Microbial Evolutionary Genomics, Institut Pasteur, CNRS, UMR3525, Paris, France.
Mol Biol Evol. 2021 May 19;38(6):2497-2512. doi: 10.1093/molbev/msab044.
Bacteriophages (phages) evolve rapidly by acquiring genes from other phages. This results in mosaic genomes. Here, we identify numerous genetic transfers between distantly related phages and aim at understanding their frequency, consequences, and the conditions favoring them. Gene flow tends to occur between phages that are enriched for recombinases, transposases, and nonhomologous end joining, suggesting that both homologous and illegitimate recombination contribute to gene flow. Phage family and host phyla are strong barriers to gene exchange, but phage lifestyle is not. Even if we observe four times more recent transfers between temperate phages than between other pairs, there is extensive gene flow between temperate and virulent phages, and between the latter. These predominantly involve virulent phages with large genomes previously classed as low gene flux, and lead to the preferential transfer of genes encoding functions involved in cell energetics, nucleotide metabolism, DNA packaging and injection, and virion assembly. Such exchanges may contribute to the observed twice larger genomes of virulent phages. We used genetic transfers, which occur upon coinfection of a host, to compare phage host range. We found that virulent phages have broader host ranges and can mediate genetic exchanges between narrow host range temperate phages infecting distant bacterial hosts, thus contributing to gene flow between virulent phages, as well as between temperate phages. This gene flow drastically expands the gene repertoires available for phage and bacterial evolution, including the transfer of functional innovations across taxa.
噬菌体(phages)通过从其他噬菌体获取基因而快速进化。这导致了镶嵌基因组。在这里,我们鉴定了许多远缘噬菌体之间的基因转移,并旨在了解它们的频率、后果以及有利于它们的条件。基因流动倾向于发生在富含重组酶、转座酶和非同源末端连接的噬菌体之间,这表明同源重组和非同源重组都有助于基因流动。噬菌体家族和宿主门是基因交换的强大障碍,但噬菌体的生活方式不是。即使我们观察到温和噬菌体之间的最近转移比其他配对之间多四倍,但温和噬菌体和毒性噬菌体之间,以及后者之间,都有广泛的基因流动。这些主要涉及以前被归类为低基因通量的大基因组的毒性噬菌体,导致参与细胞能量学、核苷酸代谢、DNA 包装和注射以及病毒体组装的功能基因的优先转移。这种交换可能有助于解释观察到的毒性噬菌体基因组大小是温和噬菌体的两倍。我们利用在宿主共感染时发生的遗传转移来比较噬菌体的宿主范围。我们发现毒性噬菌体具有更广泛的宿主范围,并且可以介导感染遥远细菌宿主的窄宿主范围温和噬菌体之间的遗传交换,从而促进毒性噬菌体之间以及温和噬菌体之间的基因流动。这种基因流动极大地扩展了噬菌体和细菌进化可用的基因库,包括功能创新在分类群之间的转移。