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An enhanced immunochromatographic strip test using colloidal gold nanoparticle-labeled dual-type N proteins for detection of antibodies to PRRS virus

Porcine reproductive and respiratory syndrome (PRRS) is recognized as one of the most important infectious diseases causing serious economic loss in the swine industry worldwide. Due to its increasing genetic diversity, a rapid and accurate diagnosis is critical for PRRS control. The immunochromatog...

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Autores principales: Yu, Ji Eun, Ouh, In-Ohk, Kang, Hyeonjeong, Lee, Hye-young, Cheong, Kwang-Myun, Cho, In-Soo, Cha, Sang-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Veterinary Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070587/
https://www.ncbi.nlm.nih.gov/pubmed/29510472
http://dx.doi.org/10.4142/jvs.2018.19.4.519
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author Yu, Ji Eun
Ouh, In-Ohk
Kang, Hyeonjeong
Lee, Hye-young
Cheong, Kwang-Myun
Cho, In-Soo
Cha, Sang-Ho
author_facet Yu, Ji Eun
Ouh, In-Ohk
Kang, Hyeonjeong
Lee, Hye-young
Cheong, Kwang-Myun
Cho, In-Soo
Cha, Sang-Ho
author_sort Yu, Ji Eun
collection PubMed
description Porcine reproductive and respiratory syndrome (PRRS) is recognized as one of the most important infectious diseases causing serious economic loss in the swine industry worldwide. Due to its increasing genetic diversity, a rapid and accurate diagnosis is critical for PRRS control. The immunochromatographic strip test (ICST) is a rapid and convenient type of immunoassay. In this study, an on-site immunochromatographic assay-based diagnostic method was developed for detection of PRRS virus (PRRSV)-specific antibodies. The method utilized colloidal gold nanoparticle-labeled dual-type nucleocapsid proteins encoded by open reading frame 7. We evaluated 991 field samples from pig farms and 66 serum samples from experimentally PRRSV-inoculated pigs. Based on true PRRSV-specific antibody-positive or -negative sera determined by immunofluorescence assay and IgM enzyme-linked immunosorbent assay (ELISA), the specificity and sensitivity of the ICST were 97.5% and 91.1%, respectively, similar to those of a commercial ELISA (IDEXX PRRS X3 Ab). More importantly, the ICST was completed within 15 min and could detect the PRRSV-specific antibody at an earlier stage of infection (3–7 days) than that of ELISA (7+ days). The results demonstrate that the developed ICST has great potential as an on-farm diagnostic method, providing excellent diagnostic performance in a quick and convenient manner.
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spelling pubmed-60705872018-08-08 An enhanced immunochromatographic strip test using colloidal gold nanoparticle-labeled dual-type N proteins for detection of antibodies to PRRS virus Yu, Ji Eun Ouh, In-Ohk Kang, Hyeonjeong Lee, Hye-young Cheong, Kwang-Myun Cho, In-Soo Cha, Sang-Ho J Vet Sci Original Article Porcine reproductive and respiratory syndrome (PRRS) is recognized as one of the most important infectious diseases causing serious economic loss in the swine industry worldwide. Due to its increasing genetic diversity, a rapid and accurate diagnosis is critical for PRRS control. The immunochromatographic strip test (ICST) is a rapid and convenient type of immunoassay. In this study, an on-site immunochromatographic assay-based diagnostic method was developed for detection of PRRS virus (PRRSV)-specific antibodies. The method utilized colloidal gold nanoparticle-labeled dual-type nucleocapsid proteins encoded by open reading frame 7. We evaluated 991 field samples from pig farms and 66 serum samples from experimentally PRRSV-inoculated pigs. Based on true PRRSV-specific antibody-positive or -negative sera determined by immunofluorescence assay and IgM enzyme-linked immunosorbent assay (ELISA), the specificity and sensitivity of the ICST were 97.5% and 91.1%, respectively, similar to those of a commercial ELISA (IDEXX PRRS X3 Ab). More importantly, the ICST was completed within 15 min and could detect the PRRSV-specific antibody at an earlier stage of infection (3–7 days) than that of ELISA (7+ days). The results demonstrate that the developed ICST has great potential as an on-farm diagnostic method, providing excellent diagnostic performance in a quick and convenient manner. The Korean Society of Veterinary Science 2018-07 2018-07-26 /pmc/articles/PMC6070587/ /pubmed/29510472 http://dx.doi.org/10.4142/jvs.2018.19.4.519 Text en © 2018 The Korean Society of Veterinary Science http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Yu, Ji Eun
Ouh, In-Ohk
Kang, Hyeonjeong
Lee, Hye-young
Cheong, Kwang-Myun
Cho, In-Soo
Cha, Sang-Ho
An enhanced immunochromatographic strip test using colloidal gold nanoparticle-labeled dual-type N proteins for detection of antibodies to PRRS virus
title An enhanced immunochromatographic strip test using colloidal gold nanoparticle-labeled dual-type N proteins for detection of antibodies to PRRS virus
title_full An enhanced immunochromatographic strip test using colloidal gold nanoparticle-labeled dual-type N proteins for detection of antibodies to PRRS virus
title_fullStr An enhanced immunochromatographic strip test using colloidal gold nanoparticle-labeled dual-type N proteins for detection of antibodies to PRRS virus
title_full_unstemmed An enhanced immunochromatographic strip test using colloidal gold nanoparticle-labeled dual-type N proteins for detection of antibodies to PRRS virus
title_short An enhanced immunochromatographic strip test using colloidal gold nanoparticle-labeled dual-type N proteins for detection of antibodies to PRRS virus
title_sort enhanced immunochromatographic strip test using colloidal gold nanoparticle-labeled dual-type n proteins for detection of antibodies to prrs virus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070587/
https://www.ncbi.nlm.nih.gov/pubmed/29510472
http://dx.doi.org/10.4142/jvs.2018.19.4.519
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