Lucchini S, Desiere F, Brüssow H
Nestlé Research Centre, Nestec Ltd., Vers-chez-les-Blanc, Lausanne 26, CH-1000, Switzerland.
Virology. 1999 Aug 1;260(2):232-43. doi: 10.1006/viro.1999.9814.
The virulent cos-site Streptococcus thermophilus bacteriophage Sfi19 has a 37,392-bp-long genome consisting of 44 open reading frames all encoded on the same DNA strand. The genome of the temperate cos-site S. thermophilus phage Sfi21 is 3.3 kb longer (40,740 bp, 53 orfs). Both genomes are very similarly organized and differed mainly by gene deletion and DNA rearrangement events in the lysogeny module; gene replacement, duplication, and deletion events in the DNA replication module, and numerous point mutations. The level of point mutations varied from <1% (lysis and DNA replication modules) to >15% (DNA packaging and head morphogenesis modules). A dotplot analysis showed nearly a straight line over the left 25 kb of their genomes. Over the right genome half, a more variable dotplot pattern was observed. The entire lysogeny module from Sfi21 comprising 12 genes was replaced by 7 orfs in Sfi19, six showed similarity with genes from temperate pac-site S. thermophilus phages. None of the genes implicated in the establishment of the lysogenic state (integrase, superinfection immunity, repressor) or remnants of it were conserved in Sfi19, while a Cro-like repressor was detected. Downstream of the highly conserved DNA replication module 11 and 13 orfs were found in Sfi19 and phiSfi21, respectively: Two orfs from Sfi21 were replaced by a different gene and a duplication of the phage origin of replication in Sfi19; a further orf was only found in Sfi21. All other orfs from this region, which included a second putative phage repressor, were closely related between both phages. Two noncoding regions of Sfi19 showed sequence similarity to pST1, a small cryptic plasmid of S. thermophilus.
烈性粘性末端嗜热链球菌噬菌体Sfi19具有一个长度为37392 bp的基因组,由44个开放阅读框组成,所有这些开放阅读框都编码在同一条DNA链上。温和性粘性末端嗜热链球菌噬菌体Sfi21的基因组长3.3 kb(40740 bp,53个开放阅读框)。这两个基因组的组织方式非常相似,主要区别在于溶原模块中的基因缺失和DNA重排事件;DNA复制模块中的基因替换、重复和缺失事件,以及大量点突变。点突变水平从<1%(裂解和DNA复制模块)到>15%(DNA包装和头部形态发生模块)不等。点阵分析显示,在它们基因组左侧的25 kb区域几乎呈一条直线。在基因组右侧的一半区域,观察到更具变化的点阵模式。Sfi21完整的包含12个基因的溶原模块在Sfi19中被7个开放阅读框取代,其中6个与温和性pac末端嗜热链球菌噬菌体的基因具有相似性。在Sfi19中没有发现与溶原状态建立相关的基因(整合酶、超感染免疫、阻遏物)或其残余部分,不过检测到了一种类Cro阻遏物。在高度保守的DNA复制模块下游,Sfi19和phiSfi21分别发现了11个和13个开放阅读框:Sfi21的两个开放阅读框被一个不同的基因和Sfi19中噬菌体复制起点的重复所取代;另一个开放阅读框仅在Sfi21中发现。该区域的所有其他开放阅读框,包括第二个假定的噬菌体阻遏物,在这两种噬菌体之间密切相关。Sfi19的两个非编码区域与嗜热链球菌的一个小隐蔽性质粒pST1具有序列相似性。