Plant Health and Environment Laboratory, Investigation and Diagnostic Centre, MAF Biosecurity New Zealand, PO Box 2095, Auckland 1140, New Zealand.
J Virol Methods. 2010 Apr;165(1):97-104. doi: 10.1016/j.jviromet.2010.01.011. Epub 2010 Feb 1.
A PCR assay was developed for the universal detection of ilarviruses using primers designed to the RNA-dependent RNA polymerase gene in RNA2. The assay detected 32 isolates of 15 definite and 2 tentative ilarvirus species using a one-step RT-PCR. The assay was more specific, and at least as sensitive as a commercial assay, and allowed direct sequencing of amplicons. No cross-reaction was observed with neither healthy plants of 15 host species nor from isolates in other genera of the Bromoviridae. A further PCR assay targeting the helicase motif of RNA1 was able to detect all species tested within the family Bromoviridae, including members of the Alfamovirus, Anulavirus, Bromovirus, Cucumovirus and Ilarvirus. The assays provide a sensitive and cost-effective way for detecting and characterising members of the Bromoviridae and can be used for quarantine and certification programmes.
一种使用针对 RNA2 的 RNA 依赖性 RNA 聚合酶基因设计的引物的 PCR 检测法,被开发出来用于普遍检测 ilarviruses。该检测法使用一步 RT-PCR 检测了 15 种确定和 2 种暂定的 ilarvirus 种的 32 个分离物。该检测法具有更高的特异性,并且至少与商业检测法一样敏感,并且允许对扩增子进行直接测序。与 15 种宿主植物的健康植物或其他 Bromoviridae 属的分离物均未观察到交叉反应。针对 RNA1 的解旋酶基序的进一步 PCR 检测法能够检测到该科中的所有测试种,包括 Alfamovirus、Anulavirus、Bromovirus、Cucumovirus 和 Ilarvirus 的成员。这些检测法为检测和鉴定 Bromoviridae 成员提供了一种敏感且具有成本效益的方法,可用于检疫和认证计划。