首页> 外文期刊>Journal of Invertebrate Pathology >Entomopathogenic nematodes, phoretic Paenibacillus spp., and the use of real time quantitative PCR to explore soil food webs in Florida citrus groves.
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Entomopathogenic nematodes, phoretic Paenibacillus spp., and the use of real time quantitative PCR to explore soil food webs in Florida citrus groves.

机译:致病性线虫,幽闭的杆状线虫菌种以及使用实时定量PCR来探索佛罗里达柑橘园的土壤食物网。

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摘要

Quantitative real-time PCR (qPCR) is a powerful tool to detect and quantify species of cryptic organisms such as bacteria, fungi and nematodes from soil samples. As such, qPCR offers new opportunities to study the ecology of soil habitats by providing a single method to characterize communities of diverse organisms from a sample of DNA. Here we describe molecular tools to detect and quantify two bacteria (Paenibacillus nematophilus and Paenibacillus sp.) phoretically associated with entomopathogenic nematodes (EPNs) in the families Heterorhabditidae and Steinernematodae. We also extend the repertoire of species specific primers and TaqManReg. probes for EPNs to include Heterorhabditis bacteriophora, Steinernema carpocapsae, Steinernema feltiae and Steinernema scapterisci, all widely distributed species used commercially for biological control. Primers and probes were designed from the ITS rDNA region for the EPNs and the 16S rDNA region for the bacteria. Standard curves were established using DNA from pure cultures of EPNs and plasmid DNA from the bacteria. The use of TaqMan probes in qPCR resolved the non-specificity of EPN and some bacterial primer amplifications whereas those for Paenibacillus sp. also amplified Paenibacillus thiaminolyticus and Paenibacillus popilliae, two species that are not phoretically associated with nematodes. The primer-probe sets for EPNs were able to accurately detect three infective juvenile EPNs added to nematodes recovered from soil samples. The molecular set for Paenibacillus sp. detected the bacterium attached to Steinernema diaprepesi suspended in water or added to nematodes recovered from soil samples but its detection decreased markedly in the soil samples, even when a nested PCR protocol was employed. Using qPCR we detected S. scapterisci at low levels in a citrus grove, which suggested natural long-distance spread of this exotic species, which is applied to pastures and golf courses to manage mole crickets (Scapteriscus spp.). Paenibacillus sp. (but not P. nematophilus) was detected in low quantities in the same survey but was unrelated to the spatial pattern of S. diaprepesi. The results of this research validate several new tools for studying the ecology of EPNs and their phoretic bacteria.
机译:实时定量PCR(qPCR)是一种强大的工具,可以检测和量化土壤样品中的隐性生物物种,例如细菌,真菌和线虫。因此,qPCR通过提供一种从DNA样本表征多种生物群落的单一方法,为研究土壤生境的生态学提供了新的机会。在这里,我们描述了分子工具,用于检测和定量分析与杂种虫科和Steinernematodae家族中的致病性线虫(EPNs)隐喻相关的两种细菌( Paenibacillus nematophilus 和 Paenibacillus sp。)。我们还扩展了物种特异性引物和TaqManReg的库。 EPN的探针包括细菌性细菌性肝炎, Steinernema feeliae 和 Steinernema scapterisci ,它们都是广泛使用的物种商业上用于生物防治。从EPN的ITS rDNA区域和细菌的16S rDNA区域设计引物和探针。使用来自EPNs纯培养物的DNA和来自细菌的质粒DNA建立标准曲线。 TaqMan探针在qPCR中的使用解决了EPN的非特异性和某些细菌引物扩增,而 Paenibacillus sp的扩增。还扩增了thiaminolyticus虫和Paillibacillus popilliae虫,这两个物种在线虫上都不具有表象关系。 EPNs的引物探针组能够准确检测添加到从土壤样品中回收的线虫中的三种感染性幼稚EPNs。 Paenibacillus sp。的分子组。细菌检测到悬浮在水中或添加到从土壤样品中回收的线虫中的细菌,但即使在采用巢式PCR方案的情况下,其检测也明显降低。使用qPCR,我们检测到 S。 scapterisci 在柑桔树丛中处于低水平,这表明该外来物​​种在自然的远距离传播,被应用于牧场和高尔夫球场以管理mole(Scapteriscus spp。)。 Paenibacillus sp。在同一调查中少量检出(但不是 P。nematophilus ),但与 S的空间格局无关。 diaprepesi 。这项研究的结果验证了用于研究EPNs及其隐性细菌生态学的几种新工具。

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