Allison Gwen E, Angeles Dario, Tran-Dinh Nai, Verma Naresh K
School of Biochemistry and Molecular Biology, Faculty of Science, The Australian National University, Canberra ACT 0200, Australia.
J Bacteriol. 2002 Apr;184(7):1974-87. doi: 10.1128/JB.184.7.1974-1987.2002.
Bacteriophage SfV is a temperate serotype-converting phage of Shigella flexneri. SfV encodes the factors involved in type V O-antigen modification, and the serotype conversion and integration-excision modules of the phage have been isolated and characterized. We now report on the complete sequence of the SfV genome (37,074 bp). A total of 53 open reading frames were predicted from the nucleotide sequence, and analysis of the corresponding proteins was used to construct a functional map. The general organization of the genes in the SfV genome is similar to that of bacteriophage lambda, and numerous features of the sequence are described. The superinfection immunity system of SfV includes a lambda-like repression system and a P4-like transcription termination mechanism. Sequence analysis also suggests that SfV encodes multiple DNA methylases, and experiments confirmed that orf-41 encodes a Dam methylase. Studies conducted to determine if the phage-encoded methylase confers host DNA methylation showed that the two S. flexneri strains analyzed encode their own Dam methylase. Restriction mapping and sequence analysis revealed that the phage genome has cos sites at the termini. The tail assembly and structural genes of SfV show homology to those of phage Mu and Mu-like prophages in the genome of Escherichia coli O157:H7 and Haemophilus influenzae. Significant homology (30% of the genome in total) between sections of the early, regulatory, and structural regions of the SfV genome and the e14 and KpLE1 prophages in the E. coli K-12 genome were noted, suggesting that these three phages have common evolutionary origins.
噬菌体SfV是弗氏志贺菌的一种温和型血清型转换噬菌体。SfV编码参与V型O抗原修饰的因子,并且该噬菌体的血清型转换和整合-切除模块已被分离和鉴定。我们现在报告SfV基因组的完整序列(37,074 bp)。从核苷酸序列中预测出总共53个开放阅读框,并通过对相应蛋白质的分析构建了功能图谱。SfV基因组中基因的总体组织与噬菌体λ相似,并描述了该序列的许多特征。SfV的超感染免疫系统包括一个类似λ的抑制系统和一个类似P4的转录终止机制。序列分析还表明SfV编码多种DNA甲基化酶,实验证实orf-41编码一种Dam甲基化酶。为确定噬菌体编码的甲基化酶是否赋予宿主DNA甲基化而进行的研究表明,所分析的两种弗氏志贺菌菌株都编码它们自己的Dam甲基化酶。限制性图谱分析和序列分析表明,噬菌体基因组在末端具有粘性末端位点。SfV的尾部组装和结构基因与大肠杆菌O157:H7和流感嗜血杆菌基因组中的噬菌体Mu及类Mu原噬菌体的尾部组装和结构基因具有同源性。注意到SfV基因组的早期、调控和结构区域的部分与大肠杆菌K-12基因组中的e14和KpLE1原噬菌体之间存在显著同源性(总共占基因组的30%),这表明这三种噬菌体具有共同的进化起源。