Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples
- Autores
- Pluta, Aneta; Jaworski, Juan Pablo; Droscha, Casey; VanderWeele, Sophie; Taxis, Tasia M.; Valas, Stephen; Brnić, Dragan; Jungić, Andreja; Ruano, María José; Sánchez, Azucena; Murakami, Kenji; Nakamura, Kurumi; Puentes, Rodrigo; De Brun, MLaureana; Ruiz, Vanesa; Ladera Gomez, Marla Eliana; Lendez, Pamela Anahí; Dolcini, Guillermina Laura; Camargos, Marcelo Fernandes; Fonseca, Antônio; Barua, Subarna; Wang, Chengming; Giza, Aleksandra; Kuźmak, Jacek
- Año de publicación
- 2024
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Bovine leukemia virus (BLV) is the etiological agent of enzootic bovine leukosis and causes a persistent infection that can leave cattle with no symptoms. Many countries have been able to successfully eradicate BLV through improved detection and management methods. However, with the increasing novel molecular detection methods there have been few eforts to standardize these results at global scale. This study aimed to determine the interlaboratory accuracy and agreement of 11 molecular tests in detecting BLV. Each qPCR/ddPCR method varied by target gene, primer design, DNA input and chemistries. DNA samples were extracted from blood of BLV-seropositive cattle and lyophilized to grant a better preservation during shipping to all participants around the globe. Twenty nine out of 44 samples were correctly identifed by the 11 labs and all methods exhibited a diagnostic sensitivity between 74 and 100%. Agreement amongst diferent assays was linked to BLV copy numbers present in samples and the characteristics of each assay (i.e., BLV target sequence). Finally, the mean correlation value for all assays was within the range of strong correlation. This study highlights the importance of continuous need for standardization and harmonization amongst assays and the diferent participants. The results underscore the need of an international calibrator to estimate the efciency (standard curve) of the diferent assays and improve quantitation accuracy. Additionally, this will inform future participants about the variability associated with emerging chemistries, methods, and technologies used to study BLV. Altogether, by improving tests performance worldwide it will positively aid in the eradication eforts.
Fil: Pluta, Aneta. National Veterinary Research Institute; Polonia
Fil: Jaworski, Juan Pablo. Instituto Nacional de Tecnologia Agropecuaria. Centro de Investigacion En Ciencias Veterinarias y Agronomicas. Instituto de Virologia E Innovaciones Tecnologicas. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Oficina de Coordinacion Administrativa Pque. Centenario. Instituto de Virologia E Innovaciones Tecnologicas.; Argentina
Fil: Droscha, Casey. CentralStar Cooperative; Estados Unidos
Fil: VanderWeele, Sophie. CentralStar Cooperative; Estados Unidos
Fil: Taxis, Tasia M.. Michigan State University; Estados Unidos
Fil: Valas, Stephen. French Agency for Food, Environmental and Occupational Health and Safety; Francia
Fil: Brnić, Dragan. Croatian Veterinary Institute; Croacia
Fil: Jungić, Andreja. Croatian Veterinary Institute; Croacia
Fil: Ruano, María José. Ministry of Agriculture, Fisheries and Food; España
Fil: Sánchez, Azucena. Ministry of Agriculture, Fisheries and Food; España
Fil: Murakami, Kenji. Iwate University; Japón
Fil: Nakamura, Kurumi. Iwate University; Japón
Fil: Puentes, Rodrigo. Universidad de la República; Uruguay
Fil: De Brun, MLaureana. Universidad de la República; Uruguay
Fil: Ruiz, Vanesa. Instituto Nacional de Tecnologia Agropecuaria. Centro de Investigacion En Ciencias Veterinarias y Agronomicas. Instituto de Virologia E Innovaciones Tecnologicas. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Oficina de Coordinacion Administrativa Pque. Centenario. Instituto de Virologia E Innovaciones Tecnologicas.; Argentina
Fil: Ladera Gomez, Marla Eliana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina
Fil: Lendez, Pamela Anahí. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina
Fil: Dolcini, Guillermina Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina
Fil: Camargos, Marcelo Fernandes. Laboratório Federal de Defesa Agropecuária de Minas Gerais; Brasil
Fil: Fonseca, Antônio. Laboratório Federal de Defesa Agropecuária de Minas Gerais; Brasil
Fil: Barua, Subarna. Auburn University.; Estados Unidos
Fil: Wang, Chengming. Auburn University.; Estados Unidos
Fil: Giza, Aleksandra. National Veterinary Research Institute; Polonia
Fil: Kuźmak, Jacek. National Veterinary Research Institute; Polonia - Materia
-
LEUCEMIA BOVINA
BLV
qPCR
DIAGNOSTICO
VALIDACION - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/266801
Ver los metadatos del registro completo
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Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samplesPluta, AnetaJaworski, Juan PabloDroscha, CaseyVanderWeele, SophieTaxis, Tasia M.Valas, StephenBrnić, DraganJungić, AndrejaRuano, María JoséSánchez, AzucenaMurakami, KenjiNakamura, KurumiPuentes, RodrigoDe Brun, MLaureanaRuiz, VanesaLadera Gomez, Marla ElianaLendez, Pamela AnahíDolcini, Guillermina LauraCamargos, Marcelo FernandesFonseca, AntônioBarua, SubarnaWang, ChengmingGiza, AleksandraKuźmak, JacekLEUCEMIA BOVINABLVqPCRDIAGNOSTICOVALIDACIONhttps://purl.org/becyt/ford/4.3https://purl.org/becyt/ford/4Bovine leukemia virus (BLV) is the etiological agent of enzootic bovine leukosis and causes a persistent infection that can leave cattle with no symptoms. Many countries have been able to successfully eradicate BLV through improved detection and management methods. However, with the increasing novel molecular detection methods there have been few eforts to standardize these results at global scale. This study aimed to determine the interlaboratory accuracy and agreement of 11 molecular tests in detecting BLV. Each qPCR/ddPCR method varied by target gene, primer design, DNA input and chemistries. DNA samples were extracted from blood of BLV-seropositive cattle and lyophilized to grant a better preservation during shipping to all participants around the globe. Twenty nine out of 44 samples were correctly identifed by the 11 labs and all methods exhibited a diagnostic sensitivity between 74 and 100%. Agreement amongst diferent assays was linked to BLV copy numbers present in samples and the characteristics of each assay (i.e., BLV target sequence). Finally, the mean correlation value for all assays was within the range of strong correlation. This study highlights the importance of continuous need for standardization and harmonization amongst assays and the diferent participants. The results underscore the need of an international calibrator to estimate the efciency (standard curve) of the diferent assays and improve quantitation accuracy. Additionally, this will inform future participants about the variability associated with emerging chemistries, methods, and technologies used to study BLV. Altogether, by improving tests performance worldwide it will positively aid in the eradication eforts.Fil: Pluta, Aneta. National Veterinary Research Institute; PoloniaFil: Jaworski, Juan Pablo. Instituto Nacional de Tecnologia Agropecuaria. Centro de Investigacion En Ciencias Veterinarias y Agronomicas. Instituto de Virologia E Innovaciones Tecnologicas. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Oficina de Coordinacion Administrativa Pque. Centenario. Instituto de Virologia E Innovaciones Tecnologicas.; ArgentinaFil: Droscha, Casey. CentralStar Cooperative; Estados UnidosFil: VanderWeele, Sophie. CentralStar Cooperative; Estados UnidosFil: Taxis, Tasia M.. Michigan State University; Estados UnidosFil: Valas, Stephen. French Agency for Food, Environmental and Occupational Health and Safety; FranciaFil: Brnić, Dragan. Croatian Veterinary Institute; CroaciaFil: Jungić, Andreja. Croatian Veterinary Institute; CroaciaFil: Ruano, María José. Ministry of Agriculture, Fisheries and Food; EspañaFil: Sánchez, Azucena. Ministry of Agriculture, Fisheries and Food; EspañaFil: Murakami, Kenji. Iwate University; JapónFil: Nakamura, Kurumi. Iwate University; JapónFil: Puentes, Rodrigo. Universidad de la República; UruguayFil: De Brun, MLaureana. Universidad de la República; UruguayFil: Ruiz, Vanesa. Instituto Nacional de Tecnologia Agropecuaria. Centro de Investigacion En Ciencias Veterinarias y Agronomicas. Instituto de Virologia E Innovaciones Tecnologicas. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Oficina de Coordinacion Administrativa Pque. Centenario. Instituto de Virologia E Innovaciones Tecnologicas.; ArgentinaFil: Ladera Gomez, Marla Eliana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; ArgentinaFil: Lendez, Pamela Anahí. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; ArgentinaFil: Dolcini, Guillermina Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; ArgentinaFil: Camargos, Marcelo Fernandes. Laboratório Federal de Defesa Agropecuária de Minas Gerais; BrasilFil: Fonseca, Antônio. Laboratório Federal de Defesa Agropecuária de Minas Gerais; BrasilFil: Barua, Subarna. Auburn University.; Estados UnidosFil: Wang, Chengming. Auburn University.; Estados UnidosFil: Giza, Aleksandra. National Veterinary Research Institute; PoloniaFil: Kuźmak, Jacek. National Veterinary Research Institute; PoloniaBioMed Central2024-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/266801Pluta, Aneta; Jaworski, Juan Pablo; Droscha, Casey; VanderWeele, Sophie; Taxis, Tasia M.; et al.; Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples; BioMed Central; BMC Veterinary Research; 20; 1; 8-2024; 1-191746-6148CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://bmcvetres.biomedcentral.com/articles/10.1186/s12917-024-04228-zinfo:eu-repo/semantics/altIdentifier/doi/10.1186/s12917-024-04228-zinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T14:57:50Zoai:ri.conicet.gov.ar:11336/266801instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-15 14:57:50.844CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples |
| title |
Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples |
| spellingShingle |
Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples Pluta, Aneta LEUCEMIA BOVINA BLV qPCR DIAGNOSTICO VALIDACION |
| title_short |
Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples |
| title_full |
Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples |
| title_fullStr |
Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples |
| title_full_unstemmed |
Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples |
| title_sort |
Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples |
| dc.creator.none.fl_str_mv |
Pluta, Aneta Jaworski, Juan Pablo Droscha, Casey VanderWeele, Sophie Taxis, Tasia M. Valas, Stephen Brnić, Dragan Jungić, Andreja Ruano, María José Sánchez, Azucena Murakami, Kenji Nakamura, Kurumi Puentes, Rodrigo De Brun, MLaureana Ruiz, Vanesa Ladera Gomez, Marla Eliana Lendez, Pamela Anahí Dolcini, Guillermina Laura Camargos, Marcelo Fernandes Fonseca, Antônio Barua, Subarna Wang, Chengming Giza, Aleksandra Kuźmak, Jacek |
| author |
Pluta, Aneta |
| author_facet |
Pluta, Aneta Jaworski, Juan Pablo Droscha, Casey VanderWeele, Sophie Taxis, Tasia M. Valas, Stephen Brnić, Dragan Jungić, Andreja Ruano, María José Sánchez, Azucena Murakami, Kenji Nakamura, Kurumi Puentes, Rodrigo De Brun, MLaureana Ruiz, Vanesa Ladera Gomez, Marla Eliana Lendez, Pamela Anahí Dolcini, Guillermina Laura Camargos, Marcelo Fernandes Fonseca, Antônio Barua, Subarna Wang, Chengming Giza, Aleksandra Kuźmak, Jacek |
| author_role |
author |
| author2 |
Jaworski, Juan Pablo Droscha, Casey VanderWeele, Sophie Taxis, Tasia M. Valas, Stephen Brnić, Dragan Jungić, Andreja Ruano, María José Sánchez, Azucena Murakami, Kenji Nakamura, Kurumi Puentes, Rodrigo De Brun, MLaureana Ruiz, Vanesa Ladera Gomez, Marla Eliana Lendez, Pamela Anahí Dolcini, Guillermina Laura Camargos, Marcelo Fernandes Fonseca, Antônio Barua, Subarna Wang, Chengming Giza, Aleksandra Kuźmak, Jacek |
| author2_role |
author author author author author author author author author author author author author author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
LEUCEMIA BOVINA BLV qPCR DIAGNOSTICO VALIDACION |
| topic |
LEUCEMIA BOVINA BLV qPCR DIAGNOSTICO VALIDACION |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/4.3 https://purl.org/becyt/ford/4 |
| dc.description.none.fl_txt_mv |
Bovine leukemia virus (BLV) is the etiological agent of enzootic bovine leukosis and causes a persistent infection that can leave cattle with no symptoms. Many countries have been able to successfully eradicate BLV through improved detection and management methods. However, with the increasing novel molecular detection methods there have been few eforts to standardize these results at global scale. This study aimed to determine the interlaboratory accuracy and agreement of 11 molecular tests in detecting BLV. Each qPCR/ddPCR method varied by target gene, primer design, DNA input and chemistries. DNA samples were extracted from blood of BLV-seropositive cattle and lyophilized to grant a better preservation during shipping to all participants around the globe. Twenty nine out of 44 samples were correctly identifed by the 11 labs and all methods exhibited a diagnostic sensitivity between 74 and 100%. Agreement amongst diferent assays was linked to BLV copy numbers present in samples and the characteristics of each assay (i.e., BLV target sequence). Finally, the mean correlation value for all assays was within the range of strong correlation. This study highlights the importance of continuous need for standardization and harmonization amongst assays and the diferent participants. The results underscore the need of an international calibrator to estimate the efciency (standard curve) of the diferent assays and improve quantitation accuracy. Additionally, this will inform future participants about the variability associated with emerging chemistries, methods, and technologies used to study BLV. Altogether, by improving tests performance worldwide it will positively aid in the eradication eforts. Fil: Pluta, Aneta. National Veterinary Research Institute; Polonia Fil: Jaworski, Juan Pablo. Instituto Nacional de Tecnologia Agropecuaria. Centro de Investigacion En Ciencias Veterinarias y Agronomicas. Instituto de Virologia E Innovaciones Tecnologicas. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Oficina de Coordinacion Administrativa Pque. Centenario. Instituto de Virologia E Innovaciones Tecnologicas.; Argentina Fil: Droscha, Casey. CentralStar Cooperative; Estados Unidos Fil: VanderWeele, Sophie. CentralStar Cooperative; Estados Unidos Fil: Taxis, Tasia M.. Michigan State University; Estados Unidos Fil: Valas, Stephen. French Agency for Food, Environmental and Occupational Health and Safety; Francia Fil: Brnić, Dragan. Croatian Veterinary Institute; Croacia Fil: Jungić, Andreja. Croatian Veterinary Institute; Croacia Fil: Ruano, María José. Ministry of Agriculture, Fisheries and Food; España Fil: Sánchez, Azucena. Ministry of Agriculture, Fisheries and Food; España Fil: Murakami, Kenji. Iwate University; Japón Fil: Nakamura, Kurumi. Iwate University; Japón Fil: Puentes, Rodrigo. Universidad de la República; Uruguay Fil: De Brun, MLaureana. Universidad de la República; Uruguay Fil: Ruiz, Vanesa. Instituto Nacional de Tecnologia Agropecuaria. Centro de Investigacion En Ciencias Veterinarias y Agronomicas. Instituto de Virologia E Innovaciones Tecnologicas. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Oficina de Coordinacion Administrativa Pque. Centenario. Instituto de Virologia E Innovaciones Tecnologicas.; Argentina Fil: Ladera Gomez, Marla Eliana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina Fil: Lendez, Pamela Anahí. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina Fil: Dolcini, Guillermina Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina Fil: Camargos, Marcelo Fernandes. Laboratório Federal de Defesa Agropecuária de Minas Gerais; Brasil Fil: Fonseca, Antônio. Laboratório Federal de Defesa Agropecuária de Minas Gerais; Brasil Fil: Barua, Subarna. Auburn University.; Estados Unidos Fil: Wang, Chengming. Auburn University.; Estados Unidos Fil: Giza, Aleksandra. National Veterinary Research Institute; Polonia Fil: Kuźmak, Jacek. National Veterinary Research Institute; Polonia |
| description |
Bovine leukemia virus (BLV) is the etiological agent of enzootic bovine leukosis and causes a persistent infection that can leave cattle with no symptoms. Many countries have been able to successfully eradicate BLV through improved detection and management methods. However, with the increasing novel molecular detection methods there have been few eforts to standardize these results at global scale. This study aimed to determine the interlaboratory accuracy and agreement of 11 molecular tests in detecting BLV. Each qPCR/ddPCR method varied by target gene, primer design, DNA input and chemistries. DNA samples were extracted from blood of BLV-seropositive cattle and lyophilized to grant a better preservation during shipping to all participants around the globe. Twenty nine out of 44 samples were correctly identifed by the 11 labs and all methods exhibited a diagnostic sensitivity between 74 and 100%. Agreement amongst diferent assays was linked to BLV copy numbers present in samples and the characteristics of each assay (i.e., BLV target sequence). Finally, the mean correlation value for all assays was within the range of strong correlation. This study highlights the importance of continuous need for standardization and harmonization amongst assays and the diferent participants. The results underscore the need of an international calibrator to estimate the efciency (standard curve) of the diferent assays and improve quantitation accuracy. Additionally, this will inform future participants about the variability associated with emerging chemistries, methods, and technologies used to study BLV. Altogether, by improving tests performance worldwide it will positively aid in the eradication eforts. |
| publishDate |
2024 |
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2024-08 |
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http://hdl.handle.net/11336/266801 Pluta, Aneta; Jaworski, Juan Pablo; Droscha, Casey; VanderWeele, Sophie; Taxis, Tasia M.; et al.; Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples; BioMed Central; BMC Veterinary Research; 20; 1; 8-2024; 1-19 1746-6148 CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/266801 |
| identifier_str_mv |
Pluta, Aneta; Jaworski, Juan Pablo; Droscha, Casey; VanderWeele, Sophie; Taxis, Tasia M.; et al.; Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples; BioMed Central; BMC Veterinary Research; 20; 1; 8-2024; 1-19 1746-6148 CONICET Digital CONICET |
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eng |
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