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一种用于同时检测苹果锈果类病毒和植物RNA内参的双重一步法逆转录定量聚合酶链反应检测方法的开发。

Development of a duplex one-step RT-qPCR assay for the simultaneous detection of Apple scar skin viroid and plant RNA internal control.

作者信息

Khan Subuhi, Mackay John, Liefting Lia, Ward Lisa

机构信息

Plant Health and Environment Laboratory, Ministry for Primary Industries, P.O. Box 2095, Auckland 1140, New Zealand.

dnature diagnostics & research Ltd., 24 Island Road, Gisborne 4010, New Zealand.

出版信息

J Virol Methods. 2015 Sep 1;221:100-5. doi: 10.1016/j.jviromet.2015.04.032. Epub 2015 May 8.

Abstract

Apple scar skin viroid (ASSVd) is an important quarantine pathogen for international movement of pome germplasm as it can cause significant damage to pip fruit. A one-step real-time RT-PCR assay was developed for the rapid and sensitive detection of ASSVd. The assay was able to detect a wide range of ASSVd isolates and was highly specific compared to a published conventional RT-PCR. The detection limit of the new assay was estimated to be about 100 copies of the ASSVd target. The assay can be run as a duplex with the nad5 internal control primers and probe to simultaneously check the PCR competency of the samples therefore reducing the risk of false negatives. It is expected that this real-time RT-PCR assay will facilitate efficient testing for ASSVd by regulatory services, and will also have a wider use for the general detection of ASSVd in a range of pip fruit.

摘要

苹果疤痕果皮类病毒(ASSVd)是梨果种质国际流通中的一种重要检疫性病原菌,因为它会对核果造成严重损害。开发了一种一步法实时逆转录聚合酶链反应(RT-PCR)检测方法,用于快速、灵敏地检测ASSVd。该检测方法能够检测多种ASSVd分离株,与已发表的传统RT-PCR相比具有高度特异性。新检测方法的检测限估计约为100个ASSVd靶标拷贝。该检测方法可与nad5内部对照引物和探针进行双重检测,以同时检查样品的PCR扩增能力,从而降低假阴性风险。预计这种实时RT-PCR检测方法将有助于监管部门对ASSVd进行高效检测,并且在一系列核果中对ASSVd的常规检测中也将有更广泛的应用。

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