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Rapid detection of H146-like goose calicivirus using a TaqMan-based real-time PCR assay

H146-like goose-origin calicivirus (H146-like GCV) is a novel Caliciviridae family member in the Sanovirus genus that was recently discovered and proposed to cause runting-stunting syndrome and urate deposition in geese. At present, however, there is a lack of epidemiological information pertaining...

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Autores principales: Zheng, Min, Lin, Su, Zhang, Shizhong, Chen, Xiuqin, Jiang, Dandan, Chen, Shaoying, Wang, Shao, Chen, Shilong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7858078/
https://www.ncbi.nlm.nih.gov/pubmed/33518100
http://dx.doi.org/10.1016/j.psj.2020.11.016
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author Zheng, Min
Lin, Su
Zhang, Shizhong
Chen, Xiuqin
Jiang, Dandan
Chen, Shaoying
Wang, Shao
Chen, Shilong
author_facet Zheng, Min
Lin, Su
Zhang, Shizhong
Chen, Xiuqin
Jiang, Dandan
Chen, Shaoying
Wang, Shao
Chen, Shilong
author_sort Zheng, Min
collection PubMed
description H146-like goose-origin calicivirus (H146-like GCV) is a novel Caliciviridae family member in the Sanovirus genus that was recently discovered and proposed to cause runting-stunting syndrome and urate deposition in geese. At present, however, there is a lack of epidemiological information pertaining to the dynamics and distribution of H146-like GCV. The development of novel molecular diagnostic approaches capable of rapidly and accurately detecting this virus would support the strengthening, the prevention, and control of H146-like GCV infection. In the present study, we therefore used a TaqMan probe and primers specific for the viral nonstructural (NS) gene to develop a highly sensitive and specific PCR assay capable of detecting this H146-like GCV. The assay reproducibly detected 5.07 × 10(2) copies of a recombinant DNA plasmid containing the NS gene, with a dynamic range of 8 orders of magnitude (10(2)–10(9) copies). Importantly, no cross-reactivity was observed with common viruses that affected waterfowl, and when we used this assay to evaluate clinical samples, we found it to be more sensitive and faster than traditional PCR. In summary, herein, we developed a novel TaqMan-based real-time PCR approach that could reliably detect and diagnose H146-like GCV. This tool will allow for the real-time diagnosis of H146-like GCV infections, enabling researchers to better understand the epidemiology and clinical presentation of this disease.
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spelling pubmed-78580782021-02-05 Rapid detection of H146-like goose calicivirus using a TaqMan-based real-time PCR assay Zheng, Min Lin, Su Zhang, Shizhong Chen, Xiuqin Jiang, Dandan Chen, Shaoying Wang, Shao Chen, Shilong Poult Sci Genetics and Molecular Biology H146-like goose-origin calicivirus (H146-like GCV) is a novel Caliciviridae family member in the Sanovirus genus that was recently discovered and proposed to cause runting-stunting syndrome and urate deposition in geese. At present, however, there is a lack of epidemiological information pertaining to the dynamics and distribution of H146-like GCV. The development of novel molecular diagnostic approaches capable of rapidly and accurately detecting this virus would support the strengthening, the prevention, and control of H146-like GCV infection. In the present study, we therefore used a TaqMan probe and primers specific for the viral nonstructural (NS) gene to develop a highly sensitive and specific PCR assay capable of detecting this H146-like GCV. The assay reproducibly detected 5.07 × 10(2) copies of a recombinant DNA plasmid containing the NS gene, with a dynamic range of 8 orders of magnitude (10(2)–10(9) copies). Importantly, no cross-reactivity was observed with common viruses that affected waterfowl, and when we used this assay to evaluate clinical samples, we found it to be more sensitive and faster than traditional PCR. In summary, herein, we developed a novel TaqMan-based real-time PCR approach that could reliably detect and diagnose H146-like GCV. This tool will allow for the real-time diagnosis of H146-like GCV infections, enabling researchers to better understand the epidemiology and clinical presentation of this disease. Elsevier 2020-11-19 /pmc/articles/PMC7858078/ /pubmed/33518100 http://dx.doi.org/10.1016/j.psj.2020.11.016 Text en © 2020 Published by Elsevier Inc. on behalf of Poultry Science Association Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Genetics and Molecular Biology
Zheng, Min
Lin, Su
Zhang, Shizhong
Chen, Xiuqin
Jiang, Dandan
Chen, Shaoying
Wang, Shao
Chen, Shilong
Rapid detection of H146-like goose calicivirus using a TaqMan-based real-time PCR assay
title Rapid detection of H146-like goose calicivirus using a TaqMan-based real-time PCR assay
title_full Rapid detection of H146-like goose calicivirus using a TaqMan-based real-time PCR assay
title_fullStr Rapid detection of H146-like goose calicivirus using a TaqMan-based real-time PCR assay
title_full_unstemmed Rapid detection of H146-like goose calicivirus using a TaqMan-based real-time PCR assay
title_short Rapid detection of H146-like goose calicivirus using a TaqMan-based real-time PCR assay
title_sort rapid detection of h146-like goose calicivirus using a taqman-based real-time pcr assay
topic Genetics and Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7858078/
https://www.ncbi.nlm.nih.gov/pubmed/33518100
http://dx.doi.org/10.1016/j.psj.2020.11.016
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