Detection of canine parvovirus type 2 (CPV-2) by PCR in dogs from Lima, Peru

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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...

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Detalles Bibliográficos
Autores: Quino Q., Raquel, Rímac B., Rocío, Luna E., Luis, Maturrano H., Lenin, Rosadio A., Raúl
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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oai_identifier_str oai:revistasinvestigacion.unmsm.edu.pe:article/14771
network_acronym_str REVUNMSM
network_name_str 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
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv 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
identifier_str_mv 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
dc.rights.none.fl_str_mv https://creativecommons.org/licenses/by-nc-sa/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 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
instname_str Universidad Nacional Mayor de San Marcos
instacron_str UNMSM
institution UNMSM
reponame_str Revistas - Universidad Nacional Mayor de San Marcos
collection Revistas - Universidad Nacional Mayor de San Marcos
repository.name.fl_str_mv
repository.mail.fl_str_mv
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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
score 13.850303
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