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感染单链RNA噬菌体PRR1后的裂解生理学

Lysis Physiology of Infected with ssRNA Phage PRR1.

作者信息

Daugelavičius Rimantas, Daujotaitė Greta, Bamford Dennis H

机构信息

Department of Biochemistry, Vytautas Magnus University, LT-44248 Kaunas, Lithuania.

Molecular and Integrative Biosciences Research Programme, Department of Biological and Environmental Sciences and Institute of Biotechnology, University of Helsinki, FIN-00014 Helsinki, Finland.

出版信息

Viruses. 2024 Apr 21;16(4):645. doi: 10.3390/v16040645.

Abstract

The phage PRR1 belongs to the family, a group of ssRNA bacteriophages that infect Gram-negative bacteria. The variety of host cells is determined by the specificity of PRR1 to a pilus encoded by a broad host range of IncP-type plasmids that confer multiple types of antibiotic resistance to the host. Using strain PAO1 as a host, we analyzed the PRR1 infection cycle, focusing on cell lysis. PRR1 infection renders cells sensitive to lysozyme approximately 20 min before the start of a drop in suspension turbidity. At the same time, infected cells start to accumulate lipophilic anions. The on-line monitoring of the entire infection cycle showed that single-gene-mediated lysis strongly depends on the host cells' physiological state. The blockage of respiration or a reduction in the intracellular ATP concentration during the infection resulted in the inhibition of lysis. The same effect was observed when the synthesis of PRR1 lysis protein was induced in an expression system. In addition, lysis was strongly dependent on the level of aeration. Dissolved oxygen concentrations sufficient to support cell growth did not ensure efficient lysis, and a coupling between cell lysis initiation and aeration level was observed. However, the duration of the drop in suspension turbidity did not depend on the level of aeration.

摘要

噬菌体PRR1属于 科,是一类感染革兰氏阴性菌的单链RNA噬菌体。宿主细胞的多样性由PRR1对由广泛宿主范围的IncP型质粒编码的菌毛的特异性决定,这些质粒赋予宿主多种类型的抗生素抗性。以PAO1菌株作为宿主,我们分析了PRR1的感染周期,重点关注细胞裂解。PRR1感染使细胞在悬浮液浊度开始下降前约20分钟对溶菌酶敏感。同时,受感染的细胞开始积累亲脂性阴离子。对整个感染周期的在线监测表明,单基因介导的裂解强烈依赖于宿主细胞的生理状态。感染期间呼吸受阻或细胞内ATP浓度降低导致裂解受到抑制。当在 表达系统中诱导PRR1裂解蛋白的合成时,也观察到了相同的效果。此外,裂解强烈依赖于通气水平。足以支持细胞生长的溶解氧浓度并不能确保有效的裂解,并且观察到细胞裂解起始与通气水平之间存在耦合。然而,悬浮液浊度下降的持续时间并不依赖于通气水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c05c/11054506/8ed4379bad46/viruses-16-00645-g001.jpg

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