Principles of Virology. Jane Flint

lysogenic, and the phenomenon, lysogeny. Studies of lysogeny revealed many previously unrecognized features of virus-host cell interactions (Box 1.6). Recognition of this phenomenon came from the work of many scientists, but it began with the elegant experiments of André Lwoff and colleagues at the Institut Pasteur in Paris. Lwoff showed that a viral genome exists in lysogenic cells in the form of a silent genetic element called the prophage. This element determined the ability of lysogenic bacteria to produce infectious bacteriophages. Subsequent studies of the E. coli bacteriophage lambda established a paradigm for one mechanism of lysogeny, the integration of a phage genome into a specific site on the bacterial chromosome.

Bacteriophages became inextricably associated with the new field of molecular biology. Their study established many fundamental principles: for example, control of the decision to enter a lysogenic or a lytic pathway is encoded in the genome of the virus. The first mechanisms discovered for the control of gene expression, exemplified by the elegant operon theory of Nobel laureates François Jacob and Jacques Monod, were deduced in part from studies of lysogeny by phage lambda. The biology of phage lambda provided a fertile ground for work on gene regulation, but study of virulent T phages (T1 to T7, where T stands for “type”) of E. coli paved the way for many other important advances. As we shall see, these systems also provided an extensive preview of mechanisms of animal virus reproduction (Box 1.7).

       Animal Cells as Hosts

      The culture of animal cells in the laboratory was initially more of an art than a science, restricted to cells that grew out of organs or tissues maintained in nutrient solutions under sterile conditions. Cells so obtained from living tissues, called primary cells, have a finite life span. Their dependence for growth on natural components in their media such as lymph, plasma, or chicken embryo extracts, and the technical demands of sterile culture prior to the discovery of antibiotics, made reproducible experimentation very difficult. However, by 1955, the work of many investigators had led to a series of important methodological advances. These included the development of defined media optimal for growth of mammalian cells, incorporation of antibiotics into cell culture media, and development of immortal cell lines such as the mouse L and human HeLa cells that are still in widespread use. These advances allowed growth of animal cells in culture to become a routine, reproducible exercise.

BOX 1.5

      EXPERIMENTS

       The Hershey-Chase experiment

      By differentially labeling the nucleic acid and protein components of virus particles with radioactive phosphorus (³²P) and radioactive sulfur (³⁵S), respectively, Alfred Hershey and Martha Chase showed that the protein coat of the infecting virus could be removed soon after infection by agitating the bacteria for a few minutes in a blender. In contrast, ³²P-labeled phage DNA entered and remained associated with the bacterial cells under these conditions. Because such blended cells produced a normal burst of new virus particles, it was clear that the DNA contained all of the information necessary to produce progeny phages.

      The availability of a variety of well-characterized animal cell cultures had several important consequences for virology. It allowed the discovery and propagation of new human viruses, such as adenovirus, measles virus, and rubella virus, for which animal hosts were not available. In 1949, John Enders and colleagues used cell cultures to propagate poliovirus, a feat that led to the development of polio vaccines a few years later. Cell culture technology revolutionized the ability to investigate the reproduction of viruses. Viral infectious cycles could be studied under precisely controlled conditions by employing the analog of the one-step growth cycle of bacteriophages and simple methods for quantification of infectious particles described in Chapter 2.

Our current understanding of the molecular basis of viral parasitism, the focus of this volume, is based almost entirely on analyses of one-step growth cycles in cultured cells. Such studies established that viruses depend absolutely on the biosynthetic machinery of their host cells for synthesis of the components from which progeny viral particles are built. In contrast to cells, viruses are not reproduced by growth and division. Rather, the infecting genome contains the information necessary to redirect cellular systems to the production of many copies of all the components needed for the de novo assembly of new virus particles. It is remarkable, however, that while viruses lack the complex energy-generating and biosynthetic systems necessary for independent existence (Box 1.8), they are not the simplest biologically active agents: viroids, which are infectious agents of a variety of economically important plants, comprise a single small molecule of noncoding RNA, whereas agents called prions, which cause neurological disease in humans and animals, are thought to be aggregates of single protein molecules (Volume II, Chapter 13).

BOX 1.6

      BACKGROUND

       Properties of lysogeny shared with animal viruses

      Lytic versus Lysogenic Response to Infection

      Some bacterial viruses can enter into either destructive (lytic) or relatively benign (lysogenic) relationships with their host cells. Such bacteriophages were called temperate. In a lysogenic bacterial cell, viral genetic information persists but viral gene expression is repressed. Such cells are called lysogens, and the quiescent viral genome, a prophage. By analogy with the prophage, an integrated DNA copy of a retroviral genome in an animal genome is termed a provirus.

      Propagation as a Prophage

      For some bacteriophages like lambda and Mu (Mu stands for “mutator”), prophage DNA is integrated into the host genome of lysogens and passively replicated by the host. Virally encoded enzymes, known as integrase (lambda) and transposase (Mu), mediate the covalent insertion of viral DNA into the chromosome of the host bacterium, establishing it as a prophage. The prophage DNA of other bacteriophages, such as P1, exists as a plasmid, a self-replicating, autonomous chromosome in a lysogen. Both forms of propagation have been identified in certain animal viruses, for example, retroviruses and a lethal herpesvirus.

      Insertional Mutagenesis

      Bacteriophage Mu inserts its genome into many random locations on the host chromosome, causing numerous mutations by disrupting host DNA sequences. This process is called insertional mutagenesis and is a phenomenon observed with retroviruses.

      Pioneers in the study of lysogeny: Nobel laureates François Jacob, Jacques Monod, and André Lwoff, 1965. Courtesy of the U.S. National Library of Medicine.

      Gene Repression and Induction

      Prophage gene expression in lysogens is turned of by the action of viral proteins called repressors. Expression can be turned on when repressors are inactivated (a process called induction). The discovery that genes can be regulated by such trans-acting proteins, and elucidation of their mechanism, set the stage