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Development of a colloidal gold immunochromatographic assay strip using monoclonal antibody for rapid detection of porcine deltacoronavirus

Porcine deltacoronavirus (PDCoV) cause diarrhea and dehydration in newborn piglets and has the potential for cross-species transmission. Rapid and early diagnosis is important for preventing and controlling infectious disease. In this study, two monoclonal antibodies (mAbs) were generated, which cou...

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Autores principales: Wang, Wei, Fan, Baochao, Zhang, Xuehan, Guo, Rongli, Zhao, Yongxiang, Zhou, Junming, Zhou, Jinzhu, Peng, Qi, Zhu, Mingjun, Li, Jizong, Li, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9849564/
https://www.ncbi.nlm.nih.gov/pubmed/36687576
http://dx.doi.org/10.3389/fmicb.2022.1074513
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author Wang, Wei
Fan, Baochao
Zhang, Xuehan
Guo, Rongli
Zhao, Yongxiang
Zhou, Junming
Zhou, Jinzhu
Peng, Qi
Zhu, Mingjun
Li, Jizong
Li, Bin
author_facet Wang, Wei
Fan, Baochao
Zhang, Xuehan
Guo, Rongli
Zhao, Yongxiang
Zhou, Junming
Zhou, Jinzhu
Peng, Qi
Zhu, Mingjun
Li, Jizong
Li, Bin
author_sort Wang, Wei
collection PubMed
description Porcine deltacoronavirus (PDCoV) cause diarrhea and dehydration in newborn piglets and has the potential for cross-species transmission. Rapid and early diagnosis is important for preventing and controlling infectious disease. In this study, two monoclonal antibodies (mAbs) were generated, which could specifically recognize recombinant PDCoV nucleocapsid (rPDCoV-N) protein. A colloidal gold immunochromatographic assay (GICA) strip using these mAbs was developed to detect PDCoV antigens within 15 min. Results showed that the detection limit of the GICA strip developed in this study was 10(3) TCID(50)/ml for the suspension of virus-infected cell culture and 0.125 μg/ml for rPDCoV-N protein, respectively. Besides, the GICA strip showed high specificity with no cross-reactivity with other porcine pathogenic viruses. Three hundred and twenty-five fecal samples were detected for PDCoV using the GICA strip and reverse transcription-quantitative real-time PCR (RT-qPCR). The coincidence rate of the GICA strip and RT-qPCR was 96.9%. The GICA strip had a diagnostic sensitivity of 88.9% and diagnostic specificity of 98.5%. The specific and efficient detection by the strip provides a convenient, rapid, easy to use and valuable diagnostic tool for PDCoV under laboratory and field conditions.
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spelling pubmed-98495642023-01-20 Development of a colloidal gold immunochromatographic assay strip using monoclonal antibody for rapid detection of porcine deltacoronavirus Wang, Wei Fan, Baochao Zhang, Xuehan Guo, Rongli Zhao, Yongxiang Zhou, Junming Zhou, Jinzhu Peng, Qi Zhu, Mingjun Li, Jizong Li, Bin Front Microbiol Microbiology Porcine deltacoronavirus (PDCoV) cause diarrhea and dehydration in newborn piglets and has the potential for cross-species transmission. Rapid and early diagnosis is important for preventing and controlling infectious disease. In this study, two monoclonal antibodies (mAbs) were generated, which could specifically recognize recombinant PDCoV nucleocapsid (rPDCoV-N) protein. A colloidal gold immunochromatographic assay (GICA) strip using these mAbs was developed to detect PDCoV antigens within 15 min. Results showed that the detection limit of the GICA strip developed in this study was 10(3) TCID(50)/ml for the suspension of virus-infected cell culture and 0.125 μg/ml for rPDCoV-N protein, respectively. Besides, the GICA strip showed high specificity with no cross-reactivity with other porcine pathogenic viruses. Three hundred and twenty-five fecal samples were detected for PDCoV using the GICA strip and reverse transcription-quantitative real-time PCR (RT-qPCR). The coincidence rate of the GICA strip and RT-qPCR was 96.9%. The GICA strip had a diagnostic sensitivity of 88.9% and diagnostic specificity of 98.5%. The specific and efficient detection by the strip provides a convenient, rapid, easy to use and valuable diagnostic tool for PDCoV under laboratory and field conditions. Frontiers Media S.A. 2023-01-05 /pmc/articles/PMC9849564/ /pubmed/36687576 http://dx.doi.org/10.3389/fmicb.2022.1074513 Text en Copyright © 2023 Wang, Fan, Zhang, Guo, Zhao, Zhou, Zhou, Peng, Zhu, Li and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Wang, Wei
Fan, Baochao
Zhang, Xuehan
Guo, Rongli
Zhao, Yongxiang
Zhou, Junming
Zhou, Jinzhu
Peng, Qi
Zhu, Mingjun
Li, Jizong
Li, Bin
Development of a colloidal gold immunochromatographic assay strip using monoclonal antibody for rapid detection of porcine deltacoronavirus
title Development of a colloidal gold immunochromatographic assay strip using monoclonal antibody for rapid detection of porcine deltacoronavirus
title_full Development of a colloidal gold immunochromatographic assay strip using monoclonal antibody for rapid detection of porcine deltacoronavirus
title_fullStr Development of a colloidal gold immunochromatographic assay strip using monoclonal antibody for rapid detection of porcine deltacoronavirus
title_full_unstemmed Development of a colloidal gold immunochromatographic assay strip using monoclonal antibody for rapid detection of porcine deltacoronavirus
title_short Development of a colloidal gold immunochromatographic assay strip using monoclonal antibody for rapid detection of porcine deltacoronavirus
title_sort development of a colloidal gold immunochromatographic assay strip using monoclonal antibody for rapid detection of porcine deltacoronavirus
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9849564/
https://www.ncbi.nlm.nih.gov/pubmed/36687576
http://dx.doi.org/10.3389/fmicb.2022.1074513
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