Andino, R., & Domingo, E. (2015). Viral quasispecies. Virology, 479-480, 46-51. doi:10.1016/j.virol.2015.03.022
Ohshima, K., Nomiyama, R., Mitoma, S., Honda, Y., Yasaka, R., & Tomimura, K. (2016). Evolutionary rates and genetic diversities of mixed potyviruses in Narcissus. Infection, Genetics and Evolution, 45, 213-223. doi:10.1016/j.meegid.2016.08.036
Froissart, R., Roze, D., Uzest, M., Galibert, L., Blanc, S., & Michalakis, Y. (2005). Recombination Every Day: Abundant Recombination in a Virus during a Single Multi-Cellular Host Infection. PLoS Biology, 3(3), e89. doi:10.1371/journal.pbio.0030089
[+]
Andino, R., & Domingo, E. (2015). Viral quasispecies. Virology, 479-480, 46-51. doi:10.1016/j.virol.2015.03.022
Ohshima, K., Nomiyama, R., Mitoma, S., Honda, Y., Yasaka, R., & Tomimura, K. (2016). Evolutionary rates and genetic diversities of mixed potyviruses in Narcissus. Infection, Genetics and Evolution, 45, 213-223. doi:10.1016/j.meegid.2016.08.036
Froissart, R., Roze, D., Uzest, M., Galibert, L., Blanc, S., & Michalakis, Y. (2005). Recombination Every Day: Abundant Recombination in a Virus during a Single Multi-Cellular Host Infection. PLoS Biology, 3(3), e89. doi:10.1371/journal.pbio.0030089
Tromas, N., Zwart, M. P., Poulain, M., & Elena, S. F. (2014). Estimation of the in vivo recombination rate for a plant RNA virus. Journal of General Virology, 95(3), 724-732. doi:10.1099/vir.0.060822-0
Simon-Loriere, E., & Holmes, E. C. (2011). Why do RNA viruses recombine? Nature Reviews Microbiology, 9(8), 617-626. doi:10.1038/nrmicro2614
Zwart, M. P., & Elena, S. F. (2015). Matters of Size: Genetic Bottlenecks in Virus Infection and Their Potential Impact on Evolution. Annual Review of Virology, 2(1), 161-179. doi:10.1146/annurev-virology-100114-055135
Neher, R. A. (2013). Genetic Draft, Selective Interference, and Population Genetics of Rapid Adaptation. Annual Review of Ecology, Evolution, and Systematics, 44(1), 195-215. doi:10.1146/annurev-ecolsys-110512-135920
Elena, S. F., Fraile, A., & García-Arenal, F. (2014). Evolution and Emergence of Plant Viruses. Advances in Virus Research, 161-191. doi:10.1016/b978-0-12-800098-4.00003-9
Longdon, B., Brockhurst, M. A., Russell, C. A., Welch, J. J., & Jiggins, F. M. (2014). The Evolution and Genetics of Virus Host Shifts. PLoS Pathogens, 10(11), e1004395. doi:10.1371/journal.ppat.1004395
Vassilakos, N., Simon, V., Tzima, A., Johansen, E., & Moury, B. (2015). Genetic Determinism and Evolutionary Reconstruction of a Host Jump in a Plant Virus. Molecular Biology and Evolution, 33(2), 541-553. doi:10.1093/molbev/msv222
Stapleford, K. A., Coffey, L. L., Lay, S., Bordería, A. V., Duong, V., Isakov, O., … Vignuzzi, M. (2014). Emergence and Transmission of Arbovirus Evolutionary Intermediates with Epidemic Potential. Cell Host & Microbe, 15(6), 706-716. doi:10.1016/j.chom.2014.05.008
Remold, S. K., Rambaut, A., & Turner, P. E. (2008). Evolutionary Genomics of Host Adaptation in Vesicular Stomatitis Virus. Molecular Biology and Evolution, 25(6), 1138-1147. doi:10.1093/molbev/msn059
Foll, M., Poh, Y.-P., Renzette, N., Ferrer-Admetlla, A., Bank, C., Shim, H., … Jensen, J. D. (2014). Influenza Virus Drug Resistance: A Time-Sampled Population Genetics Perspective. PLoS Genetics, 10(2), e1004185. doi:10.1371/journal.pgen.1004185
Bedhomme, S., Lafforgue, G., & Elena, S. F. (2011). Multihost Experimental Evolution of a Plant RNA Virus Reveals Local Adaptation and Host-Specific Mutations. Molecular Biology and Evolution, 29(5), 1481-1492. doi:10.1093/molbev/msr314
Hillung, J., Cuevas, J. M., Valverde, S., & Elena, S. F. (2014). EXPERIMENTAL EVOLUTION OF AN EMERGING PLANT VIRUS IN HOST GENOTYPES THAT DIFFER IN THEIR SUSCEPTIBILITY TO INFECTION. Evolution, 68(9), 2467-2480. doi:10.1111/evo.12458
Acevedo, A., Brodsky, L., & Andino, R. (2013). Mutational and fitness landscapes of an RNA virus revealed through population sequencing. Nature, 505(7485), 686-690. doi:10.1038/nature12861
Foll, M., Shim, H., & Jensen, J. D. (2014). WFABC: a Wright-Fisher ABC-based approach for inferring effective population sizes and selection coefficients from time-sampled data. Molecular Ecology Resources, 15(1), 87-98. doi:10.1111/1755-0998.12280
Bordería, A. V., Isakov, O., Moratorio, G., Henningsson, R., Agüera-González, S., Organtini, L., … Vignuzzi, M. (2015). Group Selection and Contribution of Minority Variants during Virus Adaptation Determines Virus Fitness and Phenotype. PLOS Pathogens, 11(5), e1004838. doi:10.1371/journal.ppat.1004838
Kessinger, T. A., Perelson, A. S., & Neher, R. A. (2013). Inferring HIV Escape Rates from Multi-Locus Genotype Data. Frontiers in Immunology, 4. doi:10.3389/fimmu.2013.00252
SCHOLTHOF, K.-B. G., ADKINS, S., CZOSNEK, H., PALUKAITIS, P., JACQUOT, E., HOHN, T., … FOSTER, G. D. (2011). Top 10 plant viruses in molecular plant pathology. Molecular Plant Pathology, 12(9), 938-954. doi:10.1111/j.1364-3703.2011.00752.x
Karasev, A. V., & Gray, S. M. (2013). Continuous and Emerging Challenges of Potato virus Y in Potato. Annual Review of Phytopathology, 51(1), 571-586. doi:10.1146/annurev-phyto-082712-102332
Kogovšek, P., Pompe-Novak, M., Baebler, Š., Rotter, A., Gow, L., Gruden, K., … Ravnikar, M. (2010). Aggressive and mild Potato virus Y isolates trigger different specific responses in susceptible potato plants. Plant Pathology, 59(6), 1121-1132. doi:10.1111/j.1365-3059.2010.02340.x
BAEBLER, Š., KREČIČ-STRES, H., ROTTER, A., KOGOVŠEK, P., CANKAR, K., KOK, E. J., … RAVNIKAR, M. (2009). PVYNTNelicits a diverse gene expression response in different potato genotypes in the first 12 h after inoculation. Molecular Plant Pathology, 10(2), 263-275. doi:10.1111/j.1364-3703.2008.00530.x
Stare, T., Ramšak, Ž., Blejec, A., Stare, K., Turnšek, N., Weckwerth, W., … Gruden, K. (2015). Bimodal dynamics of primary metabolism-related responses in tolerant potato-Potato virus Y interaction. BMC Genomics, 16(1). doi:10.1186/s12864-015-1925-2
Kogovšek, P., Pompe-Novak, M., Petek, M., Fragner, L., Weckwerth, W., & Gruden, K. (2016). Primary Metabolism, Phenylpropanoids and Antioxidant Pathways Are Regulated in Potato as a Response to Potato virus Y Infection. PLOS ONE, 11(1), e0146135. doi:10.1371/journal.pone.0146135
Baebler, Š., Stare, K., Kovač, M., Blejec, A., Prezelj, N., Stare, T., … Gruden, K. (2011). Dynamics of Responses in Compatible Potato - Potato virus Y Interaction Are Modulated by Salicylic Acid. PLoS ONE, 6(12), e29009. doi:10.1371/journal.pone.0029009
Baebler, Š., Witek, K., Petek, M., Stare, K., Tušek-Žnidarič, M., Pompe-Novak, M., … Hennig, J. (2014). Salicylic acid is an indispensable component of the Ny-1 resistance-gene-mediated response against Potato virus Y infection in potato. Journal of Experimental Botany, 65(4), 1095-1109. doi:10.1093/jxb/ert447
Singh, D. P., Moore, C. A., Gilliland, A., & Carr, J. P. (2004). Activation of multiple antiviral defence mechanisms by salicylic acid. Molecular Plant Pathology, 5(1), 57-63. doi:10.1111/j.1364-3703.2004.00203.x
Kutnjak, D., Rupar, M., Gutierrez-Aguirre, I., Curk, T., Kreuze, J. F., & Ravnikar, M. (2015). Deep Sequencing of Virus-Derived Small Interfering RNAs and RNA from Viral Particles Shows Highly Similar Mutational Landscapes of a Plant Virus Population. Journal of Virology, 89(9), 4760-4769. doi:10.1128/jvi.03685-14
Zagordi, O., Bhattacharya, A., Eriksson, N., & Beerenwinkel, N. (2011). ShoRAH: estimating the genetic diversity of a mixed sample from next-generation sequencing data. BMC Bioinformatics, 12(1). doi:10.1186/1471-2105-12-119
Prosperi, M. C. F., & Salemi, M. (2011). QuRe: software for viral quasispecies reconstruction from next-generation sequencing data. Bioinformatics, 28(1), 132-133. doi:10.1093/bioinformatics/btr627
Prabhakaran, S., Rey, M., Zagordi, O., Beerenwinkel, N., & Roth, V. (2014). HIV Haplotype Inference Using a Propagating Dirichlet Process Mixture Model. IEEE/ACM Transactions on Computational Biology and Bioinformatics, 11(1), 182-191. doi:10.1109/tcbb.2013.145
Dynan, W., Fox, K., & Stoddard, B. (2013). Editorial: NAR Surveys the Past, Present and Future of Restriction Endonucleases. Nucleic Acids Research, 42(1), 1-2. doi:10.1093/nar/gkt1324
Töpfer, A., Marschall, T., Bull, R. A., Luciani, F., Schönhuth, A., & Beerenwinkel, N. (2014). Viral Quasispecies Assembly via Maximal Clique Enumeration. PLoS Computational Biology, 10(3), e1003515. doi:10.1371/journal.pcbi.1003515
Schirmer, M., Sloan, W. T., & Quince, C. (2012). Benchmarking of viral haplotype reconstruction programmes: an overview of the capacities and limitations of currently available programmes. Briefings in Bioinformatics, 15(3), 431-442. doi:10.1093/bib/bbs081
Lang, G. I., Rice, D. P., Hickman, M. J., Sodergren, E., Weinstock, G. M., Botstein, D., & Desai, M. M. (2013). Pervasive genetic hitchhiking and clonal interference in forty evolving yeast populations. Nature, 500(7464), 571-574. doi:10.1038/nature12344
Zwart, M. P., Daròs, J.-A., & Elena, S. F. (2012). Effects of Potyvirus Effective Population Size in Inoculated Leaves on Viral Accumulation and the Onset of Symptoms. Journal of Virology, 86(18), 9737-9747. doi:10.1128/jvi.00909-12
Ruiz-Jarabo, C. M., Arias, A., Baranowski, E., Escarmís, C., & Domingo, E. (2000). Memory in Viral Quasispecies. Journal of Virology, 74(8), 3543-3547. doi:10.1128/jvi.74.8.3543-3547.2000
Pruss, G. J., Lawrence, C. B., Bass, T., Li, Q. Q., Bowman, L. H., & Vance, V. (2004). The potyviral suppressor of RNA silencing confers enhanced resistance to multiple pathogens. Virology, 320(1), 107-120. doi:10.1016/j.virol.2003.11.027
Alamillo, J. M., Saénz, P., & García, J. A. (2006). Salicylic acid-mediated and RNA-silencing defense mechanisms cooperate in the restriction of systemic spread of plum pox virus in tobacco. The Plant Journal, 48(2), 217-227. doi:10.1111/j.1365-313x.2006.02861.x
Yu, D., Fan, B., MacFarlane, S. A., & Chen, Z. (2003). Analysis of the Involvement of an Inducible Arabidopsis RNA-Dependent RNA Polymerase in Antiviral Defense. Molecular Plant-Microbe Interactions®, 16(3), 206-216. doi:10.1094/mpmi.2003.16.3.206
Miyashita, S., Ishibashi, K., Kishino, H., & Ishikawa, M. (2015). Viruses Roll the Dice: The Stochastic Behavior of Viral Genome Molecules Accelerates Viral Adaptation at the Cell and Tissue Levels. PLOS Biology, 13(3), e1002094. doi:10.1371/journal.pbio.1002094
Kogovšek, P., Gow, L., Pompe-Novak, M., Gruden, K., Foster, G. D., Boonham, N., & Ravnikar, M. (2008). Single-step RT real-time PCR for sensitive detection and discrimination of Potato virus Y isolates. Journal of Virological Methods, 149(1), 1-11. doi:10.1016/j.jviromet.2008.01.025
Weller, S. A., Elphinstone, J. G., Smith, N. C., Boonham, N., & Stead, D. E. (2000). Detection of Ralstonia solanacearumStrains with a Quantitative, Multiplex, Real-Time, Fluorogenic PCR (TaqMan) Assay. Applied and Environmental Microbiology, 66(7), 2853-2858. doi:10.1128/aem.66.7.2853-2858.2000
Gutiérrez-Aguirre, I., Rački, N., Dreo, T., & Ravnikar, M. (2015). Droplet Digital PCR for Absolute Quantification of Pathogens. Methods in Molecular Biology, 331-347. doi:10.1007/978-1-4939-2620-6_24
Rupar, M., Faurez, F., Tribodet, M., Gutiérrez-Aguirre, I., Delaunay, A., Glais, L., … Ravnikar, M. (2015). Fluorescently Tagged Potato virus Y: A Versatile Tool for Functional Analysis of Plant-Virus Interactions. Molecular Plant-Microbe Interactions®, 28(7), 739-750. doi:10.1094/mpmi-07-14-0218-ta
Li, H., & Durbin, R. (2009). Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics, 25(14), 1754-1760. doi:10.1093/bioinformatics/btp324
Li, H., Handsaker, B., Wysoker, A., Fennell, T., Ruan, J., … Homer, N. (2009). The Sequence Alignment/Map format and SAMtools. Bioinformatics, 25(16), 2078-2079. doi:10.1093/bioinformatics/btp352
Nelson, C. W., Moncla, L. H., & Hughes, A. L. (2015). SNPGenie: estimating evolutionary parameters to detect natural selection using pooled next-generation sequencing data: Table 1. Bioinformatics, btv449. doi:10.1093/bioinformatics/btv449
Suzuki R Shimodaira H . 2015. pvclust: hierarchical clustering with P values via multiscale bootstrap resampling. R package version 2.0-0. https://cran.r-project.org/web/packages/pvclust/ .
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