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International Journal of Poultry Science

.: Home > International Journal of Poultry Science > 2014 > Volume 13 Number 8 > Ketherson Rodrigues Silva, Mariana Costa Mello Goncalves, Elisabete Schirato de Oliveira, Filipe Santos Fernando, Maria de Fatima Silva Montassier, Camila Cesario Fernandes, Maria de Lourdes Feres Tamanine, Mariana Monezi Borzi, Romeu Moreira dos Santos, Andre de Oliveira Mendonca, Dilmara Reischak, Antonio Carlos Paulillo and Helio Jose Montassier

Cloning and Expression of the Nucleoprotein Gene (NP) of Newcastle Disease Virus (NDV) in Escherichia coli for Immunodiagnosis Application

Ketherson Rodrigues Silva, Mariana Costa Mello Goncalves, Elisabete Schirato de Oliveira, Filipe Santos Fernando, Maria de Fatima Silva Montassier, Camila Cesario Fernandes, Maria de Lourdes Feres Tamanine, Mariana Monezi Borzi, Romeu Moreira dos Santos, Andre de Oliveira Mendonca, Dilmara Reischak, Antonio Carlos Paulillo and Helio Jose Montassier
Ketherson Rodrigues Silva, Mariana Costa Mello Goncalves, Elisabete Schirato de Oliveira, Filipe Santos Fernando, Maria de Fatima Silva Montassier, Camila Cesario Fernandes, Maria de Lourdes Feres Tamanine, Mariana Monezi Borzi, Romeu Moreira dos Santos, Andre de Oliveira Mendonca, Dilmara Reischak, Antonio Carlos Paulillo and Helio Jose Montassier
Abstract :

The nucleocapsid protein (NP) of newcastle disease virus (NDV) is an important antigen to develop a serologic assay on account of its highly conserved sequences and high immunogenicity. This study aimed to express the gene of the NP of NDV in a heterologous system (Escherichia coli), using the appropriate vector. The NDV-NP protein was expressed as a fusion recombinant protein containing SUMO peptide and poly-histidine tags. This recombinant nucleocapsid protein (rNP) was expressed in a soluble form which was easily purified and showed the ability to react with chicken anti-NDV polyclonal antibodies. An indirect ELISA method based on the adsorption of an antigen composed by NP (rNP-NDV-ELISA) was developed. By comparing this rNP-NDV-ELISA with haemagglutination-inhibition test (HI) high and significant correlation with the HI (r = 0.83) was found. In addition, high sensitivity (88.9%), specificity (95.5%), accuracy (90.4%) and agreement (0.85) were obtained. In conclusion the results indicated that the cloning and expression procedures used in this study provided a rNP that shared the major epitopes with the homologous viral protein and has the potential to be applied in ELISA for the immunodiagnosis of the Newcastle Disease.

Keywords :
Ketherson Rodrigues Silva, Mariana Costa Mello Goncalves, Elisabete Schirato de Oliveira, Filipe Santos Fernando, Maria de Fatima Silva Montassier, Camila Cesario Fernandes, Maria de Lourdes Feres Tamanine, Mariana Monezi Borzi, Romeu Moreira dos Santos, Andre de Oliveira Mendonca, Dilmara Reischak, Antonio Carlos Paulillo and Helio Jose Montassier

Date Deposited : 24 Mar 2015 11:01

Last Modified : 24 Mar 2015 11:01

Official URL: http://www.pjbs.org/ijps/ab2538.htm

Volume 13, Number 8, - 2014 , ISSN 1682-8356

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