Institute for Sustainable Plant Protection, National Research Council of Italy (IPSP-CNR), Strada delle Cacce 73, 10135 Turin, Italy.
Certis Belchim BV, Stadsplateau 16, 3521 AZ Utrecht, The Netherlands.
Viruses. 2024 Oct 5;16(10):1572. doi: 10.3390/v16101572.
American plum line pattern virus (APLPV) is the most infrequently reported Ilarvirus infecting stone fruit trees and is of sufficient severity to be classified as an EPPO quarantine A1 pathogen. In late spring, yellow line pattern symptoms were observed on leaves in a few flowering cherries ( Lindl.) grown in a public garden in Northwest Italy. RNA extracts from twenty flowering cherries were submitted to Ilarvirus multiplex and APLPV-specific RT-PCR assays already reported or developed in this study. One flowering cherry (T22) with mixed prunus necrotic ringspot virus (PNRSV) and prune dwarf virus (PDV) infection also showed infection with APLPV. Blastn analysis of PCR products of the full coat protein () and movement protein () genes obtained from flowering cherry T22 showed 98.23% and 98.34% nucleotide identity with reference APLPV isolate NC_003453.1 from the USA. Then, a LAMP-specific assay was designed to facilitate the fast and low-cost identification of this virus either in the laboratory or directly in the field. The developed assay allowed not only the confirmation of APLPV (PSer22IT isolate) infection in the T22 flowering cherry but also the identification of APLPV in an asymptomatic flowering cherry tree (TL1). The LAMP assay successfully worked with crude flowering cherry extracts, obtained after manually shaking a single plant extract in the ELISA extraction buffer for 3-5 min. The developed rapid, specific and economic LAMP assay was able to detect APLPV using crude plant extracts rather that RNA preparation in less than 20 min, making it suitable for in-field detection. Moreover, the LAMP assay proved to be more sensitive in APLPV detection in flowering cherry compared to the specific one-step RT-PCR assay. The new LAMP assay will permit the estimation of APLPV geographic spread in the territory, paying particular attention to surrounding gardens and propagated flowering cherries in ornamental nurseries.
美国李线纹病毒(APLPV)是感染核果类树木的 Ilarvirus 中报道较少的病毒之一,其严重程度足以被归类为 EPPO 检疫 A1 病原体。在意大利西北部的一个公共花园里,一些开花樱桃( Lindl.)的叶片在晚春出现了黄线纹症状。从 20 株开花樱桃中提取的 RNA 被提交到 Ilarvirus 多重和 APLPV 特异性 RT-PCR 检测中,这些检测方法或已在本研究中报道,或由本研究开发。一株同时感染李坏死环斑病毒(PNRSV)和李矮缩病毒(PDV)的开花樱桃(T22)也显示出 APLPV 感染。从开花樱桃 T22 获得的全长外壳蛋白()和运动蛋白()基因的 PCR 产物的 Blastn 分析显示,与美国参考 APLPV 分离株 NC_003453.1 的核苷酸同一性分别为 98.23%和 98.34%。然后,设计了一种 LAMP 特异性检测方法,以方便在实验室或直接在田间快速、低成本地鉴定这种病毒。该检测方法不仅能够确认 T22 开花樱桃中的 APLPV(PSer22IT 分离株)感染,还能够鉴定出一株无症状开花樱桃树(TL1)中的 APLPV。LAMP 检测方法能够成功地用粗制的开花樱桃提取物进行检测,这种提取物是通过手动将单株植物提取物在 ELISA 提取缓冲液中摇动 3-5 分钟获得的。该快速、特异、经济的 LAMP 检测方法能够在不到 20 分钟内使用粗制植物提取物而不是 RNA 制备物检测到 APLPV,使其适用于田间检测。此外,与特异性一步 RT-PCR 检测相比,LAMP 检测方法在检测开花樱桃中的 APLPV 时更为敏感。新的 LAMP 检测方法将能够评估 APLPV 在该地区的地理传播情况,特别关注周围花园和观赏苗圃中繁殖的开花樱桃。