Effects of tissue sampling position, primary and secondary infection, cultivar, and storage temperature and duration on the detection, concentration and distribution of three viruses within infected potato tubers
Author:
Publisher
Springer Science and Business Media LLC
Subject
Plant Science
Link
http://link.springer.com/content/pdf/10.1007/s13313-011-0108-0.pdf
Reference39 articles.
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2. Barker H, Harrison BD (1986) Restricted distribution of potato leaf roll virus in resistant potato genotypes and its effect on transmission of the virus by aphids. Ann Appl Biol 109:595–604
3. Barker H, Webster KD, Reavy B (1993) Detection of potato virus Y in potato tubers: a comparison of polymerase chain reaction and enzyme-linked immunosorbent assay. Potato Res 36:13–20
4. Boonham N, Walsh K, Mumford RA, Barker I (2000) Use of multiplex real-time PCR (TaqMan) for the detection of potato viruses. EPPO Bulletin 30:427–430
5. Casper R (1977) Detection of potato leafroll virus in potato and in Physalis floridana by enzyme-linked immunosorbent assay (ELISA). Phytopathology 90:364–368
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2. Detection of four RNA viruses in commercial and informal potato seed tubers in Antioquia (Colombia);Archives of Phytopathology and Plant Protection;2020-10-05
3. Silver-enhanced lateral flow immunoassay for highly-sensitive detection of potato leafroll virus;Food and Agricultural Immunology;2017-11-13
4. Visual detection of Potato Leafroll virus by loop-mediated isothermal amplification of DNA with the GeneFinder™ dye;Journal of Virological Methods;2013-09
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