Feline Immunodeficiency virus: Difference between revisions

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(New page: By: Emily Nutt ==Introduction== <br> Approximately 1.5 to 3 percent of all healthy cats in the United States are infected with Feline Immunodeficiency Virus or FIV. Sick cats are even ...)
 
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<br>  HIV and FIV infect their host T-cells in a similar manor because they are both retroviruses. All retroviruses use reverse transcriptase to make their RNA genome into double-stranded DNA. These types of viruses carry the protein reverse transcriptase in side the viron instead of being translated by an early gene like most proteins used by viruses. In fact the  reverse transcriptase is already bound to the viral RNA with a primer attached before the virus infects the host cell (Slonczewski, 205).  Like all viruses retroviruses bind a receptor protein on the host cell and fuse with the host membrane. Once the capsid has been uncoated the RNA is converted to double-stranded DNA through the reverse transcriptase. The new DNA copy then enters the nucleus and integrates into the host genome. At first the viral genome is able to replicate with out directly affecting the host by only creating a few virons. The host cell’s RNA polymerase FIV viral phases and ribosome create virions through transcription and translation of viral genes.  The viruses are assembled and then bud out of the host cell to go infect new host cells (Slonczewski, 205). After sometime the host cell can then generate a large amount of virions thus causing the host to show symptoms of immunodeficiency. However it is unknown how this process occurs and why viruses like FIV can  infect the host for months to years without the host showing symptoms.   
<br>  HIV and FIV infect their host T-cells in a similar manor because they are both retroviruses. All retroviruses use reverse transcriptase to make their RNA genome into double-stranded DNA. These types of viruses carry the protein reverse transcriptase in side the viron instead of being translated by an early gene like most proteins used by viruses. In fact the  reverse transcriptase is already bound to the viral RNA with a primer attached before the virus infects the host cell (Slonczewski, 205).  Like all viruses retroviruses bind a receptor protein on the host cell and fuse with the host membrane. Once the capsid has been uncoated the RNA is converted to double-stranded DNA through the reverse transcriptase. The new DNA copy then enters the nucleus and integrates into the host genome. At first the viral genome is able to replicate with out directly affecting the host by only creating a few virons. The host cell’s RNA polymerase FIV viral phases and ribosome create virions through transcription and translation of viral genes.  The viruses are assembled and then bud out of the host cell to go infect new host cells (Slonczewski, 205). After sometime the host cell can then generate a large amount of virions thus causing the host to show symptoms of immunodeficiency. However it is unknown how this process occurs and why viruses like FIV can  infect the host for months to years without the host showing symptoms.   


<br>   Due to the structure and process of lentivirus infections, FIV is characterized by three stages. The first stage of FIV is during the first two to four months after infection when the infected cat shows signs of short term illness. The infected cat may show symptoms like increased body temperature, and enlarged lymph nodes (The Cat Group Policy Statement 3). This short term illness could be a result of early and sparse virion replication in the host. In the second stage of FIV the cat appears completely healthy with no signs of illness. However in the third phase of the illness the cat expresses signs of a compromised immunsystem. Signs of immunodeficiency can take many forms including weight loss, inappetence, high body temperature, gingivitis, infected lymphnodes, and abnormal cell growth resulting in  tumors (The Cat Group).  
<br> As a result  of the structure and process of lentivirus infections, FIV is characterized by three stages. The first stage of FIV is during the first two to four months after infection when the infected cat shows signs of short term illness. The infected cat may show symptoms like increased body temperature, and enlarged lymph nodes (The Cat Group Policy Statement 3). This short term illness could be a result of early and sparse virion replication in the host. In the second stage of FIV the cat appears completely healthy with no signs of illness. However in the third phase of the illness the cat expresses signs of a compromised immunsystem. Signs of immunodeficiency can take many forms including weight loss, inappetence, high body temperature, gingivitis, infected lymphnodes, and abnormal cell growth resulting in  tumors (The Cat Group).  
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Revision as of 01:20, 14 April 2009

By: Emily Nutt

Introduction


Approximately 1.5 to 3 percent of all healthy cats in the United States are infected with Feline Immunodeficiency Virus or FIV. Sick cats are even more likely to contract FIV since they have a 15 percent chance of contracting the virus ( Cornell University College of Veterinary Medicine). FIV is a type of lentivirus, a retrovirus that propagates at a slow pace. This slow pace causes a huge gap of months to years from when the cat becomes infected with the virus and when it begins to show symptoms. A more widely known lentivirus is that of Human Immunodeficiency Virus or HIV.


HIV and FIV infect their host T-cells in a similar manor because they are both retroviruses. All retroviruses use reverse transcriptase to make their RNA genome into double-stranded DNA. These types of viruses carry the protein reverse transcriptase in side the viron instead of being translated by an early gene like most proteins used by viruses. In fact the reverse transcriptase is already bound to the viral RNA with a primer attached before the virus infects the host cell (Slonczewski, 205). Like all viruses retroviruses bind a receptor protein on the host cell and fuse with the host membrane. Once the capsid has been uncoated the RNA is converted to double-stranded DNA through the reverse transcriptase. The new DNA copy then enters the nucleus and integrates into the host genome. At first the viral genome is able to replicate with out directly affecting the host by only creating a few virons. The host cell’s RNA polymerase FIV viral phases and ribosome create virions through transcription and translation of viral genes. The viruses are assembled and then bud out of the host cell to go infect new host cells (Slonczewski, 205). After sometime the host cell can then generate a large amount of virions thus causing the host to show symptoms of immunodeficiency. However it is unknown how this process occurs and why viruses like FIV can infect the host for months to years without the host showing symptoms.


As a result of the structure and process of lentivirus infections, FIV is characterized by three stages. The first stage of FIV is during the first two to four months after infection when the infected cat shows signs of short term illness. The infected cat may show symptoms like increased body temperature, and enlarged lymph nodes (The Cat Group Policy Statement 3). This short term illness could be a result of early and sparse virion replication in the host. In the second stage of FIV the cat appears completely healthy with no signs of illness. However in the third phase of the illness the cat expresses signs of a compromised immunsystem. Signs of immunodeficiency can take many forms including weight loss, inappetence, high body temperature, gingivitis, infected lymphnodes, and abnormal cell growth resulting in tumors (The Cat Group).

The Genome of FIV


Include some current research in each topic, with at least one figure showing data.

Evolution of FIV


Include some current research in each topic, with at least one figure showing data.

Relationship of FIV to other Lentiviruses


Include some current research in each topic, with at least one figure showing data.

Conclusion


Overall paper length should be 3,000 words, with at least 3 figures.

References

[Sample reference] Takai, K., Sugai, A., Itoh, T., and Horikoshi, K. "Palaeococcus ferrophilus gen. nov., sp. nov., a barophilic, hyperthermophilic archaeon from a deep-sea hydrothermal vent chimney". International Journal of Systematic and Evolutionary Microbiology. 2000. Volume 50. p. 489-500.

Edited by student of Joan Slonczewski for BIOL 238 Microbiology, 2009, Kenyon College.


Include some current research in each topic, with at least one figure showing data. [edit] Conclusion


Overall paper length should be 3,000 words, with at least 3 figures. [edit] References


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