/8 到 16 个加标米粒),假定 DNA 在稻米中均匀分布。我们在测试的所有密度水平上都检测到了卡帕甲虫的 eDNA。逻辑模型显示,根据每个样品运行的 qPCR 技术重复次数,可以以 85% 到 97% 的确定性检测到相当于 50 千克稻米容器中约 1 只卡布拉甲虫幼虫残留的 eDNA 量。根据这一模型,我们估计,对于甲虫 DNA 分布均匀的 50 千克稻米容器,一个 100 克的样本加上 6 个技术重复,就足以>99%地确定容器中没有甲虫 eDNA(95% 可信区间:97.7%-100%)。我们的研究结果表明,eDNA 调查可作为检测贮藏谷物中卡布拉甲虫的经济有效的第一步,并提供了一种绘制卡布拉甲虫运输途径相对规模图的方法,为常规生物安全检查工作的分配提供信息。
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Can environmental DNA be used within pest insect agricultural biosecurity? Detecting khapra beetle within stored rice

Environmental DNA (eDNA) has recently emerged as an effective tool for invasive species biosecurity. We explored the use of eDNA for the detection of khapra beetle (Trogoderma granarium, Everts 1898), an invasive insect of cereal grains and other food products that has a high global economic impact. We developed a novel method for aggregating khapra beetle eDNA deposited in stored grain that entails washing a sample of rice, filtering the sample, and detecting trace beetle DNA using a standard qPCR workflow. To explore the performance of this method, we raised 500 khapra beetle larvae within 500 g of rice over a 14-day period and then removed them. We then used this “spiked” rice to create a range of simulated densities of khapra beetle larvae. This lab approach mimics conditions that are comparable to field densities of ~1.4 to 180 beetles per 50 kg of rice (1/8 to 16 spiked rice grains per 100 g sample of clean rice), assuming DNA is uniformly distributed within the rice. We detected khapra beetle eDNA from all density levels tested. Logistic models revealed that eDNA amounts equivalent to what is left by ~1 khapra beetle larva in a 50 kg container of rice can be detected with 85% to >97% certainty, depending on the number of qPCR technical replicates run per sample. Based on this model, we estimated that for one 50 kg container of rice where beetle DNA is uniformly distributed, a single sample of 100 g with six technical replicates would be sufficient to be >99% certain that the container was free of khapra beetle eDNA (95% credible intervals: 97.7%–100%). Our results suggest that eDNA surveys may be useful as a cost-effective, first-step detection of khapra beetle in stored grain and provide a means to map the relative magnitude of khapra beetle transport pathways, informing allocation of conventional biosecurity inspection efforts.

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来源期刊
Environmental DNA
Environmental DNA Agricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
11.00
自引率
0.00%
发文量
99
审稿时长
16 weeks
期刊最新文献
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