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An efficient method for zoospore production, infection and real-time quantification of Phytophthora cajani causing Phytophthora blight disease in pigeonpea under elevated atmospheric CO2

机译:大气CO 2浓度升高引起木豆疫霉病的卡萨疫霉的游动孢子产生,感染和实时定量的有效方法

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摘要

Background\udPhytophthora blight caused by Phytophthora cajani is an emerging disease of pigeonpea (Cajanus cajan L.) affecting the crop irrespective of cropping system, cultivar grown and soil types. Current detection and identification methods for Phytophthora species rely primarily on cultural and morphological characteristics, the assessment of which is time-consuming and not always suitable. Sensitive and reliable methods for isolation, identification, zoospore production and estimating infection severity are therefore desirable in case of Phytophthora blight of pigeonpea.\ud\udResults\udIn this study, protocols for isolation and identification of Phytophthora blight of pigeonpea were standardized. Also the method for zoospore production and in planta infection of P. cajani was developed. Quantification of fungal colonization by P. cajani using real-time PCR was further standardized. Phytophthora species infecting pigeonpea was identified based on mycological characters such as growth pattern, mycelium structure and sporangial morphology of the isolates and confirmed through molecular characterization (sequence deposited in GenBank). For Phytophthora disease development, zoospore suspension of 1 × 105 zoospores per ml was found optimum. Phytophthora specific real-time PCR assay was developed using specific primers based on internal transcribed spacer (ITS) 1 and 2. Use of real-time PCR allowed the quantitative estimation of fungal biomass in plant tissues. Detection sensitivities were within the range of 0.001 pg fungal DNA. A study to see the effect of elevated CO2 on Phytophthora blight incidence was also conducted which indicated no significant difference in disease incidence, but incubation period delayed under elevated CO2 as compared to ambient level.\ud\udConclusion\udThe zoospore infection method for Phytophthora blight of pigeonpea will facilitate the small and large scale inoculation experiments and thus devise a platform for rapid and reliable screening against Phytophthora blight disease of pigeonpea. qPCR allowed a reliable detection and quantification of P. cajani in samples with low pathogen densities. This can be useful in early warning systems prior to potential devastating outbreak of the disease.
机译:背景\ udyPhytophthora枯萎病是由Phytophthora cajani引起的,是一种新兴的木豆病(Cajanus cajan L.),无论作物的种植系统,栽培品种和土壤类型如何,均会影响作物。当前对疫霉属物种的检测和鉴定方法主要依赖于文化和形态特征,对其进行评估是耗时的并且并不总是合适的。因此,需要一种灵敏,可靠的隔离,鉴定,游动孢子产生和估计感染严重程度的方法,以预防木豆疫霉病。\ ud \ ud结果\ ud在本研究中,对隔离和鉴定木豆疫霉病的方法进行了标准化。还开发了游动孢子生产和卡尼亚疟原虫感染植物的方法。使用实时PCR对卡氏假单胞菌真菌定植的定量进一步标准化。根据分离株的生长特性,菌丝体结构和孢子囊形态等真菌学特征鉴定了感染木豆的疫霉菌种,并通过分子鉴定(序列已在GenBank中保存)得以确认。对于疫霉菌病的发展,发现每毫升1××105个游动孢子的游动孢子悬浮液是最佳的。使用基于内部转录间隔子(ITS)1和2的特异性引物开发了疫霉菌特异性实时PCR检测方法。使用实时PCR可以定量估计植物组织中的真菌生物量。检测灵敏度在0.001pg真菌DNA的范围内。还进行了一项研究,研究了二氧化碳浓度升高对疫霉疫病的影响,该研究表明疾病发病率无显着差异,但与环境水平相比,二氧化碳浓度升高下的潜伏期有所延迟。\ ud \ ud结论\ ud疫霉菌疫病的游动孢子感染方法木豆的分离将促进小规模和大规模的接种实验,从而为快速可靠地筛查木豆疫霉病提供一个平台。 qPCR可以可靠地检测和定量低病原体密度的样品中的卡氏假单胞菌。这在潜在破坏性疾病爆发之前的预警系统中可能会很有用。

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