Difference between revisions of "Feline Leukaemia Virus"
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Also known as '''''FeLV | Also known as '''''FeLV | ||
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==Introduction== | ==Introduction== | ||
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==Pathogenesis== | ==Pathogenesis== | ||
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*Salivary glands | *Salivary glands | ||
*Reproductive tract | *Reproductive tract | ||
− | Most kittens but only 30% of adults become ''' | + | Most kittens but only 30% of adults become '''viremic''' for life without producing antibody. The condition progresses in various forms: |
− | *20% of | + | *20% of viremic cats die of tumors |
− | *30% of | + | *30% of viremic cats die of FeLV-associated disease |
*80% die within three years of exposure | *80% die within three years of exposure | ||
− | 30% of adults exposed become '''latently infected''' and can become | + | 30% of adults exposed become '''latently infected''' and can become viremic when immunosuppressed. |
40% of exposed adults remain healthy and develop Ab and CD8+ T cells after clearing the virus, without becoming reinfected or silent carriers. | 40% of exposed adults remain healthy and develop Ab and CD8+ T cells after clearing the virus, without becoming reinfected or silent carriers. | ||
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*'''Thymic lymphosarcoma''': T cell tumors, with only the thymus enlarged -this may result in dyspnoea and can be confirmed by radiography | *'''Thymic lymphosarcoma''': T cell tumors, with only the thymus enlarged -this may result in dyspnoea and can be confirmed by radiography | ||
*'''Alimentary lymphosarcoma''': B cell tumors of the Peyer's patches | *'''Alimentary lymphosarcoma''': B cell tumors of the Peyer's patches | ||
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FeLV-associated disease: | FeLV-associated disease: | ||
*'''Immunodepression''' causing secondary disease | *'''Immunodepression''' causing secondary disease | ||
− | *'''Reproductive failure''': FeLV crosses the placenta, causing fetal resorption or | + | *'''Reproductive failure''': FeLV crosses the placenta, causing fetal resorption or viremic kittens with thymic aplasia |
==Epidemiology== | ==Epidemiology== | ||
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There are 3 antigenic subgroups which are defined by the gp70 regulated viral response: | There are 3 antigenic subgroups which are defined by the gp70 regulated viral response: | ||
− | *Group A is transmitted between cats and is monotypic: one vaccine covers all isolates. Infection with this viral subgroup leads to ''' | + | *Group A is transmitted between cats and is monotypic: one vaccine covers all isolates. Infection with this viral subgroup leads to '''lymphosarcoma'''. |
− | *Group B is recombinant with transmissible FeLV-A; infection with viruses of this subgroup increases the chance of developing ''' | + | *Group B is recombinant with transmissible FeLV-A; infection with viruses of this subgroup increases the chance of developing '''thymic tumors'''. |
− | *Group C is a mutant of subgroup A. Isolates are rare, and occur as A+C | + | *Group C is a mutant of subgroup A. Isolates are rare, and occur as A+C mixtures, leading to an increased chance of developing '''anemia'''. |
==Diagnosis== | ==Diagnosis== | ||
− | *FeLV should be suspect in any cat with '''recurrent bacterial infections''', '''anemia''' or '''weight loss''' | + | *FeLV should be suspect in any cat with '''recurrent bacterial infections''', '''anemia''' or '''weight loss''' |
− | *''' | + | *'''ELISA''' for '''Antigen''' (capsid protein p27 or envelope protein gp70) |
− | *'''Immunochromatography''' is now | + | *'''Immunochromatography''' is now trusted as ELISA testing can give false positives |
− | *'''Virus isolation''' from heparinised blood can be performed to confirm a positive diagnosis | + | *'''Virus isolation''' from heparinised blood can now be performed to confirm a positive diagnosis |
− | + | ELISA | |
− | * | + | **Rapid-Immuno-Migration |
− | *Rapid-Immuno-Migration | + | **Western Blot |
− | * | + | **Virus Isolation |
+ | **Immunofluorescence | ||
+ | **PCR | ||
==Infection Control== | ==Infection Control== | ||
− | Antigen positive cats | + | *Antigen positive sick cats should be destroyed |
+ | *Healthy positive cats should have diagnosis confirmed | ||
+ | *Vaccination: | ||
+ | **Should take place once antigen-negative status has been determined | ||
+ | **'''Leukogen''': Subunit vaccine (using envelope protein gp70) produced in ''E. coli'' mixed with Quill-A and alhydrogel | ||
+ | **Others include inactivated virus and canarypox recombinants, but all MUST include FeLV-A | ||
− | + | (FeLV) | |
− | + | [[Image:FeLV Electron Micrograph.jpg|thumb|right|150px|FeLV Electron Micrograph [http://phil.cdc.gov/phil/home.asp Public Health Image Library] Image #5610]] | |
+ | [[Image:Kinetics of FeLV 2.jpg|thumb|right|150px|Kinetics of FeLV - Copyright Dr Brian Catchpole BVetMed PhD MRCVS]] | ||
+ | *Oncogenic retrovirus | ||
+ | *Causes neoplasia (lymphoma), myelosuppression (anaemia) and immunosuppression (of [[Lymphocytes#T cells|T cells]]) | ||
+ | *2 strains: | ||
+ | **FeLV-A | ||
+ | ***Natural strain | ||
+ | **FeLV-B | ||
+ | ***Formed through FeLV-A recombining with endogenous retroviral sequences in the feline genome | ||
+ | ***Increases the risks of lymphoma | ||
+ | **FeLV-C | ||
+ | ***Formed from the spontaneous mutation of FeLV-A | ||
+ | ***Is more myelosuppressive | ||
+ | *Virus replicates in the oropharyngeal lymphoid tissue causing a viraemia (virus circulating in the bloodstream) which then spreads to the systemic lymphoid tissue | ||
+ | *Shed in saliva | ||
+ | *Passed by oronasal route, e.g. mutual grooming | ||
+ | *Kittens between 6 weeks and 6 months are most susceptible | ||
+ | *60% of cats will become immune to the disease and recover | ||
+ | *Cats that are persistently viraemic will progress to develop FeLV-associated diseases | ||
+ | *Some cats will become viraemic again if treated with corticosteroids or stressed if the infection lies dormant in the [[Bone Marrow - Anatomy & Physiology|bone marrow]] | ||
==Treatment== | ==Treatment== | ||
− | + | **Antibiotics for secondary infection | |
+ | **Anti-retroviral therapy | ||
+ | *For vaccinations see [[Vaccines#Cat Vaccinations|here]] | ||
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− | [[Category:Mammalian Type C retrovirus ]][[Category:Cat | + | [[Category:Mammalian Type C retrovirus ]][[Category:Cat]][[Category:Secondary Immunodeficiency]] |
− | [[Category: | + | [[Category:To_Do_-_Clinical/Viruses]] |
− | [[Category: | + | [[Category:To Do - Blood]][[Category:To Do - Clinical]][[Category:Lymphoreticular and Haemopoietic Diseases]] |
− | [[Category: |
Revision as of 15:40, 30 October 2010
Also known as FeLV
Introduction
Pathogenesis
FeLV is the "disease of friends": transmission usually occurs through mutual grooming. From the oropharynx, the virus spreads to most tissues in the body to replicate, notably:
- Bone marrow
- Thymus
- Salivary glands
- Reproductive tract
Most kittens but only 30% of adults become viremic for life without producing antibody. The condition progresses in various forms:
- 20% of viremic cats die of tumors
- 30% of viremic cats die of FeLV-associated disease
- 80% die within three years of exposure
30% of adults exposed become latently infected and can become viremic when immunosuppressed. 40% of exposed adults remain healthy and develop Ab and CD8+ T cells after clearing the virus, without becoming reinfected or silent carriers.
Clinical Signs
- Leukemia - a neoplastic increase in blood cell numbers - usually white blood cells
- Multicentric lymphosarcoma: B or T cell tumors, which may be palpable as enlarged lymph nodes (particularly mesenteric)
- Thymic lymphosarcoma: T cell tumors, with only the thymus enlarged -this may result in dyspnoea and can be confirmed by radiography
- Alimentary lymphosarcoma: B cell tumors of the Peyer's patches
FeLV-associated disease:
- Immunodepression causing secondary disease
- Reproductive failure: FeLV crosses the placenta, causing fetal resorption or viremic kittens with thymic aplasia
Epidemiology
Vertical transmission of FeLV-A occurs from mother to kittens either via placenta, grooming, or milk. Horizontal transmission occurs via saliva during mutual grooming. FeLV is of particular concern for intensively bred cats because of close living conditions shared with other cats.
Recovery is linked to age and the presence of maternal antibody
Antigenicity
Viral subgroups have been categorised based on the different abnormalities detected in the host cellular envelope protein gp70. This protein interacts with a cellular receptor, and can prevent already infected cells from being targeted by further viral organisms.
There are 3 antigenic subgroups which are defined by the gp70 regulated viral response:
- Group A is transmitted between cats and is monotypic: one vaccine covers all isolates. Infection with this viral subgroup leads to lymphosarcoma.
- Group B is recombinant with transmissible FeLV-A; infection with viruses of this subgroup increases the chance of developing thymic tumors.
- Group C is a mutant of subgroup A. Isolates are rare, and occur as A+C mixtures, leading to an increased chance of developing anemia.
Diagnosis
- FeLV should be suspect in any cat with recurrent bacterial infections, anemia or weight loss
- ELISA for Antigen (capsid protein p27 or envelope protein gp70)
- Immunochromatography is now trusted as ELISA testing can give false positives
- Virus isolation from heparinised blood can now be performed to confirm a positive diagnosis
ELISA
- Rapid-Immuno-Migration
- Western Blot
- Virus Isolation
- Immunofluorescence
- PCR
Infection Control
- Antigen positive sick cats should be destroyed
- Healthy positive cats should have diagnosis confirmed
- Vaccination:
- Should take place once antigen-negative status has been determined
- Leukogen: Subunit vaccine (using envelope protein gp70) produced in E. coli mixed with Quill-A and alhydrogel
- Others include inactivated virus and canarypox recombinants, but all MUST include FeLV-A
(FeLV)
- Oncogenic retrovirus
- Causes neoplasia (lymphoma), myelosuppression (anaemia) and immunosuppression (of T cells)
- 2 strains:
- FeLV-A
- Natural strain
- FeLV-B
- Formed through FeLV-A recombining with endogenous retroviral sequences in the feline genome
- Increases the risks of lymphoma
- FeLV-C
- Formed from the spontaneous mutation of FeLV-A
- Is more myelosuppressive
- FeLV-A
- Virus replicates in the oropharyngeal lymphoid tissue causing a viraemia (virus circulating in the bloodstream) which then spreads to the systemic lymphoid tissue
- Shed in saliva
- Passed by oronasal route, e.g. mutual grooming
- Kittens between 6 weeks and 6 months are most susceptible
- 60% of cats will become immune to the disease and recover
- Cats that are persistently viraemic will progress to develop FeLV-associated diseases
- Some cats will become viraemic again if treated with corticosteroids or stressed if the infection lies dormant in the bone marrow
Treatment
- Antibiotics for secondary infection
- Anti-retroviral therapy
- For vaccinations see here