Diferencia entre revisiones de «Herpesvirus Bovino 1»
(Página creada con 'Also know as: '''''BHV-1 — Encephalitic Bovine Herpesvirus Type 5 or Type 1 infection in cattle — Infectious Bovine Rhinotracheitis — [[Infectious Pustular Vulvovagini...') |
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| − | + | Tambien conocido como: '''''BHV -1 — Encephalitic Bovine Herpesvirus Type 5 or Type 1 infection in cattle — [[Infectious Bovine Rhinotracheitis]] — [[Infectious Pustular Vulvovaginitis]] — Infectious Pustular Balanoposthitis — IPB''''' | |
| − | == | + | == Introducción == |
| − | + | Herpesvirus Bovino 1, produce tres enfermedades; '''[[Rinotraqueitis Bovino Infeccioso]] (IBR) y [[Vulvovaginitis Pustular Infecciosa]] (IPV) en hembras y Balanopostitis Pustular Infeccioso''' (IPB) en machos. | |
| − | + | Las manifestaciones clínicas de Herpesvirus Bovino-1 circulation in a herd depend on the virulence of the prevalent cepa. Where virulent strains circulate, '''morbidity rate is up to 100% in a naïve herd'''. Otherwise morbidity rate is approximately 20%. The mortality rate varies between 0 and 10%. | |
| − | == | + | == Distribución == |
| − | + | La distribución de la infección es '''mundial''' and has been diagnosed in all countries tested<ref name="Straub">Straub, O. C (1990) '''Infectious bovine rhinotracheitis virus'''. ''Virus infections of ruminants,'' 71-108;10</ref>. | |
| − | + | En años recientes, algunos países Europeos han podido eliminar la infección por by applying a strict culling policy, e.g. Denmark, Suecia, Finlandia, Suiza y Austria. <ref name="OIE 2005">OIE (2005) '''Terrestrial Animal Health Code'''. Paris, France: ''Office International Des Epizooties'', Chapter 2.3.5.</ref> Otros países han implementado programas de control parecidos. | |
| − | + | La infección es '''endemic in the UK'''. | |
| − | + | El Herpesvirus Bovino-1 se transmite por '''secreciones nasales o reproductivas'''. La transmisión es en forma directa, de un animal a otro, por via respiratoria o reproductiva. La transmissión indirecta tambien se puede ocurrir a través de '''equipo'''. La '''transmissión vertical''' ocurre en vacas, cuando el virus infecta al fetus a traves de la placenta. | |
In a herd, BHV-1 circulation is initiated by virus reactivation and re-excretion in a '''latently infected animal''' already present, or more often by the introduction of an acutely or latently infected animal. | In a herd, BHV-1 circulation is initiated by virus reactivation and re-excretion in a '''latently infected animal''' already present, or more often by the introduction of an acutely or latently infected animal. | ||
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Between herds transmission is a major risk of BHV-1 circulation. '''Airborne transmission''' of BHV-1 has been demonstrated over short distances and can provide an explanation of between herds transmission. | Between herds transmission is a major risk of BHV-1 circulation. '''Airborne transmission''' of BHV-1 has been demonstrated over short distances and can provide an explanation of between herds transmission. | ||
| − | == | + | == Razas Más Afectadas == |
The natural hosts are '''bovine species'''. BHV-1 has a narrow species specificity. The truly susceptible species can be defined as animals in which BHV-1 can establish a latent infection such as cattle and sheep<ref>Thiry, E et al., (2001). '''Risk evaluation of cross-infection of cattle with ruminant alphaherpesviruses related to bovine herpesvirus type 1.''' In: Körber R, ed. Tagungsbeiträge, 3. ''Internationales Symposium zur BHV-1- und BVD-Bekämpfung'', Stendal, in press</ref>, goats<ref> Six, A., Banks, M., Engels, M., Bascunana, C. R., Ackermann, M (2001) '''Latency and reactivation of bovine herpesvirus 1 (BHV-1) in goats and of caprine herpesvirus 1 (CapHV-1) in calves'''. ''Archives of Virology'', 146(7):1325-1335; 38</ref> and other species belonging to the subfamily ''Bovidae''. | The natural hosts are '''bovine species'''. BHV-1 has a narrow species specificity. The truly susceptible species can be defined as animals in which BHV-1 can establish a latent infection such as cattle and sheep<ref>Thiry, E et al., (2001). '''Risk evaluation of cross-infection of cattle with ruminant alphaherpesviruses related to bovine herpesvirus type 1.''' In: Körber R, ed. Tagungsbeiträge, 3. ''Internationales Symposium zur BHV-1- und BVD-Bekämpfung'', Stendal, in press</ref>, goats<ref> Six, A., Banks, M., Engels, M., Bascunana, C. R., Ackermann, M (2001) '''Latency and reactivation of bovine herpesvirus 1 (BHV-1) in goats and of caprine herpesvirus 1 (CapHV-1) in calves'''. ''Archives of Virology'', 146(7):1325-1335; 38</ref> and other species belonging to the subfamily ''Bovidae''. | ||
Outbreaks are most often seen in cattle between '''6 and 18 months''' of age though all ages of cattle are susceptible. Calves are usually protected by colostral antibodies until 3-4 months of age so infection before this point is uncommon. | Outbreaks are most often seen in cattle between '''6 and 18 months''' of age though all ages of cattle are susceptible. Calves are usually protected by colostral antibodies until 3-4 months of age so infection before this point is uncommon. | ||
| − | == | + | == Signos Clínicos == |
Signs of IBR vary with each particular strain but classically include '''coughing, serous nasal discharge, tachypnoea and dyspnoea'''. There may also be signs of increased '''lacrimation''' and a '''marked conjunctivitis'''. Coughing and sneezing are observed. The virus is excreted in the nasal secretions as early as 24 hours after infection. After an incubation period of 2 to 4 days, nasal secretions are more profuse and evolve from '''sero-mucous to mucopurulent discharge'''. The animal will usually be '''pyrexic''' and be weak, dull and depressed. It will usually have a reduced appetite and may show signs of weight loss. If in milk, the yield will be decreased. Young animals show ptyalism. In endemic dairy herds, it is not uncommon for animals to present with '''milk drop''' with or without pyrexia. | Signs of IBR vary with each particular strain but classically include '''coughing, serous nasal discharge, tachypnoea and dyspnoea'''. There may also be signs of increased '''lacrimation''' and a '''marked conjunctivitis'''. Coughing and sneezing are observed. The virus is excreted in the nasal secretions as early as 24 hours after infection. After an incubation period of 2 to 4 days, nasal secretions are more profuse and evolve from '''sero-mucous to mucopurulent discharge'''. The animal will usually be '''pyrexic''' and be weak, dull and depressed. It will usually have a reduced appetite and may show signs of weight loss. If in milk, the yield will be decreased. Young animals show ptyalism. In endemic dairy herds, it is not uncommon for animals to present with '''milk drop''' with or without pyrexia. | ||
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In IPV, signs will include '''pain of the vagina or penis''' and erythrematous swelling of this region, reluctance to mate, mucous discharge from the vulva or penis and signs of '''ulcers, vesicles and erosions''' on the penis or vagina. The animal may urinate frequently and have an elevated tail. | In IPV, signs will include '''pain of the vagina or penis''' and erythrematous swelling of this region, reluctance to mate, mucous discharge from the vulva or penis and signs of '''ulcers, vesicles and erosions''' on the penis or vagina. The animal may urinate frequently and have an elevated tail. | ||
| − | == | + | == Patología == |
| − | ''' | + | '''Ulceración y enrojecimiento''' son visibles en la '''mucosa nasal''', en la faringe y la traquea. Lesiones están normalmente restringidas la '''vía aérea superior'''. [[Bronquitis]] y neumonía también pueden ser observados, pero usualmente como consecuencia de infecciones bacterianas secundarias. Mucosas respiratorias son enrojecidas y edematosas, con focos de úlceras y algunos lesiones hemorrágicos.<ref>Gibbs, E. P. J., Rweyemamu, M. M (1977) '''Bovine herpesviruses. Part I. Bovine herpesvirus 1.''' ''Veterinary Bulletin', 47:317-343.</ref> <ref name="Straub" /> |
| − | ''' | + | '''Vulvovaginitis pustular infecciosa''' (IPV) y balanopostitis pustular infeccioso''' (IPB) es una inflamación pustular causando enrojecimiento y edema de la mucosa genital con '''vesículas y pústulas evolucionando a úlceras.''' |
| − | == | + | == Diagnóstico == |
| − | An outbreak of acute respiratory disease with profuse nasal discharge, fever and depression suggests IBR. In a naive herd, the epidemic progresses quickly and respiratory signs are associated with neonatal deaths and abortions at 4 to 8 months of pregnancy. | + | An outbreak of acute respiratory disease with profuse nasal discharge, fever and depression suggests IBR. In a naive herd, the epidemic progresses quickly and respiratory signs are associated with neonatal deaths and abortions at 4 to 8 months of pregnancy. Cepas hypovirulentes pueden circular sin sintomatología. The IPV form is suspected if animals have vesicular and pustular lesions of the genital mucosa and there is evidence of transmisión venérea. |
| − | + | En el laboratorio se puede aislar el virus can be isolated from nasal or vaginal swabs''', or from triturated tissue. BHV-1 DNA can also be detected by '''polymerase chain reaction (PCR).''' In an individual animal, '''técnicas serológicas paired serology''' is useful with a raised antibody response seen two weeks after clinical signs. | |
'''[[ELISA testing|ELISAs]]''' have also been developed to detect BHV-1 antibodies in '''bulk milk''', or in milk samples from individual cows. Milk ELISAs have been found to perform well when compared with standard serum ELISAs. | '''[[ELISA testing|ELISAs]]''' have also been developed to detect BHV-1 antibodies in '''bulk milk''', or in milk samples from individual cows. Milk ELISAs have been found to perform well when compared with standard serum ELISAs. | ||
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In IBR control programmes, serological diagnosis aims to identify latently infected animals. However, a few animals are seronegative latent carriers (SNLC), i.e. they are latently infected with BHV-1 without detectable antibodies. <ref>Lemaire, M., Meyer, G., Baranowski, E., Schynts, F., Wellemans, G., Kerkhofs, P., Thiry, E (2000) '''Effects of bovine herpesvirus type 1 infection in calves with maternal antibodies on immune response and virus latency'''. ''J Clin Microbiol'', 38:1885-1894</ref> | In IBR control programmes, serological diagnosis aims to identify latently infected animals. However, a few animals are seronegative latent carriers (SNLC), i.e. they are latently infected with BHV-1 without detectable antibodies. <ref>Lemaire, M., Meyer, G., Baranowski, E., Schynts, F., Wellemans, G., Kerkhofs, P., Thiry, E (2000) '''Effects of bovine herpesvirus type 1 infection in calves with maternal antibodies on immune response and virus latency'''. ''J Clin Microbiol'', 38:1885-1894</ref> | ||
| − | == | + | == Tratamiento == |
Supportive treatment is usually required for this condition. If secondary bacterial infection is present then antimicrobials can be used to treat this. | Supportive treatment is usually required for this condition. If secondary bacterial infection is present then antimicrobials can be used to treat this. | ||
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A '''[[Vaccines|vaccination]]''' is available for control and is widely used. Both '''inactivated and live attenuated''' vaccines are available. The vaccination schedule consists of two vaccinations at a 3-week interval for inactivated vaccines, starting from the age of 3-4 months to avoid interference with colostral antibodies. Live attenuated vaccines are administered either once or twice depending on the type of vaccine. Duration of immunity usually lasts from '''six months to one year'''. Vaccination is recommended for young calves to prevent clinical signs. Vaccination of calves less than 3 months of age can be achieved by intranasal administration of attenuated vaccine. This route is better for overcoming interference due to maternal immunity. Vaccinations should '''protect cattle clinically''' in case of infection and significantly '''reduce the shedding''' of field virus. Vaccinating latently infected animals may reduce the level of shedding from this group. '''Marker vaccines''' are also available and recommended. These are based on glycoprotein E (gE) deleted mutants, with detectable antibodies present to the gE antigen in marker vaccinated individuals indicating wild-type viral infection. | A '''[[Vaccines|vaccination]]''' is available for control and is widely used. Both '''inactivated and live attenuated''' vaccines are available. The vaccination schedule consists of two vaccinations at a 3-week interval for inactivated vaccines, starting from the age of 3-4 months to avoid interference with colostral antibodies. Live attenuated vaccines are administered either once or twice depending on the type of vaccine. Duration of immunity usually lasts from '''six months to one year'''. Vaccination is recommended for young calves to prevent clinical signs. Vaccination of calves less than 3 months of age can be achieved by intranasal administration of attenuated vaccine. This route is better for overcoming interference due to maternal immunity. Vaccinations should '''protect cattle clinically''' in case of infection and significantly '''reduce the shedding''' of field virus. Vaccinating latently infected animals may reduce the level of shedding from this group. '''Marker vaccines''' are also available and recommended. These are based on glycoprotein E (gE) deleted mutants, with detectable antibodies present to the gE antigen in marker vaccinated individuals indicating wild-type viral infection. | ||
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| − | == | + | == Referenciass == |
<references/> | <references/> | ||
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{{Nick Lyons | {{Nick Lyons | ||
|date = 31 August 2011}} | |date = 31 August 2011}} | ||
| − | [[ | + | [[Categoría:Enfermedades de Ganado Bovino]] |
[[Category:CABI Expert Review Completed]] | [[Category:CABI Expert Review Completed]] | ||
[[Category:Nick Lyons reviewed]] | [[Category:Nick Lyons reviewed]] | ||
Revisión del 18:37 11 sep 2011
Tambien conocido como: BHV -1 — Encephalitic Bovine Herpesvirus Type 5 or Type 1 infection in cattle — Infectious Bovine Rhinotracheitis — Infectious Pustular Vulvovaginitis — Infectious Pustular Balanoposthitis — IPB
Introducción
Herpesvirus Bovino 1, produce tres enfermedades; Rinotraqueitis Bovino Infeccioso (IBR) y Vulvovaginitis Pustular Infecciosa (IPV) en hembras y Balanopostitis Pustular Infeccioso (IPB) en machos.
Las manifestaciones clínicas de Herpesvirus Bovino-1 circulation in a herd depend on the virulence of the prevalent cepa. Where virulent strains circulate, morbidity rate is up to 100% in a naïve herd. Otherwise morbidity rate is approximately 20%. The mortality rate varies between 0 and 10%.
Distribución
La distribución de la infección es mundial and has been diagnosed in all countries tested[1].
En años recientes, algunos países Europeos han podido eliminar la infección por by applying a strict culling policy, e.g. Denmark, Suecia, Finlandia, Suiza y Austria. [2] Otros países han implementado programas de control parecidos.
La infección es endemic in the UK.
El Herpesvirus Bovino-1 se transmite por secreciones nasales o reproductivas. La transmisión es en forma directa, de un animal a otro, por via respiratoria o reproductiva. La transmissión indirecta tambien se puede ocurrir a través de equipo. La transmissión vertical ocurre en vacas, cuando el virus infecta al fetus a traves de la placenta.
In a herd, BHV-1 circulation is initiated by virus reactivation and re-excretion in a latently infected animal already present, or more often by the introduction of an acutely or latently infected animal.
Between herds transmission is a major risk of BHV-1 circulation. Airborne transmission of BHV-1 has been demonstrated over short distances and can provide an explanation of between herds transmission.
Razas Más Afectadas
The natural hosts are bovine species. BHV-1 has a narrow species specificity. The truly susceptible species can be defined as animals in which BHV-1 can establish a latent infection such as cattle and sheep[3], goats[4] and other species belonging to the subfamily Bovidae.
Outbreaks are most often seen in cattle between 6 and 18 months of age though all ages of cattle are susceptible. Calves are usually protected by colostral antibodies until 3-4 months of age so infection before this point is uncommon.
Signos Clínicos
Signs of IBR vary with each particular strain but classically include coughing, serous nasal discharge, tachypnoea and dyspnoea. There may also be signs of increased lacrimation and a marked conjunctivitis. Coughing and sneezing are observed. The virus is excreted in the nasal secretions as early as 24 hours after infection. After an incubation period of 2 to 4 days, nasal secretions are more profuse and evolve from sero-mucous to mucopurulent discharge. The animal will usually be pyrexic and be weak, dull and depressed. It will usually have a reduced appetite and may show signs of weight loss. If in milk, the yield will be decreased. Young animals show ptyalism. In endemic dairy herds, it is not uncommon for animals to present with milk drop with or without pyrexia.
IBR may cause abortion if susceptible cows or heifers are infected during pregnancy. Abortion is usually observed between 4 and 8 months of gestation. Early embryonic death can also occur. Abortion is a consequence of respiratory infection of pregnant cows. Viraemia allows the virus to enter the uterine artery and cross the placenta. Abortion is due to a lytic infection of the fetus. All internal organs of the fetus, especially the liver and renal cortex, show foci of necrosis. A generalized multifocal necrosis is diagnosed.[5] Infection of cows during the last trimester of gestation can lead to neonatal death, and death of weak calves can occur during the first 2 weeks of life.[6]
Latent infection can occur, the viral cells residing in the trigeminal nerve, and infected cattle can then shed the virus intermittently particularly after stressful episodes. Other animals recover within 14 days, due to the rise of the specific immune response. Becoming latent is a common sequelae to infection and in terms of control, all animals on an endemic farm should be considered as potential latent carriers irrespective of their antibody status. Some highly virulent BHV-1 strains induce a high mortality rate.
In IPV, signs will include pain of the vagina or penis and erythrematous swelling of this region, reluctance to mate, mucous discharge from the vulva or penis and signs of ulcers, vesicles and erosions on the penis or vagina. The animal may urinate frequently and have an elevated tail.
Patología
Ulceración y enrojecimiento son visibles en la mucosa nasal, en la faringe y la traquea. Lesiones están normalmente restringidas la vía aérea superior. Bronquitis y neumonía también pueden ser observados, pero usualmente como consecuencia de infecciones bacterianas secundarias. Mucosas respiratorias son enrojecidas y edematosas, con focos de úlceras y algunos lesiones hemorrágicos.[7] [1]
Vulvovaginitis pustular infecciosa (IPV) y balanopostitis pustular infeccioso (IPB) es una inflamación pustular causando enrojecimiento y edema de la mucosa genital con vesículas y pústulas evolucionando a úlceras.
Diagnóstico
An outbreak of acute respiratory disease with profuse nasal discharge, fever and depression suggests IBR. In a naive herd, the epidemic progresses quickly and respiratory signs are associated with neonatal deaths and abortions at 4 to 8 months of pregnancy. Cepas hypovirulentes pueden circular sin sintomatología. The IPV form is suspected if animals have vesicular and pustular lesions of the genital mucosa and there is evidence of transmisión venérea.
En el laboratorio se puede aislar el virus can be isolated from nasal or vaginal swabs, or from triturated tissue. BHV-1 DNA can also be detected by polymerase chain reaction (PCR). In an individual animal, técnicas serológicas paired serology is useful with a raised antibody response seen two weeks after clinical signs.
ELISAs have also been developed to detect BHV-1 antibodies in bulk milk, or in milk samples from individual cows. Milk ELISAs have been found to perform well when compared with standard serum ELISAs.
In IBR control programmes, serological diagnosis aims to identify latently infected animals. However, a few animals are seronegative latent carriers (SNLC), i.e. they are latently infected with BHV-1 without detectable antibodies. [8]
Tratamiento
Supportive treatment is usually required for this condition. If secondary bacterial infection is present then antimicrobials can be used to treat this.
Nonsteroidal anti-inflammatory compounds are recommended for treatment of pyrexia and for pain relief.
Control
A vaccination is available for control and is widely used. Both inactivated and live attenuated vaccines are available. The vaccination schedule consists of two vaccinations at a 3-week interval for inactivated vaccines, starting from the age of 3-4 months to avoid interference with colostral antibodies. Live attenuated vaccines are administered either once or twice depending on the type of vaccine. Duration of immunity usually lasts from six months to one year. Vaccination is recommended for young calves to prevent clinical signs. Vaccination of calves less than 3 months of age can be achieved by intranasal administration of attenuated vaccine. This route is better for overcoming interference due to maternal immunity. Vaccinations should protect cattle clinically in case of infection and significantly reduce the shedding of field virus. Vaccinating latently infected animals may reduce the level of shedding from this group. Marker vaccines are also available and recommended. These are based on glycoprotein E (gE) deleted mutants, with detectable antibodies present to the gE antigen in marker vaccinated individuals indicating wild-type viral infection.
Referenciass
- ↑ 1,0 1,1 Straub, O. C (1990) Infectious bovine rhinotracheitis virus. Virus infections of ruminants, 71-108;10
- ↑ OIE (2005) Terrestrial Animal Health Code. Paris, France: Office International Des Epizooties, Chapter 2.3.5.
- ↑ Thiry, E et al., (2001). Risk evaluation of cross-infection of cattle with ruminant alphaherpesviruses related to bovine herpesvirus type 1. In: Körber R, ed. Tagungsbeiträge, 3. Internationales Symposium zur BHV-1- und BVD-Bekämpfung, Stendal, in press
- ↑ Six, A., Banks, M., Engels, M., Bascunana, C. R., Ackermann, M (2001) Latency and reactivation of bovine herpesvirus 1 (BHV-1) in goats and of caprine herpesvirus 1 (CapHV-1) in calves. Archives of Virology, 146(7):1325-1335; 38
- ↑ Smith, K. C (1997) Herpesviral abortion in domestic animals. Vet Journal, 153(3):253-268
- ↑ Thiry, E., Detilleux, P., Vriese, A., Pirak, M., Pastoret, P-P (1984) Infectious bovine rhinotracheitis in the neonatal period: a review and a case report. Annales de Médecine Vétérinaire, 128(1):33-40; 25
- ↑ Gibbs, E. P. J., Rweyemamu, M. M (1977) Bovine herpesviruses. Part I. Bovine herpesvirus 1. Veterinary Bulletin', 47:317-343.
- ↑ Lemaire, M., Meyer, G., Baranowski, E., Schynts, F., Wellemans, G., Kerkhofs, P., Thiry, E (2000) Effects of bovine herpesvirus type 1 infection in calves with maternal antibodies on immune response and virus latency. J Clin Microbiol, 38:1885-1894
Kaashoek, M. J., Moerman, A., Madic, J., Rijsewijk, F. A. M., Quak, J., Gielkens, A. L. J., Oirschot, J. Tvan (1994) A conventionally attenuated glycoprotein E-negative strain of bovine herpesvirus type 1 is an efficacious and safe vaccine. Vaccine, 12(5):439-444; 19
Karstad, L., Jessett, D. M., Otema, J. C., Drevemo, S (1974) Vulvovaginitis in wildebeest caused by the virus of infectious bovine rhinotracheitis J Wildlife Diseases, 10:392-396.
Lemaire, M., Meyer, G., Baranowski, E., Schynts, F., Wellemans, G., Kerkhofs, P., Thiry, E (2000) Production of bovine herpesvirus type 1-seronegative latent carriers by administration of a live-attenuated vaccine in passively immunized calves. J Clin Microbiol, 38(11):4233-4238; 43 ref.
Mars, M. H et al (2000) Airborne transmission of bovine herpesvirus 1 infections in calves under field conditions. Veterinary Microbiology, 76(1):1-13.
Mars, M. H., Bruschke, C. J. M., Oirschot, J. Tvan (199) Airborne transmission of BHV 1 [bovine herpesvirus 1], BRSV [bovine respiratory virus], and BVDV [bovine virus diarrhoea virus] among cattle is possible under experimental conditions. Veterinary Microbiology, 66(3):197-207; 33
OIE, 2004. Manual of Diagnostic Tests and Vaccines for Terrestrial Animals. Paris, France: World Organisation for Animal Health. http://www.oie.int/eng/normes/mmanual/A_summry.htm. (accessed April 2011)
OIE, 2009. World Animal Health Information Database - Version: 1.4. World Animal Health Information Database. Paris, France: World Organisation for Animal Health.
Van, Oirschot, J. T., Kaashoek, M. J., Rijsewijk, F. A. M (1996) Advances in the development and evaluation of bovine herpesvirus 1 vaccines. Veterinary Microbiol, 53(1/2):43-54; 60
Wyler, R., Engels, M., Schwyzer, M (1989) Infectious Bovine Rhinotracheitis/Vulvovaginitis (BHV-1). In: Wittmann G, ed. Herpesvirus Diseases of Cattle, Horse and Pigs. Massachusetts, USA: Kluwer Academic Publishers, 1-72.
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Este artículo fue originalmente de The Animal Health & Production Compendium (AHPC) publicado en el web por CABI. Hoja(s) de datos utilizados: bovine herpesvirus 1 and bovine herpesvirus 1 infections el 3 April 2011 |
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Este artículo ha sido revisado por el experto Nick Lyons MA VetMB CertCHP MRCVS Fecha de revisión: 31 August 2011 |