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Development of a nanoparticle-assisted PCR assay for detection of bovine respiratory syncytial virus
BACKGROUND: Bovine respiratory syncytial virus (BRSV) is a common pathogen causing respiratory disease in cattle and a significant contributor to the bovine respiratory disease (BRD) complex. BRSV is widely distributed around the world, causing severe economic losses. This study we established a new...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458741/ https://www.ncbi.nlm.nih.gov/pubmed/30971257 http://dx.doi.org/10.1186/s12917-019-1858-0 |
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author | Liu, Zhankui Li, Jianyou Liu, Zeyu Li, Jiawei Li, Zhijie Wang, Chao Wang, Jianke Guo, Li |
author_facet | Liu, Zhankui Li, Jianyou Liu, Zeyu Li, Jiawei Li, Zhijie Wang, Chao Wang, Jianke Guo, Li |
author_sort | Liu, Zhankui |
collection | PubMed |
description | BACKGROUND: Bovine respiratory syncytial virus (BRSV) is a common pathogen causing respiratory disease in cattle and a significant contributor to the bovine respiratory disease (BRD) complex. BRSV is widely distributed around the world, causing severe economic losses. This study we established a new molecular detection method of BRSV pathogen NanoPCR attributed to the combination of nano-particles in traditional PCR (Polymerase chain reaction) technology. RESULTS: In this study, the BRSV NanoPCR assay was developed, and its specificity and sensitivity were investigated. The results showed that no cross-reactivity was observed for the NanoPCR assay for related viruses, including the infectious bovine rhinotracheitis virus (IBRV), bovine viral diarrhea virus (BVDV), and bovine parainfluenza virus type 3 (BPIV3), and the assay was more sensitive than the conventional PCR assay, with a detection limit of 1.43 × 10(2) copies recombinant plasmids per reaction, compared with 1.43 × 10(3) copies for conventional PCR analysis. Moreover, thirty-nine clinical bovine samples collected from two provinces in North-Eastern China, 46.15% were determined BRSV positive by our NanoPCR assay, compared with 23.07% for conventional PCR. CONCLUSIONS: This is the first report to demonstrate the application of a NanoPCR assay for the detection of BRSV. The sensitive and specific NanoPCR assay developed in this study can be applied widely in clinical diagnosis and field surveillance of BRSV infection. |
format | Online Article Text |
id | pubmed-6458741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64587412019-04-19 Development of a nanoparticle-assisted PCR assay for detection of bovine respiratory syncytial virus Liu, Zhankui Li, Jianyou Liu, Zeyu Li, Jiawei Li, Zhijie Wang, Chao Wang, Jianke Guo, Li BMC Vet Res Methodology Article BACKGROUND: Bovine respiratory syncytial virus (BRSV) is a common pathogen causing respiratory disease in cattle and a significant contributor to the bovine respiratory disease (BRD) complex. BRSV is widely distributed around the world, causing severe economic losses. This study we established a new molecular detection method of BRSV pathogen NanoPCR attributed to the combination of nano-particles in traditional PCR (Polymerase chain reaction) technology. RESULTS: In this study, the BRSV NanoPCR assay was developed, and its specificity and sensitivity were investigated. The results showed that no cross-reactivity was observed for the NanoPCR assay for related viruses, including the infectious bovine rhinotracheitis virus (IBRV), bovine viral diarrhea virus (BVDV), and bovine parainfluenza virus type 3 (BPIV3), and the assay was more sensitive than the conventional PCR assay, with a detection limit of 1.43 × 10(2) copies recombinant plasmids per reaction, compared with 1.43 × 10(3) copies for conventional PCR analysis. Moreover, thirty-nine clinical bovine samples collected from two provinces in North-Eastern China, 46.15% were determined BRSV positive by our NanoPCR assay, compared with 23.07% for conventional PCR. CONCLUSIONS: This is the first report to demonstrate the application of a NanoPCR assay for the detection of BRSV. The sensitive and specific NanoPCR assay developed in this study can be applied widely in clinical diagnosis and field surveillance of BRSV infection. BioMed Central 2019-04-11 /pmc/articles/PMC6458741/ /pubmed/30971257 http://dx.doi.org/10.1186/s12917-019-1858-0 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Article Liu, Zhankui Li, Jianyou Liu, Zeyu Li, Jiawei Li, Zhijie Wang, Chao Wang, Jianke Guo, Li Development of a nanoparticle-assisted PCR assay for detection of bovine respiratory syncytial virus |
title | Development of a nanoparticle-assisted PCR assay for detection of bovine respiratory syncytial virus |
title_full | Development of a nanoparticle-assisted PCR assay for detection of bovine respiratory syncytial virus |
title_fullStr | Development of a nanoparticle-assisted PCR assay for detection of bovine respiratory syncytial virus |
title_full_unstemmed | Development of a nanoparticle-assisted PCR assay for detection of bovine respiratory syncytial virus |
title_short | Development of a nanoparticle-assisted PCR assay for detection of bovine respiratory syncytial virus |
title_sort | development of a nanoparticle-assisted pcr assay for detection of bovine respiratory syncytial virus |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458741/ https://www.ncbi.nlm.nih.gov/pubmed/30971257 http://dx.doi.org/10.1186/s12917-019-1858-0 |
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