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Viral life cycle
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Viral entry is the earliest stage of infection in the viral life cycle, as the virus comes into contact with the host cell and introduces viral material into the cell. The major steps involved in viral entry are shown below.[1] Despite the variation among viruses, the generalities are quite similar. However, the specifics are varied.

Contents

Reducing cellular proximity [edit]

A virus floating around an enclosed space with possible host cells faces a large hurdle, the thermodynamics of diffusion. Because neutrally charged objects do not naturally clump around each other, the virus must find a way to move even near a host cell. It does this by attachment -- or adsorption --- onto a susceptible cell; a cell which holds a receptor that the virus can bind to. The receptors on the viral envelope effectively become connected to complementary receptors on the cell membrane. This attachment causes the two membranes to remain in mutual proximity, favoring further interactions between surface proteins. This is also the first requisite that must be satisfied before a cell can become infected. Satisfaction of this requisite makes the cell susceptible. Viruses that exhibit this behavior include many enveloped viruses such as HIV and Herpes simplex virus

This basic idea extends to viruses that do not contain an envelope. Well studied examples are the viruses that infect bacteria, known as bacteriophages or simply phages. Typical phages have long tails used to attach to receptors on the bacterial surface.

Viral entry [edit]

Overview [edit]

A virus must now enter the cell, which is covered by a phospholipid bilayer, a cell's natural barrier to the outside world. The process by which this barrier is breached depends upon the virus. Types of entry are:

  1. Attachment or Viral Adsorption: Receptors on the viral envelope become connected to complementary receptors on the cell membrane.
  2. Membrane Fusion or Hemifusion State: The cell membrane is punctured and made to further connect with the unfolding viral envelope.
  3. Entry Pore formation: An opening is established for the stabilization of an opening for which viral particles can then enter.
  4. Viral Penetration: The viral capsid or genome is injected into the host cell's cytoplasm.

Through the use of green fluorescent protein (GFP), virus entry and infection can be visualized in real-time. Once a virus enters a cell, replication is not immediate and indeed takes some time (seconds to hours).[2][3]

Entry via Membrane Fusion [edit]

The most well-known example is through membrane fusion. In this case, viral receptors attach to the receptors on the surface of the cell and secondary receptors may be present to initiate the puncture of the cell membrane or fusion with the host cell, followed by the unfolding of the viral envelope. In essence, the virus's envelope blends with the cell membrane, releasing its contents into the cell. Obviously, this can only be done with viruses that contain an envelope. Examples include HIV and herpes simplex virus.[4]

Entry via Endocytosis [edit]

Another example is the triggered endocytosis of a cell, in which the virus tricks the cell into thinking that the virus knocking at the door is nothing more than nutrition or harmless goods. A cell naturally takes in resources from the environment and one of the ways it does so is by attaching goods onto surface receptors and engulfing them into the cell. Once inside the cell within the vacuole by which it was taken up, the virus must now break out of the vacuole to gain access to the cytoplasm. Examples include the poliovirus, Hepatitis C virus[5] and Foot-and-mouth disease virus.[6]

Entry via Genetic Injection [edit]

A third and more specific example, is by simply attaching to the surface of the cell via receptors on the cell, and injecting only its gene into the cell, leaving the rest of the virus on the surface. This is restricted to viruses in which only the gene is required for infection of a cell (most positive-sense, single-stranded RNA viruses) and further restricted to viruses that actually exhibit this behavior. The best studied example includes the phages.[7]

Aftermath [edit]

Once a virus is in a cell, it will activate formation of proteins (either by itself or using the host) to gain full control of the host cell, if it is able to. Control mechanisms include the suppression of intrinsic cell defenses, suppression of cell signaling and suppression of host cellular transcription and translation. Often, it is these cytotoxic effects that lead to the death and decline of a cell infected by a virus.

A cell is classified as susceptible to a virus if the virus is able to enter the cell. After the introduction of the viral particle, unpacking of the contents (viral proteins in the tegument and the viral genome via some form of nucleic acid) occurs as preparation of the next stage of viral infection: viral replication.

References [edit]

  1. ^ Subramanian RP, Geraghty RJ (20 Feb 2007). "Herpes simplex virus type 1 mediates fusion through a hemifusion intermediate by sequential activity of glycoproteins D, H, L, and B". Proceedings of the National Academy of Sciences, USA 104 (8): 2903–8. doi:10.1073/pnas.0608374104. PMC 1815279. PMID 17299053. 
  2. ^ Lakadamyali, Melike; Michael J. Rust, Hazen P. Babcock, Xiaowei Zhuang (2003). "Visualizing infection of individual influenza viruses". Proceedings of the National Academy of Sciences of the United States of America 100 (16): 9280–9285. doi:10.1073/pnas.0832269100. PMC 170909. PMID 12883000. Retrieved 2009-05-21. 
  3. ^ Joo, K-I; P Wang (2008-05-15). "Visualization of Targeted Transduction by Engineered Lentiviral Vectors". Gene Ther 15 (20): 1384–1396. doi:10.1038/gt.2008.87. ISSN 0969-7128. PMC 2575058. PMID 18480844. 
  4. ^ Campadelli-Fiume G, Amasio M, Avitabile E, Cerretani A, Forghieri C, Gianni T, Menotti L. "The multipartite system that mediates entry of herpes simplex virus into the cell." Rev Med Virol. 2007 Sep-Oct;17(5):313-26. Review.
  5. ^ Helle F, Dubuisson J. "Hepatitis C virus entry into host cells." Cell Mol Life Sci. 2007 Oct 4
  6. ^ N.J. Dimmock et al. "Introduction to Modern Virology, 6th edition." Blackwell Publishing, 2007.
  7. ^ Sebestyén MG, Budker VG, Budker T, Subbotin VM, Zhang G, Monahan SD, Lewis DL, Wong SC, Hagstrom JE, Wolff JA. "Mechanism of plasmid delivery by hydrodynamic tail vein injection. I. Hepatocyte uptake of various molecules." J Gene Med. 2006 Jul;8(7):852-73.

Original courtesy of Wikipedia: http://en.wikipedia.org/wiki/Viral_entry — Please support Wikipedia.
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4 news items

 
Medical News Today
Mon, 22 Apr 2013 00:09:56 -0700

The antiviral effector IFITM3 disrupts intracellular cholesterol homeostasis to block viral entry." He explained that when a virus enters the human body the immune system is stimulated by interferon, which produces hundreds of proteins, such as the IFITM3.
 
domain-B
Thu, 25 Apr 2013 03:02:11 -0700

The study, The antiviral effector IFITM3 disrupts intra-cellular cholesterol homeostasis to block viral entry, was published in the journal Cell Host & Microbe on 17 April 2013. "We showed how this occurs," Jung says. "When a virus tries to enter, the ...
 
PR Newswire (press release)
Thu, 25 Apr 2013 04:16:12 -0700

This lytic infection leads to cognitive and motor dysfunction (the syndrome PML) and is fatal in 50 percent or more of patients. The best approach to treating the disease is to attack the virus before it enters the brain. IkT-001Pro blocks viral entry ...
 
MarketWatch (press release)
Mon, 29 Apr 2013 13:11:36 -0700

PRO 140 belongs to a new class of HIV/AIDS therapeutics -- viral-entry inhibitors -- that are intended to protect healthy cells from viral infection. PRO 140 is a humanized monoclonal antibody directed against CCR5, a molecular portal that HIV uses to ...
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