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SANA AKRAM
14-ARID-4374
VIRUS REPLICATION CYCLES
KEY POINTS
 Viruses are species specific, but almost every
species on Earth can be affected by some form
of virus.
 The lytic cycle involves the reproduction of viruses
using a host cell to manufacture more viruses; the
viruses then burst out of the cell.
 The lysogenic cycle involves the incorporation of
the viral genome into the host cell genome, infecting
it from within.
 To start with, the virus has to infect the cell. So
the virus attaches itself to the outer cell wall and
releases enzymes that weaken the cell wall.
Then, depending on whether it is a DNA virus or a
RNA virus, the virus injects its double stranded
DNA or its single stranded RNA into the cell.
TERMS
 Latency:
 The ability of a pathogenic virus to lie dormant within
a cell.
 Bacteriophage:
 A virus that specifically infects bacteria.
 lytic cycle:
 The normal process of viral reproduction involving
penetration of the cell membrane, nucleic acid
synthesis, and lysis of the host cell.
 lysogenic cycle :
 A form of viral reproduction involving the fusion of the
nucleic acid of a bacteriophage with that of a host,
followed by proliferation of the resulting prophage.
LYTIC CYCLE
 With lytic phages, bacterial cells are broken open
(lysed) and destroyed after immediate replication
of the virion. As soon as the cell is destroyed, the
phage progeny can find new hosts to infect. An
example of a lytic bacteriophage is T4, which
infects E. coli found in the human intestinal tract.
Lytic phages are more suitable for phage
therapy.
 in short, in the lytic cycle, the virus hijacks the
infected cell and then destroys it. The lytic cycle
occurs in virulent viruses.
Phage replication cycles
LYSOGENIC CYCLE
 In contrast, the lysogenic cycle does not result in
immediate lysing of the host cell. Those phages
able to undergo lysogeny are known as
temperate phages. Their viral genome will
integrate with host DNA and replicate along with it
fairly harmlessly, or may even become
established as a plasmid. The virus remains
dormant until host conditions deteriorate, perhaps
due to depletion of nutrients; then, the
endogenous phages (known as prophages)
become active.
Phage replication cycles
 . At this point they initiate the reproductive cycle,
resulting in lysis of the host cell. As the lysogenic
cycle allows the host cell to continue to survive
and reproduce, the virus is reproduced in all of
the cell’s offspring. An example of a
bacteriophage known to follow the lysogenic
cycle and the lytic cycle is the phage lambda of E.
coli.
LATENCY
 Viruses that infect plant or animal cells may also
undergo infections where they are not producing
virions for long periods. An example is the animal
herpes viruses, including herpes simplex viruses,
which cause oral and genital herpes in humans.
In a process called latency, these viruses can
exist in nervous tissue for long periods of time
without producing new virions, only to leave
latency periodically and cause lesions in the skin
where the virus replicates. Even though there are
similarities between lysogeny and latency, the
term lysogenic cycle is usually reserved to
describe bacteriophages.
Phage replication cycles
 Pseudolysogeny occurs most frequently under
nutrient-deprived conditions, when bacterial cells
cannot support DNA replication or protein
synthesis. In this situation, the phage genome
remains for an extended period of time as a non-
integrated preprophage, which resembles an
episome, until the nutritional status is restored, at
which point the phage enters either a lysogenic or
a lytic life cycle.
Citation :
 William H. Wilson*, Nicholas H. Mann .1997.
Lysogenic and lytic viral production in marine
microbial communities. Aquat microb ecol. 13, 95-
100.
 https://www.boundless.com/biology/textbooks/bou
ndless-biology-textbook/viruses-21/virus-
infections-and-hosts-137/the-lytic-and-lysogenic-
cycles-of-bacteriophages-553-11763
 Ron feiner, Tal argov, Lev rabinovich, Nadeja
segal, Ilya borovog, Anat A. Herskovits. The
phage replication cycles. Nature Reviews
Microbiology 13, 641–650 (2015).

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Phage replication cycles

  • 2. KEY POINTS  Viruses are species specific, but almost every species on Earth can be affected by some form of virus.  The lytic cycle involves the reproduction of viruses using a host cell to manufacture more viruses; the viruses then burst out of the cell.  The lysogenic cycle involves the incorporation of the viral genome into the host cell genome, infecting it from within.
  • 3.  To start with, the virus has to infect the cell. So the virus attaches itself to the outer cell wall and releases enzymes that weaken the cell wall. Then, depending on whether it is a DNA virus or a RNA virus, the virus injects its double stranded DNA or its single stranded RNA into the cell.
  • 4. TERMS  Latency:  The ability of a pathogenic virus to lie dormant within a cell.  Bacteriophage:  A virus that specifically infects bacteria.  lytic cycle:  The normal process of viral reproduction involving penetration of the cell membrane, nucleic acid synthesis, and lysis of the host cell.  lysogenic cycle :  A form of viral reproduction involving the fusion of the nucleic acid of a bacteriophage with that of a host, followed by proliferation of the resulting prophage.
  • 5. LYTIC CYCLE  With lytic phages, bacterial cells are broken open (lysed) and destroyed after immediate replication of the virion. As soon as the cell is destroyed, the phage progeny can find new hosts to infect. An example of a lytic bacteriophage is T4, which infects E. coli found in the human intestinal tract. Lytic phages are more suitable for phage therapy.  in short, in the lytic cycle, the virus hijacks the infected cell and then destroys it. The lytic cycle occurs in virulent viruses.
  • 7. LYSOGENIC CYCLE  In contrast, the lysogenic cycle does not result in immediate lysing of the host cell. Those phages able to undergo lysogeny are known as temperate phages. Their viral genome will integrate with host DNA and replicate along with it fairly harmlessly, or may even become established as a plasmid. The virus remains dormant until host conditions deteriorate, perhaps due to depletion of nutrients; then, the endogenous phages (known as prophages) become active.
  • 9.  . At this point they initiate the reproductive cycle, resulting in lysis of the host cell. As the lysogenic cycle allows the host cell to continue to survive and reproduce, the virus is reproduced in all of the cell’s offspring. An example of a bacteriophage known to follow the lysogenic cycle and the lytic cycle is the phage lambda of E. coli.
  • 10. LATENCY  Viruses that infect plant or animal cells may also undergo infections where they are not producing virions for long periods. An example is the animal herpes viruses, including herpes simplex viruses, which cause oral and genital herpes in humans. In a process called latency, these viruses can exist in nervous tissue for long periods of time without producing new virions, only to leave latency periodically and cause lesions in the skin where the virus replicates. Even though there are similarities between lysogeny and latency, the term lysogenic cycle is usually reserved to describe bacteriophages.
  • 12.  Pseudolysogeny occurs most frequently under nutrient-deprived conditions, when bacterial cells cannot support DNA replication or protein synthesis. In this situation, the phage genome remains for an extended period of time as a non- integrated preprophage, which resembles an episome, until the nutritional status is restored, at which point the phage enters either a lysogenic or a lytic life cycle.
  • 13. Citation :  William H. Wilson*, Nicholas H. Mann .1997. Lysogenic and lytic viral production in marine microbial communities. Aquat microb ecol. 13, 95- 100.  https://www.boundless.com/biology/textbooks/bou ndless-biology-textbook/viruses-21/virus- infections-and-hosts-137/the-lytic-and-lysogenic- cycles-of-bacteriophages-553-11763  Ron feiner, Tal argov, Lev rabinovich, Nadeja segal, Ilya borovog, Anat A. Herskovits. The phage replication cycles. Nature Reviews Microbiology 13, 641–650 (2015).