Validation of a Real Time PCR for Classical Swine Fever Diagnosis

Author:

Dias Natanael Lamas1,Fonseca Júnior Antônio Augusto1,Oliveira Anapolino Macedo1,Sales Érica Bravo1,Alves Bruna Rios Coelho2,Dorella Fernanda Alves1,Camargos Marcelo Fernandes1

Affiliation:

1. Laboratório de Biologia Molecular e Laboratório de Diagnóstico de Doenás Virais, Laboratório Nacional Agropecuário-Minas Gerais (LANAGRO-MG), Ministério da Agricultura, Pecuária e Abastecimento, Avenida Rômulo Joviano s/n, Fazenda Modelo, 33600-000 Pedro Leopoldo, MG, Brazil

2. Embrapa Dairy Cattle, Rua Eugênio do Nascimento 610, 36038-330 Juiz de Fora, MG, Brazil

Abstract

The viral disease classical swine fever (CSF), caused by aPestivirus, is one of the major causes of economic losses for pig farming. The aim of this work was to validate a RT-qPCR using Taqman for detection of CSF in swine tissues. The parameters for the validation followed the specifications of the Manual of Diagnostic Tests and Vaccines for Terrestrial Animals of the World Organization for Animal Health (OIE) and the guide ABNT NBR ISO/IEC 17025:2005. The analysis of the 5′NTR region of CSF virus was performed in 145 samples from 29 infected pigs and in 240 samples from 80 pigs originated in the Brazilian CSF-free zone. The tissues tested were spleen, kidney, blood, tonsils, and lymph nodes. Sequencing of the positive samples for 5′NTR region was performed to evaluate the specificity of the RT-qPCR. Tests performed for the RT-qPCR validation demonstrated that the PCR assay was efficient in detecting RNA from CSF virus in all materials from different tissues of infected animals. Furthermore, RNA from CSF virus was not detected in samples of swine originated from the Brazilian CSF-free zone. Hence, it is concluded that RT-qPCR can be used as a complementary diagnostic for CSF.

Funder

Ministério da Agricultura, Pecuária e Abastecimento

Publisher

Hindawi Limited

Subject

General Veterinary

Reference22 articles.

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