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从 Bois noir 症状和恢复的葡萄藤根系中检测到‘Candidatus Phytoplasma solani’。

Detection of 'Candidatus Phytoplasma solani' in roots from Bois noir symptomatic and recovered grapevines.

机构信息

Department of Agricultural, Food and Environmental Sciences, Marche Polytechnic University, Via Brecce Bianche, I-60131, Ancona, Italy.

出版信息

Sci Rep. 2019 Feb 14;9(1):2013. doi: 10.1038/s41598-018-38135-9.

Abstract

'Candidatus Phytoplasma solani' is the causal agent of Bois noir (BN) in grapevine (Vitis vinifera). It is usually detected in leaves, where typical disease symptoms are seen. However, little information is available on the presence of this phytoplasma in grapevine roots. Here, we investigated 'Ca. P. solani' in roots collected from 28 symptomatic, 27 recovered and eight asymptomatic grapevine plants. Protocols based on high-resolution melting (HRM) combined with real-time quantitative PCR (qPCR-HRM) and nested-qPCR-HRM were developed to identify 'Ca. P. solani' tuf-type variants with single nucleotide polymorphisms. In all, 21.4% of roots from symptomatic plants were positive to 'Ca. P. solani' using qPCR-HRM, and 60.7% with nested-qPCR HRM. Also, 7.4% of roots from recovered plants were positive using qPCR-HRM, which reached 44.4% using nested-qPCR HRM. These analyses identified tuf-type b1 on 88.2% of the positive samples from symptomatic grapevines, and 66.6% from recovered grapevines, with all other samples identified as tuf-type a. This study reports the presence of 'Ca. P. solani' in the roots of both symptomatic and recovered grapevines. These qPCR-HRM and nested-qPCR-HRM protocols can be applied to increase the sensitivity of detection of, and to simplify and speed up the screening for, 'Ca. P. solani' tuf-types.

摘要

'Candidatus Phytoplasma solani' 是葡萄(Vitis vinifera)上 Bois noir(BN)的致病因子。它通常在叶片中被检测到,在那里可以看到典型的疾病症状。然而,关于这种植原体在葡萄根系中的存在的信息很少。在这里,我们调查了 28 株有症状、27 株恢复和 8 株无症状葡萄植株根系中的 'Ca. P. solani'。开发了基于高分辨率熔解(HRM)结合实时定量 PCR(qPCR-HRM)和嵌套-qPCR-HRM 的方案,以鉴定具有单核苷酸多态性的 'Ca. P. solani' tuf 型变体。使用 qPCR-HRM 检测到 21.4%的有症状植物根系对 'Ca. P. solani' 呈阳性,使用嵌套-qPCR HRM 检测到 60.7%的植物根系呈阳性。同样,使用 qPCR-HRM 在 7.4%的恢复植物根系中检测到 'Ca. P. solani' 呈阳性,而使用嵌套-qPCR HRM 检测到 44.4%的植物根系呈阳性。这些分析在有症状葡萄藤的阳性样本中鉴定出 88.2%的 tuf-type b1,在恢复葡萄藤中鉴定出 66.6%的 tuf-type b1,其他所有样本均鉴定为 tuf-type a。本研究报告了 'Ca. P. solani' 在有症状和恢复的葡萄根系中的存在。这些 qPCR-HRM 和嵌套-qPCR-HRM 方案可用于提高 'Ca. P. solani' tuf 型检测的灵敏度,并简化和加快筛查。

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