Kohm Katharina, Floccari Valentina A, Lutz Veronika T, Nordmann Birthe, Mittelstädt Carolin, Poehlein Anja, Dragoš Anna, Commichau Fabian M, Hertel Robert
FG Synthetic Microbiology, Institute for Biotechnology, BTU Cottbus-Senftenberg, Senftenberg, 01968, Germany.
Biotechnical Faculty, University of Ljubljana, Ljubljana, 1000, Slovenia.
Environ Microbiol. 2022 Apr;24(4):2098-2118. doi: 10.1111/1462-2920.15964. Epub 2022 Mar 15.
The Bacillus phage SPβ has been known for about 50 years, but only a few strains are available. We isolated four new wild-type strains of the SPbeta species. Phage vB_BsuS-Goe14 introduces its prophage into the spoVK locus, previously not observed to be used by SPβ-like phages. Sequence data revealed the genome replication strategy and the genome packaging mode of SPβ-like phages. We extracted 55 SPβ-like prophages from public Bacillus genomes, thereby discovering three more integration loci and one additional type of integrase. The identified prophages resemble four new species clusters and three species orphans in the genus Spbetavirus. The determined core proteome of all SPβ-like prophages consists of 38 proteins. The integration cassette proved to be not conserved, even though, present in all strains. It consists of distinct integrases. Analysis of SPβ transcriptomes revealed three conserved genes, yopQ, yopR, and yokI, to be transcribed from a dormant prophage. While yopQ and yokI could be deleted from the prophage without activating the prophage, damaging of yopR led to a clear-plaque phenotype. Under the applied laboratory conditions, the yokI mutant showed an elevated virion release implying the YokI protein being a component of the arbitrium system.
芽孢杆菌噬菌体SPβ已被发现约50年,但仅有少数菌株可供研究。我们分离出了4株新的SPbeta物种野生型菌株。噬菌体vB_BsuS-Goe14将其前噬菌体导入spoVK基因座,此前未观察到类似SPβ的噬菌体使用该基因座。序列数据揭示了类似SPβ噬菌体的基因组复制策略和基因组包装模式。我们从公开的芽孢杆菌基因组中提取了55个类似SPβ的前噬菌体,从而发现了另外3个整合位点和1种额外类型的整合酶。鉴定出的前噬菌体类似于Spbetavirus属中的4个新物种簇和3个物种孤儿。所有类似SPβ的前噬菌体的核心蛋白质组由38种蛋白质组成。整合盒虽存在于所有菌株中,但并不保守,它由不同的整合酶组成。对SPβ转录组的分析揭示,有3个保守基因yopQ、yopR和yokI从休眠前噬菌体中转录。虽然yopQ和yokI可以从前噬菌体中删除而不激活前噬菌体,但破坏yopR会导致清晰噬菌斑表型。在所应用的实验室条件下,yokI突变体显示出病毒粒子释放增加,这意味着YokI蛋白是仲裁系统的一个组成部分。