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  • Anderson, C. W., and J. Eigner. 1971. Breakdown and exclusion of superinfecting T-Even Bacteriophage in Escherichia coli. Journal of Virology 8:869886.
  • Bamford, D. H., E. T. Palva, and K. Lounatmaa. 1976. Ultrastructure and life cycle of the lipid-containing bacteriophage phi 6. Journal of General Virology 32:249259.
  • Bamford, D. H., M. Romantschuk, and P. J. Somerharj. 1987. Membrane fusion in prokaryotes: bacteriophage phi 6 membrane fuses with the Pseudomonas syringae outer membrane. EMBO Journal 6:14671473.
  • Bollyky, P., A. Rambaut, P. Harvey, and E. Holmes. 1996. Recombination between sequences of hepatitis B virus from different genotypes. Journal of Molecular Evolution 42:97102.
  • Breiner, K. M. 2001. Envelope protein-mediated down-regulation of hepatitis B virus receptor in infected hepatocytes. Journal of Virology 75:143150.
  • Burch, C. L., and L. Chao. 1999. Evolution by small steps and rugged landscapes in the RNA virus phi 6. Genetics 151:921927.
  • Carbonnelle, E., S. Helaine, L. Prouvensier, X. Nassif, and V. Pelicic. 2005. Type IV pilus biogenesis in Neisseria meningitidis : PilW is involved in a step occurring after pilus assembly, essential for fibre stability and function. Molecular microbiology 55:5464.
  • Chen, J., Q. Dang, D. Unutmaz, V. K. Pathak, F. Maldarelli, D. Powell, and W. S. Hu. 2005. Mechanisms of nonrandom human immunodeficiency virus Type 1 infection and double infection: preference in virus entry is important but is not the sole factor. Journal of Virology 79:41404149.
  • Christen, L., J. Seto, and E. G. Niles. 1990. Superinfection exclusion of vaccinia virus in virus-infected cell cultures. Virology 174:3542.
  • Cicin-Sain, L., J. Podlech, M. Messerle, M. J. Reddehase, and U. H. Koszinowski. 2005. Frequent coinfection of cells explains functional in vivo complementation between cytomegalovirus variants in the multiply infected host. Journal of Virology 79:94929502.
  • Coffin, J. M. 1979. Structure, replication, and recombination of retrovirus genomes: some unifying hypotheses. Journal of General Virology 42:126.
  • Cox, N. J., and K. Subbarao. 2000. Global epidemiology of influenza: past and present. Annual Review of Medicine 51:407421.
  • Dang, Q., J. Chen, D. Unutmaz, J. M. Coffin, V. K. Pathak, D. Powell, V. N. KewalRamani et al. 2004. Nonrandom HIV-1 infection and double infection via direct and cell-mediated pathways. Proceedings of the National Academy of Sciences of the United States of America 101:632637.
  • Delbrück, M. 1945. The burst size distribution in the growth of bacterial viruses (Bacteriophages). Journal of Bacteriology 50:131135.
  • Delbrück, M., and R. Luria. 1942. Interference between bacterial viruses. I. Interference between two bacterial viruses acting upon the same host, and the mechanism of virus growth. Archives of Biochemistry 1:111141.
  • Doermann, A. H. 1948. Lysis and lysis inhibition with Escherichia coli bacteriophage. Journal of Bacteriology 55:257275.
  • Dulbecco, R. 1952. Mutual exclusion between related phages. Journal of Bacteriology 63:209217.
  • Fisher, R. A. 1930. The Genetical Theory of Natural Selection. Oxford University Press, Oxford.
  • Gandon, S., M. J. Mackinnon, S. Nee, and A. F. Read. 2001. Imperfect vaccines and the evolution of pathogen virulence. Nature 414:751756.
  • Gottlieb, P., S. Metzger, M. Romantschuk, J. Carton, J. Strassman, D. H. Bamford, N. Kalkkinen et al. 1988. Nucleotide sequence of the middle dsRNA segment of bacteriophage Φ6: placement of the genes of membrane-associated proteins. Virology 163:183190.
  • Gottlieb, P., J. Strassman, X. Qiao, M. Frilander, A. Frucht, and L. Mindich. 1992. In vitro packaging and replication of individual genomic segments of Bacteriophage Φ6 RNA. Journal of Virology 66:26112616.
  • Hershey, A. D., A. Garen, D. K. Fraser, and J. D. Hudis. 1954. Growth and inheritance in bacteriophage. Carnegie Institute of Washington Year Book 53:210225.
  • Iwabu, Y., T. Goto, S. Tsuji, J. Warachit, G. M. Li, S. Shoji, M. Kameoka et al. 2006. Superinfection of human immunodeficiency virus type 1 (HIV-1) to cell clone persistently infected with defective virus induces production of highly cytopathogenic HIV-1. Microbes and Infection 8:17731782.
  • Jakovljevic, V., S. Leonardy, M. Hoppert, and L. Søgaard-Andersen. 2008. PilB and PilT are ATPases acting antagonistically in type IV pilus function in Myxococcus xanthaus. Journal of Bacteriology 190:24112421.
  • Jetzt, A. E., H. Yu, G. J. Klarmann, Y. Ron, B. D. Preston, and J. P. Dougherty. 2000. High rate of recombination throughout the human immunodeficiency virus type 1 genome. Journal of Virology 74:12341240.
  • Kellam, P., and B. A. Larder. 1995. Retroviral recombination can lead to linkage of reverse-transcriptase mutations that confer increased Zidovudine Resistance. Journal of Virology 69:669674.
  • Kew, O. M., R. W. Sutter, E. M. De Gourville, W. R. Dowdle, and M. A. Pallansch. 2005. Vaccine-derived polioviruses and the endgame strategy for global polio eradication. Annual Review of Microbiology 59:587635.
  • Lesley, S. M., R. C. French, A. F. Graham, and C. E. Van Rooyen. 1951. Studies on the relationship between virus and host cell II. The breakdown of T2r+ bacteriophage upon infection of its host Escherichia coli. Canadian Journal of Medical Sciences 29:128143.
  • Levy, D. N., G. M. Aldrovandi, O. Kutsch, and G. M. Shaw. 2004. Dynamics of HIV-1 recombination in its natural target cells. Proceedings of the National Academy of Sciences of the United States of America 101:42044209.
  • Marschall, M., H. MeierEwert, G. Herrler, G. Zimmer, and H. F. Maassab. 1997. The cell receptor level is reduced during persistent infection with influenza C virus. Archives of Virology 142:11551164.
  • Merz, A. J., M. So, and M. P. Sheetz. 2000. Pilus retraction powers bacterial twitching motility. Nature 407:96102.
  • Michel, N., I. Allespach, S. Venzke, O. T. Fackler, and O. T. Keppler. 2005. The Nef protein of human immunodeficiency virus establishes superinfection immunity by a dual strategy to downregulate cell-surface CCR5 and CD4. Current Biology 15:714723.
  • Mindich, L., G. MacKenzie, J. Strassman, T. McGraw, S. Metzger, M. Romantschuk, and D. Bamford. 1985. cDNA cloning of portions of the bacteriophage phi 6 genome. Journal of Bacteriology 162:992999.
  • Mindich, L., X. Qiao, J. Qiao, S. Onodera, M. Romantschuk, and D. Hoogstraten. 1999. Isolation of additional bacteriophages with genomes of segmented double-stranded RNA. Journal of Bacteriology 181:45054508.
  • Monath, T. P., N. Kanesa-thasan, F. Guirakhoo, K. Pugachev, J. Almond, J. Lang, M. J. Quentin-Millet et al. 2005. Recombination and flavivirus vaccines: a commentary. Vaccine 23:29562958.
  • Moutouh, L., J. Corbeil, and D. D. Richman. 1996. Recombination leads to the rapid emergence of HIV-1 dually resistant mutants under selective drug pressure. Proceedings of the National Academy of Sciences of the United States of America 93:61066111.
  • Muller, H. J. 1932. Some genetic aspects of sex. American Naturalist 66:118128.
  • Muller, H. J. 1964. The relation of recombination to mutational advance. Mutation Research 109:29.
  • Ptashne, M. 2004, A Genetic Switch: Phage Lambda Revisited, V, 3rd edn. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
  • Robertson, D. L., P. M. Sharp, F. E. McCutchan, and B. H. Hahn. 1995. Recombination in HIV-1. Nature 374:124126.
  • Rohayem, J., J. Munch, and A. Rethwilm. 2005. Evidence of recombination in the norovirus capsid gene. Journal of Virology 79:49774990.
  • Roine, E., D. N. Nunn, L. Paulin, and M. Romantschuk. 1996. Characterization of genes required for pilus expression in Pseudomonas syringae pathovar phaseolicola. Journal of Bacteriology 178:410417.
  • Schierup, M. H., C. H. Mordhorst, C. P. Muller, and L. S. Christensen. 2005. Evidence of recombination among early-vaccination era measles virus strains. Bmc Evolutionary Biology 5:52.
  • Smith, D. R., A. P. Adams, J. L. Kenney, E. Wang, and S. C. Wagner. 2008. Venezuelan equine encephalitis virus in the mosquito vector Aedes taeniorhynchus: infection initiated by a small number of susceptible epithelial cells and a population bottleneck. Virology 372:176186.
  • Streeck, H., B. Li, A. F. Y. Poon, A. Schneidewind, A. D. Gladden, K. A. Power, D. Daskalakis et al. 2008. Immune-driven recombination and loss of control after HIV superinfection. Journal of Experimental Medicine 205:17891796.
  • Turner, P. E., and L. Chao. 1998. Sex and the evolution of intrahost competition in RNA virus phi6. Genetics 150:523532.
  • Turner, P. E., and S. Duffy. 2008. Evolutionary ecology of multiple phage adsorption and infection. In S. T.Abedon, ed. Bacteriophage Ecology: Population Growth, Evolution, and Impact of Bacterial Viruses. Cambridge University Press, Cambridge.
  • Turner, P. E., C. L. Burch, K. A. Hanley, and L. Chao. 1999. Hybrid frequencies confirm limit to coinfection in the RNA bacteriophage phi 6. Journal of Virology 73:24202424.
  • Vanderavoort, H., A. Vanderende, G. A. Vanarkel, and P. J. Weisbeek. 1984. Regions of incompatibility in single-stranded DNA bacteriophages phi X174 and G4. Journal of Virology 50:533540.
  • Vidaver, A. K., R. K. Koski, and J. L. Van Etten. 1973. Bacteriophage phi6: a lipid-containing virus of Pseudomonas phaseolicola. Journal of Virology 11:799805.
  • Whitfield, C., and M. A. Valvano. 1993. Biosynthesis and expression of cell-surface polysaccharides in gram-negative bacteria. In A. H.Rose, ed. Advances in Microbial Physiology, pp. 135246. Academic Press, London.