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Multiplex and on-site PCR detection of swine diseases based on the microfluidic chip system

BACKGROUND: At present, the process of inspection and quarantine starts with sampling at the customs port, continues with transporting the samples to the central laboratory for inspection experiments, and ends with the inspected results being fed back to the port. This process had the risks of degra...

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Autores principales: Jiang, Yan, Jiang, Shan, Wu, Yue, Zhou, Bin, Wang, Kaimin, Jiang, Luyan, Long, Yunfeng, Chen, Gan, Zeng, Dexin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953195/
https://www.ncbi.nlm.nih.gov/pubmed/33712000
http://dx.doi.org/10.1186/s12917-021-02825-w
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author Jiang, Yan
Jiang, Shan
Wu, Yue
Zhou, Bin
Wang, Kaimin
Jiang, Luyan
Long, Yunfeng
Chen, Gan
Zeng, Dexin
author_facet Jiang, Yan
Jiang, Shan
Wu, Yue
Zhou, Bin
Wang, Kaimin
Jiang, Luyan
Long, Yunfeng
Chen, Gan
Zeng, Dexin
author_sort Jiang, Yan
collection PubMed
description BACKGROUND: At present, the process of inspection and quarantine starts with sampling at the customs port, continues with transporting the samples to the central laboratory for inspection experiments, and ends with the inspected results being fed back to the port. This process had the risks of degradation of biological samples and generation of pathogenic microorganisms and did not meet the rapid on-site detection demand because it took a rather long time. Therefore, it is urgently needed to develop a rapid and high-throughput detection assay of pathogenic microorganisms at the customs port. The aim of this study was to develop a microfluidic chip to rapidly detect swine pathogenic microorganisms with high-throughput and higher accuracy. Moreover, this chip will decrease the risk of spreading infection during transportation. RESULTS: A series of experiments were performed to establish a microfluidic chip. The resulting data showed that the positive nucleic acid of four swine viruses were detected by using a portable and rapid microfluidic PCR system, which could achieve a on-site real-time quantitative PCR detection. Furthermore, the detection results of eight clinical samples were obtained within an hour. The lowest concentration that amplified of this microfluidic PCR detection system was as low as 1 copies/μL. The results showed that the high specificity of this chip system in disease detection played an important role in customs inspection and quarantine during customs clearance. CONCLUSION: The microfluidic PCR detection system established in this study could meet the requirement for rapid detection of samples at the customs port. This chip could avoid the risky process of transporting the samples from the sampling site to the testing lab, and drastically reduce the inspection cycle. Moreover, it would enable parallel inspections on one chip, which greatly raised the efficiency of inspection.
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spelling pubmed-79531952021-03-12 Multiplex and on-site PCR detection of swine diseases based on the microfluidic chip system Jiang, Yan Jiang, Shan Wu, Yue Zhou, Bin Wang, Kaimin Jiang, Luyan Long, Yunfeng Chen, Gan Zeng, Dexin BMC Vet Res Methodology Article BACKGROUND: At present, the process of inspection and quarantine starts with sampling at the customs port, continues with transporting the samples to the central laboratory for inspection experiments, and ends with the inspected results being fed back to the port. This process had the risks of degradation of biological samples and generation of pathogenic microorganisms and did not meet the rapid on-site detection demand because it took a rather long time. Therefore, it is urgently needed to develop a rapid and high-throughput detection assay of pathogenic microorganisms at the customs port. The aim of this study was to develop a microfluidic chip to rapidly detect swine pathogenic microorganisms with high-throughput and higher accuracy. Moreover, this chip will decrease the risk of spreading infection during transportation. RESULTS: A series of experiments were performed to establish a microfluidic chip. The resulting data showed that the positive nucleic acid of four swine viruses were detected by using a portable and rapid microfluidic PCR system, which could achieve a on-site real-time quantitative PCR detection. Furthermore, the detection results of eight clinical samples were obtained within an hour. The lowest concentration that amplified of this microfluidic PCR detection system was as low as 1 copies/μL. The results showed that the high specificity of this chip system in disease detection played an important role in customs inspection and quarantine during customs clearance. CONCLUSION: The microfluidic PCR detection system established in this study could meet the requirement for rapid detection of samples at the customs port. This chip could avoid the risky process of transporting the samples from the sampling site to the testing lab, and drastically reduce the inspection cycle. Moreover, it would enable parallel inspections on one chip, which greatly raised the efficiency of inspection. BioMed Central 2021-03-12 /pmc/articles/PMC7953195/ /pubmed/33712000 http://dx.doi.org/10.1186/s12917-021-02825-w Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Methodology Article
Jiang, Yan
Jiang, Shan
Wu, Yue
Zhou, Bin
Wang, Kaimin
Jiang, Luyan
Long, Yunfeng
Chen, Gan
Zeng, Dexin
Multiplex and on-site PCR detection of swine diseases based on the microfluidic chip system
title Multiplex and on-site PCR detection of swine diseases based on the microfluidic chip system
title_full Multiplex and on-site PCR detection of swine diseases based on the microfluidic chip system
title_fullStr Multiplex and on-site PCR detection of swine diseases based on the microfluidic chip system
title_full_unstemmed Multiplex and on-site PCR detection of swine diseases based on the microfluidic chip system
title_short Multiplex and on-site PCR detection of swine diseases based on the microfluidic chip system
title_sort multiplex and on-site pcr detection of swine diseases based on the microfluidic chip system
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953195/
https://www.ncbi.nlm.nih.gov/pubmed/33712000
http://dx.doi.org/10.1186/s12917-021-02825-w
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