Abstract
Lily mottle virus (LMoV; genus Potyvirus, family Potyviridae) infects plants of the genus Lilium, causing a reduction in flower and bulb quality. A rapid and sensitive loop-mediated isothermal amplification (LAMP) assay was developed to detect the coat protein gene of LMoV. This LAMP method was highly specific for LMoV, with no cross-reaction with other lily viruses. The sensitivity of LMoV using the LAMP assay was 100 times more sensitive than that using conventional polymerase chain reaction. A reverse transcription LAMP (RT-LAMP) was then successfully applied to detect LMoV RNA. The newly established LAMP and one-step RT-LAMP provide an alternative method for detecting LMoV in lily plants.
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KZ, BZ and DY participated in the design and carried out the majority of the experiments and drafted, reviewed and edited the manuscript. YZ, YX, XZ, JL, XF, QZ and XZ helped to perform the experiments. BS contributed reagents/materials/analysis tools, YC, YZ and ZZ participated in its design and coordination. YD edited the manuscript. All authors read and approved the final manuscript.
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The authors declare that they have no conflict of interest.
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This work was financially supported by the Shanghai Agriculture Applied Technology Development Program, China (Grant No. G2014070203) and the Agriculture Research System of Shanghai, China (Grant No. 201708). These funding bodies had no role in design, collection, or analysis of the study or preparation of the manuscript.
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Handling Editor: Ralf Georg Dietzgen.
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Zhao, B., Yang, D., Zhang, Y. et al. Rapid visual detection of lily mottle virus using a loop-mediated isothermal amplification method. Arch Virol 163, 545–548 (2018). https://doi.org/10.1007/s00705-017-3618-4
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DOI: https://doi.org/10.1007/s00705-017-3618-4