Temperate Bacterial Viruses Lysogeny

With most temperate phages, if the host simply makes a copy of the viral DNA, lysis does not occur but if complete virion particles are produced, then the host cell lyses. In a lysogenic bacterial culture at any one time, a small fraction of the cells, 0.1 to 0.0001 percent, 

The temperate virus does not exist in its mature, infectious state inside the cell, but rather in a latent form, called the provirus or prophage state. In considering virulent viruses we learned that the DNA of the virulent virus contains information for the synthesis of a number of enzymes and other proteins essential to virus reproduction. The prophage of the temperate virus carries similar information, but in the lysogenic cell this information remains dormant because the expression of the virus genes is blocked through the action of a specific repressor coded for by the virus. As a result of a genetic switch, the repressor is inactivated, virus reproduction occurs, the cell lyses, and virus particles are released. 

A lysogenic culture can be treated so that most or all of the cells produce virus and lyse. Such treatment, called induction, usually involves the use of agents such as ultraviolet radiation, nitrogen mustards, or X rays, known to damage DNA and activate the SOS system. However, not all prophages are inducible in some temperate viruses, prophage expression occurs only by natural events. 

Although a lysogenic bacterium may be susceptible to infection by other viruses, it cannot be infected by virus particles of the type for which it is lysogenic. This immunity, which is characteristic of lysogenized cells, is conferred by the intracellular repression mechanism under the control of virus genes. 

It is sometimes possible to eliminate the lysogenic virus (to cure the strain) by heavy irradiation or treatment with nitrogen mustards. Among the few survivors may be some cells that have been cured. Presumably the treatment causes the prophage to detach from the host chromosome and be lost during subsequent cell growth. Such a cured strain is no longer immune to the virus and can serve as a suitable host for study of virus replication. 

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