Laboratory for Foodborne Zoonoses, Public Health Agency of Canada, Guelph, ON, NIG 3W4, Canada.
Virol J. 2012 May 31;9:102. doi: 10.1186/1743-422X-9-102.
The flagellotropic phage 7-7-1 infects motile cells of Agrobacterium sp H13-3 by attaching to and traveling along the rotating flagellar filament to the secondary receptor at the base, where it injects its DNA into the host cell. Here we describe the complete genomic sequence of 69,391 base pairs of this unusual bacteriophage.
The sequence of the 7-7-1 genome was determined by pyro(454)sequencing to a coverage of 378-fold. It was annotated using MyRAST and a variety of internet resources. The structural proteome was analyzed by SDS-PAGE coupled electrospray ionization-tandem mass spectrometry (MS/MS).
Sequence annotation and a structural proteome analysis revealed 127 open reading frames, 84 of which are unique. In six cases 7-7-1 proteins showed sequence similarity to proteins from the virulent Burkholderia myovirus BcepB1A. Unique features of the 7-7-1 genome are the physical separation of the genes encoding the small (orf100) and large (orf112) subunits of the DNA packaging complex and the apparent lack of a holin-lysin cassette. Proteomic analysis revealed the presence of 24 structural proteins, five of which were identified as baseplate (orf7), putative tail fibre (orf102), portal (orf113), major capsid (orf115) and tail sheath (orf126) proteins. In the latter case, the N-terminus was removed during capsid maturation, probably by a putative prohead protease (orf114).
鞭毛噬菌体 7-7-1 通过附着在旋转的鞭毛丝上并沿着鞭毛丝移动到基部的次级受体,感染根瘤农杆菌 H13-3 的运动细胞,在那里它将其 DNA 注入宿主细胞。在这里,我们描述了这个不寻常噬菌体的 69391 个碱基对的完整基因组序列。
使用焦磷酸测序(pyro(454)sequencing)将 7-7-1 基因组的序列测序至 378 倍的覆盖率。它使用 MyRAST 和各种互联网资源进行注释。通过 SDS-PAGE 结合电喷雾电离串联质谱(MS/MS)分析结构蛋白质组。
序列注释和结构蛋白质组分析揭示了 127 个开放阅读框,其中 84 个是独特的。在六种情况下,7-7-1 蛋白与毒力旺盛的伯克霍尔德氏菌病毒 BcepB1A 的蛋白质具有序列相似性。7-7-1 基因组的独特特征是编码 DNA 包装复合物小(orf100)和大(orf112)亚基的基因的物理分离,以及明显缺乏溶菌素盒。蛋白质组分析显示存在 24 种结构蛋白,其中 5 种被鉴定为基板(orf7)、假定的尾部纤维(orf102)、门(orf113)、主要衣壳(orf115)和尾部鞘(orf126)蛋白。在后一种情况下,衣壳成熟过程中去除了 N 端,可能是由假定的头部蛋白酶(orf114)去除的。