The filamentous particle seen in electron micrographs was initially incorrectly interpreted as contaminating bacterial
pilus, but ultrasonic degradation, which breaks flexible filaments roughly in half, inactivated infectivity as predicted for a filamentous bacteriophage morphology. Three filamentous bacteriophages, fd, f1 and M13, were isolated and characterized by three different research groups in the early 1960s. Since these three phages differ by less than 2 percent in their DNA sequences, corresponding to changes in only a few dozen codons in the whole genome, for many purposes they can be considered to be identical. Further independent characterization over the subsequent half-century was shaped by the interests of these research groups and their followers. Genetic studies on M13 using conditional lethal mutants, initiated by David Pratt and colleagues, led to description of phage gene functions. Notably, the protein product of gene 5, which is required for synthesis of progeny single-stranded DNA, is made in large amounts in the infected bacteria, and it binds to the nascent DNA to form a linear intracellular complex. (The simple numbering of genes using Arabic numerals 1,2,3,4... introduced by the Pratt group is sometimes displaced by the practice of using Roman numerals I, II, III, IV... but the gene numbers defined by the two systems are the same). Longer (or shorter) DNA can be included in fd phage, since more (or fewer) protein subunits can be added during assembly as required to protect the DNA, making the phage convenient for genetic studies. The length of the phage is also affected by the positive charge per length on the inside surface of the phage capsid. The genome of fd was one of the first complete genomes to be sequenced. The taxonomy of filamentous bacteriophage was defined by
Andre Lwoff and Paul Tournier as family Inophagoviridae, genus I. inophagovirus, species Inophagovirus bacterii (Inos=fiber or filament in Greek), with phage fd (Hoffmann-Berling) as the type species. "Phagovirus" is
tautological, and the name of the family was altered to
Inoviridae and the type genus to
Inovirus. This nomenclature persisted for many decades, and for studies of p8 in membrane mimetic environments. Filamentous bacteriophage engineered to display
immunogenic peptides are useful in immunology and wider biological applications. George Smith and Greg Winter used f1 and fd for their work on
phage display for which they were awarded a share of the 2018 Nobel Prize in Chemistry. The creation and exploitation of many derivatives of M13 for a wide range of purposes, especially in materials science, has been employed by
Angela Belcher and colleagues. Filamentous bacteriophage can promote antibiotic tolerance by forming liquid crystalline domains around bacterial cells. == References ==