生态尺度上的实验进化可将病毒基因型与特定宿主菌株联系起来

María Dolores Ramos-Barbero, Borja Aldeguer-Riquelme, Tomeu Viver, Judith Villamor, Miryam Carrillo-Bautista, Cristina López-Pascual, Konstantinos T Konstantinidis, Manuel Martínez-García, Fernando Santos, Ramon Rossello-Mora, Josefa Antón
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摘要

病毒通过控制种群多样性和细胞丰度来影响微生物群落结构和活动。由于元基因组学等独立于培养的方法(并不总能提供菌株级的分辨率)和基于培养的分析(消除了生态背景和原位相互作用)的局限性,识别和监测自然界中特定病毒-宿主配对的动态受到了阻碍。在这里,我们探讨了一种特定的 "自生 "宿主菌株及其病毒在自然群落中的相互作用。将 Salinibacter ruber 菌株 M8 添加到其分离环境--沿海盐碱地的结晶池中,利用培养、元基因组学和显微镜对病毒和细胞群落进行了为期一个月的监测。元基因组测序表明,M8 丰度在加入池塘后急剧下降,这可能是由于病毒捕食以外的其他原因。不过,M8 的存在为新病毒属 Phoenicisalinivirus 挑选了两个物种,并分离出 120 株。在这次实验中,一个由密切相关的病毒基因组变种组成的群体被一个具有感染 M8 能力的单一群体所取代,这种情况与从稀有生物圈中选择基因组变种是一致的。进一步的分析表明,病毒基因组中可能编码尾纤蛋白的区域是造成 M8 特异性的原因。我们的研究结果表明,低丰度病毒基因型提供了一个病毒种子库,可以在复杂的生态背景下实现高度特化的病毒-宿主反应。
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Experimental evolution at ecological scales allows linking of viral genotypes to specific host strains
Viruses shape microbial community structure and activity through the control of population diversity and cell abundances. Identifying and monitoring the dynamics of specific virus-host pairs in nature is hampered by the limitations of culture-independent approaches such as metagenomics, which do not always provide strain-level resolution, and culture-based analyses, which eliminate the ecological background and in-situ interactions. Here, we have explored the interaction of a specific “autochthonous” host strain and its viruses within a natural community. Bacterium Salinibacter ruber strain M8 was spiked into its environment of isolation, a crystallizer pond from a coastal saltern, and the viral and cellular communities were monitored for one month using culture, metagenomics, and microscopy. Metagenome sequencing indicated that the M8 abundance decreased sharply after being added to the pond, likely due to forces other than viral predation. However, the presence of M8 selected for two species of a new viral genus, Phoenicisalinivirus, for which 120 strains were isolated. During this experiment, an assemblage of closely related viral genomic variants was replaced by a single population with the ability to infect M8, a scenario which was compatible with the selection of a genomic variant from the rare biosphere. Further analysis implicated a viral genomic region putatively coding for a tail fiber protein to be responsible for M8 specificity. Our results indicate that low abundance viral genotypes provide a viral seed bank that allows for a highly specialized virus-host response within a complex ecological background.
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