The lytic cycle ( LIT-ik) is one of the two cycles of viral reproduction (referring to bacterial viruses or bacteriophages), the other being the lysogenic cycle. The lytic cycle results in the destruction of the infected cell and its membrane. Bacteriophages that can only go through the lytic cycle are called virulent phages (in contrast to temperate phages). In the lytic cycle, the viral DNA exists as a separate free floating molecule within the bacterial cell, and replicates separately from the host bacterial DNA, whereas in the lysogenic cycle, the viral DNA is integrated into the host genome. This is the key difference between the lytic and lysogenic cycles. However, in both cases the virus/phage replicates using the host DNA machinery.
Description The lytic cycle is often separated into six stages: attachment, penetration, transcription, biosynthesis, maturation, and lysis.
Attachment – the phage attaches itself to the surface of the host cell in order to inject its DNA into the cell Penetration – the phage injects its DNA into the host cell by penetrating through the cell membrane Transcription – the host cell's DNA is degraded and the cell's metabolism is directed to initiate phage biosynthesis Biosynthesis – the phage DNA replicates inside the cell, synthesizing new phage DNA and proteins Maturation – the replicated material assembles into fully formed viral phages (each made up of a head, a tail and tail fibers) Lysis - cell wall or membrane ruptures, disintegrating it and releasing the virus in the process. The verb lyse, refers to the process of lysis.
Attachment and penetration To infect a host cell, the virus must first inject its own nucleic acid into the cell through the plasma membrane and (if present) the cell wall. The virus does so by either attaching to a receptor on the cell's surface or by simple mechanical force. The binding is due to electrostatic interactions and is influenced by pH and the presence of ions. The virus then releases its genetic material (either single- or double-stranded RNA or DNA) into the cell. In some viruses this genetic material is circular and mimics a bacterial plasmid. At this stage the cell becomes infected and can also be targeted by the immune system. It is mostly aided by receptors on the surface of the cell. The sequence of events that occur during initiation of bacteriophage infection, from adsorption (attachment) through DNA ejection from the virion into the host cell (penetration), was reviewed by Molineux.
Transcription and biosynthesis During the transcription and biosynthesis stages, the virus hijacks the cell's replication and translation mechanisms, using them to make more viruses. The virus's nucleic acid uses the host cell's metabolic machinery to make large amounts of viral components. In DNA viruses, the DNA transcribes itself into messenger RNA (mRNA) molecules that are then used to direct the cell's ribosomes. One of the first polypeptides to be translated destroys the host's DNA. In retroviruses (which inject an RNA strand), the enzyme reverse transcriptase transcribes the viral RNA into DNA, which is then transcribed again into RNA. Once the viral DNA has taken control it induces the host cell's machinery to synthesize viral DNA and proteins and begins to multiply. The biosynthesis is (e.g. T4) regulated in three phases of mRNA production followed by a phase of protein production.
Early phase Enzymes modify the host's transcriptional process by RNA polymerase. Amongst other modifications, virus T4 changes the sigma factor of the host by producing an anti-sigma factor so that the host promotors are not recognized any more but now recognize T4 middle proteins. For protein synthesis Shine-Dalgarno subsequence GAGG dominates an early genes translation. Middle phase Virus nucleic acid (DNA or RNA depending on virus type). Late phase Structural proteins including those for the head and the tail.
Maturation and lysis About 25 minutes after initial infection, approximately 200 new virions (viral bodies) are formed. Once enough virions have matured and accumulated, specialized viral proteins are used to dissolve the cells' walls. The cell bursts (i.e. it undergoes lysis) due to high internal osmotic pressure that can no longer be constrained by the cell wall. This releases progeny virions into the surrounding environment, where they can go on to infect other cells and another lytic cycle begins.
Gene regulation biochemistry There are three classes of genes in the phage genome that regulate whether the lytic or lysogenic cycles will emerge. The first class is the immediate early genes, the second is the delayed early genes and the third is the late genes. The following refers to the well-studied temperate phage lambda of E. coli.
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