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建立一种用于同时检测核桃中新壳梭孢菌和密旋腔孢菌的多重 PCR 方法。

Development of a Multiplex PCR Assay to Detect Neofusicoccum parvum and Botryosphaeria dothidea in Walnut.

机构信息

Laboratoire Universitaire de Biodiversité Et Écologie Microbienne, Univ Brest, INRAE, 29280, Plouzané, France.

出版信息

Curr Microbiol. 2024 Oct 29;81(12):432. doi: 10.1007/s00284-024-03954-9.

Abstract

In walnut orchards, frequent symptoms of cankers and dieback (fruit blight, twig and branch cankers up to tree death) are caused by different agents, in particular by Botryosphaeriaceae, primarily Neofusicoccum parvum and Botryosphaeria dothidea. This study aimed at developing a sensitive, rapid, specific and internally controlled multiplex PCR assay for the detection of these species. The ability of the multiplex PCR, with an internal inhibition control (i.e. E. coli DNA), to specifically and successfully detect members of the two targeted species was validated using 11 different isolates for each fungal target (inclusivity) and 20 tree-associated fungal species different from B. dothidea or N. parvum (exclusivity). Applicability to plant materials was further investigated and showed an absence of amplification for asymptomatic husk or twig samples while the amplification profiles of symptomatic tissues ranged from no amplification to amplification of both species, in correlation with the observed fungal contamination level. In conclusion, we developed a rapid diagnostic tool for simultaneous detection of two major fungal pathogens of walnut. Although this protocol was tailored for walnut husks and twigs, applicability to any plant sample contaminated by these pathogens can be considered.

摘要

在核桃果园中,频繁出现溃疡和枯萎(果实枯萎、嫩枝和侧枝溃疡直至树木死亡)的症状是由不同的病原体引起的,特别是由葡萄座腔菌科引起的,主要是 Neofusicoccum parvum 和 Botryosphaeria dothidea。本研究旨在开发一种敏感、快速、特异和内部对照的多重 PCR 检测方法,用于检测这些物种。使用 11 种不同的真菌目标(包容性)和 20 种与 B. dothidea 或 N. parvum 不同的树相关真菌物种(排他性)的内部抑制控制(即大肠杆菌 DNA)的多重 PCR 能够特异性和成功地检测到两个目标物种的成员,这一点得到了验证。进一步研究了该方法在植物材料上的适用性,结果表明无症状的外壳或嫩枝样本没有扩增,而症状组织的扩增图谱从没有扩增到同时扩增两种物种,这与观察到的真菌污染水平有关。总之,我们开发了一种快速诊断工具,用于同时检测核桃的两种主要真菌病原体。尽管该方案是针对核桃外壳和嫩枝量身定制的,但可以考虑将其应用于任何受到这些病原体污染的植物样本。

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