Sudhakari Pavithra Anantharaman, Ramisetty Bhaskar Chandra Mohan
Laboratory of Molecular Biology and Evolution, School of Chemical and Biotechnology, SASTRA Deemed University, 312@ASK1, Thanjavur, India.
Microb Ecol. 2023 Nov;86(4):3068-3081. doi: 10.1007/s00248-023-02301-y. Epub 2023 Oct 16.
Temperate phages integrate into the bacterial genomes propagating along with the bacterial genomes. Multiple phage elements, representing diverse prophages, are present in most bacterial genomes. The evolutionary events and the ecological dynamics underlying the accumulation of prophage elements in bacterial genomes have yet to be understood. Here, we show that the local wastewater had 7% of lysogens (hosting mitomycin C-inducible prophages), and they showed resistance to superinfection by their corresponding lysates. Genomic analysis of four lysogens and four non-lysogens revealed the presence of multiple prophages (belonging to Myoviridae and Siphoviridae) in both lysogens and non-lysogens. For large-scale comparison, 2180 Escherichia coli genomes isolated from various sources across the globe and 523 genomes specifically isolated from diverse wastewaters were analyzed. A total of 15,279 prophages were predicted among 2180 E. coli genomes and 2802 prophages among 523 global wastewater isolates, with a mean of ~ 5 prophages per genome. These observations indicate that most putative prophages are relics of past bacteria-phage conflicts; they are "grounded" prophages that cannot excise from the bacterial genome. Prophage distribution analysis based on the sequence homology suggested the random distribution of E. coli prophages within and between E. coli clades. The independent occurrence pattern of these prophages indicates extensive horizontal transfers across the genomes. We modeled the eco-evolutionary dynamics to reconstruct the events that could have resulted in the prophage accumulation accounting for infection, superinfection immunity, and grounding. In bacteria-phage conflicts, the bacteria win by grounding the prophage, which could confer superinfection immunity.
温和噬菌体整合到细菌基因组中,并随细菌基因组一起传播。大多数细菌基因组中都存在多个代表不同原噬菌体的噬菌体元件。细菌基因组中原噬菌体元件积累背后的进化事件和生态动力学尚未完全明了。在此,我们发现当地废水中有7%的溶原菌(携带丝裂霉素C诱导型原噬菌体),并且它们对相应裂解物的超感染具有抗性。对4株溶原菌和4株非溶原菌的基因组分析表明,溶原菌和非溶原菌中均存在多个原噬菌体(属于肌尾噬菌体科和长尾噬菌体科)。为了进行大规模比较,我们分析了从全球不同来源分离的2180个大肠杆菌基因组以及专门从各种废水中分离的523个基因组。在2180个大肠杆菌基因组中总共预测到15279个原噬菌体,在523个全球废水分离株中预测到2802个原噬菌体,平均每个基因组约有5个原噬菌体。这些观察结果表明,大多数推定的原噬菌体是过去细菌与噬菌体冲突的遗迹;它们是无法从细菌基因组中切除的“固定”原噬菌体。基于序列同源性的原噬菌体分布分析表明,大肠杆菌原噬菌体在大肠杆菌进化枝内部和之间呈随机分布。这些原噬菌体的独立出现模式表明它们在基因组间有广泛的水平转移。我们对生态进化动力学进行建模,以重建可能导致原噬菌体积累的事件,这些事件涉及感染、超感染免疫和固定。在细菌与噬菌体的冲突中,细菌通过使原噬菌体固定而获胜,这可以赋予超感染免疫力。