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首页> 外文期刊>Biological Control: Theory and Application in Pest Management >Interaction dynamics between endophytic biocontrol agents and pathogen in the host plant studied via quantitative real-time polymerase chain reaction (qPCR) approach
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Interaction dynamics between endophytic biocontrol agents and pathogen in the host plant studied via quantitative real-time polymerase chain reaction (qPCR) approach

机译:通过定量实时聚合酶链反应(QPCR)研究的宿主植物中内参酶生物控制剂和病原体之间的相互作用动态

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The interaction dynamics between endophytic biocontrol agents and pathogens were investigated to determine their co-existence in the host plant. The endophytes (Diaporthe phaseolorum WAA02, Trichoderma asperellum T2, Penicillium citrinum BTF08) and pathogen (Ganoderma boninense Gb) were inoculated into oil palm ramets and their relative abundance in root, stem and leaf tissues was assessed via quantitative real-time PCR. This was done using single inoculations (for every endophyte and pathogen) and co-inoculations (combined inoculation of every endophyte with Gb). In single inoculations, BTF08 (P. citrinum) was the most abundant in the host tissues (3.93 x 10(18 )ng/mg DNA concentration), followed by WAA02 (D. phaseolorum) and T2 (T. asperellum) (1.30 x 10(3) and 6.48 x 10(1) ng/mg, respectively). Pathogenic Gb was the least abundant (1.58 x 10(1) ng/mg). When co-inoculated with Gb, all endophytic isolates outcompete Gb suggesting superiority of endophytic isolates when in co-existence with Gb. All isolates favoured colonization in stem tissues (0.024-4.84 x 10(17) ng/mg), followed by root (0.045-7.30 x 10(15) ng/mg) and leaf tissues (0.072-1.16 x 10(4) ng/mg). This study represents the first report on the simultaneous monitoring of pathogen and endophytic BCA in a host plant model via real-time PCR.
机译:研究了内生生物泌体药物和病原体之间的相互作用动态,以确定它们在宿主植物中的共存。内心体(Dioporhe Phaplorulum Waa02,Trichoderma asperellum T2,Penicillium rinum Btf08)和病原体(Ganoderma Boninense Gb)接种到油棕榈槌中,并通过定量实时PCR评估它们的根,茎和叶组织中的相对丰度。这是使用单一接种(对于每个内心细胞和病原体)和共接收的(将每个内心细胞与GB接种)进行的。在单个接种中,BTF08(P. Citrinum)在宿主组织中最丰富(3.93×10(18)Ng / mg DNA浓度),然后是WaA02(D. phopaceolorum)和T2(T.Sesperellum)(1.30 x 10(3)和6.48 x 10(1)Ng / mg)。致病GB是最少的(1.58×10(1)Ng / mg)。当与GB共同接种时,所有内生分离物都是Excompete GB,表明在与GB共存时的内生分离物的优越性。所有分离物都在干组织中有利于定植(0.024-4.84×10(17)Ng / mg),然后是根(0.045-7.30×10(15)个Ng / mg)和叶组织(0.072-1.16 x 10(4)Ng / mg)。该研究代表了通过实时PCR在宿主植物模型中同时监测病原体和内生BCA的第一报告。

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