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一种高效的方法,用于生产导致羽扇豆疫病的可可球腔菌游动孢子、感染和实时定量分析,该方法在大气 CO₂升高的情况下进行。

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

机构信息

Legumes Pathology, International Crop Research Institute for the Semi-Arid Tropics, Patancheru, 502324, Telangana, India.

出版信息

BMC Plant Biol. 2015 Mar 25;15:90. doi: 10.1186/s12870-015-0470-0.

Abstract

BACKGROUND

Phytophthora 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.

RESULTS

In 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 × 10(5) 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.

CONCLUSION

The 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.

摘要

背景

由可可球二孢菌(Phytophthora cajani)引起的可可球二孢菌枯萎病是一种新兴的豇豆病害,无论种植制度、种植品种和土壤类型如何,都会对作物造成影响。目前,对可可球二孢菌物种的检测和鉴定主要依赖于培养和形态特征,而这种评估既耗时又并不总是适用。因此,在发生豇豆花叶病的情况下,需要一种敏感可靠的方法来分离、鉴定、产生游动孢子并估计感染严重程度。

结果

本研究标准化了豇豆花叶病的分离和鉴定方案。还开发了可可球二孢菌游动孢子产生和体内感染的方法。进一步标准化了使用实时 PCR 对可可球二孢菌真菌定殖的定量。根据分离物的生长模式、菌丝体结构和孢子囊形态等真菌学特征,对感染豇豆的可可球二孢菌等可可球二孢菌物种进行了鉴定,并通过分子特征(保存在 GenBank 中的序列)进行了确认。对于可可球二孢菌病害的发展,发现 1×10(5)个游动孢子/ml 的游动孢子悬浮液为最佳。使用基于内部转录间隔区(ITS)1 和 2 的特异性引物,开发了可可球二孢菌特异性实时 PCR 检测方法。实时 PCR 的使用允许对植物组织中的真菌生物量进行定量估计。检测灵敏度在 0.001 pg 真菌 DNA 范围内。还进行了一项研究,以观察高浓度 CO₂对可可球二孢菌枯萎病发病率的影响,结果表明,发病率没有显著差异,但与环境水平相比,高浓度 CO₂下的潜伏期延迟。

结论

豇豆花叶病的游动孢子感染方法将促进小型和大型接种实验,从而为快速可靠地筛选豇豆花叶病提供平台。qPCR 允许在低病原体密度的样本中可靠地检测和定量可可球二孢菌。这在疾病潜在破坏性爆发之前的早期预警系统中可能很有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f077/4377013/2d9f2692e599/12870_2015_470_Fig1_HTML.jpg

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