作为生命史开关的溶解/溶原转变

IF 5.5 2区 医学 Q1 VIROLOGY Virus Evolution Pub Date : 2024-04-03 eCollection Date: 2024-01-01 DOI:10.1093/ve/veae028
Joan Roughgarden
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引用次数: 0

摘要

溶解性生命周期和溶解性生命周期之间的过渡是温带病毒生命史的最重要特征。为了解释这种转变,我们提供了一个基于噬菌体/细菌种群动态离散时间表述的最佳生命史模型,该模型的特点是通过对环境中的病毒进行泊松采样来感染细菌。时间步长为病毒潜伏期。在这一模型中,细菌表面对病毒的吸收取决于密度,因此病毒/细菌共存,而细菌的生长则不需要取决于密度。溶解期和溶酶期之间的转换公式称为 "适应性转换"。根据该模型,当病毒作为噬菌体的种群增长速度快于通过裂解感染细胞产生的病毒时,病毒就会从溶解期转入溶生期;反之,病毒也会从溶生期转入溶解期。对所感染细菌有益的噬菌体在退出细菌基因组时会自动产生较低的适合度,从而被锁定在细菌基因组中,这里称之为 "噬菌体锁定"。这种适应性转换从本质上预测了生态地理学规则,即环境富集导致微生物化,同时溶解基因增加;波动的环境条件促进病毒介导的水平基因转移;含有噬菌体的细菌可以整合到真核宿主的微生物组中,形成功能整合的三方全生物体。这些预测更符合病毒生态学中的 "捎带赢家 "假说,而不是 "杀死赢家 "假说。
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Lytic/Lysogenic Transition as a Life-History Switch.

The transition between lytic and lysogenic life cycles is the most important feature of the life-history of temperate viruses. To explain this transition, an optimal life-history model is offered based a discrete-time formulation of phage/bacteria population dynamics that features infection of bacteria by Poisson sampling of virions from the environment. The time step is the viral latency period. In this model, density-dependent viral absorption onto the bacterial surface produces virus/bacteria coexistence and density dependence in bacterial growth is not needed. The formula for the transition between lytic and lysogenic phases is termed the 'fitness switch'. According to the model, the virus switches from lytic to lysogenic when its population grows faster as prophage than as virions produced by lysis of the infected cells, and conversely for the switch from lysogenic to lytic. A prophage that benefits the bacterium it infects automatically incurs lower fitness upon exiting the bacterial genome, resulting in its becoming locked into the bacterial genome in what is termed here as a 'prophage lock'. The fitness switch qualitatively predicts the ecogeographic rule that environmental enrichment leads to microbialization with a concomitant increase in lysogeny, fluctuating environmental conditions promote virus-mediated horizontal gene transfer, and prophage-containing bacteria can integrate into the microbiome of a eukaryotic host forming a functionally integrated tripartite holobiont. These predictions accord more with the 'Piggyback-the-Winner' hypothesis than with the 'Kill-the-Winner' hypothesis in virus ecology.

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来源期刊
Virus Evolution
Virus Evolution Immunology and Microbiology-Microbiology
CiteScore
10.50
自引率
5.70%
发文量
108
审稿时长
14 weeks
期刊介绍: Virus Evolution is a new Open Access journal focusing on the long-term evolution of viruses, viruses as a model system for studying evolutionary processes, viral molecular epidemiology and environmental virology. The aim of the journal is to provide a forum for original research papers, reviews, commentaries and a venue for in-depth discussion on the topics relevant to virus evolution.
期刊最新文献
Dimensionality reduction distills complex evolutionary relationships in seasonal influenza and SARS-CoV-2. Enhanced detection and molecular modeling of adaptive mutations in SARS-CoV-2 coding and non-coding regions using the c/µ test. Community-level variability in Bronx COVID-19 hospitalizations associated with differing population immunity during the second year of the pandemic. A phylogenetics and variant calling pipeline to support SARS-CoV-2 genomic epidemiology in the UK. Genomic epidemiology reveals the variation and transmission properties of SARS-CoV-2 in a single-source community outbreak.
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