Meir Moran, Kahn Arielle, Farage Carmel, Maoz Yael, Harel Noam, Ben Zvi Adi, Segev Shir, Volkov Maria, Yahud Ravit, Gophna Uri, Stern Adi
The Shmunis School of Biomedicine and Cancer Research, Tel Aviv University, Tel Aviv, Israel.
Edmond J. Safra Center for Bioinformatics, Tel Aviv University, Tel Aviv, Israel.
Mol Biol Evol. 2025 Jan 6;42(1). doi: 10.1093/molbev/msae258.
Cheater viruses cannot replicate on their own yet replicate faster than the wild type (WT) when the 2 viruses coinfect the same cell. Cheaters must possess dual genetic features: a defect, which leads to their inability to infect cells on their own, and a selective advantage over WT during coinfection. Previously, we have discovered 2 point-mutant cheaters of the MS2 bacteriophage. Here, we set out to discover the possible repertoire of cheater MS2 viruses by performing experimental evolution at a very high multiplicity of infection. Our results revealed a third point-mutant cheater that arose in 8 biological replicas. Each of the 3 primary cheaters disrupts the fine balance necessary for phage replication, in different ways that create a defect + advantage. We found that over time, the point-mutant cheaters accumulate additional secondary mutations, which alter other stages of the viral replication cycle, complementing the disruptions created by the original cheater. Intriguingly, cheater and secondary mutations almost always reside in very close proximity on the genome. This region encodes for multiple functions: overlapping reading frames as well as overlapping RNA structures critical for transitioning from one stage to another in the viral replication cycle. This region of overlap explains the dual functions of cheaters, as one mutation can have pleiotropic effects. Overall, these findings underscore how viruses, whose dense genomes often have overlapping functions, can easily evolve point-mutant cheaters, and how cheaters can evolve to alter the intricate balance of the viral replication cycle.
欺骗性病毒自身无法复制,但当与野生型(WT)病毒共同感染同一细胞时,其复制速度比野生型病毒更快。欺骗性病毒必须具备双重遗传特征:一是存在缺陷,导致其无法独自感染细胞;二是在共同感染期间相对于野生型具有选择性优势。此前,我们已经发现了MS2噬菌体的两种点突变型欺骗性病毒。在此,我们通过在极高的感染复数下进行实验进化,试图发现欺骗性MS2病毒可能的种类。我们的结果揭示了在8个生物学重复样本中出现的第三种点突变型欺骗性病毒。这3种主要的欺骗性病毒均以不同方式破坏了噬菌体复制所需的精细平衡,从而产生了缺陷 + 优势。我们发现,随着时间的推移,点突变型欺骗性病毒会积累额外的二级突变,这些突变会改变病毒复制周期的其他阶段,从而弥补原始欺骗性病毒造成的破坏。有趣的是,欺骗性突变和二级突变几乎总是在基因组上非常接近的位置。该区域编码多种功能:重叠阅读框以及对病毒复制周期中从一个阶段过渡到另一个阶段至关重要的重叠RNA结构。这种重叠区域解释了欺骗性病毒的双重功能,因为一个突变可能具有多效性。总体而言,这些发现强调了基因组密集且功能常常重叠的病毒是如何轻易进化出点突变型欺骗性病毒的,以及欺骗性病毒是如何进化以改变病毒复制周期的复杂平衡的。