Sanjuán Rafael
Institute for Integrative Systems Biology (I2SysBio), Universitat de València and Consejo Superior de Investigaciones Científicas València, Spain; Departament de Genètica, Universitat de València, València, Spain.
Trends Microbiol. 2017 May;25(5):402-412. doi: 10.1016/j.tim.2017.02.003. Epub 2017 Mar 3.
Increasing evidence indicates that viruses do not simply propagate as independent virions among cells, organs, and hosts. Instead, viral spread is often mediated by structures that simultaneously transport groups of viral genomes, such as polyploid virions, aggregates of virions, virion-containing proteinaceous structures, secreted lipid vesicles, and virus-induced cell-cell contacts. These structures increase the multiplicity of infection, independently of viral population density and transmission bottlenecks. Collective infectious units may contribute to the maintenance of viral genetic diversity, and could have implications for the evolution of social-like virus-virus interactions. These may include various forms of cooperation such as immunity evasion, genetic complementation, division of labor, and relaxation of fitness trade-offs, but also noncooperative interactions such as negative dominance and interference, potentially leading to conflict.
越来越多的证据表明,病毒并非简单地以独立病毒粒子的形式在细胞、器官和宿主之间传播。相反,病毒传播通常由同时运输病毒基因组群的结构介导,如多倍体病毒粒子、病毒粒子聚集体、含病毒粒子的蛋白质结构、分泌的脂质囊泡以及病毒诱导的细胞间接触。这些结构增加了感染复数,与病毒种群密度和传播瓶颈无关。集体感染单位可能有助于维持病毒遗传多样性,并可能对类似社会的病毒 - 病毒相互作用的进化产生影响。这些相互作用可能包括各种合作形式,如免疫逃避、基因互补、分工以及适应性权衡的放松,但也包括非合作相互作用,如负显性和干扰,这可能导致冲突。