Visualizing the structural changes of bacteriophage Epsilon15 and its Salmonella host during infection.

摘要

The efficient mechanism by which double-stranded DNA bacteriophages deliver their chromosome across the outer membrane, cell wall, and inner membrane of Gram-negative bacteria remains obscure. Advances in single-particle electron cryomicroscopy have recently revealed details of the organization of the DNA injection apparatus within the mature virion for various bacteriophages, including epsilon15 (varepsilon15) and P-SSP7. We have used electron cryotomography and three-dimensional subvolume averaging to capture snapshots of varepsilon15 infecting its host Salmonella anatum. These structures suggest the following stages of infection. In the first stage, the tailspikes of varepsilon15 attach to the surface of the host cell. Next, varepsilon15's tail hub attaches to a putative cell receptor and establishes a tunnel through which the injection core proteins behind the portal exit the virion. A tube spanning the periplasmic space is formed for viral DNA passage, presumably from the rearrangement of core proteins or from cellular components. This tube would direct the DNA into the cytoplasm and protect it from periplasmic nucleases. Once the DNA has been injected into the cell, the tube and portal seals, and the empty bacteriophage remains at the cell surface.