A highly sensitive method for the detection of Chrysanthemum virus B

Shinoyama, 2012, Genetic engineering of chrysanthemum (Chrysanthemum morifolium): Current progress and perspectives, Plant Biotechnol, 29, 323, 10.5511/plantbiotechnology.12.0521a Palma, 2013, Optimization of a chemiluminescent dot-blot immunoassay for detection of potato viruses, Am J Potato Res, 90, 306, 10.1007/s12230-013-9305-4 Verma, 2009, Molecular studies on Tomato aspermy virus isolates infecting chrysanthemums, Arch Phytopathol Plant Protect, 42, 99, 10.1080/03235400600951779 Rybicki, 1999, Plant virus disease problems in the developing world, Adv Virus Res, 53, 127, 10.1016/S0065-3527(08)60346-2 Singh, 2012, Genomic sequence analysis of four new chrysanthemum virus B isolates: Evidence of RNA recombination, Arch Virol, 157, 531, 10.1007/s00705-011-1190-x Levay, 1991, Nucleotide-sequence and gene organization of the 3′-terminal region of chrysanthemum virus-b genomic RNA, J Gen Virol, 72, 2333, 10.1099/0022-1317-72-10-2333 Song, 2013, An isoform of eukaryotic initiation factor 4e from Chrysanthemum morifolium interacts with chrysanthemum virus b coat protein, PLoS One, 8 Hollings, 1975, Serological and immunoelectrophoretic relationships among viruses in the tombusvirus group, Ann Appl Biol, 80, 37, 10.1111/j.1744-7348.1975.tb01598.x Singh, 2007, Coat protein gene diversity among Chrysanthemum virus B isolates from India, Arch Virol, 152, 405, 10.1007/s00705-006-0854-4 Crosslin, 2005, Serological and molecular detection of tobacco veinal necrosis isolates of Potato virus Y (PVYN) from potatoes grown in the western United States, Am J Potato Res, 82, 263, 10.1007/BF02871955 Kumar, 1999, Sensitivity of polyvalent DOT-ELISA in comparison to DOT and DAS-ELISA for detection of potato viruses, J Indian Potato Assoc, 26, 39 X-l, 2014, Multiplex reverse transcription loop-mediated isothermal amplification for the simultaneous detection of CVB and CSVd in chrysanthemum, J Virol Methods, 210, 26, 10.1016/j.jviromet.2014.09.008 Mori, 2004, Real-time turbidimetry of LAMP reaction for quantifying template DNA, J Biochem Biophys Methods, 59, 145, 10.1016/j.jbbm.2003.12.005 Hosokawa, 2006, Direct RT-PCR method for detecting two chrysanthemum viroids using minimal amounts of plant tissue, J Virol Methods, 131, 28, 10.1016/j.jviromet.2005.07.001 Coiras, 2004, Simultaneous detection of fourteen respiratory viruses in clinical specimens by two multiplex reverse transcription nested-PCR assays, J Med Virol, 72, 484, 10.1002/jmv.20008 Zhao, 2015, A multiplex RT-PCR for simultaneous detection and identification of five viruses and two viroids infecting chrysanthemum, Arch Virol, 160, 1145, 10.1007/s00705-015-2360-z Papayiannis, 2014, Diagnostic real-time RT-PCR for the simultaneous detection of Citrus exocortis viroid and Hop stunt viroid, J Virol Methods, 197, 93, 10.1016/j.jviromet.2013.11.001 Song, 2013, A multiplex RT-PCR for rapid and simultaneous detection of viruses and viroids in chrysanthemum, Lett Appl Microbiol, 56, 8, 10.1111/lam.12007 Chen, 2013, Development of a real-time fluorescent quantitative PCR assay for detection of Impatiens necrotic spot virus, J Virol Methods, 189, 299, 10.1016/j.jviromet.2013.02.012 Agindotan, 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, 10.1016/j.jviromet.2006.12.012 Schmutzhard, 2004, Detection of herpes simplex virus type 1, herpes simplex virus type 2 and varicella-zoster virus in skin lesions. Comparison of real-time PCR, nested PCR and virus isolation, J Clin Virol, 29, 120, 10.1016/S1386-6532(03)00113-6 Cha, 1995, 37 Nam, 2002, Oligo(dT) primer generates a high frequency of truncated cDNAs through internal poly(A) priming during reverse transcription, Proc Natl Acad Sci U S A, 99, 6152, 10.1073/pnas.092140899 Resuehr, 2003, A real-time polymerase chain reaction-based evaluation of cDNA synthesis priming methods, Anal Biochem, 322, 287, 10.1016/j.ab.2003.07.017 Zhang, 1999, Differential priming of RNA templates during cDNA synthesis markedly affects both accuracy and reproducibility of quantitative competitive reverse-transcriptase PCR, Biochem J, 337, 231, 10.1042/bj3370231 Manome, 2008, Quantification of potato common scab pathogens in soil by quantitative competitive PCR with fluorescent quenching-based probes, Plant Pathol, 57, 887, 10.1111/j.1365-3059.2008.01881.x Schaad, 2002, Real-time PCR and its application for rapid plant disease diagnostics, Can J Plant Pathol, 24, 250, 10.1080/07060660209507006 Kim, 2015, Evaluation of viroid extraction methods and application of a one-step reverse transcription real-time polymerase chain reaction assay (RT-qPCR) for the rapid detection of Chrysanthemum stunt viroid (CSVd) infection, Can J Plant Pathol, 37, 221, 10.1080/07060661.2015.1012742