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首页> 外文期刊>Frontiers in Microbiology >Bacteriophage T4 Infection of Stationary Phase E. coli: Life after Log from a Phage Perspective
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Bacteriophage T4 Infection of Stationary Phase E. coli: Life after Log from a Phage Perspective

机译:静止期<斜体> E的噬菌体T4感染。大肠菌:从噬菌体角度看日志后的生活

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Virtually all studies of phage infections investigate bacteria growing exponentially in rich media. In nature, however, phages largely encounter non-growing cells. Bacteria entering stationary phase often activate well-studied stress defense mechanisms that drastically alter the cell, facilitating its long-term survival. An understanding of phage-host interactions in such conditions is of major importance from both an ecological and therapeutic standpoint. Here, we show that bacteriophage T4 can efficiently bind to, infect and kill E. coli in stationary phase, both in the presence and absence of a functional stationary-phase sigma factor, and explore the response of T4-infected stationary phase cells to the addition of fresh nutrients 5 or 24 h after that infection. An unexpected new mode of response has been identified. “Hibernation” mode is a persistent but reversible dormant state in which the infected cells make at least some phage enzymes, but halt phage development until appropriate nutrients become available before producing phage particles. Our evidence indicates that the block in hibernation mode occurs after the middle-mode stage of phage development; host DNA breakdown and the incorporation of the released nucleotides into phage DNA indicate that the enzymes of the nucleotide synthesizing complex, under middle-mode control, have been made and assembled into a functional state. Once fresh glucose and amino acids become available, the standard lytic infection process rapidly resumes and concentrations of up to 10~(11)progeny phage (an average of about 40 phage per initially present cell) are produced. All evidence is consistent with the hibernation-mode control point lying between middle mode and late mode T4 gene expression. We have also observed a “scavenger” response, where the infecting phage takes advantage of whatever few nutrients are available to produce small quantities of progeny within 2 to 5 h after infection. The scavenger response seems able to produce no more than an average of one phage per originally available cell, and few if any further progeny are produced by cells in this mode even if fresh nutrients are made available later.
机译:几乎所有有关噬菌体感染的研究都对细菌在富媒体中成倍增长的情况进行了调查。然而,在自然界中,噬菌体主要遇到不生长的细胞。进入静止期的细菌通常会激活经过充分研究的应激防御机制,从而极大地改变细胞,促进其长期存活。从生态学和治疗学的观点来看,对在这种条件下的噬菌体-宿主相互作用的理解都是至关重要的。在这里,我们表明噬菌体T4可以在存在和不存在功能性固定相西格玛因子的情况下,有效地结合,感染和杀死固定相中的大肠杆菌,并探索感染了T4的固定相细胞对大肠杆菌的反应。感染后5或24小时添加新鲜营养素。已经确定了意外的新响应方式。 “休眠”模式是一种持久但可逆的休眠状态,在这种状态下,受感染的细胞会产生至少一些噬菌体酶,但会在产生噬菌体颗粒之前停止噬菌体的发育直至获得适当的营养。我们的证据表明,冬眠模式下的阻滞发生在噬菌体发育的中间模式阶段之后。宿主DNA的分解和释放的核苷酸掺入噬菌体DNA表明,在中间模式控制下,核苷酸合成复合物的酶已经制成并组装成功能状态。一旦获得新鲜的葡萄糖和氨基酸,标准的裂解感染过程就会迅速恢复,并产生高达10〜(11)个子代噬菌体的​​浓度(每个最初存在的细胞平均约40个噬菌体)。所有证据均与处于中间模式和晚期模式T4基因表达之间的休眠模式控制点一致。我们还观察到了“清道夫”反应,在这种情况下,感染噬菌体会利用几乎所有可利用的营养物在感染后2至5小时内产生少量后代。清除剂应答似乎能够为每个原始可利用的细胞产生平均不超过一个噬菌体,并且即使后来提供了新鲜的营养素,这种模式下的细胞也几乎不会产生任何后代。

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