Optimization of a simple, low-cost one-step reverse transcription recombinase polymerase amplification method for real-time detection of potato virus A in potato leaves and tubers
Author:
Publisher
Springer Science and Business Media LLC
Subject
Agricultural and Biological Sciences (miscellaneous),Environmental Science (miscellaneous),Biotechnology
Link
https://link.springer.com/content/pdf/10.1007/s13205-023-03791-w.pdf
Reference58 articles.
1. Agindotan BO, Shiel PJ, Berger PH (2007) Simultaneous detection of potato viruses, PLRV, PVA, PVX and PVY from dormant potato tubers by TaqMan®real-time RT-PCR. J Virol Methods 142:1–9. https://doi.org/10.1016/j.jviromet.2006.12.012
2. Babu B, Washburn BK, Miller SH et al (2017) A rapid assay for detection of Rose rosette virus using reverse transcription-recombinase polymerase amplification using multiple gene targets. J Virol Methods 240:78–84. https://doi.org/10.1016/j.jviromet.2016.11.014
3. Babujee L, Witherell RA, Mikami K et al (2019) Optimization of an isothermal recombinase polymerase amplification method for real-time detection of Potato virus Y O and N types in potato. J Virol Methods 267:16–21. https://doi.org/10.1016/j.jviromet.2019.02.006
4. Chi YK, Zhao W, Di YM et al (2020) Evaluation of recombinase polymerase amplification assay for detecting meloidogyne javanica. Plant Dis 104:801–807. https://doi.org/10.1094/PDIS-07-19-1473-RE
5. Chikh-Ali M, Karasev AV (2023) Virus diseases of potato and their control. Potato Prod Worldw. https://doi.org/10.1016/B978-0-12-822925-5.00008-6
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