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病毒之战:利用一种病毒阻止另一种病毒的传播。

Virus wars: using one virus to block the spread of another.

作者信息

Paff Matthew L, Nuismer Scott L, Ellington Andrew, Molineux Ian J, Bull James J

机构信息

Department of Integrative Biology, University of Texas, Austin, TX, United States; The Institute for Cellular and Molecular Biology, University of Texas, Austin, TX, United States.

Department of Biological Sciences, University of Idaho , Moscow , ID , United States.

出版信息

PeerJ. 2016 Jun 29;4:e2166. doi: 10.7717/peerj.2166. eCollection 2016.

Abstract

The failure of traditional interventions to block and cure HIV infections has led to novel proposals that involve treating infections with therapeutic viruses-infectious viruses that specifically inhibit HIV propagation in the host. Early efforts in evaluating these proposals have been limited chiefly to mathematical models of dynamics, for lack of suitable empirical systems. Here we propose, develop and analyze an empirical system of a therapeutic virus that protects a host cell population against a lethal virus. The empirical system uses E. coli bacteria as the host cell population, an RNA phage as the lethal virus and a filamentous phage as the therapeutic virus. Basic dynamic properties are established for each virus alone and then together. Observed dynamics broadly agree with those predicted by a computer simulation model, although some differences are noted. Two cases of dynamics are contrasted, differing in whether the therapeutic virus is introduced before the lethal virus or after the lethal virus. The therapeutic virus increases in both cases but by different mechanisms. With the therapeutic virus introduced first, it spreads infectiously without any appreciable change in host dynamics. With the therapeutic virus introduced second, host abundance is depressed at the time therapy is applied; following an initial period of therapeutic virus spread by infection, the subsequent rise of protection is through reproduction by hosts already protected. This latter outcome is due to inheritance of the therapeutic virus state when the protected cell divides. Overall, the work establishes the feasibility and robustness to details of a viral interference using a therapeutic virus.

摘要

传统干预措施在阻断和治愈HIV感染方面的失败催生了一些新的提议,这些提议涉及用治疗性病毒(即能特异性抑制HIV在宿主体内传播的感染性病毒)来治疗感染。由于缺乏合适的实证系统,早期评估这些提议的工作主要局限于动力学数学模型。在此,我们提出、构建并分析一个治疗性病毒的实证系统,该系统可保护宿主细胞群体免受致死性病毒的侵害。这个实证系统以大肠杆菌作为宿主细胞群体,以一种RNA噬菌体作为致死性病毒,以一种丝状噬菌体作为治疗性病毒。先分别确定了每种病毒单独存在时以及共同存在时的基本动力学特性。观察到的动力学特性大致与计算机模拟模型预测的结果相符,不过也注意到了一些差异。对比了两种动力学情况,区别在于治疗性病毒是在致死性病毒之前引入还是在致死性病毒之后引入。在这两种情况下治疗性病毒都会增加,但机制不同。如果先引入治疗性病毒,它会通过感染进行传播,宿主动力学没有明显变化。如果后引入治疗性病毒,在应用治疗时宿主数量会减少;在治疗性病毒最初通过感染进行传播的一段时间之后,随后保护作用的增强是通过已受保护的宿主进行繁殖实现的。后一种结果是由于受保护的细胞分裂时治疗性病毒状态的遗传。总体而言,这项工作证实了使用治疗性病毒进行病毒干扰在细节方面的可行性和稳健性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1bb/4933091/b03ee2d39996/peerj-04-2166-g001.jpg

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