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Abstract
Phages are viruses that infect bacteria and dominate every ecosystem on our planet. As well as impacting microbial ecology, physiology and evolution, phages are exploited as tools in molecular biology and biotechnology. This is particularly true for the Ff (f1, fd or M13) phages, which represent a widely distributed group of filamentous viruses. Over nearly five decades, Ffs have seen an extraordinary range of applications, yet the complete structure of the phage capsid and consequently the mechanisms of infection and assembly remain largely mysterious. In this work, we use cryo-electron microscopy and a highly efficient system for production of short Ff-derived nanorods to determine a structure of a filamentous virus including the tips. We show that structure combined with mutagenesis can identify phage domains that are important in bacterial attack and for release of new progeny, allowing new models to be proposed for the phage lifecycle.
In this work, the authors report a system for production of short versions of a filamentous phage enables the structure to be determined by cryo-electron microscopy. Structure combined with mutagenesis allows the identification of phage domains that are important in bacterial attack and for release of new viral progeny.
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1 University of Exeter, Living Systems Institute, Exeter, UK (GRID:grid.8391.3) (ISNI:0000 0004 1936 8024); University of Exeter, Faculty of Health and Life Sciences, Exeter, UK (GRID:grid.8391.3) (ISNI:0000 0004 1936 8024)
2 Massey University, School of Natural Sciences, Palmerston North, New Zealand (GRID:grid.148374.d) (ISNI:0000 0001 0696 9806); Nanophage Technologies, Palmerston North, New Zealand (GRID:grid.148374.d)
3 Massey University, School of Natural Sciences, Palmerston North, New Zealand (GRID:grid.148374.d) (ISNI:0000 0001 0696 9806)