Bustin, S. A. 2000. Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays. J. Mol. Endrocrinol. 25:169-193.
Clark, M. F., and Adams, A. N. 1977. Characteristics of the microplate method of enzyme-linked immunosorbent assay for the detection of plant viruses. J. Gen. Virol. 34:475-483.
Crosslin, J. M., and Mink, G. 1992. Biophysical differences among Prunus necrotic ringspot Ilarviruses. Phytopathology 82:200-206.
Dal Zotto, A., and Nome, S. F. 1999. Fluctuations of Prunus necrotic ringspot virus (PNRSV) at various phenological stages in peach cultivars. Plant Dis. 83:1055-1057.
Fulton, R. W. 1983. Ilarvirus group. C.M.I./A.A.B. Description of Plant Viruses, 260.
Grüntzig, M., Fuchs, E., Pfleistetter, E., Al Kai, B., and Otto, F. 1994. Untersuchungen zur Verleitung Mechanish Übertragbarer Viren in Bäumen des Kern-und Steinobstes. Arch. Phytopathol. Pflanzenschutz 29:217-248.
Helguera, P. R., Taborda, R., Docampo, D. M., and Ducasse, D. A. 2001. Immunocapture reverse transcription-polymerase chain reaction combined with nested PCR greatly increases the detection of Prunus necrotic ringspot virus in the peach. J. Virol. Methods 95:93-100.
Holland, P. M., Abramson, R. D., Watson, R., and Gelfand, D. H. 1991. Detection of specific polymerase chain reaction products by utilizing 5′-3′ exonuclease activity of Thermus aquaticus DNA polymerase. Proc. Natl. Acad. Sci. USA 88:7276-7280.
Howell, W. E., and Mink, G. I. 1988. Natural spread of cherry rugose mosaic disease and two Prunus necrotic ringspot virus biotypes in a Central Washington sweet cherry orchard. Plant Dis. 72:636-640.
Korimbocus, J., Coates, D., Barker, I., and Boonham, N. 2002. Improved detection of Sugarcane yellow leaf virus using a real-time fluorescent (TaqMan) RT-PCR assay. J. Virol. Methods 103:109-120.
Kummert, J., Vendrame, M., Steyer, S., and Lepoivre, P. 2001. Development of routine RT-PCR tests for certification of fruit tree multiplication material. Acta Hortic. 550:45-52.
Kutyavin, I. V., Afonina, I. A., Mills, A., Gorn, V. V., Lukhtanov, E. A., Belousov, E. S., Singer, M. J., Walburger, D. K., Lokhov, S. G., Gall, A. A., Dempcy, R., Reed, M. W., Meyer, R. B., and Hedgpeth, J. 2000. 3′-Mi-nor groove binder-DNA probes increase sequence specificity at PCR extension temperature. Nucleic Acids Res. 28:655-661.
Lie, Y. S., and Petropoulos, C. J. 1998. Advances in quantitative PCR technology: 5′ nuclease assay. Curr. Opin. Biotechnol. 9:43-48.
Livak, K., Flood, S. J. A., Marmaro, J., Giusti, W., and Deetz, K. 1995. Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization. PCR Methods Appl. 4:357-362.
Livak, K., Marmaro, J., and Flood, S. 1996. Guidelines for designing TaqMan fluorogenic probes for 5′ nuclease assays. Perkin-Elmer Res. News 57:1-5.
Roberts, C. A., Dietzgen, R. G., Heelan, L. A., and Maclean, D. J. 2000. Real-time RT-PCR fluorescent detection of tomato spotted wilt virus. J. Virol. Methods 88:1-8.
Rosner, A., Malesnin, L., and Spiegel, S. 1997. The use of short and long PCR products for improved detection of Prunus necrotic ringspot virus in woody plants. J. Virol. Methods 67:135-141.
Salmon, M., Vendrame, M., Kummert, J., and Lepoivre, P. 2002. Detection of Apple chlorotic leaf spot virus using a fluorogenic 3′ minor groove binder-DNA probe. J. Virol. Methods 104:99-106.
Salmon, M., Vendrame, M., Kummert, J., and Lepoivre, P. 2002. Rapid and homogenous detection of Apple stem pitting virus by RT-PCR and a fluorogenic 3′ minor groove binder-DNA probe. Eur. J. Plant. Pathol. 108:755-762.
Scott, S. W., Barnett, O. W., and Burrows, P. M. 1989. Incidence of Prunus necrotic ringspot virus in Selected Peach Orchards of South Carolina. Plant Dis. 73:913-916.
Spiegel, S., Scott, S. W., Bowman-Vance, V., Tam, Y., Galiakparov, N. N., and Rosner, A. 1996. Improved detection of Prunus necrotic ringspot virus by the polymerase chain reaction. Eur. J. Plant Pathol. 102:681-685.
Spiegel, S., Tam, T., Maslenin, L., Kolber, M., Nemeth, M., and Rosner, A. 1999. Typing Prunus necrotic ringspot virus isolates by serology and restriction endonuclease analysis of PCR products. Ann. Appl. Biol. 135:395-400.
Torrance, L., and Dolby, C. A. 1984. Sampling conditions for reliable routine detection by enzyme-linked immunosorbent assay of three ilarviruses in fruit trees. Ann. Appl. Biol. 104:267-276.
Uyemoto, J. K., Asai, W. K., and Luhn, C. F. 1992. Ilarviruses: Evidence for rapid spread and effects on vegetative growth and fruit yields of peach trees. Plant Dis. 76:71-74.
Uyemoto, J. K., and Scott, S. 1992. Important diseases of Prunus caused by viruses and other graft-transmissible pathogens in California and South Carolina. Plant Dis. 76:5-11.
Weller, S. A., Elphinstone, J. G., Smith, N. C., and Stead, D. E. 2000. Detection of Ralstonia solanacearum from potato tissue by post-enrichment TaqMan PCR. OEPP/EPPO Bull. 30:381-383.