Serotyping and genetic detection of Salmonella spp of avian origin

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The aim of this study was to molecularly and serologically identify Salmonella spp present in isolates from avian eggs, carcasses, and viscera. In total, 46 isolates of avian origin identified as Salmonella spp were evaluated through cultures and biochemical tests in the period 2012-2017 from variou...

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Detalles Bibliográficos
Autores: Huarcaya R., Freshia, Calle E., Sonia, Siuce M., Juan, Sedano S., André, Huamaní P., Jhonatan, García B., Arturo, Álvarez V., Luis, Gonzales M., Sofía
Formato: artículo
Fecha de Publicación:2022
Institución:Universidad Nacional Mayor de San Marcos
Repositorio:Revistas - Universidad Nacional Mayor de San Marcos
Lenguaje:español
OAI Identifier:oai:ojs.csi.unmsm:article/22893
Enlace del recurso:https://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/22893
Nivel de acceso:acceso abierto
Materia:Salmonella
serovar
invA gene
PCR
serotyping
gen invA
serotipificación
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oai_identifier_str oai:ojs.csi.unmsm:article/22893
network_acronym_str REVUNMSM
network_name_str Revistas - Universidad Nacional Mayor de San Marcos
repository_id_str
dc.title.none.fl_str_mv Serotyping and genetic detection of Salmonella spp of avian origin
Serotipificación y detección genética de Salmonella spp de origen aviar
title Serotyping and genetic detection of Salmonella spp of avian origin
spellingShingle Serotyping and genetic detection of Salmonella spp of avian origin
Huarcaya R., Freshia
Salmonella
serovar
invA gene
PCR
serotyping
Salmonella
serovar
gen invA
PCR
serotipificación
title_short Serotyping and genetic detection of Salmonella spp of avian origin
title_full Serotyping and genetic detection of Salmonella spp of avian origin
title_fullStr Serotyping and genetic detection of Salmonella spp of avian origin
title_full_unstemmed Serotyping and genetic detection of Salmonella spp of avian origin
title_sort Serotyping and genetic detection of Salmonella spp of avian origin
dc.creator.none.fl_str_mv Huarcaya R., Freshia
Calle E., Sonia
Siuce M., Juan
Sedano S., André
Huamaní P., Jhonatan
García B., Arturo
Álvarez V., Luis
Gonzales M., Sofía
Huarcaya R., Freshia
Calle E., Sonia
Siuce M., Juan
Sedano S., André
Huamaní P., Jhonatan
García B., Arturo
Álvarez V., Luis
Gonzales M., Sofía
author Huarcaya R., Freshia
author_facet Huarcaya R., Freshia
Calle E., Sonia
Siuce M., Juan
Sedano S., André
Huamaní P., Jhonatan
García B., Arturo
Álvarez V., Luis
Gonzales M., Sofía
author_role author
author2 Calle E., Sonia
Siuce M., Juan
Sedano S., André
Huamaní P., Jhonatan
García B., Arturo
Álvarez V., Luis
Gonzales M., Sofía
author2_role author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Salmonella
serovar
invA gene
PCR
serotyping
Salmonella
serovar
gen invA
PCR
serotipificación
topic Salmonella
serovar
invA gene
PCR
serotyping
Salmonella
serovar
gen invA
PCR
serotipificación
description The aim of this study was to molecularly and serologically identify Salmonella spp present in isolates from avian eggs, carcasses, and viscera. In total, 46 isolates of avian origin identified as Salmonella spp were evaluated through cultures and biochemical tests in the period 2012-2017 from various districts of Lima. These isolates are kept in the Bacteriology Laboratory stock of the Universidad Nacional Mayor de San Marcos. The strains were reactivated, and suspicious Salmonella spp colonies were reconfirmed by culturing on selective media. Subsequently, the PCR was performed on the suspicious samples as a method of genetic diagnosis of Salmonella. The invasiveness gene invA, a gene involved with the virulence of Salmonella, was detected. Serotyping was performed with polyvalent and monovalent antisera for serogroup and serovar in the Enteropathogens Laboratory of the National Institute of Health (INS), and finally the serovars were determined according to the scheme proposed by Kauffmann-White. The 46 strains showed molecular weight bands corresponding to the invA gene (244 bp). All strains were identified by serotyping, obtaining S. Infantis (34.8%), S. Pullorum (34.8%), S. Gallinarum (15.2%), S. Enteritidis (8.7%) and S. Typhimurium (6.5%). The results reveal the predominance of circulating serovars in avian samples, as well as their implication in public health.
publishDate 2022
dc.date.none.fl_str_mv 2022-06-29
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/22893
10.15381/rivep.v33i3.22893
url https://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/22893
identifier_str_mv 10.15381/rivep.v33i3.22893
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/22893/18199
dc.rights.none.fl_str_mv http://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
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. 33 Núm. 3 (2022); e22893
Revista de Investigaciones Veterinarias del Perú; Vol. 33 No. 3 (2022); e22893
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 Serotyping and genetic detection of Salmonella spp of avian originSerotipificación y detección genética de Salmonella spp de origen aviarHuarcaya R., FreshiaCalle E., SoniaSiuce M., JuanSedano S., AndréHuamaní P., JhonatanGarcía B., ArturoÁlvarez V., LuisGonzales M., SofíaHuarcaya R., FreshiaCalle E., SoniaSiuce M., JuanSedano S., AndréHuamaní P., JhonatanGarcía B., ArturoÁlvarez V., LuisGonzales M., SofíaSalmonellaserovarinvA genePCRserotypingSalmonellaserovargen invAPCRserotipificaciónThe aim of this study was to molecularly and serologically identify Salmonella spp present in isolates from avian eggs, carcasses, and viscera. In total, 46 isolates of avian origin identified as Salmonella spp were evaluated through cultures and biochemical tests in the period 2012-2017 from various districts of Lima. These isolates are kept in the Bacteriology Laboratory stock of the Universidad Nacional Mayor de San Marcos. The strains were reactivated, and suspicious Salmonella spp colonies were reconfirmed by culturing on selective media. Subsequently, the PCR was performed on the suspicious samples as a method of genetic diagnosis of Salmonella. The invasiveness gene invA, a gene involved with the virulence of Salmonella, was detected. Serotyping was performed with polyvalent and monovalent antisera for serogroup and serovar in the Enteropathogens Laboratory of the National Institute of Health (INS), and finally the serovars were determined according to the scheme proposed by Kauffmann-White. The 46 strains showed molecular weight bands corresponding to the invA gene (244 bp). All strains were identified by serotyping, obtaining S. Infantis (34.8%), S. Pullorum (34.8%), S. Gallinarum (15.2%), S. Enteritidis (8.7%) and S. Typhimurium (6.5%). The results reveal the predominance of circulating serovars in avian samples, as well as their implication in public health.El objetivo del presente estudio fue identificar molecular y serológicamente Salmonella spp presentes en aislados de huevos, canales y vísceras aviares. Se evaluaron 46 aislados de origen aviar identificados como Salmonella spp mediante cultivos y pruebas bioquímicas en el periodo 2012-2017, procedentes de varios distritos de la ciudad de Lima. Estos aislados son conservados en el cepario de Laboratorio de Bacteriología de la Universidad Nacional Mayor de San Marcos. Se reactivaron las cepas, y se reconfirmaron las colonias sospechosas a Salmonella spp mediante el cultivo en medios selectivos. Posteriormente se realizó el PCR a las muestras sospechosas como método de diagnóstico genético de Salmonella. Se detectó el gen de invasividad invA, gen involucrado con la virulencia de Salmonella. Se realizó la serotipificación con antisueros polivalentes y monovalentes para serogrupo y serovar en el Laboratorio de Enteropatógenos del Instituto Nacional de Salud (INS), y finalmente se determinaron las serovariedades de acuerdo con el esquema propuesto por Kauffmann-White. Las 46 cepas evidenciaron bandas de peso molecular correspondientes al gen invA (244 pb). Todas las cepas fueron identificadas mediante serotipificación, obteniendo: S. Infantis (34.8%), S. Pullorum (34.8%), S. Gallinarum (15.2%), S. Enteritidis (8.7%) y S. Typhimurium (6.5%). Los resultados revelan la predominancia de los serovares circulantes en muestras aviares, así como su implicancia en la salud pública.Universidad Nacional Mayor de San Marcos, Facultad de Medicina Veterinaria2022-06-29info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/2289310.15381/rivep.v33i3.22893Revista de Investigaciones Veterinarias del Perú; Vol. 33 Núm. 3 (2022); e22893Revista de Investigaciones Veterinarias del Perú; Vol. 33 No. 3 (2022); e228931682-34191609-9117reponame:Revistas - Universidad Nacional Mayor de San Marcosinstname:Universidad Nacional Mayor de San Marcosinstacron:UNMSMspahttps://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/22893/18199Derechos de autor 2022 Freshia Huarcaya R., Sonia Calle E., Juan Siuce M., André Sedano S., Jhonatan Huamaní P., Arturo García B., Luis Álvarez V., Sofía Gonzales M.http://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessoai:ojs.csi.unmsm:article/228932022-07-07T14:32:35Z
score 13.959468
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