Feline panleukopenia virus: Difference between revisions
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==Genome Structure== | ==Genome Structure== | ||
The genome of feline panleukopenia virus contains approximately 5123 nucleotides and 4 open-reading frames that encode NS1 and NS1 (non-structural proteins) and VP1 and VP2 (structural proteins). The first open-reading frame contributes to replication, transcription and cell death of the host's cells. The second open-reading frame directs the formation and translation of capsid proteins. The third open-reading frame consist of VP2's sequence and contributes to cell infection and nuclear transport of capsids. The fourth open-reading frame encodes VP2 which is considered major capsid protein since it makes up approximately 90% of the whole capsid. The amount of base pairs in the DNA sequence varies depending on the specific strain of the virus. Due to the Y-type structure at the 3-terminal and the U-shaped structure at the 5-terminal, it is challenging for researchers to amplify the full-length genome of this virus and many others in the parvovirus genus. | The genome of feline panleukopenia virus contains approximately 5123 nucleotides and 4 open-reading frames that encode NS1 and NS1 (non-structural proteins) and VP1 and VP2 (structural proteins). The first open-reading frame contributes to replication, transcription and cell death of the host's cells. The second open-reading frame directs the formation and translation of capsid proteins. The third open-reading frame consist of VP2's sequence and contributes to cell infection and nuclear transport of capsids. The fourth open-reading frame encodes VP2 which is considered major capsid protein since it makes up approximately 90% of the whole capsid. The amount of base pairs in the DNA sequence varies depending on the specific strain of the virus. Due to the Y-type structure at the 3-terminal and the U-shaped structure at the 5-terminal, it is challenging for researchers to amplify the full-length genome of this virus and many others in the parvovirus genus. | ||
==Cell Structure, Metabolism and Life Cycle== | ==Cell Structure, Metabolism and Life Cycle== | ||
Parvoviruses, including FPV, do not have DNA polymerases and cannot promote cell division. FPV relies on its host for its metabolic processes and use the host's cell division machinery, specifically cells in S-phase, to complete their lytic cycle. The virus usually attacks bone marrow, lymphatic tissue, and intestinal epithelial cells. The virus has an incubation period of 2 to 7 days. It can remain in an environment for days to months and possibly years. Due to its resistance to most disinfectants it is a difficult virus to eliminate from the environment making it more possible for other vulnerable animals to contract it. | Parvoviruses, including FPV, do not have DNA polymerases and cannot promote cell division. FPV relies on its host for its metabolic processes and use the host's cell division machinery, specifically cells in S-phase, to complete their lytic cycle. The virus usually attacks bone marrow, lymphatic tissue, and intestinal epithelial cells. The virus has an incubation period of 2 to 7 days. It can remain in an environment for days to months and possibly years. Due to its resistance to most disinfectants it is a difficult virus to eliminate from the environment making it more possible for other vulnerable animals to contract it. | ||
==Ecology and Pathogenesis== | ==Ecology and Pathogenesis== | ||
The virus can be transmitted either by the fecal-oral route or by indirect transmission via fomites contaminated by infected individuals, as well as from humans that have the virus on their hands or clothes. The virus can live in an environment for months to a year and in some instances over a year. FPV is also highly resistant to certain disinfectants making it difficult for owners to remove it from their household. Using transferrin receptors FPV can enter cells and replicate inside of cells that are currently in the synthesis phase of mitosis. | The virus can be transmitted either by the fecal-oral route or by indirect transmission via fomites contaminated by infected individuals, as well as from humans that have the virus on their hands or clothes. The virus can live in an environment for months to a year and in some instances over a year. FPV is also highly resistant to certain disinfectants making it difficult for owners to remove it from their household. Using transferrin receptors FPV can enter cells and replicate inside of cells that are currently in the synthesis phase of mitosis. | ||
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==References== | ==References== | ||
[ | [https://www.kjvr.org/journal/view.php?number=3880 Yang, D.K, Park,Y.R, Park, Y., An, S., Choi, S.S., Park, J., and Hyun, B.H. "Isolation and molecular characterization of feline panleukopenia viruses from Korean cats". ''Korean Journal of Veterinary Research 2022''. 2022. Volume 62. ] | ||
[https://www.mdpi.com/1999-4915/14/6/1248 Rehme, T., Hartmann, K., Truyen, U., Zablotski, Y., and Bergmann, M. "Feline Panleukopenia outbreaks and risk factors in cats in animal shelters". ''Viruses'' 2022. Volume 6. ] | |||
[https://www. | [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6964837/#:~:text=FPLV%20has%20a%20single%2Dstranded,%2Dshaped%20structure%20%5B29%5D Leal, E., Liang, R., Liu, Q., Villanova, F., Shi, L., Liang, L., Li, J., Witkin, S., and Cui, S. "Regional adaptations and parallel mutations in Feline panleukopenia virus strains from China revealed by nearly-full length genome analysis". ''PLoS One''2020. Volume 15.] | ||
[https://www-sciencedirect-com.liblink.uncw.edu/science/article/pii/S109002331400224X Stuetzer, B. and Hartmann, K. "Feline parvovirus infection and associated diseases". ''The Veterinary Journal'' 2014. Volume 201. Pages 150-155.] | |||
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979488/ Kolangath, S.M., Upadhye, S.V., Dhoot, V.M., Pawshe, M.D., Bhadane, B.K., Gawande, A.P., and Kolangath, R.M. "Molecular investigation of Feline Panleukopenia in an endangered leopard (Panthera pardus)-a case report". ''BMC Veterinary Research'' 2023. Volume 19.] | |||
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9227120/ Rehme, T., Hartmann, K., Truyen, U., Zablotski, Y., and Bergmann, M. "Feline Panleukopenia outbreaks and risk factors in cats in animal shelters". ''Vruses'' 2020. Volume 14.] | |||
[https://www. | [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7151839/ Sykes, J.E. "Feline Panleukopenia virus infection and other viral enteritides". ''Canine and Feline Infectious Diseases'' 2014. Pages 187-194.] | ||
==Author== | ==Author== | ||
Latest revision as of 17:36, 6 December 2023
Classification
Viruses; Monodnaviria; Shotokuvirae; Cossaviricota; Quintoviricetes; Piccovirales; Parvoviridae; Parvovirinae; Protoparvovirus; Protoparvovirus carnivoran 1; Feline panleukopenia virus (genogroup)
Species
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NCBI: [1] |
Protoparvovirus Protoparvovirus carnivoran 1
Description and Significance
Feline panleukopenia virus (FPV or FPLV) is a non-enveloped, icosahedral, single-stranded DNA virus and is sometimes referred to as feline distemper, cat plague, or feline parvovirus. FPV was first identified in the 1920s and has maintained genomic stability to a degree. FPV is a serious, highly contagious and potentially fatal issue among unvaccinated felines. Following proper vaccine guidelines can prevent felines from getting infected.
Genome Structure
The genome of feline panleukopenia virus contains approximately 5123 nucleotides and 4 open-reading frames that encode NS1 and NS1 (non-structural proteins) and VP1 and VP2 (structural proteins). The first open-reading frame contributes to replication, transcription and cell death of the host's cells. The second open-reading frame directs the formation and translation of capsid proteins. The third open-reading frame consist of VP2's sequence and contributes to cell infection and nuclear transport of capsids. The fourth open-reading frame encodes VP2 which is considered major capsid protein since it makes up approximately 90% of the whole capsid. The amount of base pairs in the DNA sequence varies depending on the specific strain of the virus. Due to the Y-type structure at the 3-terminal and the U-shaped structure at the 5-terminal, it is challenging for researchers to amplify the full-length genome of this virus and many others in the parvovirus genus.
Cell Structure, Metabolism and Life Cycle
Parvoviruses, including FPV, do not have DNA polymerases and cannot promote cell division. FPV relies on its host for its metabolic processes and use the host's cell division machinery, specifically cells in S-phase, to complete their lytic cycle. The virus usually attacks bone marrow, lymphatic tissue, and intestinal epithelial cells. The virus has an incubation period of 2 to 7 days. It can remain in an environment for days to months and possibly years. Due to its resistance to most disinfectants it is a difficult virus to eliminate from the environment making it more possible for other vulnerable animals to contract it.
Ecology and Pathogenesis
The virus can be transmitted either by the fecal-oral route or by indirect transmission via fomites contaminated by infected individuals, as well as from humans that have the virus on their hands or clothes. The virus can live in an environment for months to a year and in some instances over a year. FPV is also highly resistant to certain disinfectants making it difficult for owners to remove it from their household. Using transferrin receptors FPV can enter cells and replicate inside of cells that are currently in the synthesis phase of mitosis. FPV can occur in cats younger than 1 year old, or unvaccinated or improperly vaccinated cats of any age. Severity of the virus depends on age, immunity of the individual and infections from other bacteria or viruses. FPV causes feline infections enteritis (FIE) which is a severe infection of the gut that is fatal and highly contagious making it spread rapidly in a multiple cat household. In addition to domestic cats, FPV can infect wild cats, raccoons, foxes, and mink. Clinical symptoms of infected individuals are lethargy, diarrhea, inappetence, fever (103°F to 107°F or 39.5°C to 42.5°C), vomiting, weight loss. In severe cases, cats can have ulcers in the mouth as well as exhibit mucosal pallor. In terminal cases, cats can be hypothermic, bradycardic, and comatose. If left untreated or if the virus has progressed too far then death can occur usually because of dehydration, low blood sugar, imbalanced electrolytes, hemorrhaging, or bacteria in the bloodstream.
References
Author
Page authored by Phoebe Chambers, student of Prof. Bradley Tolar at UNC Wilmington.
