Detection of canine parvovirus type 2 (CPV-2) by PCR in dogs from Lima, Peru
Descripción del Articulo
The objective of the study was the detection of canine parvovirus type 2 (CPV-2) in young dogs of Lima city with and without clinical symptoms compatible with parvovirus by the PCR technique using primers that can allow the amplification of a fragment of the gene coding for the protein VP2. Rectal s...
| Autores: | , , , , |
|---|---|
| Formato: | artículo |
| Fecha de Publicación: | 2018 |
| Institución: | Universidad Nacional Mayor de San Marcos |
| Repositorio: | Revistas - Universidad Nacional Mayor de San Marcos |
| Lenguaje: | español |
| OAI Identifier: | oai:revistasinvestigacion.unmsm.edu.pe:article/14771 |
| Enlace del recurso: | https://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/14771 |
| Nivel de acceso: | acceso abierto |
| Materia: | parvovirus canino hisopados rectales diagnóstico clínico PCR canine parvovirus rectal swabs clinic diagnosis |
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Revistas - Universidad Nacional Mayor de San Marcos |
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| dc.title.none.fl_str_mv |
Detection of canine parvovirus type 2 (CPV-2) by PCR in dogs from Lima, Peru Detección de parvovirus canino tipo 2 (CPV-2) en perros de Lima Metropolitana, Perú, mediante PCR |
| title |
Detection of canine parvovirus type 2 (CPV-2) by PCR in dogs from Lima, Peru |
| spellingShingle |
Detection of canine parvovirus type 2 (CPV-2) by PCR in dogs from Lima, Peru Quino Q., Raquel parvovirus canino hisopados rectales diagnóstico clínico PCR canine parvovirus rectal swabs clinic diagnosis PCR |
| title_short |
Detection of canine parvovirus type 2 (CPV-2) by PCR in dogs from Lima, Peru |
| title_full |
Detection of canine parvovirus type 2 (CPV-2) by PCR in dogs from Lima, Peru |
| title_fullStr |
Detection of canine parvovirus type 2 (CPV-2) by PCR in dogs from Lima, Peru |
| title_full_unstemmed |
Detection of canine parvovirus type 2 (CPV-2) by PCR in dogs from Lima, Peru |
| title_sort |
Detection of canine parvovirus type 2 (CPV-2) by PCR in dogs from Lima, Peru |
| dc.creator.none.fl_str_mv |
Quino Q., Raquel Rímac B., Rocío Luna E., Luis Maturrano H., Lenin Rosadio A., Raúl |
| author |
Quino Q., Raquel |
| author_facet |
Quino Q., Raquel Rímac B., Rocío Luna E., Luis Maturrano H., Lenin Rosadio A., Raúl |
| author_role |
author |
| author2 |
Rímac B., Rocío Luna E., Luis Maturrano H., Lenin Rosadio A., Raúl |
| author2_role |
author author author author |
| dc.subject.none.fl_str_mv |
parvovirus canino hisopados rectales diagnóstico clínico PCR canine parvovirus rectal swabs clinic diagnosis PCR |
| topic |
parvovirus canino hisopados rectales diagnóstico clínico PCR canine parvovirus rectal swabs clinic diagnosis PCR |
| description |
The objective of the study was the detection of canine parvovirus type 2 (CPV-2) in young dogs of Lima city with and without clinical symptoms compatible with parvovirus by the PCR technique using primers that can allow the amplification of a fragment of the gene coding for the protein VP2. Rectal swabs were collected from 78 dogs younger than one year old and without a history of previous vaccinations, of which 39 individuals had a clinical diagnosis of canine parvovirus and the other 39 were clinically healthy animals. For the extraction of viral DNA, the fast boiling method was used. Samples were boiled at 100 °C for 10 minutes and then centrifuged to extract the supernatant, which was used as a template for the PCR reaction. Specific primers that amplify a 1316 base pair fragment of the VP2 gene of the CPV-2 virus were used, using a commercial vaccine as a positive control. The virus was detected in 62% of animals with clinical diagnosis of the disease with conventional PCR, not being detected in clinically healthy dogs. The non-detection of CPV-2 in animals with a clinical diagnosis compatible with parvovirus in 38% of cases would indicate the presence of another etiological agent as the cause of the clinical signs, and therefore, recommending the use of complementary techniques for the correct diagnosis of the disease. |
| publishDate |
2018 |
| dc.date.none.fl_str_mv |
2018-09-06 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
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https://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/14771 10.15381/rivep.v29i3.14771 |
| url |
https://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/14771 |
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10.15381/rivep.v29i3.14771 |
| dc.language.none.fl_str_mv |
spa |
| language |
spa |
| dc.relation.none.fl_str_mv |
https://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/14771/13095 https://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/14771/13906 |
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https://creativecommons.org/licenses/by-nc-sa/4.0 info:eu-repo/semantics/openAccess |
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https://creativecommons.org/licenses/by-nc-sa/4.0 |
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openAccess |
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application/pdf text/html |
| dc.publisher.none.fl_str_mv |
Universidad Nacional Mayor de San Marcos, Facultad de Medicina Veterinaria |
| publisher.none.fl_str_mv |
Universidad Nacional Mayor de San Marcos, Facultad de Medicina Veterinaria |
| dc.source.none.fl_str_mv |
Revista de Investigaciones Veterinarias del Perú; Vol. 29 No. 3 (2018); 972-979 Revista de Investigaciones Veterinarias del Perú; Vol. 29 Núm. 3 (2018); 972-979 1682-3419 1609-9117 reponame:Revistas - Universidad Nacional Mayor de San Marcos instname:Universidad Nacional Mayor de San Marcos instacron:UNMSM |
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Universidad Nacional Mayor de San Marcos |
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UNMSM |
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UNMSM |
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Revistas - Universidad Nacional Mayor de San Marcos |
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Revistas - Universidad Nacional Mayor de San Marcos |
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1848424238404337664 |
| spelling |
Detection of canine parvovirus type 2 (CPV-2) by PCR in dogs from Lima, PeruDetección de parvovirus canino tipo 2 (CPV-2) en perros de Lima Metropolitana, Perú, mediante PCRQuino Q., RaquelRímac B., RocíoLuna E., LuisMaturrano H., LeninRosadio A., Raúlparvovirus caninohisopados rectalesdiagnóstico clínicoPCRcanine parvovirusrectal swabsclinic diagnosisPCRThe objective of the study was the detection of canine parvovirus type 2 (CPV-2) in young dogs of Lima city with and without clinical symptoms compatible with parvovirus by the PCR technique using primers that can allow the amplification of a fragment of the gene coding for the protein VP2. Rectal swabs were collected from 78 dogs younger than one year old and without a history of previous vaccinations, of which 39 individuals had a clinical diagnosis of canine parvovirus and the other 39 were clinically healthy animals. For the extraction of viral DNA, the fast boiling method was used. Samples were boiled at 100 °C for 10 minutes and then centrifuged to extract the supernatant, which was used as a template for the PCR reaction. Specific primers that amplify a 1316 base pair fragment of the VP2 gene of the CPV-2 virus were used, using a commercial vaccine as a positive control. The virus was detected in 62% of animals with clinical diagnosis of the disease with conventional PCR, not being detected in clinically healthy dogs. The non-detection of CPV-2 in animals with a clinical diagnosis compatible with parvovirus in 38% of cases would indicate the presence of another etiological agent as the cause of the clinical signs, and therefore, recommending the use of complementary techniques for the correct diagnosis of the disease.El objetivo del estudio fue la detección de parvovirus canino tipo 2 (CPV-2) en perros jóvenes con/sin sintomatología clínica compatible con parvovirosis mediante la técnica de PCR, usando cebadores que pueden permitir la amplificación de un fragmento del gen codificante de la proteína VP2. Se colectaron hisopados rectales de 78 perros menores a un año y sin historia de vacunaciones previas, de los cuales 39 individuos tuvieron un diagnóstico clínico de parvovirosis canina y los otros 39 fueron animales clínicamente sanos. Para la extracción de ADN viral se usó el método fast boiling, donde las muestras fueron sometidas a un hervido a 100 °C por 10 minutos con posterior centrifugación para extraer el sobrenadante, el cual fue usado como molde para la reacción de PCR. Se usaron cebadores específicos que amplifican un fragmento de 1316 pares de bases del gen VP2 del virus CPV-2, utilizando como control positivo una vacuna comercial. El virus fue detectado en el 62% de animales con diagnóstico clínico de la enfermedad con PCR convencional, no siendo detectado en perros clínicamente sanos. La no detección de CPV-2 en animales con diagnóstico clínico compatibles a parvovirosis en el 38% de los casos indicaría la presencia de otro agente etiológico como causante del cuadro sintomatológico, recomendándose el uso de técnicas complementarias para el correcto diagnóstico de la enfermedad.Universidad Nacional Mayor de San Marcos, Facultad de Medicina Veterinaria2018-09-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdftext/htmlhttps://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/1477110.15381/rivep.v29i3.14771Revista de Investigaciones Veterinarias del Perú; Vol. 29 No. 3 (2018); 972-979Revista de Investigaciones Veterinarias del Perú; Vol. 29 Núm. 3 (2018); 972-9791682-34191609-9117reponame:Revistas - Universidad Nacional Mayor de San Marcosinstname:Universidad Nacional Mayor de San Marcosinstacron:UNMSMspahttps://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/14771/13095https://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/14771/13906Derechos de autor 2018 Raquel Quino Q., Rocío Rímac B., Luis Luna E., Lenin Maturrano H., Raúl Rosadio A.https://creativecommons.org/licenses/by-nc-sa/4.0info:eu-repo/semantics/openAccessoai:revistasinvestigacion.unmsm.edu.pe:article/147712018-12-21T09:58:01Z |
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13.850303 |
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La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).