Univ. Grenoble Alpes, CNRS, CEA, Institute for Structural Biology, F-38000 Grenoble, France.
Hockmeyer Hall of Structural Biology, Purdue University, West Lafayette, IN 47907, USA.
Curr Opin Virol. 2020 Dec;45:34-42. doi: 10.1016/j.coviro.2020.06.010. Epub 2020 Aug 7.
Bacteriophages, viruses that infect bacteria, are the most abundant biological entities on Earth. Siphophages, accounting for ∼60% of known phages, bear a long, flexible tail that allows host recognition and safe delivery of the DNA from the capsid to the cytoplasm of the infected cell. Independently from their host (Gram positive or Gram negative) and the nature of their receptor at its surface (polysaccharide or protein), the core tail architecture of all caudophages and of bacterial phage-derived contractile injection systems share the same structural organisation and are thought to be homologous. Here, we review the recent advances in the structure, function and assembly of the core tail architecture of siphophages.
噬菌体是感染细菌的病毒,是地球上最丰富的生物实体。长尾噬菌体,占已知噬菌体的约 60%,具有一条长而灵活的尾巴,允许宿主识别并将 DNA 从衣壳安全地递送到感染细胞的细胞质中。长尾噬菌体的核心尾部结构与所有尾部收缩性注射系统的核心尾部结构相同,无论它们的宿主(革兰氏阳性或革兰氏阴性)和表面受体的性质(多糖或蛋白质)如何,它们都具有相同的结构组织,并且被认为是同源的。在这里,我们回顾了长尾噬菌体核心尾部结构的结构、功能和组装的最新进展。