Lysogenic cycle, or lysogeny, is one of the two alternative life cycles of a virus inside a host cell, whereby the virus that has infected a cell attaches itself to the host DNA and, acting like an inert segment of the DNA, replicates when the host cell divides. This method of replication is contrasted with the lytic cycle, whereby the virus that has entered a cell takes over the cell's replication mechanism, makes viral DNA and viral proteins, and then lyses (breaks open) the cell, allowing the newly produced viruses to leave the now disintegrated host cell to infect other cells. While the lysogenic cycle causes no harm to the host cell, an induction event, such as exposure to ultraviolet light, can cause this latent stage to enter the lytic cycle.
The lysogenic cycle is one strategy for replication of the virus without destruction of the host. The discovery of this cycle has important medical implications. Sometimes expression of the genes of a lysogenic bacteriophage can alter the phenotype of the host bacteria. This phenomenon, called lysogenic conversion, can have medical significance for humans. For example, the bacteria that causes diptheria, Corynebacterium diphtheriae, is harmless to humans unless it is infected by the phage β. Then the genes of the incorporated DNA of the bacteriophage induce the host bacteria to produce toxins.
Viral reproduction is most fully understood through studying viruses that infect bacteria, known as bacteriophages (or, commonly, phages). The lysogenic cycle and the lytic cycle are two fundamental reproductive processes that have been identified. The following is a description of these cycles based on bacteriophages.
The lytic cycle involves the virus entering a host cell, taking control of the host DNA to produce viral DNA and the viral proteins that provide the structural component of the bacteriophage, and then, when the cell has many new virus particles assembled, digesting the host cell wall from within and releasing the new viruses. For example, the bacteriophage lambda, after infecting an E. coli host cell, normally multiplies until several hundred progeny are produced, at which time the bacterial cell is lysed and the progeny released (Alberts et al. 1989).
The lysogenic cycle involves the virus entering the cell, and instead of creating new virus particles, is characterized by integration of the bacteriophage nucleic acid into the host bacterium's genome. The newly integrated genetic material acts as an additional set of genes that can be replicated when the DNA of the host cell is replicated and the host cell divides. The virus is thus transmitted to daughter cells at each subsequent cell division, although the phages remain inert, causing no harm to the host cells. Lysogenic cycles can also occur in eukaryotes, although the method of incorporation of DNA is not fully understood.
Prophage is the term for a phage DNA in its dormant state, typically integrated into the host bacteria's chromosome, but also can include the rare cases where the phage exists as a stable plasmid within the host cell.
The lysogenic bacterium multiples normally until some environmental induction, such as ionizing radiation or ultraviolet light threatens the bacterial cell and induces the prophage to initiate the lytic cycle. The prophage expresses gene(s) that repress the phage's lytic action, and the phage enters the lytic cycle when this suppression is disrupted.
Temperate phages are those phages able to undergo both a lytic cycle and a lysogenic cycle, such as the lambda phage. They lyse a small fraction of bacterial cells; in the remaining majority of the bacteria, the phage DNA becomes integrated into the bacterial chromosome and replicates along with it. In this lysogenic state, the information contained in the viral nucleic acid is not expressed.
In some interactions between lysogenic phages and bacteria, lysogenic conversion may occur. It is when a temperate phage induces a change in the phenotype of the bacteria infected that is not part of a usual phage cycle. Changes can often involve the external membrane of the cell by making it impervious to other phages or even by increasing the pathogenic capability of the bacteria for a host.
Extra genes present in prophage genomes that do not have a phage function but (may) act as fitness factors for the bacterial host are termed "morons" (Canchaya et al. 2003).
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