Mahichi Faezeh, Synnott Aidan John, Yamamichi Keiko, Osada Toshiya, Tanji Yasunori
Department of Life science, Tokyo Institute of Technology, Midori-ku, Yokohama, Japan.
FEMS Microbiol Lett. 2009 Jun;295(2):211-7. doi: 10.1111/j.1574-6968.2009.01588.x. Epub 2009 Apr 21.
The application of bacteriophages (phages) in therapy urgently requires the production of wide-host-range recombinant phages that possess strong lytic activity. The wide-host-range IP008 phage was classified by transmission electron microscopy analysis as an A2 morphotype member of the Myoviridae family of the order Caudovirales. IP008 showed a high homology (99.4% similarity in the amino acid alignment of the major capsid protein Gp 23) with KEP10, another wide-host-range phage. The long tail fiber genes (genes 37 and 38) from the genome of T2 were replaced with those of the IP008 phage by homologous recombination. The host range of the recombinant phages was identical to that of IP008. Furthermore, the recombinant phage bacterial lytic activity was restored. Future analyses of host-range mutants of the closely related phages T2 and IP008 could lead to a more precise localization of the genetic factors responsible for receptor specificity.
噬菌体在治疗中的应用迫切需要生产具有强裂解活性的广宿主范围重组噬菌体。通过透射电子显微镜分析,广宿主范围的IP008噬菌体被归类为尾病毒目肌尾噬菌体科的A2形态型成员。IP008与另一种广宿主范围的噬菌体KEP10具有高度同源性(主要衣壳蛋白Gp 23的氨基酸比对中相似度为99.4%)。通过同源重组,将T2基因组中的长尾纤维基因(基因37和38)替换为IP008噬菌体的相应基因。重组噬菌体的宿主范围与IP008相同。此外,重组噬菌体的细菌裂解活性得以恢复。对密切相关的噬菌体T2和IP008的宿主范围突变体的进一步分析可能会更精确地定位负责受体特异性的遗传因素。